Nothing Special   »   [go: up one dir, main page]

You seem to have javascript disabled. Please note that many of the page functionalities won't work as expected without javascript enabled.
 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

Article Types

Countries / Regions

Search Results (45)

Search Parameters:
Keywords = Myristica fragrans

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
14 pages, 1562 KiB  
Article
GC-MS Profiling of Ethanol-Extracted Polyherbal Compounds from Medicinal Plant (Citrullus colocynthis, Curcuma longa, and Myristica fragrans): In Silico and Analytical Insights into Diabetic Neuropathy Therapy via Targeting the Aldose Reductase
by Mohd Adnan Kausar, Sadaf Anwar, Halima Mustafa Elagib, Kehkashan Parveen, Malik Asif Hussain, Mohammad Zeeshan Najm, Abhinav Nair and Subhabrata Kar
Curr. Issues Mol. Biol. 2025, 47(2), 75; https://doi.org/10.3390/cimb47020075 - 23 Jan 2025
Viewed by 757
Abstract
Diabetic neuropathy is one of the severe complications of diabetes, which affects the quality of life in a patient and increases the risk of amputations and chronic wounds. Current therapeutic approaches are symptomatically oriented, focusing on comfort and non-inflammatory aspects without addressing the [...] Read more.
Diabetic neuropathy is one of the severe complications of diabetes, which affects the quality of life in a patient and increases the risk of amputations and chronic wounds. Current therapeutic approaches are symptomatically oriented, focusing on comfort and non-inflammatory aspects without addressing the mechanism or molecular target of the disease. The present study investigates the therapeutic effects of an ethanolic polyherbal extract from Citrullus colocynthis (Bitter Apple), Curcuma longa (Turmeric), and Myristica fragrans (Nutmeg) using advanced in silico and analytical methods. According to the findings, PHE showed the presence of a total of 39 bioactive compounds in GC–MS analysis, which include alcohols, fatty acids, terpenoids, esters, neolignans, phenylpropanoids, and steroids. Three of the compounds—-4-isopropyl-1,6-dimethyl-1,2,3,4-tetrahydronaphthalene (−11.4 kcal/mol), (1S,2R)-2-(4-allyl-2,6-dimethoxyphenoxy)-1-(3,4,5-trimethoxyphenyl)-1-propanol (−9.8 kcal/mol) and (S)-5-Allyl-2-((1-(3,4-dimethoxyphenyl)propan-2-yl)oxy)-1,3-dimethoxybenzene (−10.3 kcal/mol)—followed the Lipinski rule and showed the binding affinity with aldol reductase. Docking experiments showed that compound 4-isopropyl-1,6-dimethyl-1,2,3,4-tetrahydronaphthalene (−11.4 kcal/mol) has high-affinity binding to aldose reductase, an enzyme involved in diabetic neuropathy pathophysiology, whereas molecular dynamics simulations show long-range persistence of the interaction of (S)-5-Allyl-2-((1-(3,4-dimethoxyphenyl)propan-2-yl)oxy)-1,3-dimethoxybenzene with aldol reductase in physiological conditions. Therefore, this combination of herbal therapy and advanced computational/analytical techniques could be leading towards innovative, multi-targeted therapies against diabetic neuropathy. Nevertheless, further studies in vivo are required to confirm the efficacy, safety, and pharmacokinetics of the PHE in biological systems. Full article
Show Figures

Figure 1

Figure 1
<p>Schematic representation of polyol pathway of glucose metabolism, accumulation of sorbitol causes osmotic stress, which leads to the pathogenesis of diabetic complication.</p>
Full article ">Figure 2
<p>GC-MS chromatogram of PHE showing the presence of different compounds at different retention times. * Tentatively Identified Compounds (TIC).</p>
Full article ">Figure 3
<p>Presents a representative image illustrating the docking analysis of selected ligands with high binding affinity for aldol reductase. (i) The 3D interaction of the ligands with aldol reductase is depicted, with each ligand represented in stick form and shown in different colors: (<b>A</b>) (i) 4-isopropyl-1,6-dimethyl-1,2,3,4-tetrahydronaphthalene (in magenta); (<b>B</b>) (i) (1S,2R)-2-(4-allyl-2,6-dimethoxyphenoxy)-1-(3,4,5-trimethoxyphenyl)-1-propanol (in cyan); and (<b>C</b>) (i) (S)-5-Allyl-2-((1-(3,4-dimethoxyphenyl)propan-2-yl)oxy)-1,3-dimethoxybenzene (in blue). (<b>A</b>) (ii), (<b>B</b>) (ii), (<b>C</b>) (ii) The 2D interaction of the ligands with aldol reductase is generated by LigPlot v2.2.</p>
Full article ">Figure 4
<p>(<b>A</b>) Represents the RMSD graph of unbound protein (blue color) and protein-bound ligand (red color) over 200 ns of simulation. (<b>B</b>) Represents the RMSF graph of unbound protein (red color) and protein-bound ligand complex (green color) over 200 ns of simulation.</p>
Full article ">
18 pages, 2252 KiB  
Review
The Strong Inhibition of Pancreatic Lipase by Selected Indonesian Medicinal Plants as Anti-Obesity Agents
by Min Rahminiwati, Dyah Iswantini, Trivadila, Rut Novalia Rahmawati Sianipar, Rani Melati Sukma, Susi Indariani and Anggia Murni
Curr. Issues Mol. Biol. 2025, 47(1), 39; https://doi.org/10.3390/cimb47010039 - 9 Jan 2025
Viewed by 723
Abstract
Obesity is characterized by the accumulation of excessive fat, potentially leading to degenerative diseases. Pancreatic lipase, an enzyme responsible for converting 50–70% of dietary fat into monoglycerides, free fatty acids, and various other smaller molecules, plays a crucial role in fat metabolism. Therefore, [...] Read more.
Obesity is characterized by the accumulation of excessive fat, potentially leading to degenerative diseases. Pancreatic lipase, an enzyme responsible for converting 50–70% of dietary fat into monoglycerides, free fatty acids, and various other smaller molecules, plays a crucial role in fat metabolism. Therefore, this study aimed to review selected Indonesian medicinal plants with the potential to inhibit the activity of the pancreatic lipase enzyme. The results showed that kunci pepet (Kaempferiae angustifolia Rosc.), asam gelugur (Garcinia atroviridis), temulawak (Curcuma xanthorrhiza), jombang (Taraxacum officinale F. H. Wigg), pegagan (Centella asiatica), and pala (Myristica fragrans) had strong inhibitory effects, exceeding 50% for both in vitro and in vivo studies. Therefore, further studies are needed to explore the potential of these medicinal plants as anti-obesity treatments. Full article
(This article belongs to the Special Issue New Insight: Enzymes as Targets for Drug Development, 2nd Edition)
Show Figures

Figure 1

Figure 1
<p>The chemical structure of orlistat (PubChem ID: 3034010).</p>
Full article ">Figure 2
<p>Catalysis reaction of pancreatic lipase enzyme (Modification [<a href="#B25-cimb-47-00039" class="html-bibr">25</a>]. License number: 5924750703740).</p>
Full article ">Figure 3
<p>The chemical structures of benzoic acid, <span class="html-italic">o</span>-Coumaric acid, and stigmasterol.</p>
Full article ">Figure 4
<p>The chemical structure of flavokawain A (PubChem ID: 5355469).</p>
Full article ">Figure 5
<p>The chemical structure of hydroxycitric acid (HCA). (PubChem ID: 123908).</p>
Full article ">Figure 6
<p>The chemical structures of diarylheptanoids, curcumin, demethoxycurcumin, and bisdemethoxycurcumin.</p>
Full article ">Figure 7
<p>The chemical structure of xanthorrhizol (PubChem ID: 93135).</p>
Full article ">Figure 8
<p>Structure of taraxerol, taraxacin, β-sitosterol, campesterol, and chicoric acid.</p>
Full article ">Figure 9
<p>Structure of asiaticoside, madecassoside, madecassic acid, and asiatic acid.</p>
Full article ">Figure 10
<p>Structure of tetrahydrofuran.</p>
Full article ">
24 pages, 1590 KiB  
Article
Effect of Nutmeg (Myristica fragrans) and Tea Tree (Melaleuca alternifolia) Essential Oils on the Oxidative and Microbial Stability of Chicken Fillets During Refrigerated Storage
by Sushmita Moirangthem, Gopal Patra, Subhasish Biswas, Annada Das, Santanu Nath, Arun K. Verma, Srija Pal, Niloy Chatterjee, Samiran Bandyopadhyay, Pramod K. Nanda, Geetanjali Sharma and Arun K. Das
Foods 2024, 13(24), 4139; https://doi.org/10.3390/foods13244139 - 20 Dec 2024
Viewed by 704
Abstract
The current study investigated the impact of nutmeg essential oil (NEO) and tea tree essential oil (TTEO) on the preservation of raw chicken fillets during nine days of refrigerated storage study. The primary aim was to explore the antioxidant and antimicrobial properties of [...] Read more.
The current study investigated the impact of nutmeg essential oil (NEO) and tea tree essential oil (TTEO) on the preservation of raw chicken fillets during nine days of refrigerated storage study. The primary aim was to explore the antioxidant and antimicrobial properties of these essential oils (EOs) and assess their ability to extend the shelf life of poultry meat. Gas chromatography–mass spectrometry (GC-MS) was utilized to identify the chemical compositions of NEO and TTEO, revealing the presence of compounds like myristicin and terpenoids, known for their antimicrobial and antioxidant activities. Antioxidant properties were evaluated using DPPH and ABTS radical scavenging assays, where both oils exhibited potent free radical scavenging abilities, with NEO showing higher efficacy than TTEO. The EOs showed their antimicrobial potential, exhibiting significant antibacterial activities against tested Gram-positive and Gram-negative pathogens, such as Staphylococcus aureus and Escherichia coli, respectively. Raw chicken fillets treated with either NEO or TTEO at 1% were analyzed for physico-chemical, microbiological, and sensory attributes. Results demonstrated that both NEO- and TTEO-treated samples maintained better microbiological qualities, with lower total viable counts and enhanced sensory attributes, such as color and odor, compared to the control samples. Furthermore, NEO and TTEO effectively delayed spoilage, extending the shelf life of chicken fillets by up to seven days. This study concludes that both the test’s essential oils can be considered natural preservatives for enhancing the safety and quality of meat. Full article
(This article belongs to the Section Food Packaging and Preservation)
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>Gas chromatography and mass spectrometry analysis of nutmeg essential oil with major compounds.</p>
Full article ">Figure 2
<p>Gas chromatography and mass spectrometry analysis of tree tea essential oil with major compounds.</p>
Full article ">Figure 3
<p>Zone of inhibition of NEO and TTEO by agar well diffusion method against different pathogenic bacterial strains (SA—<span class="html-italic">Staphylococcus aureus</span>; LM—<span class="html-italic">Listeria monocytogenes</span>; EC—<span class="html-italic">Escherichia coli</span>; ST—<span class="html-italic">Salmonella</span> Typhimurium).</p>
Full article ">Figure 4
<p>Effect of essential oils on TBARS values of chicken fillets during storage at 4 °C. Bars with different superscript (a–d) between days and (a–c) between treatments differ significantly (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">
14 pages, 5398 KiB  
Article
Attenuating Oxidative Damage with Macelignan in Glutamate-Induced HT22 Hippocampal Cells
by Mei Tong He, Kiwon Jung, Chan-Woong Park, Young-Won Chin and Ki Sung Kang
Appl. Sci. 2024, 14(23), 11408; https://doi.org/10.3390/app142311408 - 7 Dec 2024
Viewed by 709
Abstract
Macelignan, from Myristica fragrans (nutmeg), is a bioactive compound with various pharmacological properties, including anti-inflammatory and neuroprotective activities. The purpose of this work was to investigate the antioxidant and anti-apoptotic effects of macelignan in glutamate-treated HT22 mouse hippocampal neurons. Macelignan was extracted and [...] Read more.
Macelignan, from Myristica fragrans (nutmeg), is a bioactive compound with various pharmacological properties, including anti-inflammatory and neuroprotective activities. The purpose of this work was to investigate the antioxidant and anti-apoptotic effects of macelignan in glutamate-treated HT22 mouse hippocampal neurons. Macelignan was extracted and identified in a methanol extract of M. fragrans seeds. The DPPH was used to assess the antioxidative activity of macelignan. Glutamate (5 mM) was used to induce neurotoxicity in the HT22 cells. Neuroprotective effects were measured using relevant biochemical and imaging assays, including cell viability, ROS production, nuclear staining, apoptotic cell death, and protein expression. Macelignan markedly and concentration-dependently enhanced DPPH radical scavenging activity. In the HT22 cell model, glutamate induced cell damage by decreasing cell viability, promoting ROS generation, and increasing apoptotic cell death according to cell morphological changes. However, macelignan treatment restored cell viability, inhibited ROS generation concentration-dependently, and reduced apoptosis. Moreover, glutamate significantly up-regulated the phosphorylation of MAPK-pathway-related proteins, which was reversed by macelignan treatment. In conclusion, macelignan shows notable neuroprotective effects on oxidative stress and apoptotic cell death in glutamate-induced cells, and this study provides useful information on its potential therapeutic implications in neurological disorders. Full article
Show Figures

Figure 1

Figure 1
<p>Chemical structure (<b>a</b>) and DPPH scavenging activity of macelignan (<b>b</b>). Value represents the mean ± S.D. (<span class="html-italic">n</span> = 4). Mac, macelignan.</p>
Full article ">Figure 2
<p>Effect of macelignan on cytotoxicity in HT22 cells. (<b>a</b>) Cell viability of Mac (1, 5, 10, and 20 µM) pretreatment in glutamate (5 mM)-treated HT22 cells; (<b>b</b>) cell viability of NAC (the positive control at 0.5, 1, and 2 mM) pretreatment in glutamate-treated HT22 cells; (<b>c</b>) morphology of HT22 cells after exposure to glutamate for 24 h. Scale bar, 50 µm. Value represents the mean ± S.D. (<span class="html-italic">n</span> = 3). # <span class="html-italic">p</span> &lt; 0.05 compared to the untreated cells, * <span class="html-italic">p</span> &lt; 0.05 compared to glutamate-treated cells (ANOVA, Tukey’s test). Mac, macelignan; NAC, N-acetylcysteine; CTL, control; Glu, glutamate.</p>
Full article ">Figure 3
<p>Effect of macelignan on ROS generation in HT22 cells. Cells were pretreated with Mac (5 and 10 µM) for 2 h, followed by exposure to glutamate (5 mM) for 8 h. (<b>a</b>) Mac (5 µM, 1.92-fold; 10 µM, 1.62-fold) inhibited the generation of ROS in glutamate-treated cells; (<b>b</b>) NAC, the positive control, inhibited the generation of ROS in glutamate-treated cells; (<b>c</b>) fluorescence images of HT22 cells exposed to glutamate were captured using fluorescence microscopy. Scale bar, 50 µm. Value represents the mean ± S.D. (<span class="html-italic">n</span> = 3). # <span class="html-italic">p</span> &lt; 0.05 in comparison to the untreated cells, * <span class="html-italic">p</span> &lt; 0.05 in comparison with glutamate-treated cells (ANOVA, Tukey’s test). Mac, macelignan; NAC, N-acetylcysteine; CTL, control; Glu, glutamate.</p>
Full article ">Figure 4
<p>Effect of macelignan on apoptotic cell death in HT22 cells. Cells were pretreated with Mac (5 and 10 µM) for 2 h, followed by exposure to glutamate (5 mM) for 12 h. (<b>a</b>) Mac reduced chromatin condensation in glutamate-treated cells with Hoechst 33342 staining using a fluorescence microscope (scale bar, 50 µm); (<b>b</b>) Mac inhibited apoptosis in glutamate-treated cells with annexin V/PI staining using a Tali Image-Based Cytometer (scale bar, 5 µm); (<b>c</b>) quantification of apoptotic cells from the obtained images using TaliPCApp software (version 1.0). Values represent the mean ± S.D. (<span class="html-italic">n</span> = 3). # <span class="html-italic">p</span> &lt; 0.05 in comparison to the untreated cells, * <span class="html-italic">p</span> &lt; 0.05 in comparison with glutamate-treated cells (ANOVA, Tukey’s test). Mac, macelignan; CTL, control; Glu, glutamate.</p>
Full article ">Figure 5
<p>Effect of macelignan on glutamate-stimulated activation of MAPK pathway. (<b>a</b>) Expression of MAPK pathway-related proteins and GAPDH; (<b>b</b>) levels of p-ERK/ERK, p-JNK/JNK, and p-p38/p38. GAPDH was detected as loading control. Value represents the mean ± S.D. (<span class="html-italic">n</span> = 3). # <span class="html-italic">p</span> &lt; 0.05 compared to the untreated cells, * <span class="html-italic">p</span> &lt; 0.05 compared to glutamate-treated cells (ANOVA, Tukey’s test). Mac, macelignan; Glu, glutamate.</p>
Full article ">
18 pages, 6510 KiB  
Article
Molecular Networking, Docking, and Biological Evaluation of Licarin A from Myristica fragrans as a Potential Cancer Chemopreventive Agent
by Peter J. Blanco Carcache, Ines Y. Castro-Dionicio, Nathan P. Mirtallo Ezzone, Eric D. Salinas-Arrellano, Joshua Bahar, Steven K. Clinton and A. Douglas Kinghorn
Molecules 2024, 29(20), 4919; https://doi.org/10.3390/molecules29204919 - 17 Oct 2024
Viewed by 1334
Abstract
Currently, clinically available cancer chemopreventive drug options are limited to mostly tamoxifen and its derivatives, such as raloxifene, and approved specifically for breast cancer. Thus, the availability of chemopreventive drug molecules for other types of malignant cancers would be desirable. In previous reports, [...] Read more.
Currently, clinically available cancer chemopreventive drug options are limited to mostly tamoxifen and its derivatives, such as raloxifene, and approved specifically for breast cancer. Thus, the availability of chemopreventive drug molecules for other types of malignant cancers would be desirable. In previous reports, the arils of Myristica fragrans (mace) have been found to exhibit cancer chemopreventive activity. Therefore, the purpose of the present study was to identify a natural product from this species with potential chemopreventive activity guided by chemoinformatic sample analysis via Global Natural Products Social (GNPS) molecular networking and molecular docking. The neolignan licarin A (1) was identified as a potential chemopreventive constituent, and subsequently submitted to several in vitro bioassays and a zebrafish toxicity evaluation. In this work, 1 afforded superior phosphoNF-κBp65 phosphorylation activity in DU-145 prostate cancer cells compared to isoliquiritigenin (2), which was used as a natural product chemopreventive control. Both 1 and 2 showed a longer-lasting reduction in cellular stress in a cell oxidative stress real-time dose–response assay than the positive control using Hepa1c1c7 mouse hepatoma cells. In addition, 1 displayed similar activities to 2, while also being less toxic to zebrafish (Danio rerio) than both this chalcone and the clinically used chemopreventive drug tamoxifen. Full article
Show Figures

Figure 1

Figure 1
<p>Structures of licarin A (<b>1</b>) and isoliquiritigenin (<b>2</b>).</p>
Full article ">Figure 2
<p>LC-MS/MS chemoinformatic analysis of all chromatographic fractions obtained from the ethyl acetate partition of <span class="html-italic">M. fragrans</span> revealed the presence of <b>1</b> in region A (see <a href="#app1-molecules-29-04919" class="html-app">Supplementary Figure S1</a>) of the molecular network. (Relevant data: GNPS library hit, Bronze: 0.81c.)</p>
Full article ">Figure 3
<p>Molecular docking of licarin A (<b>1</b>) based on binding energy and structural similarity. The binding pocket of <b>1</b> to NF-<span class="html-italic">κ</span>Bp65 is shown in a 3D perspective. The 2D perspective displays all binding interactions with relevant amino acids. (Relevant data: in silico binding affinity, 10.66 μM; binding energy, −6.78).</p>
Full article ">Figure 4
<p>Molecular docking for the SIRIUS CSI: FingerID structural predictions with NF-<span class="html-italic">κ</span>Bp65. (<b>A</b>) Structures of <b>3</b>–<b>6</b>. (<b>B</b>–<b>E</b>) Docking profiles for <b>3</b> (blue, <b>B</b>), <b>4</b> (gray, <b>C</b>), <b>5</b> (pink, <b>D</b>), and <b>6</b> (cyan, <b>E</b>) with NF-<span class="html-italic">κ</span>Bp65.</p>
Full article ">Figure 5
<p>Molecular docking for the GNPS library hits with NF-<span class="html-italic">κ</span>Bp65. (<b>A</b>) Structures of <b>7</b>–<b>10</b>. (<b>B</b>–<b>E</b>) Docking profiles for <b>7</b> (dark green, <b>B</b>), <b>8</b> (yellow, <b>C</b>), <b>9</b> (neon green, <b>D</b>), and <b>10</b> (blue, <b>E</b>) with NF-<span class="html-italic">κ</span>Bp65.</p>
Full article ">Figure 6
<p>(<b>A</b>) Crystal violet viability data for compounds <b>1</b> and <b>2</b>, and the rocaglamide positive control, with the DU-145 prostate cancer cell line. (<b>B</b>–<b>D</b>) Cell oxidative stress real-time dose–response assay profiles of <b>1</b>, <b>2</b>, and vitamin C, respectively, using Hepa1c1c7 mouse hepatoma cells.</p>
Full article ">Figure 7
<p>(<b>A</b>) Phosphorylated NF-<span class="html-italic">κ</span>Bp65 levels after treatment with 150 μM of <b>1</b>, <b>2</b>, and rocaglamide with the DU-145 prostate cancer cell line. (<b>B</b>–<b>D</b>) Individual phosphorylated NF-<span class="html-italic">κ</span>Bp65 levels after treatment with <b>1</b>, <b>2</b>, and rocaglamide, respectively, using the DU-145 prostate cancer cell line.</p>
Full article ">Figure 8
<p>Representative images of the observed morphological toxicity of tamoxifen, licarin A (<b>1</b>), and isoliquiritigenin (<b>2</b>) in a zebrafish model.</p>
Full article ">Figure 9
<p>Representative histograms showing the condition of zebrafish after separate exposure to tamoxifen, licarin A (<b>1</b>), and isoliquiritigenin (<b>2</b>).</p>
Full article ">
16 pages, 857 KiB  
Article
Evaluation of the Shelf Life of Myristica-fragrans Powder-Flavored Oils Obtained through the Application of Two Processes: Infusion and Co-Pressing Technology
by Irene Maria Grazia Custureri, Monica Rosa Loizzo, Vincenzo Sicari, Roberta Pino, Rosa Tundis, Ana Cristina Soria and Angelo Maria Giuffrè
Molecules 2024, 29(15), 3588; https://doi.org/10.3390/molecules29153588 - 30 Jul 2024
Cited by 1 | Viewed by 1034
Abstract
This work aimed to evaluate the impact of enrichment processing on the quality parameters, bioactivity and sensorial aspects of Myristica fragrans (mace)-flavored olive oil storage for one year. The mace powder was added to extra virgin olive oil through two different processes: immediately [...] Read more.
This work aimed to evaluate the impact of enrichment processing on the quality parameters, bioactivity and sensorial aspects of Myristica fragrans (mace)-flavored olive oil storage for one year. The mace powder was added to extra virgin olive oil through two different processes: immediately after crushing the olives by mixing mace (1% weight/weight (w/w)) with the olive paste (MAVOO-M) and by adding mace to extra virgin olive oil (C) (2% w/w) (MAVOO-I). A multi-analytical approach was applied to measure the main qualitative indexes, such as the free acidity, peroxide value and ultraviolet parameters. The total phenolic and carotenoid contents (TPC and TCC, respectively) and α-tocopherol were also evaluated, as well as the sensory attributes. The radical scavenging potential was estimated by using two different in vitro tests, namely, 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH). A significant increase in the free acidity parameter was found in all the flavored oils, and particularly in the MAVOO-M (1.27% oleic acid); at the same time, this oil was the sample with the lowest peroxide value (i.e., 9.68 meqO2/kg) after 360 days of storage. At the end of the storage, an increase in L* values was found in both the MAVOO-M and -I vs. the C (43.88 and 43.02, respectively, vs. 42.62). The TCC was strongly influenced by the addition of mace, especially when the infusion process was used. In fact, after one year of storage, the TCC in the MAVOO-I resulted in ~34.7% more than the MAVOO-M. A promising DPPH radical scavenging activity was observed independently by the applied aromatization process, with IC50 values of 19.77 and 17.80 μg/mL for the MAVOO-M and MAVOO-I, respectively. However, this activity decreased during storage, and a similar trend was observed using the ABTS test. In conclusion the infusion as enrichment methodology led to more promising results in terms of functionality compared with the co-mixing one. Full article
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>Quantitative parameters of the unaromatized olive oil (C), aromatized olive oil by co-mixing 1% (MAVOO-M) and aromatized olive oil by infusion 2% (MAVOO-I). (<b>a</b>) Total carotenoid content (TCC); (<b>b</b>) total chlorophyll content (TChlC); (<b>c</b>) total phenolic content (TPC); (<b>d</b>) α-tocopherol content (α-Toc). Data are expressed as the mean ± standard deviation (<span class="html-italic">n</span> = 3). Statistical analysis was followed by Tukey’s test, which were used to evaluate any differences at the same time of analysis (lowercase letters) or during the considered storage (uppercase letters). Results followed by different letters were significant at <span class="html-italic">p</span> ≤ 0.01. ** <span class="html-italic">p</span> ≤ 0.01.</p>
Full article ">Figure 2
<p>Sensory attributes of the unaromatized olive oil (C), aromatized olive oil by co-mixing 1% (MAVOO-M) and aromatized olive oil by infusion 2% (MAVOO-I).</p>
Full article ">Figure 3
<p>Antioxidant and antiradical activities of the unaromatized olive oil (C), aromatized olive oil by co-mixing 1% (MAVOO-M) and aromatized olive oil by infusion 2% (MAVOO-I). (<b>a</b>) DPPH test (AA: ascorbic acid positive control); (<b>b</b>) ABTS test (AA: ascorbic acid positive control); (<b>c</b>) FRAP test (BHT: butylated hydroxytoluene positive control); (<b>d</b>) β-carotene bleaching test (PG: propyl gallate positive control). Data are expressed as the mean ± standard deviation (<span class="html-italic">n</span> = 3). Statistical analysis was followed by Tukey’s test, which were used to evaluate any differences at the same time of analysis (lowercase letters) or during the considered storage (uppercase letters). Results followed by letters were significant at <span class="html-italic">p</span> ≤ 0.01. * <span class="html-italic">p</span> ≤ 0.05; ** <span class="html-italic">p</span> ≤ 0.01.</p>
Full article ">
18 pages, 2923 KiB  
Article
In Vitro and In Vivo Wide-Spectrum Dual Antimycetomal Activity of Eight Essential Oils Coupled with Chemical Composition and Metabolomic Profiling
by Shereen O. Abd Algaffar, Prabodh Satyal, Naglaa S. Ashmawy, Annelies Verbon, Wendy W. J. van de Sande and Sami A. Khalid
Microbiol. Res. 2024, 15(3), 1280-1297; https://doi.org/10.3390/microbiolres15030086 - 22 Jul 2024
Cited by 2 | Viewed by 1124
Abstract
Mycetoma, a neglected infection of subcutaneous tissues, poses a significant health burden, especially in tropical regions. It is caused by fungal (eumycetoma) and bacterial (actinomycetoma) pathogens, with current treatments often providing unsatisfactory outcomes. This study aims to discover novel broad-spectrum antimicrobial agents to [...] Read more.
Mycetoma, a neglected infection of subcutaneous tissues, poses a significant health burden, especially in tropical regions. It is caused by fungal (eumycetoma) and bacterial (actinomycetoma) pathogens, with current treatments often providing unsatisfactory outcomes. This study aims to discover novel broad-spectrum antimicrobial agents to circumvent the lengthy and costly diagnostic procedures. Eight essential oils (EOs) from the roots and aerial parts of Geigeria alata, Lavandula angustifolia, Melaleuca alternifolia, Myristica fragrans, Pimpinella anisum, Syzigum aromaticum, and Thymus vulgaris were prepared using steam distillation. The in vitro antimycetomal activity against Madurella mycetomatis and Actinomadura madurae strains was assessed using resazurin assays. The chemical compositions of the EOs were analyzed using gas chromatography and mass spectrometry (GC–MS). Promising EOs underwent further in vivo toxicity and efficacy testing in Galleria mellonella larvae models. EOs of G. alata roots, M. fragrans, P. anisum, S. aromaticum, and T. vulgaris showed wide-spectrum dual in vitro antimycetomal activity against all tested strains, with minimum inhibitory concentrations (MICs) ranging from 0.004 to 0.125% v/v. G. alata aerial parts and L. angustifolia EOs demonstrated activity predominantly against A. madurae, while M. alternifolia EO did not inhibit any tested strains. M. fragrans and P. anisum EOs significantly enhanced the survival of M. mycetomatis-infected larvae without inducing toxicity in uninfected larvae. Notably, P. anisum EO tended to enhance the survival of A. madurae-infected larvae, ranking it as the most promising EO among those tested. The investigated EOs, particularly P. anisum, exhibited promising broad-spectrum antimycetomal activity against fungal and bacterial pathogens responsible for mycetoma. These findings highlight the potential of essential oils as a basis for developing novel antimycetomal agents, offering hope for improved treatment strategies for this neglected disease. Full article
(This article belongs to the Special Issue Antifungal Activities of Plant Extracts)
Show Figures

Figure 1

Figure 1
<p>Toxicity of (<b>A</b>) <span class="html-italic">M. fragrans</span>, (<b>B</b>) <span class="html-italic">P. anisum</span>, (<b>C</b>) <span class="html-italic">S. aromaticum</span>, and (<b>D</b>) <span class="html-italic">T. vulgaris</span> EOs in the <span class="html-italic">G. mellonella</span> model.</p>
Full article ">Figure 2
<p>Efficacy of (<b>A</b>) <span class="html-italic">M. fragrans</span> and (<b>B</b>) <span class="html-italic">P. anisum</span> EOs in the <span class="html-italic">G. mellonella</span> infected with <span class="html-italic">M. mycetomatis</span> (SO1).</p>
Full article ">Figure 3
<p>Efficacy of (<b>A</b>) <span class="html-italic">M. fragrans</span> and (<b>B</b>) <span class="html-italic">P. anisum</span> EOs in <span class="html-italic">G. mellonella</span> infected with <span class="html-italic">A. madurae</span> (DSM 44005).</p>
Full article ">Figure 4
<p>(<b>A</b>) PCA loading plot, (<b>B</b>) VIP score plot, (<b>C</b>) Hierarchical cluster analysis (HCA), (<b>D</b>) Heat map. GR: <span class="html-italic">Geigeria alata</span> root, TV: <span class="html-italic">Thymus vulgaris</span>, MF: <span class="html-italic">Myristica fragrans</span>, SA: <span class="html-italic">Syzigum aromaticum</span>, PA: <span class="html-italic">Pimpinella anisum</span>, LA: <span class="html-italic">Lavandula angustifolia</span>, GA: <span class="html-italic">Geigeria alata</span> aerial parts, MA: <span class="html-italic">Melaleuca alternifolia</span>.</p>
Full article ">
26 pages, 43920 KiB  
Article
Herbal Spices as Food and Medicine: Microscopic Authentication of Commercial Herbal Spices
by Amjad Khan, Mushtaq Ahmad, Amir Sultan, Raees Khan, Jamil Raza, Sheikh Zain Ul Abidin, Siraj Khan, Muhammad Zafar, Mohammad N. Uddin and Mohsin Kazi
Plants 2024, 13(8), 1067; https://doi.org/10.3390/plants13081067 - 10 Apr 2024
Cited by 6 | Viewed by 3203
Abstract
Herbal spices are an agricultural commodity, economically very important and beneficial in primary healthcare in the food and medicine sectors. Herbal spices are used as food flavoring agents as well as in phytotherapies throughout the world and have nutritive benefits. The food and [...] Read more.
Herbal spices are an agricultural commodity, economically very important and beneficial in primary healthcare in the food and medicine sectors. Herbal spices are used as food flavoring agents as well as in phytotherapies throughout the world and have nutritive benefits. The food and medicine industries widely employ artificial or natural adulteration to retard the deterioration and utilization of these adulterants in food and medicine products has given rise to significant apprehension among consumers, primarily stemming from the potential health risks that they pose. Thus, their characterization for the purpose of identification, origin, and quality assurance is mandatory for safe human consumption. Here, we studied 22 samples of commonly traded herbal spices that belong to 20 different genera and 21 species comprising 14 families, investigated macroscopically or organoleptically as well as histologically under microscopic examination. In this study, we provide details on organoleptic features including appearance, taste, odor, color, shape, size, fractures, types of trichomes, and the presence of lenticels among the examined herbal spices and these features have great significance in the detection of both natural as well as artificial deterioration. In terms of microscopic characterization, each examined plant part comprising different anatomical characteristics has taxonomic importance and also provides useful information for authentication from natural adulterants. Furthermore, the studied taxa were also described with nutritive and therapeutic properties. For condiments, herbal beverages and medicinal purposes, different herbal parts such as leaves, floral buds, seeds, fruit, and accessory parts like mericarp, rhizome, bulbs, and bark were used and commercially traded. Similarly, in this study, the leaves of Cinnamomum tamala and Mentha spicata, the floral buds of Syzygium aromaticum, the seeds of Amomum subulatum, Brassica nigra, Punica granatum, Myristica fragrans, Phyllanthus emblica, and Elettaria cardamomum, the mericarp of Coriandrum sativum, and Cuminum cyminum were observed. As a result, we show the potential of herbal spices as a source of many valuable phytochemicals and essential nutrients for food, nutraceutical, and homoeopathic medicine. Full article
(This article belongs to the Section Phytochemistry)
Show Figures

Figure 1

Figure 1
<p>Map showing sampling sites in the investigated area.</p>
Full article ">Figure 2
<p>(<b>a</b>) Herbal spices, (<b>b</b>) macroscopic examination, (<b>c</b>) sample preparation, (<b>d</b>) slide preparation, (<b>e</b>) microscopic examination, and (<b>f</b>) histology.</p>
Full article ">Figure 3
<p>(<b>A</b>) Micrograph of garlic bulb. (<b>B</b>) Transverse section of <span class="html-italic">Allium sativum</span> bulb: Cu—cuticle, Ep—epidermis, Co—cortex, En—endodermis, Vb—vascular bundles and Mt—mesophyll tissues. (<b>C</b>) Micrograph of greater cardamom. (<b>D</b>) Transverse section of <span class="html-italic">Amomum subulatum</span> fruit: Te—Testa, Sc—sclerenchymatous region, Og—oil globules and En—endospermic region.</p>
Full article ">Figure 4
<p>(<b>A</b>) Micrograph of mustard seed. (<b>B</b>) Transverse section of <span class="html-italic">Brassica nigra</span> seed: Te—testa, En—endosperm, Co—cotyledon, Em—embryo and Cen—chalazal endosperm. (<b>C</b>) Micrograph of pepper seed. (<b>D</b>) Transverse section of <span class="html-italic">Capsicum annuum</span> Seed: Sc—seed coat, Rg—ridges, Co—separately localized cotyledons, En—endosperm and Em—embryo.</p>
Full article ">Figure 5
<p>(<b>A</b>) Micrograph of malabar leaf. (<b>B</b>) Transverse section of <span class="html-italic">Cinnamomum tamala</span> leaf (<b>a</b>) leaf lamina, (<b>b</b>) leaf base and (<b>c</b>) leaf petiole: (<b>b</b>,<b>c</b>) Cu—cuticle, Ep—epidermis, Mc—mucilage cells, Vc—volatile oil cavity, Lp—lignified parenchyma, Pp—pitted parenchyma, Sc—sclerenchyma, Co—collenchyma, Pc—pericycle, Mc—mesophyll cell, Pc—palisade, Xy—xylem, Mc—mucilage cavity, Ph—phloem, Stc—stone cell with tannin and Sc—sclerenchyma. (<b>C</b>) Micrograph of cinnamon bark. (<b>D</b>) Transverse section of <span class="html-italic">Cinnamomum verum</span> bark: Ct—cork tissues, Pf—pericyclic fibers, Sc—sclereids, Sp—secondary phloem, Mr—medullary ray, Mc—mucilage cells, Pf—phloem fibers and Oc—oil cavity.</p>
Full article ">Figure 6
<p>(<b>A</b>) Micrograph of coriander mericarp. (<b>B</b>) Transverse section of <span class="html-italic">Coriandrum sativum</span> mericarp: Rd-ridges, Ep—epicarp, Me—mesocarp, Ec—endocarp, Cp—carpophore, Ts—testa and En—endosperm. (<b>C</b>) Micrograph of cumin mericarp. (<b>D</b>) Transverse section of <span class="html-italic">Cuminum cyminum</span> mericarp: Rd—ridges, Ep—epicarp, Vt—vittae, Me—mesocarp, Ec—endocarp, Ts—testa, Cp—carpophore and En—endosperm.</p>
Full article ">Figure 7
<p>(<b>A</b>) Micrograph of turmeric rhizome. (<b>B</b>) Transverse section of <span class="html-italic">Curcuma longa</span> rhizome: (<b>a</b>) Fb—fibers and Vs—vessels. (<b>b</b>) Oc.c—outer cork cells, Pt—parenchymatous tissue, Ic.c—inner cork cells, Sg—starch grains and Oc—oleoresin cells. (<b>C</b>) Micrograph of cardamom fruit. (<b>D</b>) Transverse section of <span class="html-italic">Elettaria cardamomum</span> fruit: (<b>c</b>) Ep—epidermis, Lu—lumen and Oc—oil cellular layer (<b>d</b>) Sc—sclerenchymatous layer, En—endosperm, Rh—raphe and Ps—palisade sclerenchyma.</p>
Full article ">Figure 8
<p>(<b>A</b>) Micrograph of fennel mericarp. (<b>B</b>) Transverse section of <span class="html-italic">Foeniculum vulgare</span> mericarp: Rd—ridges, Ep—epicarp, Vt—vittae, Rp—raphe, Me—mesocarp, Ec—endocarp, Vb—vascular bundle and En—endosperm. (<b>C</b>) Micrograph of star anise fruit. (<b>D</b>) Transverse section of <span class="html-italic">Illicium verum</span> fruit: (<b>a</b>) Ep—epicarp, Gt—ground tissue, Ec—endocarp region, and Co—cotyledon. (<b>b</b>) Ts—testa, Oc—oil cavity Lu—lumen and Me—mesocarp region.</p>
Full article ">Figure 9
<p>(<b>A</b>) Micrograph of mace seed endosperm. (<b>B</b>) Transverse section of <span class="html-italic">Myristica fragrans</span> seed endosperm: Sp—spongy parenchyma, Dp—dilated parenchyma, Oc—oil cavity, En—endosperm and Pig—perisperm inner growth. (<b>C</b>) Micrograph of fruit peel of Mace. (<b>D</b>) Cross-section of fruit peel of <span class="html-italic">Myristica fragrans</span>: Vb—vascular bundle, Gp—ground parenchyma, Oc—oil cavity, and Vo—volatile oil contents.</p>
Full article ">Figure 10
<p>(<b>A</b>) Micrograph of spearmint leaf and young twig. (<b>B</b>) Transverse section of <span class="html-italic">Mentha spicata</span> leaf and young twig: (<b>a</b>) Ep—epidermis, Cgt—capitate glandular trichomes, Co—collenchyma cells, Pt—palisade tissues, Vb—vascular bundle, Pc—pericycle and Sp—spongy parenchyma. (<b>b</b>) Ep—epidermis, Cor—collenchymatous ridges, Co—cortex, Pc—pericycle, Ph—phloem, Xy—xylem, Tr—trichomes and Pi—pith. (<b>C</b>) Micrograph of emblic fruit. (<b>D</b>) Transverse section of <span class="html-italic">Phyllanthus emblica</span> fruit: Gt—ground tissue, C.o.c—calcium oxalate crystals, Sp—spongy parenchyma, En—endosperm, Ec—endocarp region and Vb—vascular bundle.</p>
Full article ">Figure 11
<p>(<b>A</b>) Micrograph of black pepper fruit. (<b>B</b>) Transverse section of <span class="html-italic">Piper nigrum</span> fruit: Pc—pericap, Ps—perisperm, Rd—ridges, Og—oil globules, and En—endosperm. (<b>C</b>) Micrograph of Pomegranate seed. (<b>D</b>) Transverse section of <span class="html-italic">Punica granatum</span> seed: (<b>a</b>) Sc—seed coat, En—endosperm and Em—embryo. (<b>b</b>) P.La—pigmented layer and C.co—coiled cotyledons.</p>
Full article ">Figure 12
<p>(<b>A</b>) Micrograph of Clove flower bud. (<b>B</b>) Transverse section of <span class="html-italic">Syzygium aromaticum</span> flower bud: CU—cuticle, EP—epidermis, OG—oil glands, COL—columella, SPH—sphaeraphide, VB—vascular bundles and AER—aerenchyma. (<b>C</b>) Micrograph of Carom Mericarp. (<b>D</b>) Transverse section of <span class="html-italic">Trachyspermum ammi</span> mericarp: Rd—ridges, Ep—epicarp, VT—vittae, SC—secretory cells, ME—mesocarp, EC—endocarp, CP—carpophore and EN—endosperm.</p>
Full article ">Figure 13
<p>(<b>A</b>) Micrograph of fenugreek seed. (<b>B</b>) Transverse section of <span class="html-italic">Trigonella foenum-graecum</span> seed: Ts—testa, En—endosperm, Cen—chalazal endosperm, Em—embryo and Co—both the cotyledon. (<b>C</b>) Micrograph of ginger rhizome. (<b>D</b>) Transverse section of <span class="html-italic">Zingiber officinale</span> rhizome: (<b>a</b>,<b>b</b>) Oc—outer cork Co—cortex and Gt—ground tissues (<b>b</b>) Oc—outer cork, Ic—inner cork, Co—cortex, Sg—starch grains, Fvb—fibro—vascular bundles, Fb—fibers and Oc—oleoresin cells.</p>
Full article ">Figure 14
<p>Representative plant families (numbers of taxa and its percentage).</p>
Full article ">Figure 15
<p>Representative plant parts traded (including frequency and its percentage).</p>
Full article ">
23 pages, 3589 KiB  
Article
The Identification and Cytotoxic Evaluation of Nutmeg (Myristica fragrans Houtt.) and Its Substituents
by Suthiwat Khamnuan, Ampai Phrutivorapongkul, Pornsiri Pitchakarn, Pensiri Buacheen, Jirarat Karinchai, Chuda Chittasupho, Mingkwan Na Takuathung, Tinnakorn Theansungnoen, Kannika Thongkhao and Aekkhaluck Intharuksa
Foods 2023, 12(23), 4211; https://doi.org/10.3390/foods12234211 - 22 Nov 2023
Cited by 4 | Viewed by 2905
Abstract
The aril and seed of nutmeg, Myristica fragrans Houtt. (Myristicaceae), hold significant value in various industries globally. Our preliminary research found two morphological variations: a globose shape and an oval shape. Due to these different characteristics, the safety of consumers is of primary [...] Read more.
The aril and seed of nutmeg, Myristica fragrans Houtt. (Myristicaceae), hold significant value in various industries globally. Our preliminary research found two morphological variations: a globose shape and an oval shape. Due to these different characteristics, the safety of consumers is of primary concern. Thus, authentication and comparative pharmacological and toxicity analyses are necessary. In this study, pharmacognostic and advanced phytochemical analyses, DNA barcoding, cytotoxicity, and the anti-nitric oxide production of commercial Thai nutmeg were examined. Via morphologic examinations and TLC fingerprinting, all the sampled aril and seed were categorized into globose and oval-shaped groups. The results of HPLC, GC-MS, and LC-MS/MS experiments revealed distinct differences between these groups. The DNA barcoding of the trnH-psbA region using the BLAST method and neighbor-joining tree analyses confirmed the globose nutmeg as M. fragrans and the oval-shaped variant as M. argentea. A comparison was then carried out between the potential toxicity and anti-inflammatory capabilities of M. fragrans and M. argentea. Cytotoxicity tests on HaCaT, 3T3-L1, Caco-2, HEK293, and RAW264.7 were performed using both methanolic extracts and volatile oil from the arils and seeds of both species. This study concludes that blending or substituting these two species maintains their therapeutic integrity without posing safety concerns. Full article
Show Figures

Figure 1

Figure 1
<p>Morphologic characteristics of <span class="html-italic">M. fragrans</span> Houtt.: (<b>a</b>) habit, (<b>b</b>) leaves, (<b>c</b>) ripened fruit displaying the aril, (<b>d</b>) ground nutmeg, (<b>e</b>) flowers, (<b>f</b>) seeds, (<b>g</b>) fruits, (<b>h</b>) dried arils, and (<b>i</b>) Thai massaman curry.</p>
Full article ">Figure 2
<p>The methodological framework employed in this study.</p>
Full article ">Figure 3
<p>Macroscopic features of nutmeg arils and seeds divided in two groups: globose (<b>a</b>,<b>b</b>) and oval-shaped groups (<b>c</b>,<b>d</b>).</p>
Full article ">Figure 4
<p>TLC fingerprints of authentic <span class="html-italic">M. fragrans</span> arils (AA1–AA3) and seeds (AS1–AS3), along with commercial nutmeg arils (PA1–PA10) and seeds (PS1–PS12), were developed using hexane: ethyl acetate (70:30) as the mobile phase. All samples were compared using the standard myristicin (Std.). The TLC chromatograms of aril and seed samples, detected under UV at 254 nm ((<b>a</b>) for arils and (<b>c</b>) for seeds) and after being derivatized with 10% <span class="html-italic">v</span>/<span class="html-italic">v</span> sulfuric acid ((<b>b</b>) for arils and (<b>d</b>) for seeds), are presented. Black arrows indicate the presence of bands at hRf = 65 in all oval-shaped samples.</p>
Full article ">Figure 5
<p>HPLC fingerprints of the methanolic extracts (<b>a</b>–<b>d</b>) and volatile oils (<b>e</b>–<b>h</b>) from representative nutmeg samples of a globose (<b>a</b>,<b>b</b>,<b>e</b>,<b>f</b>) and an oval shape (<b>c</b>,<b>d</b>,<b>g</b>,<b>h</b>). The green and red arrows indicate distinct peaks at retention times of 11.00 and 18.30 min, respectively, distinguishing the globose nutmeg samples from the oval-shaped ones.</p>
Full article ">Figure 6
<p>Neighbor-joining tree constructed using MEGA 11.0.10 Software, showcasing authentic <span class="html-italic">M. fragrans</span>, globose nutmeg (PS1), and oval-shaped nutmeg (PS3), alongside various <span class="html-italic">Myristica</span> spp. retrieved from the GenBank database. The <span class="html-italic">Myristica</span> species from the GenBank database include <span class="html-italic">M. fragrans</span> (highlighted in red), <span class="html-italic">M. yunnanensis</span> (black), <span class="html-italic">M. argentea</span> (yellow), <span class="html-italic">M. andamanica</span> (blue), <span class="html-italic">M. malabarica</span> (grey), <span class="html-italic">M. fatua</span> (green), and <span class="html-italic">M. beddomei</span> (violet). The orange dots represent the identified <span class="html-italic">Myristica</span> specimens from our study. The dendrogram was constructed based on the aligned nucleotide sequences from the <span class="html-italic">trn</span>H-<span class="html-italic">psb</span>A region. Numerical values at the nodes represent bootstrap values derived from 10,000 replications.</p>
Full article ">Figure 7
<p>Assessment of the cytotoxic effects of methanolic extracts and volatile oils extracted from <span class="html-italic">M. fragrans</span> and its substituent, <span class="html-italic">M. argentea</span>: representations include <span class="html-italic">M. fragrans</span> aril (AA1; blue) and seed (AS1; green), along with <span class="html-italic">M. argentea</span> aril (PA4; orange) and seed (PS3; red). After 24 h treatment, the SRB assay illustrates the effect of the methanolic extracts and volatile oils of <span class="html-italic">M. fragrans</span> and <span class="html-italic">M. argentea</span> on the viability of HaCaT (<b>a</b>,<b>b</b>) and RAW 264.7 (<b>c</b>,<b>d</b>) cells, and illustrates the effect after 48 h treatment on 3T3-L1 (<b>e</b>,<b>f</b>), Caco-2 (<b>g</b>,<b>h</b>), HEK 293 (<b>i</b>,<b>j</b>), and RAW264.7 (<b>k</b>,<b>l</b>) cells.</p>
Full article ">Figure 8
<p>Results of NO production inhibition (%relative to LPS-treated control) for methanolic extracts and volatile oils in RAW 264.7 cells with an IC<sub>20</sub> or non-toxic concentration. The bar graph illustrates the LPS-untreated group (black), the LPS-treated group (grey), the LPS+methanolic extract of AA, PA, AS, PS-treated group (green), and the LPS+volatile oil of AA, PA, AS, PS-treated group (yellow), and the LPS+myristicin-treated group (red). Each value representes as mean ± SD of three independent experiments. * <span class="html-italic">p</span> &lt; 0.033, ** <span class="html-italic">p</span> &lt; 0.002 compared to control group, ns means not statistically significant between the groups.</p>
Full article ">
14 pages, 1291 KiB  
Article
Effect of Simmering Technology on Components and Activity of Myristica fragrans Houtt.
by Jiaqi Sun, Fuyin Zhao, Zhenlei Wang, Weina Zhang, Xiudong Yang, Hongli Zhou and Peng Wan
Molecules 2023, 28(22), 7627; https://doi.org/10.3390/molecules28227627 - 16 Nov 2023
Cited by 2 | Viewed by 1316
Abstract
This study aims to optimize the processing of Myristica fragrans Houtt. by talcum powder simmering using single-factor and orthogonal experimental methods, and the overall desirability values of dehydrodiisoeugenol and essential oils content were selected as indicators of the process. The new process reduced [...] Read more.
This study aims to optimize the processing of Myristica fragrans Houtt. by talcum powder simmering using single-factor and orthogonal experimental methods, and the overall desirability values of dehydrodiisoeugenol and essential oils content were selected as indicators of the process. The new process reduced the total content of the three toxic components, namely myristicin, safrole and elemicin, from 1.91% to 1.16% before and after processing, indicating that the toxic components were reduced by 39%. The IC50 of the essential oils before and after processing were 1.002 ± 0.05 and 0.233 ± 0.05 mg/mL for DPPH scavenging activity and 0.132 ± 0.04 and 0.057 ± 0.05 mg/mL for ABTS scavenging activity, respectively. And the absorbance of the antioxidant activity against Ferric reducing power ranged from 0.213 to 0.709 and from 0.225 to 0.755, respectively. The minimum inhibitory concentration for Staphylococcus aureus, Bacillus pumilus and Escherichia coli were all lower after processing than before. The antioxidant activity and antibacterial activity of the essential oils after processing were better than before. The results of the survival of zebrafish embryos at different concentrations of essential oils at 0–168 h post fertilisation were higher after processing than before. These findings suggest that processing plays the role of reducing toxicity and increasing beneficial effects. They provide a scientific basis not only for the processing of M. fragrans, but also for the processing of other foods. Full article
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>SEM images of the <span class="html-italic">M. fragrans</span> powder before and after processing. (<b>a</b>) Images of <span class="html-italic">M. fragrans</span> powder at 1000 magnification. (<b>b</b>) Images of <span class="html-italic">M. fragrans</span> powder at 3000 magnification. (<b>c</b>) Images of <span class="html-italic">M. fragrans</span> powder after processing at 1000 magnification. (<b>d</b>) Images of the <span class="html-italic">M. fragrans</span> powder after processing at 3000 magnification.</p>
Full article ">Figure 2
<p>IR spectra of OMB and OMA.</p>
Full article ">Figure 3
<p>(<b>A</b>–<b>C</b>) represent the antioxidant capacities of OMB and OMA against DPPH radicals, ABTS·<sup>+</sup> and Ferric reducing antioxidant power (FRAP), respectively. The significance of the difference between the two sets of data is represented as ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001, respectively.</p>
Full article ">
13 pages, 1291 KiB  
Article
Rapid Determination of Nutmeg Shell Content in Ground Nutmeg Using FT-NIR Spectroscopy and Machine Learning
by Alissa Drees, Bernadette Bockmayr, Michael Bockmayr and Markus Fischer
Foods 2023, 12(15), 2939; https://doi.org/10.3390/foods12152939 - 2 Aug 2023
Cited by 2 | Viewed by 2303
Abstract
Nutmeg is a popular spice often used in ground form, which makes it highly susceptible to food fraud. Therefore, the aim of the present study was to detect adulteration of ground nutmeg with nutmeg shell via Fourier transform near-infrared (FT-NIR) spectroscopy. For this [...] Read more.
Nutmeg is a popular spice often used in ground form, which makes it highly susceptible to food fraud. Therefore, the aim of the present study was to detect adulteration of ground nutmeg with nutmeg shell via Fourier transform near-infrared (FT-NIR) spectroscopy. For this purpose, 36 authentic nutmeg samples and 10 nutmeg shell samples were analyzed pure and in mixtures with up to 50% shell content. The spectra plot as well as a principal component analysis showed a clear separation trend as a function of shell content. A support vector machine regression used for shell content prediction achieved an R2 of 0.944 in the range of 0–10%. The limit of detection of the prediction model was estimated to be 1.5% nutmeg shell. Based on random sub-sampling, the likelihood was found to be 2% that a pure nutmeg sample is predicted with a nutmeg shell content of >1%. The results confirm the suitability of FT-NIR spectroscopy for rapid detection and quantitation of the shell content in ground nutmeg. Full article
(This article belongs to the Special Issue Analytical Methods in Detecting Food Fraud and Food Authenticity)
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>Overview of authentic nutmeg and nutmeg shell samples; (<b>A</b>) NIR spectra (MSC-corrected); (<b>B</b>) PCA scores plot after MSC correction including first and second principal component.</p>
Full article ">Figure 2
<p>(<b>A</b>) Average spectra of nutmeg, nutmeg shell, and different mixtures of nutmeg with 10%, 20%, 30%, 40%, or 50% nutmeg shell proportion after MSC correction, bold type: spectrum of pure nutmeg and pure shell.; (<b>B</b>) PCA scores plot of nutmeg, nutmeg shell samples, and different mixtures of nutmeg with 1–50% nutmeg shell content (variances based on pure nutmeg and shell samples).</p>
Full article ">Figure 3
<p>(<b>A</b>) Scatter plot of predicted vs. true nutmeg shell percentage in nutmeg samples based on 100-fold repeated SVM prediction; (<b>B</b>) Histogram showing the frequency of predicted shell percentages in pure nutmeg samples taken from the scatter plot (<b>A</b>); (<b>C</b>) Scatter plot of predicted vs. true shell percentage in nutmeg samples based on the average of 100-fold repeated SVM prediction; (<b>D</b>) Histogram showing the frequency of predicted shell percentage in pure nutmeg samples taken from the scatter plot (<b>C</b>). The orange dotted lines of both histograms visualize the standard deviation (σ).</p>
Full article ">Figure 4
<p>Sankey plot showing the relationship between true (<b>left</b>) and predicted shell percentage (<b>right</b>) based on the average predictions shown in <a href="#foods-12-02939-f003" class="html-fig">Figure 3</a>C,D.</p>
Full article ">
15 pages, 4295 KiB  
Article
Widely Targeted Volatilomics and Metabolomics Analysis Reveal the Metabolic Composition and Diversity of Zingiberaceae Plants
by Youjin Zhang, Rongxiu Su, Honglun Yuan, Haihong Zhou, Yiding Jiangfang, Xianqing Liu and Jie Luo
Metabolites 2023, 13(6), 700; https://doi.org/10.3390/metabo13060700 - 27 May 2023
Cited by 10 | Viewed by 2782
Abstract
Zingiberaceae plants are widely used in the food and pharmaceutical industries; however, research on the chemical composition and interspecific differences in the metabolome and volatilome of Zingiberaceae plants is still limited. In this study, seven species of Zingiberaceae plants were selected, including Curcuma [...] Read more.
Zingiberaceae plants are widely used in the food and pharmaceutical industries; however, research on the chemical composition and interspecific differences in the metabolome and volatilome of Zingiberaceae plants is still limited. In this study, seven species of Zingiberaceae plants were selected, including Curcuma longa L., Zingiber officinale Rosc., Alpinia officinarum Hance, Alpinia tonkinensis Gagnep, Amomum tsaoko Crevost et Lemarie, Alpinia hainanensis K. Schum. and Amomum villosum Lour. Myristica fragrans Houtt. was also selected due to its flavor being similar to that of the Zingiberaceae plant. The metabolome and volatilome of selected plants were profiled by widely targeted approaches; 542 volatiles and 738 non-volatile metabolites were detected, and β-myrcene, α-phellandrene and α-cadinene were detected in all the selected plants, while chamigren, thymol, perilla, acetocinnamone and cis-α-bisabolene were exclusively detected in certain Zingiberaceae plants. Differential analysis showed that some terpenoids, such as cadalene, cadalene-1,3,5-triene, cadalene-1,3,8-triene and (E)-β-farnesene, and some lipids, including palmitic acid, linoleic acid and oleic acid were amongst the most varied compounds in Zingiberaceae plants. In conclusion, this study provided comprehensive metabolome and volatilome profiles for Zingiberaceae plants and revealed the metabolic differences between these plants. The results of this study could be used as a guide for the nutrition and flavor improvement of Zingiberaceae plants. Full article
(This article belongs to the Section Plant Metabolism)
Show Figures

Figure 1

Figure 1
<p>Phylogenetic tree analysis of seven species of Zingiberaceae plants.</p>
Full article ">Figure 2
<p>Classification of metabolome and volatilome data of Zingiberaceae plants. (<b>A</b>) Volatilome data. (<b>B</b>) Metabolome data.</p>
Full article ">Figure 3
<p>Venn diagram of metabolome and volatilome data of Zingiberaceae plants. (<b>A</b>) Volatilome data. (<b>B</b>) Metabolome data. Red number indicates the number of exclusive metabolites.</p>
Full article ">Figure 4
<p>Principal component analysis (PCA) of metabolome and volatilome data of Zingiberaceae plants. (<b>A</b>) PCA plot of volatilome data. (<b>B</b>) Loading score of volatiles. (<b>C</b>) PCA plot of metabolome data. (<b>D</b>) Loading score of metabolites.</p>
Full article ">Figure 5
<p>Heatmap obtained after hierarchical cluster analysis of amino acids, lipids and vitamins in Zingiberaceae plants. Two biological replicates were used for metabolomics analysis, expressed as 1 and 2, respectively. The relative intensity of metabolite was log2-transformed.</p>
Full article ">Figure 6
<p>Heatmap obtained after hierarchical cluster analysis of monoterpenes and sesquiterpenes in Zingiberaceae plants. (<b>A</b>) Heatmap of monoterpenes. (<b>B</b>) Heatmap of sesquiterpenes. Two biological replicates were used for volatilomics analysis, expressed as 1 and 2, respectively. The relative intensity of metabolite was log<sub>2</sub>-transformed.</p>
Full article ">Figure 7
<p>The synthetic pathway of geraniol and geranial. The relative intensity of metabolite was log<sub>2</sub>-transformed.</p>
Full article ">
18 pages, 3453 KiB  
Article
Myristica fragrans Extract Inhibits Platelet Desialylation and Activation to Ameliorate Sepsis-Associated Thrombocytopenia in a Murine CLP-Induced Sepsis Model
by Seong-Hun Jeong, Ji-Young Park, Young Bae Ryu, Woo Sik Kim, In-Chul Lee, Ju-Hong Kim, Dohoon Kim, Ji-Hye Ha, Ba-Wool Lee, Jiyoung Nam, Kyoung-Oh Cho and Hyung-Jun Kwon
Int. J. Mol. Sci. 2023, 24(10), 8863; https://doi.org/10.3390/ijms24108863 - 16 May 2023
Cited by 3 | Viewed by 2387
Abstract
Sepsis, characterized by an uncontrolled host inflammatory response to infections, remains a leading cause of death in critically ill patients worldwide. Sepsis-associated thrombocytopenia (SAT), a common disease in patients with sepsis, is an indicator of disease severity. Therefore, alleviating SAT is an important [...] Read more.
Sepsis, characterized by an uncontrolled host inflammatory response to infections, remains a leading cause of death in critically ill patients worldwide. Sepsis-associated thrombocytopenia (SAT), a common disease in patients with sepsis, is an indicator of disease severity. Therefore, alleviating SAT is an important aspect of sepsis treatment; however, platelet transfusion is the only available treatment strategy for SAT. The pathogenesis of SAT involves increased platelet desialylation and activation. In this study, we investigated the effects of Myristica fragrans ethanol extract (MF) on sepsis and SAT. Desialylation and activation of platelets treated with sialidase and adenosine diphosphate (platelet agonist) were assessed using flow cytometry. The extract inhibited platelet desialylation and activation via inhibiting bacterial sialidase activity in washed platelets. Moreover, MF improved survival and reduced organ damage and inflammation in a mouse model of cecal ligation and puncture (CLP)-induced sepsis. It also prevented platelet desialylation and activation via inhibiting circulating sialidase activity, while maintaining platelet count. Inhibition of platelet desialylation reduces hepatic Ashwell–Morell receptor-mediated platelet clearance, thereby reducing hepatic JAK2/STAT3 phosphorylation and thrombopoietin mRNA expression. This study lays a foundation for the development of plant-derived therapeutics for sepsis and SAT and provides insights into sialidase-inhibition-based sepsis treatment strategies. Full article
(This article belongs to the Special Issue Sepsis: Molecular Research)
Show Figures

Figure 1

Figure 1
<p>RCA-I, ECA, SNA, and MAL-II binding and inhibitory effects of MF on platelet desialylation in washed platelets exposed to sialidase. Washed platelets were subjected to treatment without sialidase (−Sia) or with varying concentrations of sialidase (+Sia; 1, 2.5, 5, and 10 mU) for 30 min at 37 °C. Following the treatment, the binding of platelets to (<b>a</b>) RCA-I, (<b>b</b>) ECA, (<b>c</b>) SNA, and (<b>d</b>) MAL-II was confirmed using flow cytometry (FACS). (<b>e</b>) Washed platelets were treated with sialidase and MF or OS, and RCA-I binding was measured. Representative FACS data from one of three separate experiments are shown. The bar graphs presented indicate mean ± standard deviation (SD) of three samples. All experiments were repeated thrice, and similar outcomes were observed. ** <span class="html-italic">p</span> &lt; 0.01 compared with the Sia 5 mU group. RCA-I, <span class="html-italic">Ricinus communis</span>-1 agglutinin lectin; ECA, <span class="html-italic">Erythrina crista-galli</span> lectin; SNA, <span class="html-italic">Sambucus nigra</span> lectin; MAL-II, <span class="html-italic">Maackia amurensis</span> lectin II; MFI, mean fluorescence intensity; MF, <span class="html-italic">Myristica fragrans</span>; OS, oseltamivir phosphate; NC, negative control.</p>
Full article ">Figure 2
<p>Effects of MF on the suppression of sialidase-mediated platelet hyper-reactivity and activation in washed platelets. (<b>a</b>) CD62P expression in washed platelets was measured after stimulation with 5 mU sialidase and 125 μM ADP in the presence of MF or OS at different concentrations. Representative FACS data from one of three separate experiments are shown. (<b>b</b>) Inhibition of CD62P expression using OS in Sia + ADP-stimulated washed platelets. (<b>c</b>) Inhibition of CD62P expression using MF in Sia + ADP-stimulated washed platelets. The bar graphs presented indicate mean ± standard deviation (SD) of three samples. All experiments were repeated thrice, and similar outcomes were observed. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 compared with the Sia + ADP group. ADP, adenosine diphosphate; MF, <span class="html-italic">Myristica fragrans</span>; OS, oseltamivir phosphate; Sia, sialidase.</p>
Full article ">Figure 3
<p>Effects of MF on the survival of and inflammation in cecal ligation and puncture (CLP)-induced septic mice. (<b>a</b>) MF (200 mg/kg) and OS (20 mg/kg) were administered orally for 3 days before the CLP procedure, and survival was monitored every 8 h daily for up to 4 days after CLP. (<b>b</b>,<b>c</b>) Serum TNF-α and IL-6 levels in each group were measured using ELISA. Values are presented as mean ± SD (n = 5 mice). * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 compared with the CLP group. MF, <span class="html-italic">Myristica fragrans</span>; OS, oseltamivir phosphate.</p>
Full article ">Figure 4
<p>Effect of MF on platelet desialylation and thrombocytopenia in cecal ligation and puncture (CLP)-induced septic mice. (<b>a</b>) Circulating platelet count. (<b>b</b>) Sialidase activity was measured in the serum of each group of mice. (<b>c</b>) Platelets isolated and washed from mice in each group were stained for CD41, ECA, and RCA-I, and platelet desialylation was analyzed using flow cytometry. (<b>d</b>) Bar graphs for the percentage of ECA binding and MFI on platelet surface in each group. (<b>e</b>) Bar graphs for the percentage of RCA-I binding and MFI on platelet surface in each group. The data are presented as mean ± standard deviation (SD) with a sample size of five mice per group. Representative FACS data from one of three separate experiments are shown. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 compared with the CLP group. MF, <span class="html-italic">Myristica fragrans</span>; OS, oseltamivir phosphate; ECA, <span class="html-italic">Erythrina crista-galli</span> lectin; RCA-I, <span class="html-italic">Ricinus communis</span>-1 agglutinin lectin.</p>
Full article ">Figure 5
<p>Effect of MF on the suppression of platelet activation in mice with CLP-induced sepsis. (<b>a</b>) Platelet activation was determined based on CD41 and CD62P (P-selectin) expression. (<b>b</b>) Bar graphs for the percentage of CD62P-positive platelets in each group. Percentages of CD62P-positive platelets are presented as mean ± SD (n = 5 mice). Representative FACS data from one of three separate experiments are shown. ** <span class="html-italic">p</span> &lt; 0.01 compared with the CLP group. MF, <span class="html-italic">Myristica fragrans</span>; OS, oseltamivir phosphate.</p>
Full article ">Figure 6
<p>Effects of MF on organ damage and fibrin deposition in CLP-induced septic mice. (<b>a</b>) Histopathological analysis of lung and liver tissues was performed using H&amp;E and immunohistochemical staining to determine inflammation and fibrin deposition. Representative sections are shown at ×200 (lung section) and ×400 (liver section) magnifications; scale bar: 60 and 30 μm, respectively. Representative images from each group were selected (n = 5). (<b>b</b>) Bar graphs for the lung injury scores of each group. Lung damage was assessed via scoring necrosis, inflammatory cell infiltration, hemorrhage, and congestion. (<b>c</b>) Bar graphs for liver injury scores of each group. Liver damage was assessed via scoring vacuolization, swollen hepatocytes, hepatocellular necrosis, and inflammatory cell infiltration. (<b>d</b>) Bar graphs for lung fibrin deposition scores. (<b>e</b>) Bar graphs for liver fibrin deposition scores. Semi-quantitative analysis of immunohistochemical images using ImageJ software was performed. The data are presented as mean ± standard deviation (SD) with a sample size of five mice. ** <span class="html-italic">p</span> &lt; 0.01 compared with the CLP group. MF, <span class="html-italic">Myristica fragrans</span>; OS, oseltamivir phosphate.</p>
Full article ">Figure 7
<p>Effects of MF on hepatic JAK2/STAT3 signaling and TPO expression in CLP-induced septic mice. (<b>a</b>) Phosphorylated JAK2 and STAT3 levels in the liver tissue were analyzed using Western blotting (<b>b</b>) Western blot signals of phosphorylated JAK2 and STAT3 were normalized to those of total JAK2 and STAT3. Relative expression of phosphorylated JAK2 and STAT3 was quantified based on three independent experiments. (<b>c</b>) The expression of liver TPO mRNA was determined using qPCR. (<b>d</b>) The serum TPO level was quantified using ELISA. The data are presented as mean ± standard deviation (SD) with a sample size of five mice. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 compared with the CLP group. MF, <span class="html-italic">Myristica fragrans</span>; OS, oseltamivir phosphate; JAK2, Janus kinase 2; STAT3, signal transducer and activator of transcription 3; TPO, thrombopoietin.</p>
Full article ">
16 pages, 755 KiB  
Article
Essential Oils and Sustainability: In Vitro Bioactivity Screening of Myristica fragrans Houtt. Post-Distillation By-Products
by Adriana Trifan, Gokhan Zengin, Izabela Korona-Glowniak, Krystyna Skalicka-Woźniak and Simon Vlad Luca
Plants 2023, 12(9), 1741; https://doi.org/10.3390/plants12091741 - 23 Apr 2023
Cited by 13 | Viewed by 2797
Abstract
The essential oil of Myristica fragrans Hutt. (nutmeg) is an important commodity used as a flavoring agent in the food, pharmaceutical, and cosmetic fields. Hydrodistillation is chiefly employed at the industrial scale for nutmeg essential oil isolation, but such a technique generates large [...] Read more.
The essential oil of Myristica fragrans Hutt. (nutmeg) is an important commodity used as a flavoring agent in the food, pharmaceutical, and cosmetic fields. Hydrodistillation is chiefly employed at the industrial scale for nutmeg essential oil isolation, but such a technique generates large quantities of post-distillation by-products (e.g., spent plant material and residual distillation water). Therefore, our work aimed to propose a novel strategy for the valorization of nutmeg wastes, with beneficial economic and ecological advantages. Thus, the current study assessed the phytochemical (GC-MS, LC-HRMS/MS) and biological (antioxidant, enzyme inhibitory, antimicrobial) profile of nutmeg crude materials (essential oil and total extract) and post-distillation by-products (residual water and spent material extract). Identified in these were 43 volatile compounds, with sabinene (21.71%), α-pinene (15.81%), myristicin (13.39%), and β-pinene (12.70%) as the main constituents. LC-HRMS/MS analysis of the nutmeg extracts noted fifteen metabolites (e.g., organic acids, flavonoids, phenolic acids, lignans, and diarylnonanoids). Among the investigated nutmeg samples, the spent material extract was highlighted as an important source of bioactive compounds, with a total phenolic and flavonoid content of 63.31 ± 0.72 mg GAE/g and 8.31 ± 0.06 mg RE/g, respectively. Moreover, it showed prominent radical-scavenging and metal-reducing properties and significantly inhibited butyrylcholinesterase (4.78 ± 0.03 mg GALAE/g). Further, the spent material extract displayed strong antimicrobial effects against Streptococcus pneumoniae, Micrococcus luteus, and Bacillus cereus (minimum inhibitory concentrations of 62.5 mg/L). Overall, our study brings evidence on the health-promoting (antioxidant, anti-enzymatic, antimicrobial) potential of nutmeg post-distillation by-products with future reference to their valorization in the pharmaceutical, cosmeceutical, and food industries. Full article
Show Figures

Figure 1

Figure 1
<p>Chemical structures of lignans and diarylnonanoids tentatively identified by LC-HRMS/MS in nutmeg extracts.</p>
Full article ">Figure 2
<p>Pearson’s correlation between total phenolic (TPC)/total flavonoids contents (TFC) and antioxidant/enzyme inhibitory assays.</p>
Full article ">
30 pages, 5645 KiB  
Article
Screening for Neuroprotective and Rapid Antidepressant-like Effects of 20 Essential Oils
by Khoa Nguyen Tran, Nhi Phuc Khanh Nguyen, Ly Thi Huong Nguyen, Heung-Mook Shin and In-Jun Yang
Biomedicines 2023, 11(5), 1248; https://doi.org/10.3390/biomedicines11051248 - 23 Apr 2023
Cited by 20 | Viewed by 5274
Abstract
Depression is a serious psychiatric disorder with high prevalence, and the delayed onset of antidepressant effects remains a limitation in the treatment of depression. This study aimed to screen essential oils that have the potential for rapid-acting antidepressant development. PC12 and BV2 cells [...] Read more.
Depression is a serious psychiatric disorder with high prevalence, and the delayed onset of antidepressant effects remains a limitation in the treatment of depression. This study aimed to screen essential oils that have the potential for rapid-acting antidepressant development. PC12 and BV2 cells were used to identify essential oils with neuroprotective effects at doses of 0.1 and 1 µg/mL. The resulting candidates were treated intranasally (25 mg/kg) to ICR mice, followed by a tail suspension test (TST) and an elevated plus maze (EPM) after 30 min. In each effective essential oil, five main compounds were computationally analyzed, targeting glutamate receptor subunits. As a result, 19 essential oils significantly abolished corticosterone (CORT)-induced cell death and lactate dehydrogenase (LDH) leakage, and 13 reduced lipopolysaccharide (LPS)-induced tumor necrosis factor alpha (TNF-α) and interleukin 6 (IL-6). From in vivo experiments, six essential oils decreased the immobility time of mice in the TST, in which Chrysanthemum morifolium Ramat. and Myristica fragrans Houtt. also increased time and entries into the open arms of the EPM. Four compounds including atractylon, α-curcumene, α-farnesene, and selina-4(14),7(11)-dien-8-one had an affinity toward GluN1, GluN2B, and Glu2A receptor subunits surpassed that of the reference compound ketamine. Overall, Atractylodes lancea (Thunb.) DC and Chrysanthemum morifolium Ramat essential oils are worthy of further research for fast-acting antidepressants through interactions with glutamate receptors, and their main compounds (atractylon, α-curcumene, α-farnesene, and selina-4(14),7(11)-dien-8-one) are predicted to underlie the fast-acting effect. Full article
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>Effects of (<b>A</b>) CORT and (<b>B</b>) essential oils on the viability of PC12 cells. Results are presented as means ± SDs (<span class="html-italic">n</span> = 3 per experiment). * <span class="html-italic">p</span> &lt; 0.05 vs. CON.</p>
Full article ">Figure 1 Cont.
<p>Effects of (<b>A</b>) CORT and (<b>B</b>) essential oils on the viability of PC12 cells. Results are presented as means ± SDs (<span class="html-italic">n</span> = 3 per experiment). * <span class="html-italic">p</span> &lt; 0.05 vs. CON.</p>
Full article ">Figure 2
<p>Effects of essential oils on CORT-induced neurotoxicity in PC12 cells. (<b>A</b>) Effects of essential oils on the cell viability in CORT-stimulated PC12 cells. (<b>B</b>) Effects of essential oils on the LDH release in CORT-stimulated PC12 cells. Results are presented as means ± SDs (<span class="html-italic">n</span> = 3 per experiment). * <span class="html-italic">p</span> &lt; 0.05 vs. CON, # <span class="html-italic">p</span> &lt; 0.05 vs. CORT-treated cells.</p>
Full article ">Figure 2 Cont.
<p>Effects of essential oils on CORT-induced neurotoxicity in PC12 cells. (<b>A</b>) Effects of essential oils on the cell viability in CORT-stimulated PC12 cells. (<b>B</b>) Effects of essential oils on the LDH release in CORT-stimulated PC12 cells. Results are presented as means ± SDs (<span class="html-italic">n</span> = 3 per experiment). * <span class="html-italic">p</span> &lt; 0.05 vs. CON, # <span class="html-italic">p</span> &lt; 0.05 vs. CORT-treated cells.</p>
Full article ">Figure 3
<p>Effects of essential oils on the viability of BV2 cells. Results are presented as means ± SDs (<span class="html-italic">n</span> = 3 per experiment). * <span class="html-italic">p</span> &lt; 0.05 vs. CON.</p>
Full article ">Figure 4
<p>Effects of essential oils on LPS-induced neuroinflammation in BV2 cells. (<b>A</b>) TNF-α levels (pg/mL). (<b>B</b>) IL-6 levels (pg/mL). Results are presented as means ± SDs (<span class="html-italic">n</span> = 3 per experiment). * <span class="html-italic">p</span> &lt; 0.05 vs. CON, # <span class="html-italic">p</span> &lt; 0.05 vs. LPS-treated cells.</p>
Full article ">Figure 4 Cont.
<p>Effects of essential oils on LPS-induced neuroinflammation in BV2 cells. (<b>A</b>) TNF-α levels (pg/mL). (<b>B</b>) IL-6 levels (pg/mL). Results are presented as means ± SDs (<span class="html-italic">n</span> = 3 per experiment). * <span class="html-italic">p</span> &lt; 0.05 vs. CON, # <span class="html-italic">p</span> &lt; 0.05 vs. LPS-treated cells.</p>
Full article ">Figure 5
<p>Effects of essential oils on the behavioral changes of mice in TST test. The immobility time in TST was recorded. Each black triangle indicates the value of each mouse subject in groups. Results are presented as means percentage relative to control ± SDs (<span class="html-italic">n</span> = 4 mice per group). * <span class="html-italic">p</span> &lt; 0.05 vs. CON.</p>
Full article ">Figure 6
<p>Effects of essential oils on the behavioral changes of mice in EPM test. The (<b>A</b>) number of entries, (<b>B</b>) time, and (<b>C</b>) distance in open arms were recorded. Each black triangle indicates the value of each mouse subject in groups. Results are presented as means percentage relative to control ± SDs (<span class="html-italic">n</span> = 4 mice per group). * <span class="html-italic">p</span> &lt; 0.05 vs. CON.</p>
Full article ">Figure 6 Cont.
<p>Effects of essential oils on the behavioral changes of mice in EPM test. The (<b>A</b>) number of entries, (<b>B</b>) time, and (<b>C</b>) distance in open arms were recorded. Each black triangle indicates the value of each mouse subject in groups. Results are presented as means percentage relative to control ± SDs (<span class="html-italic">n</span> = 4 mice per group). * <span class="html-italic">p</span> &lt; 0.05 vs. CON.</p>
Full article ">Figure 7
<p>Superimposed zoomed-in image of native ligand and redocked native ligand in the active site of (<b>A</b>) GluN1, (<b>B</b>) GluN2B, and (<b>C</b>) GluA2 (native ligand: gray color, redocked ligand: yellow color).</p>
Full article ">Figure 8
<p>2D interactions between (<b>A</b>) ketamine, (<b>B</b>) ifenprodil, (<b>C</b>) TAK-653, (<b>D</b>) atractylon, (<b>E</b>) α-curcumene, (<b>F</b>) α-farnesene, and (<b>G</b>) selina-4(14),7(11)-dien-8-one with GluN1 protein.</p>
Full article ">Figure 8 Cont.
<p>2D interactions between (<b>A</b>) ketamine, (<b>B</b>) ifenprodil, (<b>C</b>) TAK-653, (<b>D</b>) atractylon, (<b>E</b>) α-curcumene, (<b>F</b>) α-farnesene, and (<b>G</b>) selina-4(14),7(11)-dien-8-one with GluN1 protein.</p>
Full article ">Figure 9
<p>2D interactions between (<b>A</b>) ketamine, (<b>B</b>) ifenprodil, (<b>C</b>) TAK-653, (<b>D</b>) atractylon, (<b>E</b>) α-curcumene, (<b>F</b>) α-farnesene, and (<b>G</b>) selina-4(14),7(11)-dien-8-one with GluN2B protein.</p>
Full article ">Figure 9 Cont.
<p>2D interactions between (<b>A</b>) ketamine, (<b>B</b>) ifenprodil, (<b>C</b>) TAK-653, (<b>D</b>) atractylon, (<b>E</b>) α-curcumene, (<b>F</b>) α-farnesene, and (<b>G</b>) selina-4(14),7(11)-dien-8-one with GluN2B protein.</p>
Full article ">Figure 10
<p>2D interactions between (<b>A</b>) ketamine, (<b>B</b>) ifenprodil, (<b>C</b>) TAK-653, (<b>D</b>) atractylon, (<b>E</b>) α-curcumene, (<b>F</b>) α-farnesene, and (<b>G</b>) selina-4(14),7(11)-dien-8-one with GluA2 protein.</p>
Full article ">Figure 10 Cont.
<p>2D interactions between (<b>A</b>) ketamine, (<b>B</b>) ifenprodil, (<b>C</b>) TAK-653, (<b>D</b>) atractylon, (<b>E</b>) α-curcumene, (<b>F</b>) α-farnesene, and (<b>G</b>) selina-4(14),7(11)-dien-8-one with GluA2 protein.</p>
Full article ">
Back to TopTop