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15 pages, 1638 KiB  
Review
The Role of AFB1, OTA, TCNs, and Patulin in Forensic Sciences: Applications in Autopsy, Criminal Investigations, and Public Health Prevention
by Matteo Antonio Sacco, Saverio Gualtieri, Alessandro Pasquale Tarallo, Maria Cristina Verrina, Angela Carbone, Wandamaria Mazzuca, Santo Gratteri and Isabella Aquila
Toxins 2024, 16(12), 514; https://doi.org/10.3390/toxins16120514 - 28 Nov 2024
Viewed by 230
Abstract
Mycotoxins, specifically aflatoxin B1 (AFB1), ochratoxin A (OTA), trichothecenes (TCNs), and patulin, are a group of secondary metabolites that can contaminate food, leading to severe health implications for humans. Their detection and analysis within forensic toxicology are crucial, particularly as they can be [...] Read more.
Mycotoxins, specifically aflatoxin B1 (AFB1), ochratoxin A (OTA), trichothecenes (TCNs), and patulin, are a group of secondary metabolites that can contaminate food, leading to severe health implications for humans. Their detection and analysis within forensic toxicology are crucial, particularly as they can be implicated in cases of poisoning, foodborne illnesses, or lethal chronic exposure. However, little is known about the application that mycotoxins could have in forensic investigations and especially about the possibility of extracting and quantifying these molecules on tissues or post-mortem fluids collected at autopsy. We propose a review of the scientific literature on autopsy case studies in which the presence of mycotoxins on cadavers in cases of acute and chronic exposure has been investigated and identified. This review demonstrates how the analysis of mycotoxins on cadavers could be fundamental in the study of mushroom poisonings or even in the investigation of the chronic effects of mycotoxins on the human organism, by virtue of the known carcinogenic and mutagenic effects of many of them. This paper aims to explore the multifaceted role of mycotoxins within forensic sciences, focusing on their detection methods, implications in criminal contexts, and their potential as forensic evidence, thereby underscoring the critical importance they could assume in post-mortem toxicology, public health prevention, and forensic investigations. Full article
(This article belongs to the Section Mycotoxins)
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<p>Effects due to poisoning in case of aflatoxicosis (created with <a href="http://Biorender.com" target="_blank">Biorender.com</a>, accessed on 1 October 2024).</p>
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<p>Protocol for post-mortem investigations in suspects of mycotoxin related death (created with <a href="http://Biorender.com" target="_blank">Biorender.com</a>, accessed on 1 October 2024).</p>
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<p>Medico-legal applications of mycotoxins (created with <a href="http://Biorender.com" target="_blank">Biorender.com</a>, accessed on 13 November 2024).</p>
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13 pages, 2629 KiB  
Article
Exposure Assessment of Essential and Potentially Toxic Elements (PTEs) from Chia Seeds
by Dailos González-Weller, Elena Bethencourt-Barbuzano, Katarzyna Siedzik, Soraya Paz-Montelongo, Ángel J. Gutiérrez-Fernández, Arturo Hardisson, Samuel Alejandro-Vega, Juan R. Jáudenes-Marrero and Carmen Rubio
J. Xenobiot. 2024, 14(4), 1836-1848; https://doi.org/10.3390/jox14040098 - 28 Nov 2024
Viewed by 282
Abstract
The increasing consumption of chia seeds is followed by a growing interest in their nutritional and toxicological characterization. To assess the characterization of the essential and PTEs of this novel food, 20 samples of conventional and organic chia seeds available on the European [...] Read more.
The increasing consumption of chia seeds is followed by a growing interest in their nutritional and toxicological characterization. To assess the characterization of the essential and PTEs of this novel food, 20 samples of conventional and organic chia seeds available on the European market were analyzed using ICP-OES. Then, the dietary exposure to these elements was assessed. An exhaustive investigation into the metal content of this food serves to elucidate the paucity of existing knowledge. The results show that the levels of essential elements are similar in both types of production, while the levels of PTEs are higher in the organic samples. The exposure assessment indicates that Mn contributes the most among the essential elements, followed by Cu in women. Exposure to PTEs through doses of 50 g/day of chia seeds analyzed would hardly pose short-term health risks as the contributions are below 10%, except for Sr, although they could produce a long-term toxicological risk. To promote safety in chia seed consumption, it is recommended to encourage responsible and moderate consumption, continue monitoring PTE levels in this novel food, and establish concentration limits for PTEs in future European regulations. Full article
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<p>Box plot of the Mo concentrations detected in the organic (orange) and conventional (blue) chia seeds.</p>
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<p>Box plot of the Mn and Cu concentrations detected in the organic (orange) and conventional (blue) chia seeds.</p>
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<p>Box plot of the Mg concentrations detected in the organic (orange) and conventional (blue) chia seeds.</p>
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13 pages, 2157 KiB  
Article
Analysis of the Energy Potential of Waste Biomass Generated from Fruit Tree Seedling Production
by Natalia Matłok, Grzegorz Zaguła, Józef Gorzelany and Maciej Balawejder
Energies 2024, 17(23), 5964; https://doi.org/10.3390/en17235964 - 27 Nov 2024
Viewed by 290
Abstract
The depletion of conventional fuels and the state of the natural environment have influenced global policy, dictating a new direction for development and approaches to the use of renewable resources. One such resource is woody biomass, which can be used for energy purposes. [...] Read more.
The depletion of conventional fuels and the state of the natural environment have influenced global policy, dictating a new direction for development and approaches to the use of renewable resources. One such resource is woody biomass, which can be used for energy purposes. A type of raw material with an unrecognized potential for utilization is waste biomass from the production of fruit tree seedlings. In this study, thirteen popular species of rootstock produced in Poland were collected and subjected to comprehensive analyses. After determining the calorific value of the collected wood waste, a comprehensive analysis of their suitability for energy purposes was conducted. The highest calorific value of 19.51 MJkg−1 was recorded for waste biomass obtained from Mahaleb Cherry rootstocks in the first year of research, compared to P14 with 17.96 MJkg−1. The content of other elements was also advantageous for Mahaleb Cherry. Considering the relatively large production of this type of waste biomass, it can be concluded that it has great energy potential and can largely meet energy needs in regions where fruit tree seedlings are mass-produced. Implementing the use of such raw materials in energy production will result in a reduction of anthropogenic impacts on the environment by decreasing the demand for standard energy resources. Full article
(This article belongs to the Section B: Energy and Environment)
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<p>Scheme for obtaining waste biomass from the production of one-year-old fruit tree seedlings.</p>
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<p>Mean humidity (Wa) (<b>A</b>), ash (<b>B</b>) and volatile substances (<b>C</b>) in waste biomass (d.m.) from various species of fruit tree rootstocks. Mean values ± standard deviation. Identical superscripts denote no significant (<span class="html-italic">p</span> &lt; 0.05) differences between the experimental objects according to the post-hoc Tukey HSD test.</p>
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<p>Mean content of carbon (<b>A</b>), hydrogen (<b>B</b>) and nitrogen (<b>C</b>) in waste biomass from various species of fruit tree rootstocks. Mean values ± standard deviation. Identical superscripts denote no significant (<span class="html-italic">p</span> &lt; 0.05) differences between the experimental objects according to the post-hoc Tukey HSD test.</p>
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<p>Mean percentage grams of chlorine (Cl) (<b>A</b>) and sulfur (S) (<b>B</b>) in the dry mass of various types of waste biomass from nursery production. Mean values ± standard deviation. Identical superscripts denote no significant (<span class="html-italic">p</span> &lt; 0.05) differences between the experimental objects according to the post-hoc Tukey HSD test.</p>
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<p>Ratio of mean grams S:Cl in dry waste mass after harvesting of selected species of fruit tree rootstocks. Mean values ± standard deviation.</p>
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13 pages, 1266 KiB  
Article
The Impact of Complementary Feeding on Fecal Microbiota in Exclusively Breast-Fed Infants with Cystic Fibrosis (A Descriptive Study)
by Andrea Asensio-Grau, María Garriga, Saioa Vicente, Ana Andrés, Carmen Ribes-Koninckx and Joaquim Calvo-Lerma
Nutrients 2024, 16(23), 4071; https://doi.org/10.3390/nu16234071 - 27 Nov 2024
Viewed by 247
Abstract
Background/Objectives: Early life gut microbiota plays a pivotal role in shaping immunity, metabolism, and overall health outcomes. This is relevant in healthy infants but may be even more crucial in infants with chronic devastating diseases, such as cystic fibrosis (CF). While the introduction [...] Read more.
Background/Objectives: Early life gut microbiota plays a pivotal role in shaping immunity, metabolism, and overall health outcomes. This is relevant in healthy infants but may be even more crucial in infants with chronic devastating diseases, such as cystic fibrosis (CF). While the introduction of solid foods in healthy infants modifies the composition of colonic microbiota, less knowledge is available on those with CF. The aim of this descriptive observational study was to assess the composition of fecal microbiota in six exclusively breast-fed infants with CF, and then explore the changes induced upon the introduction of different foods. Methods: two types of fecal samples were collected from each subject: one during the exclusive-breastfeeding period, and the other after incorporating each new food in the ad libitum diet. The microbiota composition was analyzed by 16S rRNA amplicon sequencing. Results: Wide heterogenicity in the composition at the phylum level (variable proportions of Actinobacteriota, Proteobacteria, and Firmicutes, and the absence of Bacteroidota in all subjects) was found, and different enterotypes were characterized in each subject by the main presence of one genus: Bifidobacterium in Subject 1 (relative abundance of 54.4%), Klebsiella in Subject 3 (49.1%), Veillonella in Subjects 4 and 5 (32.7% and 36.9%, respectively), and Clostridium in Subject 6 (48.9%). The transition to complementary feeding induced variable changes in microbiota composition, suggesting a subject-specific response and highlighting the importance of inter-individual variation. Conclusions: Further studies are required to identify which foods contribute to shaping colonic microbiota in the most favorable way for patients with CF using a personalized approach. Full article
(This article belongs to the Special Issue Nutrition and Cystic Fibrosis in Children)
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<p>Baseline microbiota compositions in the study subjects at the phylum taxonomic level (<b>a</b>) and genus level (<b>b</b>).</p>
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<p>Evolution of microbiota composition over the complementary feeding follow-up period in study subjects 1 (<b>a</b>), 2 (<b>b</b>), and 3 (<b>c</b>), expressed as the relative abundance (%) at the genus taxonomic level. n.d., non-determined.</p>
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<p>Fecal microbiota alpha diversity expressed as richness (observed ASVs) and evenness during the breastfeeding period ((<b>a</b>) and (<b>b</b>), respectively) and over the complementary feeding period ((<b>c</b>) and (<b>d</b>), respectively). Beta diversity (Bray–Curtis) expressed with PCoA and two groups of samples (breastfeeding and complementary feeding) (<b>e</b>).</p>
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18 pages, 1558 KiB  
Article
Nutrients and Quality Aspects Characterizing Ostrea edulis Cultivated in Valli di Comacchio (Northern Italy) Across Different Seasons
by Francesco Chiefa, Paola Tedeschi, Mirco Cescon, Valentina Costa, Elena Sarti, Manuel Salgado-Ramos, Noelia Pallarés, Natasha Damiana Spadafora, Leonardo Aguiari and Luisa Pasti
Molecules 2024, 29(23), 5546; https://doi.org/10.3390/molecules29235546 - 24 Nov 2024
Viewed by 602
Abstract
The quality aspects of Ostrea edulis (O. edulis) cultured in Valli di Comacchio were examined across different seasons. Nutritional quality parameters, antioxidant activity, total carotenoids, and contaminants were determined in winter, summer, and autumn (December, June, and October). Seasonal variations in [...] Read more.
The quality aspects of Ostrea edulis (O. edulis) cultured in Valli di Comacchio were examined across different seasons. Nutritional quality parameters, antioxidant activity, total carotenoids, and contaminants were determined in winter, summer, and autumn (December, June, and October). Seasonal variations in nutritional parameters were observed. In particular, in the winter samples, proteins, eicosapentaenoic acid, docosahexaenoic acid, threonine, tyrosine, valine and methionine, isoleucine, potassium, and carotenoids showed the highest values, whereas oleic acid, linolenic acid, lysine, and magnesium exhibited the maximum values in the summer. Finally, lipids, carbohydrates, histidine, and magnesium were present at high values in the autumn. The antioxidant activity values differed between the two methods used (DPPH and photochemiluminescence assays); however, the oysters collected in June presented lower antioxidant capacity. Contaminant levels were always below the imposed concentration limits; however, higher levels of toxic metals were detected in the winter, while polycyclic aromatic hydrocarbons were detected in the summer and autumn. It is important to monitor the nutritional and toxicological quality of Ostrea edulis throughout the cultivation seasons, not only to enhance knowledge of this species and improve its cultivation systems but also to determine the optimal period for human consumption from both nutritional and toxicological perspectives. Full article
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<p>Loading plots of <span class="html-italic">Ostrea edulis</span> from the principal component analysis of the biochemical components (proximate composition, fatty acids, amino acids, and minerals) and environmental parameters (oxygen percentage, salinity, and temperature).</p>
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<p>Results regarding the seasonal quantitative determination of total amino acids in <span class="html-italic">Ostrea edulis</span>. The results are expressed as means (<span class="html-italic">n</span> = 3) ± SD. Results from ANOVA show significant differences between the means. Means that share a common letter (A, B, C) are not significantly different from each other (Tukey’s test, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Pearson’s correlation between antioxidant capacity assays (photochemiluminescence and DPPH assay) and fatty acids, amino acids, and total carotenoids.</p>
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15 pages, 1038 KiB  
Article
Determination of 16 Hydroxyanthracene Derivatives in Food Supplements Using LC-MS/MS: Method Development and Application
by Svetlana V. Malysheva, Benoît Guillaume, Céline Vanhee and Julien Masquelier
Toxins 2024, 16(12), 505; https://doi.org/10.3390/toxins16120505 - 23 Nov 2024
Viewed by 490
Abstract
Hydroxyanthracene derivatives (HADs) are plant substances produced by a variety of plant species, including different Aloe, Rheum, and Rhamnus species and Cassia senna. These plants are often used in food supplements to improve bowel function. However, recently, the European Commission prohibited [...] Read more.
Hydroxyanthracene derivatives (HADs) are plant substances produced by a variety of plant species, including different Aloe, Rheum, and Rhamnus species and Cassia senna. These plants are often used in food supplements to improve bowel function. However, recently, the European Commission prohibited a number of HADs due to toxicological concerns. These HADs included aloin (aloin A and aloin B), aloe-emodin, emodin, and danthron. Most of the currently available analytical methods are restricted to the analysis of only these compounds and do not include other HADs. In this view, a multi-analyte method could be useful for both regulatory analysis and dietary intake studies. To this end, such a method, employing liquid chromatography–tandem mass spectrometry and targeting 16 different HADs, was developed and validated in this study. Limits of quantification were in the range from 0.025 mg kg−1 to 1 mg kg−1. The recovery of the method was within the acceptable range of 80% to 120%, with the exception of physcion. Repeatability varied from 0.5% to 11.6%, and the range for within-laboratory reproducibility was from 3.4% to 16.3%. The expanded measurement uncertainty was below 50% for all HADs. Subsequently, 24 commercial samples of food supplements and herbal infusions sourced in Belgium were analyzed. The results indicated that although the industry put a great effort into minimizing the amount of aloin and danthron present in food supplements, more than half of the products still exceeded the maximum tolerated levels suggested for aloe-emodin and emodin. Full article
(This article belongs to the Special Issue Multi Methods for Detecting Natural Toxins)
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<p>LC-MS/MS multiple reaction monitoring (MRM) chromatograms of a blank food supplement fortified with 16 HADs at the limit of quantification (LOQ) level. The LOQ levels for each HAD are specified in <a href="#toxins-16-00505-t002" class="html-table">Table 2</a>. For each analyte, the most abundant MRM transition is displayed. The vertical axes represent relative peak intensity (normalized to 100%), while the horizontal axes display retention time (in min). The chromatographic conditions used were as described in <a href="#sec4dot4-toxins-16-00505" class="html-sec">Section 4.4</a>.</p>
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<p>Distribution of HAD content in commercial food supplements and herbal infusions. The bottom and top of the box correspond to the lower quartile (25th percentile) and the upper quartile (75th percentile), respectively. The line inside the box represents the median (50th percentile). The ends of the whiskers correspond to the lowest and highest observations that are still within 1.5-fold of the interquartile range (corresponding to the length of the box). Observations beyond the ends of the whiskers are marked with an asterisk and labeled with a sample code. The spacings between the different parts of the box give an indication of the degree of spread and skewness of the data. Given the large distribution in HAD concentrations, a logarithmic scale is applied to the y-axis for better visualization.</p>
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16 pages, 2718 KiB  
Article
NMR Analysis of Pulegone in Food Products
by Yifei Yu, Thomas Kuballa and Dirk W. Lachenmeier
Appl. Sci. 2024, 14(23), 10838; https://doi.org/10.3390/app142310838 - 22 Nov 2024
Viewed by 309
Abstract
Pulegone is a monoterpene ketone found in a variety of mint species. It has been classified as possibly carcinogenic to humans (Group 2B) by the International Agency for Research on Cancer (IARC). In previous studies, pulegone in food was analyzed exclusively via GC-MS, [...] Read more.
Pulegone is a monoterpene ketone found in a variety of mint species. It has been classified as possibly carcinogenic to humans (Group 2B) by the International Agency for Research on Cancer (IARC). In previous studies, pulegone in food was analyzed exclusively via GC-MS, while 1H NMR methods were limited to essential oils. The aim of this study was to develop an NMR method for the detection and quantification of pulegone in essential oils and foods. A mixture of methanol-d4/chloroform-d1 in a 1:1 ratio (v/v) was identified as the most effective solvent for separating pulegone signals. The essential oils were subjected to analysis at this solvent-mixture ratio. The extraction of pulegone was required for food analysis, and the steam distillation method proved to be more effective than the ultrasonic-assisted extraction method. The highest pulegone concentrations were identified in pennyroyal oil and muña oil, whereas lower levels were observed in other matrices, including corn mint oil and select food items. A toxicological assessment showed that the amount consumed did not exert any adverse effects on human health. Full article
(This article belongs to the Special Issue Recent Applications of Plant Extracts in the Food Industry)
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<p>Comparison of <sup>1</sup>H NMR spectra of pulegone in chloroform-<span class="html-italic">d</span><sub>1</sub> (CDCl<sub>3</sub>) (upper panel, blue line) and pulegone in methanol-<span class="html-italic">d</span><sub>4</sub> (MeOD) (lower panel, red line). The inset shows a detailed enlargement of the range <span class="html-italic">δ</span><sub>H</sub> = 1.81–2.04 ppm for a better view of the differences between the spectra.</p>
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<p>Comparison of <sup>1</sup>H NMR spectrum of pure pulegone in a solvent mixture consisting of methanol-<span class="html-italic">d</span><sub>4</sub> (MeOD) and chloroform-<span class="html-italic">d</span><sub>1</sub> (CDCl<sub>3</sub>) at mixing ratios of 1:4, 1:1, and 4:1 (<span class="html-italic">v/v</span>) (blue line, green line, red line, from top to bottom). The inset shows an enlargement of the range <span class="html-italic">δ</span><sub>H</sub> = 1.85–2.05 ppm for a better view of the differences between the spectra.</p>
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<p><sup>1</sup>H NMR (400 MHz, 300 K, methanol-<span class="html-italic">d</span><sub>4</sub>/chloroform-<span class="html-italic">d</span><sub>1</sub> 1:1; <span class="html-italic">v/v</span>) spectrum of pure pulegone and the assignment of all signals. The inset shows the chemical structure with numbering.</p>
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<p><sup>13</sup>C-NMR (100 MHz, 300 K, methanol-<span class="html-italic">d</span><sub>4</sub>/chloroform-<span class="html-italic">d</span><sub>1</sub> 1:1; <span class="html-italic">v/v</span>) spectrum of pulegone and the assignment of the signals (206.2 ppm (1), 143.8 ppm (2), 29.01 ppm (3), 32.04 ppm (4), 33.12 ppm (5), 51.1 ppm (6), 132.2 ppm (7), 23.26 ppm (8), 22.37 ppm (9), and 21.86 ppm (10)). For carbon numbering, see <a href="#applsci-14-10838-f003" class="html-fig">Figure 3</a>.</p>
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<p>Section of the HSQC spectrum of pure pulegone recorded in methanol-<span class="html-italic">d</span><sub>4</sub>/chloroform-<span class="html-italic">d</span><sub>1</sub> (1:1; <span class="html-italic">v/v</span>).</p>
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<p>Section of a <sup>1</sup>H NMR spectrum of spearmint essential oil (dark blue line) overlaid with a spectrum spiked with pulegone (thin gray line); both were recorded in MeOD/CDCl<sub>3</sub> (1:1; <span class="html-italic">v/v</span>).</p>
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<p>Section of a spectrum of herb mint 3, recorded in CDCl<sub>3</sub>. The signal marked in green is pulegone, and to the left is the signal of carvone. I: integral, <span class="html-italic">δ</span>: chemical shift.</p>
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16 pages, 2267 KiB  
Article
Ornamental Barberry Twigs as an Underexploited Source of Berberine-Rich Extracts—Preliminary Research
by Michał Miłek, Małgorzata Dżugan, Natalia Pieńkowska, Sabina Galiniak, Mateusz Mołoń and Wojciech Litwińczuk
Curr. Issues Mol. Biol. 2024, 46(11), 13193-13208; https://doi.org/10.3390/cimb46110787 - 18 Nov 2024
Viewed by 379
Abstract
Berberine is a natural substance obtained from the roots of common barberry which, due to its strong pharmacological activity, is a commonly tested ingredient of dietary supplements. However, ornamental barberries, which are widely available, have not been considered as a source of berberine [...] Read more.
Berberine is a natural substance obtained from the roots of common barberry which, due to its strong pharmacological activity, is a commonly tested ingredient of dietary supplements. However, ornamental barberries, which are widely available, have not been considered as a source of berberine so far. The research aimed to check whether the ornamental barberry leaves and twigs could be used as an easily accessible raw material for obtaining natural berberine-rich extract with biological activity. Twigs and leaves of seven cultivars of ornamental barberry extracts were assessed for their polyphenol content, antioxidant potential (FRAP and DPPH), and berberine content using high-performance thin layer chromatography (HPTLC). As a reference, commercially available roots of Berberis vulgaris were used. For the next step, selected extracts (two with high and two with low berberine content) were tested on three cell lines (HaCaT, A375, Caco-2) using neutral red assay, and pure berberine sulfate (1–100 μg mL−1) was used as a control. Although the antioxidant potential of aqueous–methanol extracts of tested barberry was higher for the leaves than for the twigs, the berberine content was determined only in the twig extracts (from 42 to 676 mg 100 g−1). Studies on cell lines have shown the general toxicity of barberry extracts, but the observed effect was not directly correlated with the content of the alkaloid. However, the extract showed greater activity compared to an analogous dose of pure berberine, suggesting a significant effect of the matrix composition. For the first time, it was shown that the twigs of selected cultivars of ornamental barberry can be considered as a promising berberine source for the pharmaceutical industry to develop new effective formulations. However, these findings require further studies. Full article
(This article belongs to the Special Issue Phytochemicals in Cancer Chemoprevention and Treatment)
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<p>Berberine structure.</p>
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<p>HPTLC analysis of berberine content in twig extracts. Top visible in 366 nm UV light, bottom in visible light. Tracks: 1—‘NN’, 2—‘Superba’, 3—‘Powwow’, 4—‘Golden Carpet’, 5—‘Red Pillar’, 6—‘Golden Ring’, 7—‘Red Tears’, 8—root bark, 9—<span class="html-italic">Berberis vulgaris</span> (organic) root bark, 10—berberine standard.</p>
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<p>Berberine content in twigs of tested barberry cultivars compared to reference material (<span class="html-italic">B. vulgaris</span> root bark). The bars represent standard deviation; a,b,c—means marked with different letters are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Cultivar-dependent effect of selected barberry extracts (‘Superba’, ‘Golden carpet’, ‘Red Tears’, ‘Golden ring’) on the viability of human keratinocytes HaCaT cells estimated by the Neutral Red assay. The cells were treated with extracts in concentrations of 62.5, 125, 250 and 500 μg mL<sup>−1</sup>. Non-treated cells were used as a control (C). Data are expressed as median from at least three independent experiments. Error bars represent 25% and 75% percentiles. Statistical significance was assessed using one-way ANOVA and Dunnett’s post hoc test (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>Cultivar-dependent effect of selected barberry extracts (‘Superba’, ‘Golden carpet’, ‘Red Tears’, ‘Golden ring’) on the viability of human malignant melanoma A375 cells estimated by the Neutral Red assay. The cells were treated with extracts in concentrations of 62.5, 125, 250, and 500 μg mL<sup>−1</sup>. Non-treated cells were used as a control (C). Data are expressed as median from at least three independent experiments. Error bars represent 25% and 75% percentiles. Statistical significance was assessed using one-way ANOVA and Dunnett’s post hoc test (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>Cultivar-dependent effect of selected barberry extracts (‘Superba’, ‘Golden carpet’, ‘Red Tears’, ‘Golden ring’) on the viability of human colorectal adenocarcinoma cells Caco-2 estimated by the Neutral Red assay. The cells were treated with extracts in concentrations of 62.5, 125, 250 and 500 μg mL<sup>−1</sup> Non-treated cells were used as a control (C). Data are expressed as median from at least three independent experiments. Error bars represent 25% and 75% percentiles. Statistical significance was assessed using one-way ANOVA and Dunnett’s post hoc test (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001).</p>
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17 pages, 1822 KiB  
Review
Domoic Acid: A Review of Its Cytogenotoxicity Within the One Health Approach
by Goran Gajski, Marko Gerić, Ana Baričević and Mirta Smodlaka Tanković
Antioxidants 2024, 13(11), 1366; https://doi.org/10.3390/antiox13111366 - 8 Nov 2024
Viewed by 637
Abstract
In this review, we toxicologically assessed the naturally occurring toxin domoic acid. We used the One Health approach because the impact of domoic acid is potentiated by climate change and water pollution on one side, and reflected in animal health, food security, human [...] Read more.
In this review, we toxicologically assessed the naturally occurring toxin domoic acid. We used the One Health approach because the impact of domoic acid is potentiated by climate change and water pollution on one side, and reflected in animal health, food security, human diet, and human health on the other. In a changing environment, algal blooms are more frequent. For domoic acid production, the growth of Pseudo-nitzschia diatoms is of particular interest. They produce this toxin, whose capability of accumulation and biomagnification through the food web impacts other organisms in the ecosystem. Domoic acid targets nervous system receptors inducing amnestic shellfish poisoning, among other less severe health-related problems. However, the impact of domoic acid on non-target cells is rather unknown, so we reviewed the currently available literature on cytogenetic effects on human and animal cells. The results of different studies indicate that domoic acid has the potential to induce early molecular events, such as oxidative imbalance and DNA damage, thus posing an additional threat which needs to be thoroughly addressed and monitored in the future. Full article
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<p>Structure (2D structure (<b>A</b>) and 3D conformer (<b>B</b>)) of domoic acid. National Center for Biotechnology Information. PubChem Compound Summary for CID 5282253, Domoic acid. <a href="https://pubchem.ncbi.nlm.nih.gov/compound/5282253" target="_blank">https://pubchem.ncbi.nlm.nih.gov/compound/5282253</a> (accessed on 31 August 2024).</p>
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<p>Light micrographs of <span class="html-italic">Pseudo-nitzschia</span> species (#CIM1078) from the Adriatic Sea. Culture Collection of the Center for Marine Research, Ruđer Bošković Institute (Rovinj, Croatia; scale 10 μm).</p>
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<p>The rationale of evaluating the domoic acid case using the One Health approach, where climate change and increased pollution are major drivers of algal blooms and potential of domoic acid production. The presence of particulate and dissolved domoic acid leads to food contamination, thus impacting animal health, food quality, costs, and human health.</p>
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31 pages, 1729 KiB  
Review
Dietary Mycotoxins: An Overview on Toxicokinetics, Toxicodynamics, Toxicity, Epidemiology, Detection, and Their Mitigation with Special Emphasis on Aflatoxicosis in Humans and Animals
by James Kibugu, Leonard Munga, David Mburu, Fredrick Maloba, Joanna E. Auma, Delia Grace and Johanna F. Lindahl
Toxins 2024, 16(11), 483; https://doi.org/10.3390/toxins16110483 - 8 Nov 2024
Viewed by 760
Abstract
Mycotoxins are secondary metabolites of filamentous fungi and ubiquitous dietary contaminants. Aflatoxins, a group of mycotoxins with high prevalence and toxicity, have raised a high level of public health concern, the most prevalent and toxic being aflatoxin B1 (AFB1). Many aspects appertaining to [...] Read more.
Mycotoxins are secondary metabolites of filamentous fungi and ubiquitous dietary contaminants. Aflatoxins, a group of mycotoxins with high prevalence and toxicity, have raised a high level of public health concern, the most prevalent and toxic being aflatoxin B1 (AFB1). Many aspects appertaining to AFB1 poisoning are not well understood. Yet this information is necessary to devise appropriate surveillance and mitigation strategies against human and animal aflatoxicosis. This review provides an in-depth update of work carried out on mycotoxin poisoning, particularly aflatoxicosis in humans and animals, to identify gaps in knowledge. Hypotheses explaining the functional significance of mycotoxins in fungal biology and their dietary epidemiological data are presented and briefly discussed. The toxicology of aflatoxins and the challenges of their mitigation are discussed in depth. It was concluded that the identification of potential mycotoxin-hazard-prone food items and quantification of the associated risk of cancer ailments in humans is a prime priority. There is a dearth of reliable sampling methodologies for estimating AFB1 in animal feed. Data update on AFB1 in animal feed and its implication in animal production, mitigation strategies, and elucidation of risk factors to this hazard is required. To reduce the burden of aflatoxins, surveillance employing predictive technology, and biocontrol strategies seem promising approaches. Full article
(This article belongs to the Special Issue Occurrence, Toxicity, Metabolism, Analysis and Control of Mycotoxins)
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<p>Basic structures of primary aflatoxins. (<b>A</b>) Difurocoumarocyclopentenones: B-aflatoxins; (<b>B</b>) difurocoumarolactones: G-aflatoxins. The bifuran moiety (highlighted in blue) associated with AFB1, G1, and other aflatoxins have an unsaturated C8=C9 double bond, which is prone to enzymatic insult (bio-activation), conferring the molecule’s high toxicity and carcinogenicity. The backbone of the molecule is the coumarin nucleus (shown in green). Highlighted in red are cyclo-pentene ring (for difurocoumarocyclopentenones) and lactone ring (for difurocoumarolactones). (Source: Benkerroum [<a href="#B5-toxins-16-00483" class="html-bibr">5</a>]).</p>
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<p>Schematic illustration of toxicokinetic events of AFB1 in animals and humans after exposure via oral and respiratory routes. The toxin is absorbed through mucosal cells, distributed to various body compartments, and undergoes phase I and II reactions. The hallmark of this pathway is the bio-activation of AFB1 into highly reactive electrophile AFBO.</p>
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<p>Illustration of toxicodynamic events of AFB1 poisoning and its outcomes in animals and humans. Bio-activation to highly reactive metabolites and oxidative stress are the twin modes of action responsible for AFB1-mediated insults on macromolecules, leading to genotoxicity, acute toxicity, and immunotoxicity.</p>
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17 pages, 2038 KiB  
Article
Integrated Approach to Cyclopiazonic Acid Cytotoxicity Using In Vitro (2D and 3D Models) and In Silico Methods
by Carmen Martínez-Alonso, Luana Izzo, Yelko Rodríguez-Carrasco and María-José Ruiz
Toxins 2024, 16(11), 473; https://doi.org/10.3390/toxins16110473 - 3 Nov 2024
Viewed by 728
Abstract
Cyclopiazonic acid (CPA) is an indole-tetramic acid neurotoxin produced by Aspergillus and Penicillium genera present mainly in fruit, cereals and nuts. This study compares the cytotoxicity produced by CPA after 24, 48 and 72 h of exposure using both monolayers and 3D spheroids [...] Read more.
Cyclopiazonic acid (CPA) is an indole-tetramic acid neurotoxin produced by Aspergillus and Penicillium genera present mainly in fruit, cereals and nuts. This study compares the cytotoxicity produced by CPA after 24, 48 and 72 h of exposure using both monolayers and 3D spheroids in human neuroblastoma SH-SY5Y cells. Furthermore, CPA toxicokinetics was evaluated using in silico models. Cytotoxicity increased dose- and time-dependently, as shown by the MTT assay. The lowest CPA IC50 values were found in the monolayer study compared to the 3D spheroids at all exposure times (24 h: 864.01 vs. 1132; 48 h: 437 vs. 1069; 72 h: 392 vs. 567 nM). The CPA exposure on SH-SY5Y spheroid organization and morphology was also studied. Morphological changes, including spheroid disaggregation, were observed after mycotoxin exposure. The in silico methods, SwissADME and admetSAR, were used for short and full ADMEt profiles of CPA. The ADMEt predictive profile shows high gastrointestinal absorption and ability to penetrate the blood–brain barrier. Including in silico studies emphasizes the comprehensive approach to understanding mycotoxin toxicity and risk assessment. By combining in vitro 3D spheroid models with computational simulations, this study aims to provide a holistic perspective on the effects of CPA, enhancing the accuracy and relevance of our findings. Full article
(This article belongs to the Special Issue Toxins: 15th Anniversary)
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<p>SH-SY5Y spheroids growth in ULA 96-well round-bottom plates. (<b>a</b>) Bright-field images of SH-SY5Y spheroids growth from 0 to 7 days. Images were obtained using the Light Microscope Zeiss Axio Observer (Zeiss Microscopy, Oberkochen, Germany) at 10× magnification. Scale bars: 100 μm; (<b>b</b>) Diameter of SH-SY5Y spheroids plotted over time (7 days). Values are expressed as means ± SD (<span class="html-italic">n</span> = 3 spheroids/timepoint). Diameters were calculated using Zen Lite version 3.8 software.</p>
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<p>Cytotoxic effects of CPA in SH-SY5Y monolayer cultures obtained by MTT assay after 24, 48 and 72 h of exposure. Data are expressed as mean ± SEM of three independent experiments (<span class="html-italic">n</span> = 3). (*) <span class="html-italic">p</span> ≤ 0.05 indicates a significant difference compared to the control.</p>
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<p>Cytotoxic effects of CPA in 3D SH-SY5Y spheroids by MTT (<b>a</b>) and ATP (<b>b</b>) assays. Data are expressed as mean ± SEM of three independent experiments (<span class="html-italic">n</span> = 3). (*) <span class="html-italic">p</span> ≤ 0.05 indicates a significant difference with respect to the control.</p>
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<p>Bright-field images of SH-SY5Y spheroids after 24, 48 and 72 h of exposure to increasing concentrations of CPA (500–1500 nM). Spheroids exposed to DMSO (≤1%) were used as control (CRL). Scale bar: 50 μm. Images were obtained using the Light Microscope Zeiss Axio Observer (Zeiss Microscopy, Germany).</p>
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<p>Diameter of SH-SY5Y spheroids after CPA (500–1500 nM) exposure for 24, 48 and 72 h. Quantitative analysis was performed using the software Zen Lite version 3.8 (Zeiss Microscopy, Germany). Results are expressed as the mean ± SEM of four independent spheroids for each concentration and time (<span class="html-italic">n</span> = 4). CRL: control. (*) <span class="html-italic">p</span> ≤ 0.05 indicates a significant difference compared to the control.</p>
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<p>BOILED-Egg predictive model constructed using the CPA SMILES. The ‘yolk’ area represents the physicochemical space where molecules are likely to penetrate the blood–brain barrier (BBB), while the white region denotes the physicochemical space where molecules are likely to be absorbed by the gastrointestinal tract (HIA). The grey area indicates low permeability and absorption. CPA is represented as a single point based on its specific lipophilicity and polarity values. The blue circle indicates that CPA is probably a substrate of P-glycoprotein.</p>
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18 pages, 4822 KiB  
Article
Effects of Licorice Functional Components Intakes on Blood Pressure: A Systematic Review with Meta-Analysis and NETWORK Toxicology
by Tianyu Wu, Jingyi Yang, Jiayue Xia and Guiju Sun
Nutrients 2024, 16(21), 3768; https://doi.org/10.3390/nu16213768 - 2 Nov 2024
Viewed by 882
Abstract
Objective: To investigate the effects of licorice functional ingredient intake on blood pressure, explore its potential mechanisms of action, and provide safety information for personalized nutritional interventions in special populations and for the application of licorice-derived functional foods. Methods: PubMed, Cochrane Library, Medline, [...] Read more.
Objective: To investigate the effects of licorice functional ingredient intake on blood pressure, explore its potential mechanisms of action, and provide safety information for personalized nutritional interventions in special populations and for the application of licorice-derived functional foods. Methods: PubMed, Cochrane Library, Medline, Embase, EBSCO, ScienceDirect, and Web of Science databases were searched from inception to 31 August 2024. Randomized controlled trials (RCTs) investigating the intake of licorice or its functional components were included. The range of continuous variables was assessed using the weighted mean difference (WMD) with 95% confidence intervals. Genes associated with hypertension were screened using an online database. Machine learning, receiver operating characteristic(ROC) curve analysis, molecular docking, and gene set enrichment analysis (GSEA) were employed to explore the potential mechanisms underlying licorice-induced blood pressure fluctuations. Results: Eight RCTs (541 participants) were included in the meta-analysis, which indicated interventions containing glycyrrhizic acid (GA) as the main component increased systolic blood pressure (SBP) and diastolic blood pressure (DBP) (SBP: WMD [95% CI] = 3.48 [2.74, 4.21], p < 0.001; DBP: WMD [95% CI] = 1.27 [0.76, 1.78], p < 0.001). However, interventions dominated by licorice flavonoids(LF) had no significant effect on SBP or DBP (SBP: WMD [95% CI] = 0.58 [−1.15, 2.31], p = 0.511; DBP: WMD [95% CI] = 0.17 [−1.53, 1.88], p = 0.843). Three machine learning algorithms identified five biomarkers associated with hypertension: calmodulin 3 (CALM3), cluster of differentiation 9 (CD9), growth factor independence 1B transcriptional repressor (GFI1B), myosin light chain kinase (MYLK), and Ras suppressor-1 (RSU1). After removing biomarkers with lower validity and reliability, GFI1B, MYLK, and RSU1 were selected for subsequent analysis. The network toxicology results suggested that GA and its metabolite glycyrrhetinic acid may act on GFI1B, MYLK, and RSU1, influencing blood pressure fluctuations by modulating nitrogen metabolism signaling pathways. Conclusions: There were distinct differences in the effects of licorice functional components on blood pressure. Functional constituents dominated by GA were shown to increase both SBP and DBP, whereas those dominated by LF did not exhibit significant effects on blood pressure. The hypertensive mechanism of GA may involve the modulation of GFI1B, MYLK, and RSU1 to regulate nitrogen metabolic pathways. Full article
(This article belongs to the Section Phytochemicals and Human Health)
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<p>Research scheme. Step 1: We conducted a comprehensive search across multiple databases for RCTs on licorice and blood pressure. Relevant studies were classified into two groups based on the primary licorice components, and duplicates were removed. Articles were then screened by abstract, with eight studies ultimately included. The publication bias of the included studies was assessed using the RevMan tool, and a quantitative analysis was performed using Stata. Step 2: Hypertension-associated genes were identified from TTD, OMIM, and GeneCards databases, complemented by transcriptomic data to screen additional hypertension-related genes. The intersection of these genes was further refined to identify hypertension biomarkers using machine learning methods. Step 3: Step 1 revealed a blood pressure-elevating effect of GA; therefore, toxicology prediction, molecular docking, and GSEA were employed to explore the potential mechanisms underlying this effect.</p>
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<p>Study screening flowchart.</p>
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<p>Forest plot of weight difference and 95% confidence intervals for the effect of GA or LF intake on SBP and DBP. (<b>A</b>,<b>B</b>) WMD and 95% CI of the effects of GA-based interventions on SBP and DBP. (<b>C</b>,<b>D</b>) WMD and 95% CI of the effects of LF-based interventions on SBP and DBP [<a href="#B20-nutrients-16-03768" class="html-bibr">20</a>,<a href="#B28-nutrients-16-03768" class="html-bibr">28</a>,<a href="#B29-nutrients-16-03768" class="html-bibr">29</a>,<a href="#B30-nutrients-16-03768" class="html-bibr">30</a>,<a href="#B31-nutrients-16-03768" class="html-bibr">31</a>,<a href="#B32-nutrients-16-03768" class="html-bibr">32</a>,<a href="#B33-nutrients-16-03768" class="html-bibr">33</a>,<a href="#B34-nutrients-16-03768" class="html-bibr">34</a>].</p>
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<p>Subgroup analysis of the effect of GA-based interventions on blood pressure. (<b>A</b>,<b>B</b>) Effect of GA-based interventions intake on SBP at different doses and intervention times. (<b>C</b>,<b>D</b>) Effect of GA-based interventions intake on DBP at different doses and intervention times [<a href="#B20-nutrients-16-03768" class="html-bibr">20</a>,<a href="#B28-nutrients-16-03768" class="html-bibr">28</a>,<a href="#B32-nutrients-16-03768" class="html-bibr">32</a>].</p>
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<p>Toxicological prediction results based on Pro Tox-3.0. (<b>A</b>) Oral toxic effect class of GA. (<b>B</b>) Basic chemical properties of GA. (<b>C</b>) Prediction of toxic effects of GA. Dili: drug-induced liver injury; Neuro: neurotoxicity; Nephro: nephrotoxicity; Respi: respiratory toxicity; Cardio: cardiotoxicity; Immuno: immunotoxicity; Nutri: nutritional toxicity; Mie_ache: achetylcholinesterase; Mie_pxr: pregnane X receptor; Mie_nadhox: NADH-quinone oxidoreductase.</p>
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<p>Network analysis and gene module selection related to hypertension. (<b>A</b>) Selection of the soft threshold power for WGCNA. (<b>B</b>) Screening of gene modules associated with hypertensive traits. (<b>C</b>) Gene modules showing high correlation with hypertension phenotypes. (<b>D</b>) Correlation plot of gene-trait relationships for the MEpink module. (<b>E</b>) Identification of hypertension-associated and effector genes.</p>
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<p>Identify key signature genes for hypertension by machine learning. (<b>A</b>,<b>B</b>) Accuracy and error rates of gene selection using the SVM-REF method. (<b>C</b>) Construction of the Lasso regression model. (<b>D</b>) Development of the Random Forest decision tree and identification of the point with minimal error. (<b>E</b>) Identification of hypertension-specific genes using the Random Forest approach. (<b>F</b>) Comparison of hypertension-specific gene selection across three machine learning algorithms.</p>
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<p>Validation of the diagnostic model for hypertension-specific signature genes. (<b>A</b>) Nomogram illustrating disease-associated genes. Expression levels of CALM3 (<b>B</b>), CD9 (<b>C</b>), MYLK (<b>D</b>), RSU1 (<b>E</b>), and GFI1B (<b>F</b>) in patients with hypertension. ROC curves for CALM3 (<b>G</b>), CD9 (<b>H</b>), MYLK (<b>I</b>), RSU1 (<b>J</b>), and GFI1B (<b>K</b>).</p>
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<p>Investigation of the potential toxicological mechanisms of GA. Molecular docking results of GFI1B (<b>A</b>), MYLK (<b>B</b>), and RSU1 (<b>C</b>) with GA; GSEA results of GFI1B (<b>D</b>), MYLK (<b>E</b>), and RSU1 (<b>F</b>).</p>
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18 pages, 2266 KiB  
Article
Comparison of In Vitro Hair Growth Promotion and Anti-Hair Loss Potential of Thai Rice By-Product from Oryza sativa L. cv. Buebang 3 CMU and Sanpatong
by Anurak Muangsanguan, Warintorn Ruksiriwanich, Chaiwat Arjin, Sansanee Jamjod, Chanakan Prom-u-Thai, Pensak Jantrawut, Pornchai Rachtanapun, Patipan Hnorkaew, Apinya Satsook, Mathukorn Sainakham, Juan Manuel Castagnini and Korawan Sringarm
Plants 2024, 13(21), 3079; https://doi.org/10.3390/plants13213079 - 1 Nov 2024
Viewed by 906
Abstract
The bioactive compounds in herbal extracts may provide effective hair loss treatments with fewer side effects compared to synthetic medicines. This study evaluated the effects of Buebang 3 CMU and Sanpatong rice bran extracts, macerated with dichloromethane or 95% ethanol, on hair growth [...] Read more.
The bioactive compounds in herbal extracts may provide effective hair loss treatments with fewer side effects compared to synthetic medicines. This study evaluated the effects of Buebang 3 CMU and Sanpatong rice bran extracts, macerated with dichloromethane or 95% ethanol, on hair growth promotion and hair loss prevention. Overall, Buebang 3 CMU extracts contained significantly higher levels of bioactive compounds, including γ-oryzanol, tocopherols, and various polyphenols such as phytic acid, ferulic acid, and chlorogenic acid, compared to Sanpatong extracts. Additionally, ethanolic extracts demonstrated greater bioactive content and antioxidant activities than those extracted with dichloromethane. These compounds enhanced the proliferation of human hair follicle dermal papilla cells (HFDPCs) by 124.28 ± 1.08% (p < 0.05) and modulated anti-inflammatory pathways by reducing nitrite production to 3.20 ± 0.36 µM (p < 0.05). Key hair growth signaling pathways, including Wnt/β-catenin (CTNNB1), Sonic Hedgehog (SHH, SMO, GLI1), and vascular endothelial growth factor (VEGF), were activated by approximately 1.5-fold to 2.5-fold compared to minoxidil. Also, in both human prostate cancer (DU-145) and HFDPC cells, the ethanolic Buebang 3 CMU extract (Et-BB3-CMU) suppressed SRD5A1, SRD5A2, and SRD5A3 expression—key pathways in hair loss—by 2-fold and 1.5-fold more than minoxidil and finasteride, respectively. These findings suggest that Et-BB3-CMU holds promise for promoting hair growth and preventing hair loss. Full article
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<p>The effects of rice bran extracts and the standard control (diclofenac sodium) at a concentration of 0.125 mg/mL on nitrite production in lipopolysaccharide (LPS)-induced RAW 264.7 (<b>A</b>) and HFDPC (<b>B</b>) cells after 24 h, compared to a solvent-treated control without LPS (blank) and an LPS-induced control (+LPS). DF: diclofenac sodium; Di-SPT: Sanpatong rice bran extracts using dichloromethane as the solvent; Et-SPT: Sanpatong rice bran extracts using ethanol as the solvent; Di-BB3-CMU: Buebang 3-CMU rice bran extracts using dichloromethane as the solvent; Et-BB3-CMU: Buebang 3-CMU rice bran extracts using ethanol as the solvent. Values are expressed as the mean ± SD for triplicate samples. Statistical analysis was performed using one-way ANOVA followed by Tukey’s HSD test. Different letters (a–f) indicate statistically significant differences (<span class="html-italic">p</span> &lt; 0.05) between samples.</p>
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<p>Effects of rice bran extracts and standard controls (L-ascorbic acid) at the concentration of 0.125 mg/mL on the malondialdehyde production in hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>)-induced HFDPCs using the thiobarbituric acid reactive substances (TBARS) assay. Di-SPT: Sanpatong rice bran extracts using dichloromethane as the solvent; Et-SPT: Sanpatong rice bran extracts using ethanol as the solvent; Di-BB3-CMU: Buebang 3-CMU rice bran extracts using dichloromethane as the solvent; Et-BB3-CMU: Buebang 3-CMU rice bran extracts using ethanol as the solvent. Values were expressed as the mean ± SD for triplicates in each sample. Statistical analysis was performed using a one-way ANOVA, followed by Tukey’s HSD test. Different letters (a–f) indicate statistical differences (<span class="html-italic">p</span> &lt; 0.05) in comparison to each sample.</p>
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<p>The effects of rice bran extracts on the gene expression in the androgen pathway; (<b>A</b>) <span class="html-italic">SRD5A1</span>, (<b>B</b>) <span class="html-italic">SRD5A2</span>, and (<b>C</b>) <span class="html-italic">SRD5A3</span> in DU-145 cells; and (<b>D</b>) <span class="html-italic">SRD5A1</span>, (<b>E</b>) <span class="html-italic">SRD5A2</span>, and (<b>F</b>) <span class="html-italic">SRD5A3</span> in HFDPCs were compared to the standard controls (minoxidil, dutasteride, and finasteride) at a concentration of 0.125 mg/mL. Di-SPT: Sanpatong rice bran extracts using dichloromethane as the solvent; Et-SPT: Sanpatong rice bran extracts using ethanol as the solvent; Di-BB3-CMU: Buebang 3-CMU rice bran extracts using dichloromethane as the solvent; Et-BB3-CMU: Buebang 3-CMU rice bran extracts using ethanol as the solvent. The results were shown as a fold change in gene expression relative to the control (untreated). Statistical analysis was performed using one-way ANOVA, followed by Tukey’s HSD test. Different letters (a–g) within each sample indicate significant differences (<span class="html-italic">p</span>-value &lt; 0.05).</p>
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<p>The effects of rice bran extracts on the gene expression in the androgen pathway; (<b>A</b>) <span class="html-italic">SRD5A1</span>, (<b>B</b>) <span class="html-italic">SRD5A2</span>, and (<b>C</b>) <span class="html-italic">SRD5A3</span> in DU-145 cells; and (<b>D</b>) <span class="html-italic">SRD5A1</span>, (<b>E</b>) <span class="html-italic">SRD5A2</span>, and (<b>F</b>) <span class="html-italic">SRD5A3</span> in HFDPCs were compared to the standard controls (minoxidil, dutasteride, and finasteride) at a concentration of 0.125 mg/mL. Di-SPT: Sanpatong rice bran extracts using dichloromethane as the solvent; Et-SPT: Sanpatong rice bran extracts using ethanol as the solvent; Di-BB3-CMU: Buebang 3-CMU rice bran extracts using dichloromethane as the solvent; Et-BB3-CMU: Buebang 3-CMU rice bran extracts using ethanol as the solvent. The results were shown as a fold change in gene expression relative to the control (untreated). Statistical analysis was performed using one-way ANOVA, followed by Tukey’s HSD test. Different letters (a–g) within each sample indicate significant differences (<span class="html-italic">p</span>-value &lt; 0.05).</p>
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<p>Effects of rice bran extracts and standard control (minoxidil and purmorphamine) (0.125 mg/mL) on the relative mRNA expression of genes associated with the Wnt/β-catenin signaling (<b>A</b>) <span class="html-italic">CTNNB1</span>; Sonic Hedgehog pathways (<b>B</b>) <span class="html-italic">SHH</span>; (<b>C</b>) <span class="html-italic">SMO</span>; (<b>D</b>); <span class="html-italic">GLI1</span>; and angiogenesis (<b>E</b>) <span class="html-italic">VEGF</span> in HFDPCs. Di-SPT: Sanpatong rice bran extracts using dichloromethane as the solvent; Et-SPT: Sanpatong rice bran extracts using ethanol as the solvent; Di-BB3-CMU: Buebang 3-CMU rice bran extracts using dichloromethane as the solvent; Et-BB3-CMU: Buebang 3-CMU rice bran extracts using ethanol as the solvent. Statistical analysis was performed using one-way ANOVA, followed by Tukey’s HSD test. Different letters (a–g) above the bars indicated significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effects of rice bran extracts and standard control (minoxidil and purmorphamine) (0.125 mg/mL) on the relative mRNA expression of genes associated with the Wnt/β-catenin signaling (<b>A</b>) <span class="html-italic">CTNNB1</span>; Sonic Hedgehog pathways (<b>B</b>) <span class="html-italic">SHH</span>; (<b>C</b>) <span class="html-italic">SMO</span>; (<b>D</b>); <span class="html-italic">GLI1</span>; and angiogenesis (<b>E</b>) <span class="html-italic">VEGF</span> in HFDPCs. Di-SPT: Sanpatong rice bran extracts using dichloromethane as the solvent; Et-SPT: Sanpatong rice bran extracts using ethanol as the solvent; Di-BB3-CMU: Buebang 3-CMU rice bran extracts using dichloromethane as the solvent; Et-BB3-CMU: Buebang 3-CMU rice bran extracts using ethanol as the solvent. Statistical analysis was performed using one-way ANOVA, followed by Tukey’s HSD test. Different letters (a–g) above the bars indicated significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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24 pages, 934 KiB  
Review
Effects of Bisphenol A on the Risk of Developing Obesity
by Mónica García García, Yolanda Picó and María Morales-Suárez-Varela
Nutrients 2024, 16(21), 3740; https://doi.org/10.3390/nu16213740 - 31 Oct 2024
Viewed by 738
Abstract
Background: Every year the global incidence of obesity increases considerably and among the factors that favor it is bisphenol A (BPA), an endocrine disruptor widely used in plastics and omnipresent in many everyday objects. Methods: A total of 19 studies published between 2018 [...] Read more.
Background: Every year the global incidence of obesity increases considerably and among the factors that favor it is bisphenol A (BPA), an endocrine disruptor widely used in plastics and omnipresent in many everyday objects. Methods: A total of 19 studies published between 2018 and 2023 that addressed the relationship between BPA exposure and obesity were included in this review in order to better understand its behavior and mechanisms of action. Results: The studies reviewed conclude that BPA is an obesogen that alters the function of hormonal receptors, promotes metabolic syndrome, affects certain genes, etc., leading to a greater risk of developing obesity. With important emphasis on the ability to cause epigenetic changes, thus transmitting the effects to offspring when exposure has occurred during critical stages of development such as during gestation or the perinatal period. Conclusions: There is sufficient evidence to show that BPA is a risk factor in the development of obesity. Even so, further research is necessary to exhaustively understand the causal relationship between the two in order to develop prevention measures and avoid possible future adverse effects. Full article
(This article belongs to the Section Nutrition and Obesity)
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<p>Chemical structure of bisphenol A (<b>A</b>), bisphenol S (<b>B</b>), and bisphenol F (<b>C</b>).</p>
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<p>Study selection flow diagram.</p>
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13 pages, 1061 KiB  
Article
Assessment of the Quality, Bioactive Compounds, and Antimicrobial Activity of Egyptian, Ethiopian, and Syrian Black Cumin Oils
by Adel Gabr Abdel-Razek, Minar Mahmoud M. Hassanein, Shimaa Moawad, Amr Farouk, Ahmed Noah Badr, Mohamed Gamal Shehata, Aleksander Siger, Anna Grygier and Magdalena Rudzińska
Molecules 2024, 29(21), 4985; https://doi.org/10.3390/molecules29214985 - 22 Oct 2024
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Abstract
Background: The oils obtained from the seeds of Nigella sativa, also named black cumin, are rich in bioactive compounds that strengthen immunity and support human health. This study aimed to compare Nigella sativa oils pressed from Egyptian (Eg-NSSO), Ethiopian (Et-NSSO), and Syrian [...] Read more.
Background: The oils obtained from the seeds of Nigella sativa, also named black cumin, are rich in bioactive compounds that strengthen immunity and support human health. This study aimed to compare Nigella sativa oils pressed from Egyptian (Eg-NSSO), Ethiopian (Et-NSSO), and Syrian (Sy-NSSO) seeds. Methods: The analyzed oils were obtained from a local company. The content of phenolic compounds, tocochromanols, phytosterols, volatile compounds, triglycerides, and fatty acids composition was determined using chromatographic methods. The oxidative stability was determined by Rancimat technique as well as the determination of DPPH and ABTS scavenging activity. As an assessment of bioactivity, the antimicrobial and anti-aflatoxigenic properties of oils were evaluated. Results: Ethiopian oil had highest content of phenolic compounds, flavonoids, phytosterols, and tocochromanols and was characterized by the longest induction period (IP = 7.89 h). The share of thymoquinone was the highest in Ethiopian oil (34.84%), followed by Egyptian (27.36%), then Syrian (22.59%). Ethiopian oil recorded a high antibacterial activity, while Egyptian oil showed a unique antifungal activity against toxigenic fungi. Aflatoxins’ secretion into liquid medium containing NSSO was reduced, especially with Egyptian oil. Full article
(This article belongs to the Special Issue New Insight into Edible Oil: From Food Chemistry to Health Benefits)
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Figure 1
<p>Total phenolic compounds (<b>A</b>), flavonoids (<b>B</b>), and antioxidant activities determined as DPPH (<b>C</b>), ABTS<sup>+</sup> (<b>D</b>) against standard of ascorbic acid. Results are expressed as mean ± SD, means with different letters differ significantly (<span class="html-italic">n</span> = 5; <span class="html-italic">p</span> ≤ 0.05). Eg-NSSO: Egyptian <span class="html-italic">Nigella sativa</span> seed oil; Et-NSSO: Ethiopian <span class="html-italic">Nigella sativa</span> seed oil; Sy-NSSO: Syrian <span class="html-italic">Nigella sativa</span> seed oil.</p>
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<p>Anti-pathogenicity (<b>A</b>), antifungal (<b>B</b>), and dissimilarity of aflatoxin-fungi inhibition efficiency (<b>C</b>) by <span class="html-italic">Nigella sativa</span> seed oils.</p>
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