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13 pages, 2731 KiB  
Article
EPR Spectroscopy Coupled with Spin Trapping as an Alternative Tool to Assess and Compare the Oxidative Stability of Vegetable Oils for Cosmetics
by Giulia Di Prima, Viviana De Caro, Cinzia Cardamone, Giuseppa Oliveri and Maria Cristina D’Oca
Appl. Sci. 2024, 14(22), 10766; https://doi.org/10.3390/app142210766 - 20 Nov 2024
Viewed by 264
Abstract
Antioxidants are the most popular active ingredients in anti-aging cosmetics as they can restore the physiological radical balance and counteract the photoaging process. Instead of adding pure compounds into the formulations, some “precious” vegetable oils could be used due to their content of [...] Read more.
Antioxidants are the most popular active ingredients in anti-aging cosmetics as they can restore the physiological radical balance and counteract the photoaging process. Instead of adding pure compounds into the formulations, some “precious” vegetable oils could be used due to their content of tocopherols, phenols, vitamins, etc., constituting a powerful antioxidant unsaponifiable fraction. Here, electron paramagnetic resonance (EPR) spectroscopy coupled with spin trapping was proven to provide a valid method for evaluating the antioxidant properties and the oxidative resistance of vegetable oils which, following UV irradiation, produce highly reactive radical species although hardly detectable. Extra virgin olive oil, sweet almond oil, apricot kernel oil, and jojoba oil were then evaluated by using N-t-butyl-α-phenylnitrone as a spin trapper and testing different UV irradiation times followed by incubation for 5 to 180 min at 70 °C. The EPR spectra were manipulated to obtain quantitative information useful for comparing the different tested samples. As a result, the knowledge acquired via the EPR analyses demonstrated jojoba oil as the best of the four considered oils in terms of both starting antioxidant ability and oxidative stability overtime. The obtained results confirmed the usefulness of the EPR spin trapping technique for the main proposed purpose. Full article
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<p>EPR spectra of the PBN spin adducts in EVOO after 30 min of incubation at 70 °C with the not-irradiated (black line) sample and UV-irradiated ones (30 min: green line; 60 min: blue line; 120 min: red line). Results are reported as means (n = 6).</p>
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<p>Determination of the induction time (IT) for EVOO (sample not irradiated). Results are reported as means (n = 6).</p>
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<p>H<sub>p/p</sub> intensity against incubation time at 70 °C for EVOO samples. Means (n = 6) ± SD.</p>
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<p>H<sub>p/p</sub> intensity against incubation time at 70 °C for SAO samples. Means (n = 6) ± SD.</p>
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<p>H<sub>p/p</sub> intensity against incubation time at 70 °C for AKO samples. Means (n = 6) ± SD.</p>
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<p>H<sub>p/p</sub> intensity against incubation time at 70 °C for JO samples. Means (n = 6) ± SD.</p>
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<p>Slope of the linear portion of the H<sub>p/p</sub> intensity against incubation time at 70 °C graphs as a function of UV irradiation time for EVOO, SAO, AKO, and JO samples. Means (n = 6).</p>
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30 pages, 2905 KiB  
Article
(Photo)toxicity of Partially Oxidized Docosahexaenoate and Its Effect on the Formation of Lipofuscin in Cultured Human Retinal Pigment Epithelial Cells
by Linda M. Bakker, Michael E. Boulton and Małgorzata B. Różanowska
Antioxidants 2024, 13(11), 1428; https://doi.org/10.3390/antiox13111428 - 20 Nov 2024
Viewed by 236
Abstract
Docosahexaenoate is a cytoprotective ω-3 polyunsaturated lipid that is abundant in the retina and is essential for its function. Due to its six unsaturated double bonds, docosahexaenoate is highly susceptible to oxidation and the formation of products with photosensitizing properties. This study aimed [...] Read more.
Docosahexaenoate is a cytoprotective ω-3 polyunsaturated lipid that is abundant in the retina and is essential for its function. Due to its six unsaturated double bonds, docosahexaenoate is highly susceptible to oxidation and the formation of products with photosensitizing properties. This study aimed to test on cultured human retinal pigment epithelial cells ARPE-19 the (photo)cytotoxic potential of partly oxidized docosahexaenoate and its effect on the formation of lipofuscin from phagocytosed photoreceptor outer segments (POSs). The results demonstrate that the cytoprotective effects of docosahexaenoate do not counteract the deleterious effects of its oxidation products, leading to the concentration-dependent loss of cell metabolic activity, which is exacerbated by concomitant exposure to visible light. Partly oxidized docosahexaenoate does not cause permeability of the cell plasma membrane but does cause apoptosis. While vitamin E can provide partial protection from the (photo)toxicity of partly oxidized docosahexaenoate, zeaxanthin undergoes rapid photodegradation and can exacerbate the (photo)toxicity. Feeding cells with POSs enriched in partly oxidized docosahexaenoate results in a greater accumulation of intracellular fluorescent lipofuscin than in cells fed POSs without the addition. In conclusion, partly oxidized docosahexaenoate increases the accumulation of lipofuscin-like intracellular deposits, is cytotoxic, and its toxicity increases during exposure to light. These effects may contribute to the increased progression of geographic atrophy observed after long-term supplementation with docosahexaenoate in age-related macular degeneration patients. Full article
(This article belongs to the Special Issue Antioxidants and Retinal Diseases—2nd Edition)
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<p>Monitoring oxidation of 22:6PC in liposomes. (<b>A</b>): Representative absorption spectra of the chloroform-soluble components extracted from liposomes at indicated times of incubation with air and dissolved in acetonitrile–methanol mixture (20:1 <span class="html-italic">v</span>/<span class="html-italic">v</span>). (<b>B</b>): Changes in absorbance at indicated wavelengths obtained from spectra shown in graph (<b>A</b>). (<b>C</b>): HPLC chromatograms of docosahexanoate hydrolyzed from PC before and after 18 days of oxidation of 22:6PC as liposomes. Inset: absorption spectra at maxima shown in the chromatogram. (<b>D</b>): Absorption spectrum of the 22:6PC oxidation products extracted from the liposomes into the chloroform-enriched phase after 18 days of liposome oxidation, corresponding to 3.75 mM concentration of the original 22:6PC.</p>
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<p>Comparison of metabolic activity of cells measured by MTT immediately after (<b>A</b>) and 24 h after (<b>B</b>) the exposure to partly oxidized 22:6PC (Pox22:6PC) in dark (Dark) or during concomitant exposure to 15 mW/cm<sup>2</sup> visible light (Light). Symbols indicate the means; error bars indicate SEM from at least three independent experiments.</p>
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<p>Plasma membrane integrity of ARPE-19 cells immediately after (0 h) and 2 h after 1-h exposure to lipid vesicles containing partly oxidized 22:6PC (Pox22:6PC) at indicated concentrations in the presence of 15 mW/cm<sup>2</sup> visible light assessed by propidium iodide (PI) assay. Representative images of fluorescence of cells stained with Hoechst (blue) and PI (pink) immediately after the exposure (<b>A</b>) and 2 h post-exposure (<b>B</b>). All micrographs are taken at the same magnification. (<b>C</b>): The ratio of nuclei stained with PI to total nuclei per image expressed as a percentage as a function of Pox22:6PC concentration. Symbols indicate the means, and the error bars indicate SEMs.</p>
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<p>Assays of apoptosis by evaluation of nuclear condensation and TUNEL of cells remaining attached 12 h after the exposure. (<b>A</b>): Representative fluorescence images of Hoechst (blue) and TUNEL (pink) of cells fixed 12 h after exposure to indicated concentrations of partly oxidized 22:6PC (Pox22:6PC). All micrographs were taken at the same magnification. (<b>B</b>): Quantification of normal and condensed nuclei of remaining attached cells. (<b>C</b>): Quantification of TUNEL positive and negative nuclei of remaining attached cells. In (<b>B</b>,<b>C</b>), the heights of rectangles indicate the means; the error bars indicate SDs.</p>
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<p>Effect of indicated micromolar concentrations of antioxidants, zeaxanthin or α-tocopherol, on (photo)toxicity of liposomes containing 0.5 mM partly oxidized 22:6PC (Pox22:6PC). (Photo)toxicity was measured by MTT assay of metabolic activity of ARPE-19 cells 24 h after a 1 h exposure to liposomes in the dark or under irradiation with visible light (15 mW/cm<sup>2</sup>). # indicates the mean metabolic activity is significantly different from that of the control cells under corresponding light/dark conditions. The heights of rectangles indicate the means; the error bars indicate SEMs; # indicates the mean metabolic activity significantly different from that of the control cells under the corresponding light/dark conditions; * indicates the mean metabolic activity significantly different from that of the cells exposed to Pox22:6PC without antioxidants under the corresponding light/dark conditions.</p>
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<p>(<b>A</b>): Absorption spectra of liposomal extracts obtained after 1-h exposure of zeaxanthin-containing liposomes to light or incubation in the dark in PBS containing 0.2% DMSO. The liposomes contained partly oxidized 1.5 mM 22:6PC (Pox22:6PC) and 4 µM zeaxanthin in the absence or presence of 40 µM α-tocopherol (TOH). The control spectrum of zeaxanthin was obtained by extraction of zeaxanthin delivered into PBS solution directly with DMSO. (<b>B</b>): Effect of α-tocopherol and/or zeaxanthin at indicated micromolar concentrations on (photo)toxicity when added to Pox22:6PC liposomes from a solution in DMSO immediately before adding to cells in the culture wells. (Photo)toxicity was measured by MTT assay of metabolic activity of ARPE-19 cells 24 h after 1 h exposure to liposomes in the dark or under irradiation with visible light (15 mW/cm<sup>2</sup>). The heights of rectangles indicate the means; the error bars indicate SEMs; # indicates the mean metabolic activity significantly different from that of the control cells under the corresponding light/dark conditions; there are no statistically significant differences between the mean metabolic activities of the cells exposed to Pox22:6PC in the absence and presence of antioxidants under the corresponding light/dark conditions.</p>
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<p>MTT assay of metabolic activity carried out after supplementing cells for 2 or 3 weeks with POSs in the absence or presence of indicated micromolar concentrations of partly oxidized 22:6PC (Pox22:6PC). All treatments were normalized to control cells from the same culture plate. The heights of bars indicate the means; error bars indicate SEMs; # indicates the mean metabolic activity significantly different from that of the corresponding control cells.</p>
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<p>Accumulation of lipofuscin-like material in ARPE-19 cells fed 3 times per week with POSs supplemented with indicated concentrations of partly oxidized 22:6PC (Pox22:6PC) and evaluated by its fluorescence by flow cytometry (<b>A</b>) and by transmission electron microscopy (TEM; (<b>B</b>)). (<b>A</b>): The graphs on the left are representative histograms of fluorescent cells after indicated weeks of feeding; the graph on the right shows the geometric means of fluorescence as a function of time of supplementation with POSs with indicated concentrations of Pox22:6. A total of 10,000 cells was counted for each condition and time point. Fluorescence refers to the intensity of green fluorescence (arbitrary units). Symbols indicate the means; error bars indicate SEMs. Most cells fed POSs supplemented with 20 μM Pox22:6PC (blue lines) died in the 4th week of feeding, so the accumulation of lipofuscin-like fluorescence could not be evaluated at the end of that week. (<b>B</b>): on the left, a representative TEM micrograph of a control cell cross-section; in the middle: a representative TEM micrograph of a POS-supplemented cell with green arrows pointing to membraneous deposits and red arrows pointing to the homogenous deposits; on the right: a bar chart depicting the numbers of homogenous and membraneous deposits per cell cross-section after 2 weeks of supplementation with POSs and/or 20 μM Pox22:6PC. The heights of rectangles indicate the means; error bars indicate SDs based on 10 different cells for each treatment.</p>
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17 pages, 556 KiB  
Article
Effect of Different Dietary Doses of Black Soldier Fly Meal on Performance and Egg Quality in Free-Range Reared Laying Hens
by Carlos Romero, Juan Carlos Cenalmor, Susana Chamorro and César Redondo
Animals 2024, 14(22), 3340; https://doi.org/10.3390/ani14223340 - 20 Nov 2024
Viewed by 247
Abstract
(1) Background: Given the problems currently posed by the use of soybean meal in poultry feeding, its replacement with black soldier fly (BSF) meal may be a suitable strategy. Therefore, this study evaluated the effect of this dietary replacement on laying performance, egg [...] Read more.
(1) Background: Given the problems currently posed by the use of soybean meal in poultry feeding, its replacement with black soldier fly (BSF) meal may be a suitable strategy. Therefore, this study evaluated the effect of this dietary replacement on laying performance, egg quality, and yolk nutritional composition in free-range reared hens. (2) Methods: Three diets were formulated: a control diet with 210 g/kg of soybean meal, a diet with 105 g/kg of soybean meal and 80 g/kg of BSF meal, and a diet with 160 g/kg of BSF meal. This eight-week-long study was performed with 126 Bovans Brown hens aged 36 weeks (six replicates of seven hens each per dietary treatment); (3) Results: The laying performance of hens was not influenced by the diet consumed. Neither was the yolk content in fat, protein, cholesterol, choline, B vitamins, and cholecalciferol affected. The dietary inclusion of BSF meal made yolk colour score and albumen Haugh units decrease (p < 0.001) by 51.1% and 12.0%, respectively. It also reduced the yolk content in retinol (by 10.1%, p = 0.0037), but it increased that of α- and γ-tocopherol (by 27.6%, p = 0.014, and 25.8%, p = 0.0077, respectively). A negative linear effect (p < 0.001) was observed on yolk zinc concentration and on the proportions of polyunsaturated and ω-3 fatty acids with increasing dietary dose of BSF meal; (4) Conclusions: Soybean meal could be fully replaced by BSF meal in the diet of hens without affecting the laying rate or the egg weight. However, the dietary inclusion of BSF meal led to paler yolks and impaired albumen quality, while it decreased the content of retinol and zinc and the proportions of polyunsaturated and ω-3 fatty acids in egg yolk. Full article
(This article belongs to the Section Poultry)
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<p>Effect of egg storage time on albumen Haugh units depending on the diet consumed (SEM = 1.27; n = 108 eggs at each day; <span class="html-italic">p</span> <sub>time</sub> &lt; 0.001; <span class="html-italic">p</span> <sub>diet</sub> &lt; 0.001; <span class="html-italic">p</span> <sub>time x diet</sub> = 0.042). Diets: Control diet; 8% BSF meal: diet including 80 g/kg of defatted black soldier fly meal; 16% BSF meal: diet including 160 g/kg of defatted black soldier fly meal. Eggs were stored in darkness at a constant temperature of 4 °C. <sup>a–d</sup> Means with different superscripts differ significantly (<span class="html-italic">p</span> &lt; 0.05).</p>
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13 pages, 991 KiB  
Article
Fatty Acid Composition, Oxidative Status, and Content of Biogenic Elements in Raw Oats Modified Through Agricultural Practices
by Michał Wojtacki, Krystyna Żuk-Gołaszewska, Robert Duliński, Joanna Giza-Gołaszewska, Barbara Kalisz and Janusz Gołaszewski
Foods 2024, 13(22), 3622; https://doi.org/10.3390/foods13223622 - 13 Nov 2024
Viewed by 380
Abstract
The chemical composition of raw oat grain is responsible for the high dietary value and health-promoting properties of oat products. This article presents the results of a study investigating the biofortification of grain in two oat genotypes—hulless and hulled—through agronomic treatments: chemical plant [...] Read more.
The chemical composition of raw oat grain is responsible for the high dietary value and health-promoting properties of oat products. This article presents the results of a study investigating the biofortification of grain in two oat genotypes—hulless and hulled—through agronomic treatments: chemical plant protection against weeds and fungi and mineral nitrogen fertilization. The applied agronomic treatments induced different changes in the fatty acid profiles, content of tocopherols, macronutrients, and micronutrients in the grain of hulled and hulless oats. Plant health contributed to higher concentrations of unsaturated fatty acids and potassium in oat grain. In turn, nitrogen fertilization decreased the content of unsaturated fatty acids, potassium, and copper and increased the content of saturated fatty acids, calcium, and manganese in oat grain. At the same time, agronomic treatments reduced the tocopherol content of the grain, which implies that the nutritional value of oats increases in the absence of chemical plant protection agents. The correlations between the content of desirable chemical compounds and agronomic treatments were stronger in hulless oat grain, which may suggest that the agronomic modification of oat-based foods is more effective in this genotype. The content of exogenous alpha-linoleic acid C18:3 n-3 and alpha-tocopherol was higher in grain harvested from the control treatment (without chemical plant protection), whereas grain harvested from fully protected treatments accumulated more essential gamma-linolenic acid C18:3 n-6. The content of gamma-tocopherol and copper in oat grain was higher in the absence of nitrogen fertilization. Full article
(This article belongs to the Section Food Nutrition)
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<p>Groups of fatty acids in the grain of different oat morphotypes, and <span class="html-italic">oat morphotype</span> x <span class="html-italic">plant protection</span> and <span class="html-italic">oat morphotype</span> x <span class="html-italic">nitrogen fertilization</span> interactions. C—control without plant protection; H—herbicide; HF—herbicide and fungicide; N0, N60, N120—nitrogen rate of 0, 60, and 120 kg ha<sup>−1</sup>, respectively; SFAs—saturated fatty acids; MUFAs—monounsaturated fatty acids; PUFAs—polyunsaturated fatty acids.</p>
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<p>Interaction effects of agronomic treatments on the content of tocopherol in the grain of hulled and hulless oats. C—control without plant protection; H—herbicide; HF—herbicide and fungicide; N0, N60, N120—nitrogen rates of 0, 60, and 120 kg ha<sup>−1</sup>, respectively.</p>
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<p>Significant effects of (<b>A</b>) the <span class="html-italic">nitrogen fertilization</span> x <span class="html-italic">oat morphotype</span> interaction on the calcium content of oat grain and (<b>B</b>) the <span class="html-italic">plant protection</span> x <span class="html-italic">oat morphotype</span> interaction on the zinc content of oat grain. The same lower-case letters next to the bars indicate a statistically insignificant difference according to Tukey’s test.</p>
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<p>Principal component analysis (PCA)—the first two principal components (PC1 and PC2) describe the relationships between agronomic treatments and the chemical properties of hulless (<b>left</b>) and hulled oat (<b>right</b>) grain. Inner and outer dotted circles represent correlation coefficients of 0.7 and 1, respectively. Black circles denote agronomic treatments: {C}—control without chemical plant protection, {H}—herbicide application, {HF}—herbicide and fungicide application, {N0}—without mineral nitrogen fertilization, {N60} and {N120}—nitrogen fertilization applied at 60 and 120 kg ha<sup>−1</sup>, respectively. Blue circles—macronutrients and micronutrients. Yellow circles—saturated fatty acids. Red circles—unsaturated fatty acids. White circles—proximates. Gray circles—tocopherols.</p>
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12 pages, 1039 KiB  
Article
Cold-Pressed Aristotelia chilensis (Mol.) Stuntz Seed Oil Prevents Metabolic-Dysfunction-Associated Steatotic Liver Disease (MASLD) in a High-Fat-Diet-Induced Obesity Murine Model
by Benjamín Claria, Alejandra Espinosa, Alicia Rodríguez, Gretel Dovale-Rosabal, José Luis Bucarey, María Elsa Pando, Nalda Romero, Francisca Reinoso, Camila Sánchez, Rodrigo Valenzuela, Carolina H. Ribeiro and Santiago P. Aubourg
Antioxidants 2024, 13(11), 1384; https://doi.org/10.3390/antiox13111384 - 13 Nov 2024
Viewed by 381
Abstract
This study evaluated the effects of cold-pressed maqui (Aristotelia chilensis (Mol.) Stuntz) seed oil (MO) on liver metabolism and biochemical markers in a high-fat diet (HFD) murine model. In it, the fatty acid profile, tocopherol and tocotrienol contents, and antioxidant capacity of [...] Read more.
This study evaluated the effects of cold-pressed maqui (Aristotelia chilensis (Mol.) Stuntz) seed oil (MO) on liver metabolism and biochemical markers in a high-fat diet (HFD) murine model. In it, the fatty acid profile, tocopherol and tocotrienol contents, and antioxidant capacity of MO were analyzed. Male C57BL/6 mice were divided into four groups (i.e., a, b, c, and d groups) and supplemented for 12 weeks according to the following distribution: (a) control diet (CD)-sunflower oil (SO), (b) CD+MO, (c) HFD+SO, and (d) HFD+MO. Total body and organ weights, serum markers, and liver fat infiltration were assessed. MO contained 32.31% oleic acid, 46.41% linoleic acid, and 10.83% α-linolenic acid; additionally, α- and γ-tocopherol levels were 339.09 ± 5.15 and 135.52 ± 38.03 mg/kg, respectively, while β-, δ-tocopherol, and α-tocotrienol were present in trace amounts and the antioxidant capacity measured was 6.66 ± 0.19 μmol Trolox equivalent/g. MO supplementation significantly reduced the visceral fat (0.76 ± 0.06 g vs. 1.32 ± 0.04 g) and GPT (glutamate pyruvate transaminase) levels (71.8 ± 5.0 vs. 35.2 ± 2.6 U/L), and the liver fat infiltration score (6 vs. 3) in the HFD+MO group compared to HFD+SO. It is suggested that MO may effectively prevent fatty liver disease, warranting further research on its potential benefits for human health. Full article
(This article belongs to the Special Issue Phenolic Antioxidants)
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<p>Effect of cold-pressed maqui seed oil (MO) on total and adipose tissue weight of mice under an HFD. Animals were weighed before euthanasia (<b>a</b>), followed by an immediate measure of the liver (<b>b</b>), visceral fat (<b>c</b>), and epididymal fat (<b>d</b>) weight. Abbreviations: CD (control diet), HFD (high-fat diet), and SO (sunflower oil). Data are presented as the mean ± standard error of the mean (SEM). Statistical differences were determined using ordinary two-way ANOVA test, followed by Tukey’s comparative 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; **** <span class="html-italic">p</span> &lt; 0.0001; ns: no significant differences; <span class="html-italic">n</span> = 6 mice for each group.</p>
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<p>Histology of liver steatosis prevention by cold-pressed maqui seed oil supplementation. (<b>a</b>) Hematoxylin and eosin (H&amp;E) staining of paraffin liver sections displaying general architecture and cellular morphology. White arrows indicate macrovesicular steatosis and black arrows microvesicular steatosis. (<b>b</b>) Bodipy staining on a representative liver cryosection for lipid detection (green fluorescence) merged with DAPI stain (blue). Abbreviations: CD (control diet), HFD (high-fat diet), SO (sunflower oil), and MO (cold-pressed maqui seed oil); <span class="html-italic">n</span> = 6 mice for each group. Magnification of the figure is 400×.</p>
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18 pages, 1714 KiB  
Review
Potential Vitamin E Signaling Mediators in Skeletal Muscle
by Elisabetta Meacci, Antony Chirco and Mercedes Garcia-Gil
Antioxidants 2024, 13(11), 1383; https://doi.org/10.3390/antiox13111383 - 13 Nov 2024
Viewed by 391
Abstract
Vitamin E (Vit E) deficiency studies underline the relevance of this vitamin in skeletal muscle (SkM) homeostasis. The knowledge of the effectors and modulators of Vit E action in SkM cells is limited, especially in aging and chronic diseases characterized by a decline [...] Read more.
Vitamin E (Vit E) deficiency studies underline the relevance of this vitamin in skeletal muscle (SkM) homeostasis. The knowledge of the effectors and modulators of Vit E action in SkM cells is limited, especially in aging and chronic diseases characterized by a decline in musculoskeletal health. Vit E comprises eight fat-soluble compounds grouped into tocopherols and tocotrienols, which share the basic chemical structure but show different biological properties and potentials to prevent diseases. Vit E has antioxidant and non-antioxidant activities and both favorable and adverse effects depending on the specific conditions and tissues. In this review, we focus on the actual knowledge of Vit E forms in SkM functions and new potential signaling effectors (i.e., bioactive sphingolipids and myokines). The possible advantages of Vit E supplementation in counteracting SkM dysfunctions in sarcopenia and under microgravity will also be discussed. Full article
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Graphical abstract
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<p>(<b>A</b>) Stereochemical structures of tocotrienols and tocopherols. The four isoforms of both tocopherols and tocotrienols differ in the degree and position of methyl groups on the chromanol ring: the α-isomers are trimethylated, the β- and γ-isomers are dimethylated, and the δ-isomers are monomethylated. (<b>B</b>) Most relevant biological differences between tocotrienols and tocopherols.</p>
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<p>Effects of tocopherols and tocotrienols on skeletal muscle. The figure shows the potential molecular mechanisms (blue arrows) by which tocopherols and tocotrienols act in SkM cells, leading to the modulation of biochemical processes (blue boxes) and tissue regeneration or atrophy. The double yellow arrows indicate an unknown relationship. Green arrow: decrease; red arrow: increase.</p>
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<p>Sphingolipid structure, metabolism, and function in SkM. (<b>A</b>) The stereochemical structure of the sphingolipids sphingosine, ceramide, and sphingomyelin. (<b>B</b>) Balance between ceramide (Cer) and S1P content can affect the cellular fate. In SkM, S1P is a pro-survival and pro-myogenic factor, whereas ceramide inhibits myogenesis and promotes cell atrophy. (<b>C</b>) Sphingolipid metabolism. The de novo SL pathway occurs in the endoplasmic reticulum, where the condensation of serine and palmitoyl CoA by serine palmitoyltransferase (SPT) generates ceramide, which is then shuttled to the Golgi apparatus. Here, it is used as the building structure for the synthesis of sphingomyelin and other complex sphingolipids. Cer can also be generated by sphingomyelin hydrolysis catalyzed by sphingomyelinase (SMase) activity. Ceramide is then converted reversibly to sphingosine by ceramidase (CDase) or phosphorylated to ceramide-1-phosphate (C1P) by ceramide kinase (CERK) activity. Successively, sphingosine is phosphorylated by two isoforms of sphingosine kinases, SPHK1 and SPHK2, to S1P. The exit from the sphingolipid synthesis pathways occurs through S1P lyase, which promotes the degradation of S1P into hexadecenal and phosphoethanolamine. The latter is further metabolized into palmitoyl CoA. S1P is also a substrate of specific S1P phosphatases, which generate sphingosine. CERS: ceramide synthase; DEGS: sphingolipid delta 4-desaturases; SMS: sphingomyelin synthase; KDS: 3-ketodihydrosphingosine reductase. (<b>D</b>) S1P produced by the active membrane-bound SPHK from sphingosine (Sph) can be transported outside the cell by an ATP-binding cassette transporter named spinster homolog 2 (Spns2) and, acting as a ligand for specific GTP-binding protein-coupled receptors (S1PRs), can affect different signaling pathways. The orange boxes indicate the metabolites that are affected by Vit E.</p>
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17 pages, 319 KiB  
Article
Comparative Evaluation of Camelina Seed Oils Obtained by Cold-Pressing and Solvent Extraction
by Slađana Rakita, Nedeljka Spasevski, Ivan Savić, Ivana Savić Gajić, Jasmina Lazarević, Danka Dragojlović and Olivera Đuragić
Foods 2024, 13(22), 3605; https://doi.org/10.3390/foods13223605 - 11 Nov 2024
Viewed by 539
Abstract
This study aimed to analyze the physicochemical properties and nutritional quality of oil extracted from the camelina seed genotypes NS Zlatka and NS Slatka, grown in Serbia, using both Soxhlet extraction with n-hexane and the cold-pressing technique. Extraction technique did not have [...] Read more.
This study aimed to analyze the physicochemical properties and nutritional quality of oil extracted from the camelina seed genotypes NS Zlatka and NS Slatka, grown in Serbia, using both Soxhlet extraction with n-hexane and the cold-pressing technique. Extraction technique did not have an effect on oil yield. Camelina oils exhibited satisfactory physicochemical characteristics, which were influenced by the extraction methods. The oils were rich in polyunsaturated fatty acids, with α-linolenic acid being the most abundant. They were characterized by a balanced ω-6 to ω-3 ratio (0.5), low atherogenicity index and thrombogenicity index values, and a relatively high hypocholesterolemic/hypercholesterolemic ratio. Cold-pressed oils contained significantly higher amounts of α- and γ-tocopherols and showed greater oxidative stability at moderate temperatures, as confirmed by the Schaal oven test. Despite this, their oxidative stability decreased at elevated temperatures (Rancimat test) compared to solvent-extracted oils. Conversely, solvent-extracted oils had higher levels of β-carotene and showed superior resistance to high-temperature conditions. Due to its unique characteristics, nutritional properties, and health-promoting attributes, cold-pressed camelina oil presents significant potential for application in food, nutraceutical, feed, and cosmetic industries. Full article
(This article belongs to the Special Issue Edible Oils: Composition, Processing and Nutritional Properties)
28 pages, 3460 KiB  
Article
Antioxidant Valorization of PLE Extracts from Macroalgae (Cladophora glomerata): In Vitro Assessment of Nanoemulsions Against Oxidative Stress
by Lucía Sáez-González, Marcos Carreño-Díaz, Gema Blázquez-Abellán, Manuel J. Santander-Ortega, Rosa M. Martínez-García, Luis A. Martínez, Jose A. Carbajal and Lucía Castro-Vázquez
Antioxidants 2024, 13(11), 1370; https://doi.org/10.3390/antiox13111370 - 8 Nov 2024
Viewed by 385
Abstract
Driven by a growing global interest in natural products, macroalgae have emerged as a prime source for nutraceuticals and pharmaceutical applications. In the current research, the effect of oven-drying (OD) and freeze-drying (FD), as well as the pressurized liquid extraction (PLE) conditions, were [...] Read more.
Driven by a growing global interest in natural products, macroalgae have emerged as a prime source for nutraceuticals and pharmaceutical applications. In the current research, the effect of oven-drying (OD) and freeze-drying (FD), as well as the pressurized liquid extraction (PLE) conditions, were investigated in relation to the polyphenols, flavonoids, carotenoids, chlorophylls, and tocochromanols levels in Cladophora glomerata extracts. The ethanol–water extracts (1:1) obtained with PLE-150 °C from macroalgae oven-dried (OD)-80 °C displayed the highest total polyphenol content (TPC) and total flavonoid contents (TFCs), reaching 29.62 mg GAE/g and 5.92 mg QE/g. Aqueous extracts using PLE-200 °C were also an excellent environmentally friendly option for TPC and TFC isolation, which were the main factors accounting for the ABTS, DPPH, and FRAP antioxidant activity of the extracts. The remarkable effects of drying conditions positively affect the carotenoids, chlorophyll α-tocopherol, and α-tocotrienol levels from extracts showing 1.3–6 times higher amounts in extracts of Cladophora glomerata OD at 80 °C compared with other research approaches. Nanotechnology approaches allowed the formulation of antioxidant-loaded nanoemulsions from Cladophora glomerata extracts, providing stability and a great internalization rate that ameliorates to 85% the ROS levels, attenuating the oxidative stress induced by H2O2 in J774.1 macrophage cell line. Full article
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<p>(<b>a</b>–<b>c</b>) show the total phenolic compounds (TPCs) regarding gallic acid equivalent (GAE) for all the solvents and temperatures tested in <span class="html-italic">Cladophora glomerata.</span> (<b>d</b>) shows differences between the macroalgae drying method. Different letters in the same column (a–d) denote a significant difference according to the Student–Newman–Keuls test, at <span class="html-italic">p</span> ≤ 0.05.</p>
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<p>Mean concentration of flavonoids in <span class="html-italic">Cladophora glomerata</span> algae, freeze-dried, oven-dried (60 °C, 80 °C). No significant differences were observed between samples with the same color of asterisks (*) of every solvent, according to the Student–Newman–Keuls test, at <span class="html-italic">p</span> ≤ 0.05. QE—quercetin equivalent.</p>
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<p>Chromatographic profile of tocopherols (T) and tocotrienols (T3) from <span class="html-italic">Cladophora glomerata</span>, previously oven-dried at 60 °C (using PLE at 150 °C). Mass spectrometry parameters for the isomer’s identification.</p>
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<p>Correlation between total phenols content (TPC) and total flavonoids content (TFC) with the antioxidant activity (DPPH, FRAP, and ABTS assay) in <span class="html-italic">Cladophora glomerata</span> algae oven-dried at 80 °C and submitted to PLE extraction at 50 °C, 100 °C, 150 °C, and 200 °C using ethanol–water (1:1) (<b>a</b>,<b>b</b>) and water (<b>c</b>,<b>d</b>).</p>
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<p>Hydrodynamic mean size of the nanoemulsions formulated either with Mygliol © or Soybean oils with the three different <span class="html-italic">Cladophora glomerata</span> extracts (<b>a</b>). Z-Potential of the nanoemulsions formulated either with Mygliol © or Soybean oils with 3 different <span class="html-italic">Cladophora glomerata</span> extracts (<b>b</b>). 1:1 150°: PLE <span class="html-italic">Cladophora</span> G. extracts obtained with ethanol–water (1:1) at 150 °C 1:1 100°: PLE <span class="html-italic">Cladophora</span> G. extracts obtained with ethanol–water (1:1) at 100 °C 1:1 100°: PLE <span class="html-italic">Cladophora</span> G. extracts obtained with water at 200 °C.</p>
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<p>Antioxidant effect of the three free extracts from <span class="html-italic">Cladophora glomerata</span> at different concentrations on the intracellular ROS generation in J774.1 macrophage cells after oxidative stress induced by H<sub>2</sub>O<sub>2</sub>. The ROS percentages were calculated considering 123.5 mM of H<sub>2</sub>O<sub>2</sub> in relation to 100% ROS. Significant difference <span class="html-italic">p</span> ≤ 0.001 (***), <span class="html-italic">p</span> ≤ 0.0001 (****).</p>
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<p>Effect of the type of nanoemulsion from <span class="html-italic">Cladophora glomerata</span> on the intracellular ROS in J774.1 macrophage cells after oxidative stress induced by H<sub>2</sub>O<sub>2</sub>. Cladoph. Ext: free <span class="html-italic">Cladophora glomerata</span> extracts from hydroalcoholic PLE-150 °C Miglyol ©: nanoemulsion of <span class="html-italic">Cladophora glomerata</span> using Miglyol Soybean: nanoemulsion of <span class="html-italic">Cladophora glomerata</span> using soybean oil. <span class="html-italic">p</span> ≤ 0.0001 (****).</p>
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24 pages, 4261 KiB  
Review
Perilla Seed Oil and Protein: Composition, Health Benefits, and Potential Applications in Functional Foods
by Lijun Guan, Ling Zhu, Xindi Zhang, Yaxi Han, Kunlun Wang, Nina Ji, Xinmiao Yao, Ye Zhou, Bo Li, Qing Chen, Jing Fan, Dixin Sha and Shuwen Lu
Molecules 2024, 29(22), 5258; https://doi.org/10.3390/molecules29225258 - 7 Nov 2024
Viewed by 1014
Abstract
Perilla (Perilla frutescens) seeds are emerging as a valuable resource for functional foods and medicines owing to their rich oil and protein content with diverse nutritional and health benefits. Perilla seed oil (PSO) possesses a high level of a-linolenic acid (ALA), [...] Read more.
Perilla (Perilla frutescens) seeds are emerging as a valuable resource for functional foods and medicines owing to their rich oil and protein content with diverse nutritional and health benefits. Perilla seed oil (PSO) possesses a high level of a-linolenic acid (ALA), a favorable ratio of unsaturated to saturated fatty acids, and other active ingredients such as tocopherols and phytosterols, which contribute to its antioxidant, anti-inflammatory, and cardiovascular protective effects. The balanced amino acid ratio and good functional properties of perilla seed protein make it suitable for a variety of food applications. The chemical composition, health benefits, and potential applications of PSO as well as the structural characterization, functional properties, modification methods, bioactivities, and application scenarios of perilla seed protein are comprehensively presented in this paper. Furthermore, the challenges as well as future prospects and research focus of PSO and perilla seed protein are discussed. The growing interest in plant-based diets and functional foods has made PSO and perilla seed protein promising ingredients for the development of novel foods and health products. The purpose of this paper is to highlight implications for future research and development utilizing these two untapped resources to improve human health and nutrition. Full article
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<p>The plant (<b>a</b>) and seed (<b>b</b>) of perilla.</p>
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<p>Chemical structure of fatty acids, phytosterols, and tocopherols in PSO.</p>
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<p>Activation and negative regulation of JAK-STAT and NF-κB signaling pathways after PSO treatment.</p>
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15 pages, 1792 KiB  
Article
Nutritional Quality, Functional Properties, and Biological Characterization of Watermeal (Wolffia globosa)
by Parinya Boonarsa, Apichaya Bunyatratchata, Theeraphan Chumroenphat, Pornpisanu Thammapat, Tipaukson Chaikwang, Tarathep Siripan, Hua Li and Sirithon Siriamornpun
Horticulturae 2024, 10(11), 1171; https://doi.org/10.3390/horticulturae10111171 - 5 Nov 2024
Viewed by 859
Abstract
Watermeal (Wolffia globosa) has emerged as a promising candidate as an alternative protein source due to its outstanding nutritional profile. This study evaluated the nutritional quality, functional properties, and biological characteristics of W. globosa. The protein content was found to be [...] Read more.
Watermeal (Wolffia globosa) has emerged as a promising candidate as an alternative protein source due to its outstanding nutritional profile. This study evaluated the nutritional quality, functional properties, and biological characteristics of W. globosa. The protein content was found to be high at 26.76 g/100 g of dry weight (DW). Functional properties, including water and oil holding capacities, protein solubility, foaming, and emulsifying abilities across different pH levels, were assessed to determine optimal conditions. Amino acid profiling revealed that essential amino acids constitute 67% of the total amino acids. Polyunsaturated fatty acids (PUFAs), particularly α-linolenic (18:3 n-3) and linoleic acids (18:2 n-6), were identified as the predominant fatty acids. Additionally, watermeal was found to contain significant amounts of α-tocopherol (699 µg/g) and γ-oryzanol (100 µg/g), which contribute to its antioxidant capacity, as confirmed by DPPH and FRAP assays. The prominent protein bands were observed at around 62–67 kDa, likely representing a structural, metabolic protein (vicilin-like protein) of 38% of the total protein content. Overall, W. globosa demonstrates significant potential as a functional food ingredient, offering a rich nutrient profile and health-promoting properties, making it a promising choice for future diets. Full article
(This article belongs to the Section Processed Horticultural Products)
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<p>Appearance of watermeal (<span class="html-italic">W. globosa</span>) samples.</p>
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<p>The protein solubility (<b>A</b>), foaming capacity (<b>B</b>), foaming stability (<b>C</b>), emulsion capacity (<b>D</b>), and emulsion stability (<b>E</b>) as a function of the pH of watermeal (<span class="html-italic">W. globosa</span>).</p>
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<p>Molecular weight distribution of protein in watermeal (<span class="html-italic">W. globosa</span>).</p>
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16 pages, 1431 KiB  
Article
Effect of Extracted Walnut Pomace Cake Edible Coating and Packaging Type on Quality Parameters of Walnut (Juglans regia L.) Kernels During Long Storage Periods
by Pradeep Kumar, Lilla Szalóki-Dorkó, Beatrix Szabó-Nótin, Julianna Kereszturi, Judit Tormási, László Abrankó, István Dalmadi, Dóra Székely and Mónika Máté
Appl. Sci. 2024, 14(22), 10120; https://doi.org/10.3390/app142210120 - 5 Nov 2024
Viewed by 504
Abstract
Walnuts are highly valued for their rich nutritional content, but their quality degrades during storage due to oxidation and other quality reducing processes. This study investigated the use of bioactive compounds extracted from walnut pomace, a by-product of walnut oil production, to develop [...] Read more.
Walnuts are highly valued for their rich nutritional content, but their quality degrades during storage due to oxidation and other quality reducing processes. This study investigated the use of bioactive compounds extracted from walnut pomace, a by-product of walnut oil production, to develop an edible coating that extends the shelf life of ‘Milotai 10’ walnut kernels. Walnut kernels were stored for eight months in four different packaging materials (PE, PP, MPP, PLA) and three treatments were used (air or without treatment, nitrogen gas, and walnut pomace extract coating). The effects of these combinations on walnut quality parameters, including polyphenol content, vitamin E, fatty acids, peroxide value, and color, were analyzed. The results show that the combination of metallized polypropylene packaging under nitrogen treatment or with atmospheric air and walnut pomace extract (MPP-A-E+) best preserves walnut quality, making it a promising option for extending shelf-life. Full article
(This article belongs to the Special Issue Extraction of Functional Ingredients and Their Application)
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<p>ΔE* values for the different packaging treatments and packaging materials for ‘Milotai 10’ cultivar. PE (polyethylene), PP (polypropylene), MPP (metallized polypropylene), PLA (polylactic acid), A–E- (air without edible coating), A–E+ (air, with edible coating), N–E- (nitrogen without edible coating).</p>
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<p>Tocopherol content of the MPP and PP packaging samples during storage (µg/g). MPP (metallized polypropylene), PP (polypropylene), A–E- (air without edible coating), A–E+ (air, with edible coating), N–E- (nitrogen without edible coating).</p>
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<p>Tocopherol content of the PE and PLA packaging samples during storage (µg/g). PE (polyethylene), PLA (polylactic acid), A–E- (air without edible coating), A–E+ (air, with edible coating), N–E- (nitrogen without edible coating).</p>
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<p>Fatty acid content of the MPP and PP packaging samples during storage (%). MPP (metallized polypropylene), PP (polypropylene), A–E- (air without edible coating), A–E+ (air, with edible coating), N–E- (nitrogen without edible coating).</p>
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<p>Fatty acid content of the PE and PLA packaging samples during storage (%). PE (polyethylene), PLA (polylactic acid), A–E- (air without edible coating), A–E+ (air, with edible coating), N–E- (nitrogen without edible coating).</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 812
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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14 pages, 664 KiB  
Article
Day-to-Day Fluctuation in Micronutrient Content in Human Milk Relative to Maternal Diet
by Noelia Ureta-Velasco, Adriana Montealegre-Pomar, Kristin Keller, Diana Escuder-Vieco, José C. E. Serrano, Nadia Raquel García-Lara and Carmen R. Pallás-Alonso
Nutrients 2024, 16(21), 3727; https://doi.org/10.3390/nu16213727 - 31 Oct 2024
Viewed by 588
Abstract
Background/Objectives: The impact of daily variations in habitual maternal intake on human milk (HM) composition has been poorly studied. We aimed to investigate the associations between day-to-day fluctuation in the micronutrient concentration in HM and daily maternal diet. Methods: To this end, an [...] Read more.
Background/Objectives: The impact of daily variations in habitual maternal intake on human milk (HM) composition has been poorly studied. We aimed to investigate the associations between day-to-day fluctuation in the micronutrient concentration in HM and daily maternal diet. Methods: To this end, an observational longitudinal study was carried out. A total of 143 lactating women each compiled a five-day weighed dietary record and concomitantly expressed milk for four successive days. Maternal daily intakes of micronutrients and food groups were analyzed. Free thiamine, free riboflavin, nicotinamide, pantothenic acid, pyridoxal, folic acid, cobalamin, ascorbic and dehydroascorbic acids, retinol, alpha- and gamma-tocopherol, cholecalciferol, and calcidiol in HM were determined for each of the four investigated days. A longitudinal data analysis with generalized estimating equation models was performed. Results: For each daily serving of meat, fish, and eggs, total vitamin D3 levels increased by 243.2 pg/mL (p = 0.027) and selenium levels increased by 0.16 ppb (p = 0.031) in HM. For every 1 mg/day of riboflavin supplementation, free riboflavin levels in HM increased by 28.6 mcg/L (p = 0.019). Pyridoxal levels in HM increased by 6.3 mcg/L per 1 mg/day of vitamin B6 supplementation (p = 0.001), and by 2 mcg/L per daily fruit ration (p = 0.016). Conclusions: In conclusion, we were able to quantify the impact of the usual day-to-day variations in the diet and in the intake of commonly used supplements on the fluctuation of vitamin D, free riboflavin, pyridoxal, and selenium concentration in the milk of lactating women. Full article
(This article belongs to the Section Nutrition in Women)
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<p>Protocol for completion of the dietary record and collection of milk samples over time.</p>
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<p>Distribution of participants (<span class="html-italic">n</span> = 143) by group. Abbreviations: D, human milk donors; P, mothers of preterm infants less than 32 weeks gestational age admitted to the neonatal service; V, vegetarian or vegan mothers. Number of total human milk donors = 113 (108 + 2 + 3). Number of total mothers of preterm infants less than 32 weeks of gestational age admitted to the neonatal service = 15 (12 + 3). Number of total vegetarian or vegan mothers = 20 (18 + 2).</p>
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18 pages, 5024 KiB  
Article
Impact of Buriti Oil from Mauritia flexuosa Palm Tree on the Rheological, Thermal, and Mechanical Properties of Linear Low-Density Polyethylene for Improved Sustainability
by Odilon Leite-Barbosa, Marcelo Ferreira Leão de Oliveira, Fernanda Cristina Fernandes Braga, Sergio Neves Monteiro, Marcia Gomes de Oliveira and Valdir Florêncio Veiga-Junior
Polymers 2024, 16(21), 3037; https://doi.org/10.3390/polym16213037 - 29 Oct 2024
Viewed by 547
Abstract
Recent advancements highlight the utilization of vegetable oils as additives in polymeric materials, particularly for replacing conventional plasticizers. Buriti oil (BO), extracted from the Amazon’s Mauritia flexuosa palm tree fruit, boasts an impressive profile of vitamins, minerals, proteins, carotenoids, and tocopherol. This study [...] Read more.
Recent advancements highlight the utilization of vegetable oils as additives in polymeric materials, particularly for replacing conventional plasticizers. Buriti oil (BO), extracted from the Amazon’s Mauritia flexuosa palm tree fruit, boasts an impressive profile of vitamins, minerals, proteins, carotenoids, and tocopherol. This study investigates the impact of incorporating buriti oil as a plasticizer in linear low-density polyethylene (LLDPE) matrices. The aim of this research was to evaluate how buriti oil, a bioactive compound, influences the thermal and rheological properties of LLDPE. Buriti oil/LLDPE compositions were prepared via melt intercalation techniques, and the resulting materials were characterized through thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), mechanical property testing, and contact angle measurement. The addition of buriti oil was found to act as a processing aid and plasticizer, enhancing the fluidity of LLDPE polymer chains. TGA revealed distinct thermal stabilities for buriti oil/LLDPE under different degradation conditions. Notably, buriti oil exhibited an initial weight loss temperature of 402 °C, whereas that of LLDPE was 466.4 °C. This indicated a minor reduction in the thermal stability of buriti oil/LLDPE compositions. The thermal stability, as observed through DSC, displayed a nuanced response to the oil’s incorporation, suggesting a complex interaction between the oil and polymer matrix. Detailed mechanical testing indicated a marked increase in tensile strength and elongation at break, especially at optimal concentrations of buriti oil. SEM analysis showcased a more uniform and less brittle microstructure, correlating with the enhanced mechanical properties. Contact angle measurements revealed a notable shift in surface hydrophobicity, indicating a change in the surface chemistry. This study demonstrates that buriti oil can positively influence the processability and thermal properties of LLDPE, thus expanding its potential applications as an effective plasticizer. Full article
(This article belongs to the Special Issue Physicochemical Properties of Polymer Composites)
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<p>FTIR spectra of buriti oil.</p>
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<p>Torque (<b>a</b>) and specific energy (<b>b</b>) curves as a function of processing time for the LLDPE and compositions.</p>
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<p>Thermogravimetric analysis (<b>a</b>) and differential thermal gravimetry (<b>b</b>) of buriti oil, pure LLDPE, and LLDPE/buriti oil compositions.</p>
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<p>DSC analysis of LLDPE and its compositions with buriti oil: (<b>a</b>) LLDPE, (<b>b</b>) LLDPE/buriti oil—0.1%, (<b>c</b>) LLDPE/buriti oil—0.3%, (<b>d</b>) LLDPE/buriti oil—0.5%, (<b>e</b>) LLDPE/buriti oil—1.0%. Note: Crystallization temperature (Tc).</p>
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<p>DSC analysis of LLDPE and its compositions with buriti oil: (<b>a</b>) LLDPE, (<b>b</b>) LLDPE/buriti oil—0.1%, (<b>c</b>) LLDPE/buriti oil—0.3%, (<b>d</b>) LLDPE/buriti oil—0.5%, (<b>e</b>) LLDPE/buriti oil—1.0%. Note: Crystalline melting temperature (Tm).</p>
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<p>SEM images of LLDPE and LLDPE/buriti oil compositions: (<b>a</b>) Pure LLDPE showing rough surface morphology; (<b>b</b>) LLDPE/buriti oil composition displaying smoother and more homogeneous surface; (<b>c</b>–<b>e</b>) LLDPE/buriti oil compositions with dispersed particles of varying sizes, indicating partial agglomeration within the matrix.</p>
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<p>Effect of buriti oil addition on the mechanical properties of LLDPE composites, including tensile strength (<b>a</b>), elongation at break (<b>b</b>), and elastic modulus (<b>c</b>). Error bars represent standard deviations.</p>
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Review
Anticancer Potential of Tocopherols-Containing Plants and Semi-Synthetic Tocopherols
by Nesti Fronika Sianipar, Zidni Muflikhati, Dave Mangindaan and Khoirunnisa Assidqi
Plants 2024, 13(21), 2994; https://doi.org/10.3390/plants13212994 - 26 Oct 2024
Viewed by 628
Abstract
Tocopherols, potent bioactive compounds with anticancer properties, remain understudied in herbal medicinal plants, presenting a significant knowledge gap in the field of natural anticancer agents. This review evaluates tocopherol-containing plants for their anticancer potential, analyzing Scopus publications from 2016 to 2024. Fifteen herbal [...] Read more.
Tocopherols, potent bioactive compounds with anticancer properties, remain understudied in herbal medicinal plants, presenting a significant knowledge gap in the field of natural anticancer agents. This review evaluates tocopherol-containing plants for their anticancer potential, analyzing Scopus publications from 2016 to 2024. Fifteen herbal medicinal plants were identified as promising candidates, including Bulbine anguistifolia Poelln, Punica granatum L., Moringa oleifera, Kigelia pinnata, and Typhonium flagelliforme Lodd. The review explores tocopherols’ anticancer mechanisms, including apoptosis induction and cell cycle arrest. Factors influencing tocopherols’ anticancer effects are examined, such as their forms (α, β, γ, δ), concentrations, plant parts utilized, and their stability in various plants. Additionally, emerging research on semi-synthetic tocopherol derivatives is analyzed, highlighting their potential as adjuvants in chemotherapy and their role in enhancing drug delivery and reducing side effects. This comprehensive analysis aims to advance the development of plant-based anticancer pharmaceuticals and improve cancer treatment strategies. By elucidating the mechanisms and potential of tocopherol-containing plants, this review provides a foundation for future research in plant-based anticancer therapies. It emphasizes the need for further investigation into these plants’ anticancer properties, potentially leading to novel, more effective, and less toxic cancer therapies. The findings presented here contribute to a nuanced understanding of how tocopherol-containing plants can be leveraged in the development of future anticancer drugs. Full article
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Figure 1

Figure 1
<p>Chemical structures of tocopherols (<b>1</b>–<b>3</b>, <b>6</b>–<b>8</b>), tocotrienols (<b>4</b>–<b>5</b>), α-tocospiro B (<b>9</b>), and α-tocopherol succinate (<b>10</b>). Structure numbers correspond to the “Structure Number” column in <a href="#plants-13-02994-t001" class="html-table">Table 1</a>. α-tocopherol (<b>1</b>), γ-tocopherol (<b>2</b>), δ- tocopherol (<b>3</b>), β-tocotrienol (<b>4</b>), γ-tocotrienol (<b>5</b>), DL-α-tocopherol (<b>6</b>), tocopherol trimer IVa (<b>7</b>) tocopherol trimer IVb (<b>8</b>), α-tocospiro B (<b>9</b>), and α-tocopherol succinate (<b>10</b>).</p>
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