Effect Of Selenium Nanoparticles Research Articles

Effects of selenium nanoparticles on larval development, ontogeny of antioxidant enzymes and fatty acid profile in Arabian yellowfin seabream (Acanthopagrus arabicus)

Selenium (Se) is an essential trace element that has vital effects on growth, antioxidant capacity and early development in marine fish larvae. However, traditional livefoods such as rotifer and artemia lack of Se. In this regard, a 50-day feeding experiment was conducted in order to examine the effects of Rotifer and Artemia enrichment with selenium nanoparticles (SeNPs) on growth, antioxidant capacity and fatty acid profile of Arabian yellowfin seabream (Acanthopagrus arabicus) larvae. Four levels of SeNPs were used to prepare the experimental emulsions,including control (0), 0.5, 1.0 and 5 mg SeNPs L−1. Larvae were stocked at density of 50 larvae L−1 into twelve 250-L cylindrical tanks. Tanks supplied with seawater (23 ± 1 ºC; 40.0 ± 1.0 g L−1). Green water was used from day first until 20 days after hatch (DAH). Rotifers (15 ml−1) were offered to larvae from day 2–21 DAH and Artemia metanauplii (1–3 Artemia ml−1) were offered to larvae from day 18–45 DAH. Fish were sampled at 0, 7, 10, 15, 22, 30, 40, 45, 50 DAH. The Se concentration in the livefoods and larval whole body linearly increased with the increment of SeNPs level in the experimental emulsions. Larvae wet weight showed quadratic response and increased with SeNPs up to 1 mg mg SeNPs/L, then decreased in SeNPs (5.0) group. The activity of antioxidant enzymes including catalase, superoxide dismutase glutathione peroxidase, and total antioxidant capacity increased but malondialdehyde level decreased in larvae fed the SeNPs-enriched livefoods and showed both linear and quadratic responses. Lysozyme activity in the whole body of larvae fed SeNPs-enriched livefoods had both linear and quadratic responses and in the most of the sampling times was higher than the control group. Docosahexaenoic acid (DHA) level in the livefoods and larval whole body increased with SeNPs. In conclusion, livefoods enrichment with SeNPs at 1 mg L−1 is recommended to elevate the antioxidant capacity and non-specific immune response in A. arabicus larvae.

Evaluation of biological selenium nanoparticles on growth performance, histopathology of vital organs and genotoxicity in Japanese quails (coturnix coturnix japonica)

Research on the effects of selenium nanoparticles (Se-NPs), particularly in Japanese quails, is lacking, especially regarding the potential for DNA damage. Therefore, this study aimed to investigate the impact of administering 0.2 and 0.4 mg/kg of Se-NPs on the growth performance, DNA integrity, and histopathological alterations of the liver, lung, kidney, and heart in quails. A total of 480 one-day-old Japanese quails were divided into three experimental groups as follows: Group 1 served as the control and received only basic feed, while Group 2 and 3 received 0.2 mg/kg and 0.4 mg/kg of Se-NPs via oral gavage. Our results suggested that, birds fed with Se-NPs at both levels significantly (p < .01) reduced feed intake, however, weight gain was significantly (p < .01) increased in quails supplemented with 0.2 mg/kg. Similarly, feed conversion ratio (FCR) was significantly (p < .01) reduced in group supplemented with 0.2 mg/kg Se-NPs. White blood cells increased significantly (P0.01) in 0.4 mg/kg while haemoglobin and red cell distribution width decreased (p < .01) in the same group. Both treatment regimens resulted in DNA damage and histopathological alterations; however, the adverse effects were more prominent in the group receiving the higher dose of 0.4 mg/kg. These findings indicate that the lower dose of 0.2 mg/kg may have beneficial effects on growth. However, the higher dose of 0.4 mg/kg not only negatively impacts growth but also leads to histopathological alterations in major organs of the body and DNA damage as well.

Effect of selenium nanoparticles on the quality and fertility of short-term preserved boar semen.

This study was carried out to investigate the effect of different concentrations of selenium nanoparticles (Se-NPs) in the Beltsville Thawing Solution (BTS) extender on the semen quality and fertility of Hampshire crossbred pigs. For the study, semen was collected from four boars (10 ejaculates/boar) by the gloved hand method. Each ejaculate was extended @ 1:2 with the BTS extender and split into four aliquots. The control (C) samples were without the supplementation of Se-NPs, whereas the other three were supplemented with 0.5 (T1), 1 (T2), and 2 μg ml-1 of Se-NPs (T3) and stored at 15°C in a BOD incubator. Extended semen was evaluated at 0 (immediately after dilution), 24, 48, 72, and 96 h of storage for sperm motility, live sperm, plasma membrane integrity, acrosome integrity, DNA integrity, and mitochondrial membrane potential (MMP). The mean percentage of sperm motility, live sperm, and sperm with intact plasma membrane and acrosome, and MMPs were significantly (p < 0.01) higher in all treated groups in comparison to control at 24, 48, 72, and 96 h of storage. Sperm with intact DNA in all treated groups increased significantly at 48 (p < 0.05), and 72 and 96 (p < 0.01) h of storage in comparison to the control group. The concentration of 1 μg ml-1 of Se-NPs was found to be the best among other concentrations. In each group, 10 sows were artificially inseminated with the liquid semen preserved for 72 h at 15°C. Supplementation of 1 μg ml-1 of Se-NPs yielded the highest conception rate in comparison to other groups. In conclusion, supplementation of 1 μg ml-1 of Se-NPs in the BTS extender resulted in the best semen quality and conception rate during the short-time liquid preservation of boar semen.

A screening for optimal selenium enrichment additives for selenium-enriched fish production: Application of a HPLC-ICP-MS method

The production of selenium-enriched fish contributes to alleviating selenium deficiency for humans. In this study, selenium nanoparticles (SeNPs) comparable in bioavailability to selenomethionine (SeMet), increased SeMet content in O. macrolepis (Onychostoma macrolepis) muscle. Additionally, dietary SeNPs significantly enhanced selenocysteine (SeCys2) and methylselenocysteine (MeSeCys) levels in O. macrolepis muscle. The effect of SeNPs on selenium speciation in grass carp muscle was consistent with O. macrolepis results. SeCys2 and MeSeCys showed antioxidant capacity in HEK293T cells, indicating enhanced health benefits of Se-enriched fish produced using SeNPs. Furthermore, the addition of 0.3 mg/kg SeNPs significantly improved the flesh quality of O. macrolepis by reducing the content of crude fat and heavy metals, as well as increasing the levels of crude protein, eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), and the ratio of n-3/n-6 polyunsaturated fatty acids (PUFAs). Therefore, selenium-enriched fish produced from SeNPs is a good source for improving human dietary selenium intake.

Effect of Selenium Nanoparticles and Aqueous Almond Extract on Isolated Bacteria

This study was conducted in the laboratories of the University of Tikrit / College of Agricultural Sciences / Department of Food Industries. The study began in the period 1/10/2022 to 1/6/2023. The study included the preparation of a biofilm of whey proteins combined with selenium nanoparticles (2 w/%) and (4) w/v%) as a coating of biocomposites to estimate the antibacterial effect against both Staphylococcus aureus and E.coli, and the total bacterial count (TBC) in soft cheese samples stored in the refrigerator at 4 °C during 14 days. To reach the goal of the study, the chemical parameters such as the pH value and the physical information that includes the water holding capacity (WHC), as well as the total number of bacteria and colon. In addition to the sensory properties of soft cheese samples without coating (control T1), coated with a biofilm of whey proteins T2, whey protein coatings mixed with selenium nanoparticles (2 w/v %) T3, whey protein coatings mixed with aqueous almond extract at (2 w/v %) T4, whey protein coatings mixed with Se NPs with aqueous almond extract at (2 w/v %) %) T5 The results showed that TBC and the total number of coliforms in samples coated with the mixture of whey proteins and nano-biofilms decreased significantly (P < 0.05), and TBC appeared in 14 days in T1, T2, T3, T4 and T5: 16.34, 15.12, 13.58, 11.28, and 12.84 (CFU.g-1) respectively compared to the number at the beginning of the experiment 8.6 9, 8.80, 8.87, 8.74, and 8.81 (CFU.g-1), respectively. An increase in the amount of ph and the value of TBA was observed with an increase in the storage period in all groups of soft cheese samples, while the rate of increase was significantly lower in the T5, T4 and T3 groups compared to the T2 and T1 groups. The percentage of water retention (WHC) decreased significantly with the increase in the storage period, and the decreasing rate was significantly less in the samples coated with a vital membrane of the spray proteins only and a vital membrane of the spray proteins integrated with the nano-selenium particles, which appeared in 14 days of storage in T2, T3, T4, T5 55.41, 56.71, 58.46 and 57.11 % Completely compared to the T1 53.32 % console. She was. The results of the sensory characteristics evaluation showed that the soft cheese samples coated with whey protein coatings combined with selenium nanoparticles and aqueous almond extract preserved their sensory properties until the end of the storage periods. Similarly, samples coated with a whey protein biofilm for nine days maintained their sensory characteristics. In contrast, the unwrapped samples maintained sensory features for only four days. It was concluded that the antibacterial and antioxidant effect of the mixture of biowhey proteins with selenium nanoparticles and aqueous almond extract enhanced the increase in the preservation periods of soft cheese samples for a period of 14 days inside the refrigerator at 4 °C without any effect on the sensory properties.

Effect of Nano-selenium on exosomes secretion associated with sperm maturation within the epididymis

Selenium is commonly used as a supplement in the poultry diet and plays an important role in male fertility. However, the effect of selenium nanoparticles (Se-NPs) on exosome secretion associated with spermatozoa in the epididymis is largely unknown. H&E staining, Immunohistochemistry, Immunofluorescence and Western blot were performed to study the effect of Se-NPs on exosomes secretion associated with sperm maturation in epididymis. The results indicated that the Se-NPs showed a significant contribution to sperm concentration by light microscopy. It was observed that there was an increase in the spermatozoa concentration in the epididymis of the treated group as compared to the control group. Furthermore, exosome secretion, the expression of tumor susceptibility gene-101 (TSG-101) and cluster of differentiation (CD-63) proteins was identified by immunochemistry, immunofluorescence assay, and western blotting. After nano-selenium treatment, the exosome markers TSG-101 and CD-63 were strong positive immunoreactivity and immunosignaling in the lumen followed by epithelial lining of the epididymis. However weak positive immunoreactivity and immunosignaling were seen of TSG-101 and CD63 in the control group. In addition, highly significant protein expression of TSG-101 and CD63 in the treated group as compared to the control group was confirmed by western blotting. In conclusion, the above findings provide rich evidence about the Se-NPs play a dynamic role in exosome secretion that might be essential for sperm motility and maturation within epididymis.

(-)-Epigallocatechin-3-Gallate Attenuates the Adverse Reactions Triggered by Selenium Nanoparticles without Compromising Their Suppressing Effect on Peritoneal Carcinomatosis in Mice Bearing Hepatocarcinoma 22 Cells.

Increasing evidence shows that selenium and polyphenols are two types of the most reported compounds in tumor chemoprevention due to their remarkable antitumor activity and high safety profile. The cross-talk between polyphenols and selenium is a hot research topic, and the combination of polyphenols and selenium is a valuable strategy for fighting cancer. The current work investigated the combination anti-peritoneal carcinomatosis (PC) effect of selenium nanoparticles (SeNPs) and green tea (Camellia sinensis) polyphenol (-)-epigallocatechin-3-gallate (EGCG) in mice bearing murine hepatocarcinoma 22 (H22) cells. Results showed that SeNPs alone significantly inhibited cancer cell proliferation and extended the survival time of mice bearing H22 cells. Still, the potential therapeutic efficacy is accompanied by an approximately eighty percent diarrhea rate. When EGCG was combined with SeNPs, EGCG did not affect the tumor proliferation inhibition effect but eliminated diarrhea triggered by SeNPs. In addition, both the intracellular selectively accumulated EGCG without killing effect on cancer cells and the enhanced antioxidant enzyme levels in ascites after EGCG was delivered alone by intraperitoneal injection indicated that H22 cells were insensitive to EGCG. Moreover, EGCG could prevent SeNP-caused systemic oxidative damage by enhancing serum superoxide dismutase, glutathione, and glutathione peroxidase levels in healthy mice. Overall, we found that H22 cells are insensitive to EGCG, but combining EGCG with SeNPs could protect against SeNP-triggered diarrhea without compromising the suppressing efficacy of SeNPs on PC in mice bearing H22 cells and attenuate SeNP-caused systemic toxicity in healthy mice. These results suggest that EGCG could be employed as a promising candidate for preventing the adverse reactions of chemotherapy including chemotherapy-induced diarrhea and systemic toxicity in cancer individuals.

Structurally natural chitosan films decorated with Andrographis paniculata extract and selenium nanoparticles: Properties and strawberry preservation

In this study, selenium nanoparticles (SeNPs) were synthesized using Annona glabra leaf extract as a reducing agent. In addition, the solution-casting method was employed to prepare the food preservation film from the chitosan-Andrographis paniculata extract-selenium nanoparticles (CS-APE-Se). The effects of SeNPs with different contents (equivalent to 1, 2, 3, and 4% of chitosan mass) on fundamental properties and bioactivities of the films were also tested. According to the results, the prepared films possess good biodegradability after 30 days of burial. Besides, the antioxidant activity of the material was also investigated via free radical scavenging toward 2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), which showed the inhibition rate up to 45 and 82%, respectively. Additionally, the antibacterial performance of the films was assessed against Staphylococcus aureus and Pseudomonas aeruginosa, which indicated the highest antibacterial capacity with the inhibition diameter of 18.1 ± 0.03 and 19.25 ± 0.01 mm, respectively. Furthermore, the coating of the CS-APE-Se films also effectively prevented physical damage and prolonged the shelf life of the strawberries by up to 10 days. The aforementioned results demonstrated the potential for applying chitosan (CS) film in combination with Andrographis paniculata leaf extract and SeNPs as a secure alternative to the harmful chemicals currently used in food preservation.

Effect of Selenium Nanoparticles and/or Bee Venom against STZ-Induced Diabetic Cardiomyopathy and Nephropathy.

The main purpose of our study was to examine the role of selenium nanoparticles (SeNPs) and/or bee venom (BV) in ameliorating diabetic cardiomyopathy (DCM) and nephropathy (DN) at the biochemical, histopathological and molecular levels. Fifty male albino rats were used in this experiment, divided into five groups: control, Streptozocin (STZ) diabetic, STZ-diabetic treated with SeNPs, STZ-diabetic treated with BV, and STZ-diabetic treated with SeNPs and BV. Biochemically, STZ injection resulted in a significant increase in serum glucose, BUN, creatinine, CRP, CK-MB, AST, LDH and cardiac troponins with a significant decrease in the serum insulin and albumin concentrations. Histopathologically, STZ injection resulted in diabetes, as revealed by glomerulonephritis, perivascular hemorrhage, inflammatory cell infiltrations and fibrosis, with widening of interstitial spaces of cardiomyocytes, loss of muscle cells continuity and some hyaline degeneration. At the molecular levels, the expression levels of miRNA 328, miRNA-21, TGFβ1, TGFβ1R, JAK1, STST-3, SMAD-1 and NFκβ genes were significantly up-regulated, whereas the expression levels of SMAD-7 were significantly down-regulated. It is concluded that SeNPs and/or BV administration ameliorates the deleterious effects resulting from STZ administration through improving the biochemical, histopathological and molecular effects, suggesting their protective role against the long-term diabetic complications of DCM and DN.

Carbapenem-Resistant Acinetobacter baumannii: Biofilm-Associated Genes, Biofilm-Eradication Potential of Disinfectants, and Biofilm-Inhibitory Effects of Selenium Nanoparticles.

This study aimed to investigate the biofilm-production ability of carbapenem-resistant Acinetobacter baumannii (CRAB), the biofilm-eradication potential of 70% ethanol and 0.5% sodium hypochlorite, the effects of selenium nanoparticles (SeNPs) against planktonic and biofilm-embedded CRAB, and the relationship between biofilm production and bacterial genotypes. A total of 111 CRAB isolates were tested for antimicrobial susceptibility, biofilm formation, presence of the genes encoding carbapenemases, and biofilm-associated virulence factors. The antibiofilm effects of disinfectants and SeNPs against CRAB isolates were also tested. The vast majority of the tested isolates were biofilm producers (91.9%). The bap, ompA, and csuE genes were found in 57%, 70%, and 76% of the CRAB isolates, with the csuE being significantly more common among biofilm producers (78.6%) compared to non-biofilm-producing CRAB (25%). The tested disinfectants showed a better antibiofilm effect on moderate and strong biofilm producers than on weak producers (p &lt; 0.01). The SeNPs showed an inhibitory effect against all tested planktonic (MIC range: 0.00015 to &gt;1.25 mg/mL) and biofilm-embedded CRAB, with a minimum biofilm inhibitory concentration of less than 0.15 mg/mL for 90% of biofilm producers. In conclusion, SeNPs might be used as promising therapeutic and medical device coating agents, thus serving as an alternative approach for the prevention of biofilm-related infections.

Possible protective and curative effects of selenium nanoparticles on testosterone-induced benign prostatic hyperplasia rat model.

Men over the age of 40 are more likely to develop benign prostatic hyperplasia (BPH). BPH is characterised by proliferation of the prostatic epithelium and stroma. Selenium in the form of nanoparticles is an essential metalloid mineral and antioxidant. In this study, selenium nanoparticles (SeNPs) were tested for their potential protective and curative impacts on BPH in rats. Fifty male Sprague-Dawley rats were randomly divided into five groups: Group I (Control group); Group II (Orchiectomised group): bilateral orchiectomy was conducted on rats; Group III (BPH group): testosterone (TE) enanthate injection was used to induce BPH; Group IV (Protective group): rats were given SeNPs before subjecting rats to BPH; Group V (Curative group): rats were succumbed to BPH, followed by administration of SeNPs. Measurement of prostate specific antigen (PSA) and TE in serum was performed and prostates were weighed and prepared for histological, immunohistochemical and ultrastructural examination. In the BPH group, serum TE and PSA levels, as well as prostate weight, increased significantly and significant decreases were observed in the protective and curative groups. Reduced acinar lumen, expansion of stroma and epithelial hyperplasia were noticed in the BPH group, which were ameliorated significantly in both the protective and curative groups. There was an increase in proliferating cell nuclear antigen immunoreaction in the BPH group and a decrease in both the protective and curative groups. On transmission electron microscopy of BPH group, the nuclei appeared irregular with dilated endoplasmic reticulum, loss of cell boundaries and apical microvilli. The protective group showed more improvement than the curative group. The effects of SeNPs on BPH induced by TE in rats, were both protective and curative, although the protective effects were more pronounced.

Effect of selenium nanoparticles against protoscoleces of Echinococcus granulosus in vitro and hydatid cysts in mice

This study determined the influence of selenium nanoparticles on the vitality of the protoscoleces of Echinococcus granulosus in vitro; seven concentrations were used: 50, 100, 150, 200, 250, 350, and 500 µg/ml for different exposure times: ten, twenty, thirty, and sixty minutes, respectively. Albino mice Mus musculus were injected with protoscoleces exposed to nanoparticles at 100, 150, and 200 µg/ml concentrations for 60 minutes. In contrast, control groups were injected with non-exposed protoscoleces. Mice were dissected three, four-, and five-months post infestation. Many criteria were relied on: numbers, weights, diameters of growing hydatid cysts, and their reduction proportion. The outcomes uncovered an apparent influence of selenium nanoparticles on the viability of protoscoleces of Echinococcus granlosus by the increase in exposure time in vitro, as well as diminish in the numbers of the larvae in processed mice versus the unprocessed collection; no cysts evolved inside processed mice at the concentration 200 µg/ml, three- and four-months post-infection. In contrast, the reduction rate was 90% in mice injected with exposed protoscoleces at the concentration of 150 µg/ml next 4 and 5 months of infection.

Effect of selenium nanoparticles on alternative splicing in heat-stressed rainbow trout primary hepatocytes

Alternative splicing (AS) is a ubiquitous post-transcriptional regulatory mechanism in eukaryotes that generates multiple mRNA isoforms from a single gene, increasing diversity of mRNAs and proteins that are essential for eukaryotic developmental processes and responses to environmental stress. Results showed that a total of 37,463 AS events were identified in rainbow trout hepatocytes. In addition, a total of 364 differential alternative splicing (DAS) events were identified in hepatocytes under selenium nanoparticles (SeNPs) and 3632 DAS events were identified under a combination of SeNPs and heat stress (24 °C). Gene Ontology (GO) enrichment showed that some subcategories “immune effector processes”, “response to stimuli” and “antioxidant activity” were associated with immunity, abiotic stimuli and antioxidants. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment showed that differentially expressed genes (DEGs) were significantly enriched in spliceosomes by adding SeNPs in heat-stressed hepatocytes. Splicing factor family (SRSF3, SRSF7, SRSF9, U2AF1 and U2AF2) and pre-RNA splicing factors (ACIN1 and PPRF18) were significantly upregulated and promoted AS. Furthermore, addition of SeNPs activated the phosphatidylinositol signaling system and upregulated the related genes PI4KA, DGKH, ITPK1 and Ocrl, and thus attenuated the inflammatory response to heat stress and enhanced resistance to heat stress by activating the adherent plaque kinase-PI3K-Akt signaling pathway and calcium channels. Those findings suggested that AS could be an essential regulatory mechanism in adaptation of rainbow trout to heat-stressed environments.

Selenium nanoparticles reduce Ce accumulation in grains and ameliorate yield attributes in mung bean (Vigna radiata) exposed to CeO2

Exposure of crops to CeO2 nanoparticles (nCeO2) in agricultural environments impact crop quality and human health. In this regard, the effects of selenium nanoparticles (nSe) on the yield and quality of Vigna radiata (L.) exposed to nCeO2 were investigated. The experiment was carried out as a factorial with two factors: NPs (nCeO2, and nSe) as factor one and concentrations as factor two [(0, 250, 500 and 1000 mg/L nCeO2; 0, 25, 50 and 75 mg/L nSe)]. Nanoparticles were foliar applied to 45-day old mung bean shoot in two steps and one-week interval. At 250–1000 mg/L, nCeO2 increased P, protein and Ce accumulation in grain. Additionally, at 1000 mg/L, the nCeO2, significantly decreased seed number, yield, Fe, and Zn storage in seeds. Conversely, at 25 and 50 mg/L, nSe stimulated the growth and yield of mung bean, and significantly increased P, Fe, Zn, and Se in seeds, but reduced the protein content in seeds. The Se25+Ce250 and Se50+Ce250 significantly increased pod number, seed number, grain weight, yield, Fe, Zn and Se storage in grains. In contrast, the Ce accumulation in seeds decreased in all combination treatments (nCeO2 + nSe) compared to their respective single nCeO2 treatments. Moreover, in the plants exposed to high nCeO2 concentrations, nSe application resulted in undamaged vacuoles, less starch granules' accumulation, significant yield improvement, and elevated Fe, Se, and Zn in seeds. Data suggest that selenium nanoparticles prevent nCeO2 stress in mung bean and improve grain production and quality.

Effect of Selenium Nanoparticles and Mannan Oligosaccharide Supplementation on Growth Performance, Stress Indicators, and Intestinal Microarchitecture of Broilers Reared under High Stocking Density.

The current study investigated the potential of selenium nanoparticles (SeNPs) and mannan-oligosaccharide (MOS) supplementation in ameliorating high stocking density (HSD) stress in broilers. A total of 392 day-old male chicks were divided into seven groups with eight replicates (n = 7): NSD [basal diet (BD) + normal stocking density: 10 bird/m2], HSD [BD + high stocking density: 16 bird/m2], Se-HSD [BD + Selenium (Se) 0.15 mg/kg], MOS-HSD (BD + MOS 5 gm/kg), Se-MOS-HSD (BD + Se 0.15 mg/kg and MOS 5 gm/kg), SeNPs-HSD (BD + SeNPs 0.15 mg/kg) and SeNPs-MOS-HSD (BD + SeNPs 0.15 mg/kg and MOS-5 gm/kg). HSD stress decreased (p &lt; 0.05) weekly body weight and body weight gain and increased (p &lt; 0.05) FCR compared to the NSD group. Supplementation with SeNPs and the SeNPs-MOS combination improved (p &lt; 0.05) the weekly body weight and FCR in HSD-stressed broilers during the 5th and 6th weeks. On day 21, HSD stress decreased (p &lt; 0.05) duodenal villus height (VH) and villus surface area (VSA) and increased (p &lt; 0.05) serum corticosterone and cholesterol compared to the NSD group. Supplementation with the SeNPs-MOS combination increased (p &lt; 0.05) duodenal VH and VH:CD, and jejunal total goblet cell (TGC) density and decreased (p &lt; 0.05) serum corticosterone and cholesterol and ileal intra-epithelial lymphocyte (IEL) density in HSD-stressed broilers. On day 42, HSD stress decreased (p &lt; 0.05) duodenal and jejunal VH, VSA, VH:CD, PCNA positive cell density and TGC density, Ileal VSA and TGC density, and increased (p &lt; 0.05) serum cholesterol and ileal IEL density compared to the NSD group. Supplementation with the SeNPs-MOS combination increased (p &lt; 0.05) spleen and bursa absolute weights, duodenal VH, VSA, VH:CD, PCNA positive cell density and jejunal VH, VH:CD, and decreased (p &lt; 0.05) serum cholesterol and ileal IEL density in HSD-stressed broilers. Our findings signify that HSD is stressful for broilers particularly during the finishing phase. Supplementation with the SeNPs-MOS combination mitigated HSD stress by partially improving the gut microarchitecture, gut barrier function and performance indicators.

Effect of selenium nanoparticles (SeNPs) supplementation on the sperm quality of fish after short-term storage

Selenium is a necessary trace element for animals, and it can improve the antioxidant capacity of a variety of cells. In this study, the antioxidant capacity of different concentrations of selenium nanoparticles (SeNPs) (0.1, 0.5, 1.5, and 4.5 mg/L) on Onychostoma macrolepis and Schizothorax prenanti sperm were explored during stored at 4 °C for 72 h. After 24 h, 0.5 mg/L SeNPs was more effective at improving the quality of Onychostoma macrolepis sperm by stabilizing the level of reactive oxygen species (ROS) within the sperm. A similar function of SeNPs was also found in Schizothorax prenanti sperm. RAS-selective lethal 3 (RSL3) significantly inhibited the effect of SeNPs on Onychostoma macrolepis sperm quality. Moreover, RSL3 completely abolished the effect of SeNPs which inhibited glutathione peroxidase 4 (GPX4) protein degradation in Onychostoma macrolepis sperm. The GPX4 protein is mainly located at the midpiece, where mitochondria were enriched in Onychostoma macrolepis sperm. These results revealed that GPX4 played an important role in sperm storage in vitro, and SeNPs stabilized ROS levels mainly by regulating GPX4 in Onychostoma macrolepis sperm. Furthermore, compared with the midpiece of the non-activated sperm, the midpiece of the activated sperm displayed deformation and a higher ATP content. In summary, SeNPs can effectively sustain the level of physiological reactive oxygen species (ROS) in Onychostoma macrolepis and Schizothorax prenanti sperm during storage at 4 °C, thereby SeNPs may be a potential additive for fish sperm stored in vitro.

Light enhanced the antimicrobial, anticancer, and catalytic activities of selenium nanoparticles fabricated by endophytic fungal strain, Penicillium crustosum EP-1

Selenium nanoparticles (Se-NPs) has recently received great attention over owing to their superior optical properties and wide biological and biomedical applications. Herein, crystallographic and dispersed spherical Se-NPs were green synthesized using endophytic fungal strain, Penicillium crustosum EP-1. The antimicrobial, anticancer, and catalytic activities of biosynthesized Se-NPs were investigated under dark and light (using Halogen tungsten lamp, 100 Watt, λ > 420 nm, and light intensity of 2.87 W m−2) conditions. The effect of Se-NPs was dose dependent and higher activities against Gram-positive and Gram-negative bacteria as well different Candida spp. were attained in the presence of light than obtained under dark conditions. Moreover, the viabilities of two cancer cells (T47D and HepG2) were highly decreased from 95.8 ± 2.9% and 93.4 ± 3.2% in dark than those of 84.8 ± 2.9% and 46.4 ± 3.3% under light-irradiation conditions, respectively. Significant decreases in IC50 values of Se-NPs against T47D and HepG2 were obtained at 109.1 ± 3.8 and 70.4 ± 2.5 µg mL−1, respectively in dark conditions than 19.7 ± 7.2 and 4.8 ± 4.2 µg mL−1, respectively after exposure to light-irradiation. The photoluminescence activity of Se-NPs revealed methylene blue degradation efficiency of 89.1 ± 2.1% after 210 min under UV-irradiation compared to 59.7 ± 0.2% and 68.1 ± 1.03% in dark and light conditions, respectively. Moreover, superior stability and efficient MB degradation efficiency were successfully achieved for at least five cycles.

Effects of Selenium Nanoparticles on Bleomycin-Induced Pulmonary Fibrosis in Rats

Effects of Selenium Nanoparticles on Bleomycin-Induced Pulmonary Fibrosis in Rats

Protective effects of Selenium nanoparticles and thyme extract in detoxification the toxic effects of aflatoxin B1 in rabbits

Protective effects of Selenium nanoparticles and thyme extract in detoxification the toxic effects of aflatoxin B1 in rabbits

Effects of Selenium Nanoparticles on Preventing Patulin-Induced Liver, Kidney and Gastrointestinal Damage.

Patulin (PAT) is a toxic fungal metabolite, and oxidative damage was proved to be its important toxicity mechanism. Selenium nanoparticles (SeNPs) were prepared by reducing sodium selenite with chitosan as a stabilizer and used for preventing PAT-induced liver, kidney and gastrointestinal damage. SeNPs have good dispersibility, in vitro antioxidant activity, and are much less cytotoxic than sodium selenite. Cell culture studies indicated that SeNPs can effectively alleviate PAT-induced excessive production of intracellular ROS, the decline of glutathione peroxidase activity, and the suppression of cell viability. Evaluation of serum biochemical parameters, histopathology, oxidative stress biomarkers and activities of antioxidant enzymes in a mouse model showed that pre-treatment with SeNPs (2 mg Se/kg body weight) could ameliorate PAT-induced oxidative damage to the liver and kidneys of mice, but PAT-induced gastrointestinal oxidative damage and barrier dysfunction were not recovered by SeNPs, possibly because the toxin doses suffered by the gastrointestinal as the first exposed tissues exceeded the regulatory capacity of SeNPs. These results suggested that a combination of other strategies may be required to completely block PAT toxicity.