Antioxidant-related Genes Research Articles

Effects of increasing dietary zinc oxide levels on the hepatic mitochondrial energy metabolism, oxidative balance and antioxidant system in weaned piglets.

This study compared different levels of dietary zinc oxide (ZnO) on mitochondria ATP synthesis and the cellular and systemic redox balance in weaned pigs. One hundred twenty weaned piglets (7.96 ± 1.17kg, 21 days of age) were randomly allocated in one of three diets containing different Zn levels (as ZnO); 100 (100Zn), 1000 (1000Zn) and 3000mg/kg (3000Zn), and were slaughtered at day 21, 23, 35 or 42 for the collection of blood and liver samples. Dietary copper (Cu) levels were constant at 131mg/kg. Hepatic mitochondrial concentrations of Zn and Cu, hepatic mitochondria respiration, antioxidant response and the hepatic expression of related genes were analyzed. Piglets fed 3000Zn had the highest Zn (P < 0.01) and the lowest Cu concentrations (P = 0.01) in hepatic mitochondria. The hepatic oxygen consumption rate for maximal respiration was the highest in 3000Zn piglets (P < 0.05) whereas hepatic cytochrome c oxidase activity tended to be lower (P = 0.06) and intracellular ATP concentrations was the lowest (P = 0.01). Mitochondrial Cu/Zn superoxide dismutase (Cu/Zn-SOD) activity was the lowest (P < 0.01) and glutathione peroxidase (GPx) activity tended to be the lowest (P = 0.07) for 3000Zn piglets. The mRNA expression of the antioxidant related genes copper chaperone for superoxide dismutase (CCS) was highest (P = 0.01) in 3000Zn piglets and tended to be the highest (P = 0.07) for glutathione synthetase (GSS). Plasma carbonyls concentrations (P = 0.02) and GPx activity (P = 0.01) were the highest while SOD activity was not impacted (P = 0.55) in 3000Zn piglets. In conclusion, supplementing 3000mg Zn/kg had detrimental impacts on mitochondria Zn and Cu homeostasis, resulting in a dysfunctional mitochondria respiratory chain and disturbed antioxidant response in post-weaning piglets.

A bHLH transcription factor RrUNE12 regulates salt tolerance and promotes ascorbate synthesis.

RrUNE12 binds to the RrGGP2 promoter to facilitate biosynthesis of AsA in Rosa roxburghii fruit. Furthermore, RrUNE12 upregulates antioxidant-related genes and maintains ROS homeostasis, thereby improving tolerance to salt stress. L-ascorbic acid (AsA) plays an essential role in stress defense as a major antioxidant in plant cells. GDP-L-galactose pyrophosphatase 2 (RrGGP2) has been previously identified as the key structural gene operating in AsA overproduction in Rosa roxburghii fruit. However, the transcriptional regulation of RrGGP2 in response to abiotic stress is not fully elucidated. In this study, we identified a bHLH transcription factor, RrUNE12, whose transcription level significantly correlated with RrGGP2 abundance and AsA accumulation in developing fruit. RrUNE12 is localized in the nucleus and specifically binds to the promoter of RrGGP2 to promote its transcription. The overexpression or silencing of RrUNE12 in R. roxburghii fruit and fruit callus further confirmed that RrUNE12 positively regulated RrGGP2 transcription and AsA level. Different abiotic stress treatments indicated that RrUNE12 was greatly induced by salt. Exogenous NaCl treatment on the RrUNE12-overexpressing or RrUNE12-silencing fruits also led to enhanced transcripts abundance of both RrUNE12 and RrGGP2, compared to the treatment without adding NaCl. RrUNE12 overexpression in fruit callus alleviated salt stress damage by upregulating the expression of RrGGP2 and antioxidant-related genes. Additionally, stable overexpression of RrUNE12 in tomato plants resulted in a significant increase in AsA content and antioxidant capacity, accompanied by an increased resistance to the salt stress. Collectively, the results suggest that RrUNE12 functions as an activator of AsA biosynthesis in R. roxburghii fruit and plays a positive role in mitigating salt stress by increasing both AsA level and the oxidation resistance.

Transcriptome Analysis Reveals the Key Genes and Pathways for Growth, Ion Transport, and Oxidative Stress in Post-Larval Black Tiger Shrimp (Penaeus monodon) Under Acute Low Salt Stress.

As an abiotic stress factor, salinity significantly affects the physiological activities of crustaceans. In this study, transcriptome sequencing was used to evaluate the mechanism of ion transport and the physiological response of black tiger shrimp (Penaeus monodon) under low salt stress. Four hundred post larval (PL) stage P. monodon were distributed in eight experimental tanks and exposed to 3 or 5 ppt salt concentrations for 96h. Low salinity significantly reduced the survival rate of shrimp but simultaneously activated the activity of ion transporter enzymes Na+/K+-ATPase (NKA) and Ca2+/Mg2+-ATPase), the expression of NKA, galectin 10, and cytochrompe c peroxidase genes, and the activity and expression of antioxidant-related genes (superoxide dismutase, catalase, heat shock protein 60). Low salt stress activated the urea cycle but significantly inhibited glutathione metabolization-related indicators (glutamate dehydrogenase, glutaminase, glutamic acid). RNA-seq analysis identified 221 differentially expressed genes (78 up-regulated and 143 down-regulated). Quantitative real-time PCR and RNA-seq results of 11 of them were consistent, illustrating the validity of the transcriptomic predictions. Gene set enrichment analysis results showed that calcium ion transmembrane transport, calmodulin binding, the stress-activated protein kinase signaling cascade, and regulation of the cytosolic calcium ion concentration process were significantly enriched. These results showed that low salt stress activated the calcium-dominated ion transport pathway and promoted molting growth of P. monodon. They also indicate that there is potential for larval rearing shrimp under low salt conditions.

Effects of Lysophospholipids on the Antioxidant Capacity, Digestive Performance, and Intestinal Microbiota of Litopenaeus vannamei.

This study seeks to assess the impact of varying concentrations of lysophospholipids on the antioxidant capacity, digestive performance, and intestinal microbiota of L. vannamei. A total of 840 shrimp, with an average initial weight of 2.22 ± 0.11 g, were randomly distributed across 28 aquaculture tanks (30 shrimp per tank), organized into 7 distinct treatment groups, each comprising 4 replicates. The control group (DL2) was administered a basal diet formula supplemented with 2% soy lecithin, whereas the experimental groups received lysophospholipids at varying concentrations of 0% (RL0), 0.1% (RL0.1), 0.5% (RL0.5), 1% (RL1), 1.5% (RL1.5), and 2% (RL2). The results revealed that the total antioxidant capacity (T-AOC) level in the RL0.1 group was significantly elevated compared to the DL2 and RL2 groups (p < 0.05). Furthermore, glutathione peroxidase (GSH-Px) and catalase (CAT) activities were markedly higher in the RL1 and RL1.5 groups relative to other groups (p < 0.05). Superoxide dismutase (SOD) activity exhibited a significant increase across all lysophospholipid-supplemented groups when compared to the DL2 group (p < 0.05). Malondialdehyde (MDA) levels were notably elevated in the RL0.5, RL1.5, and RL2 groups relative to the other groups (p < 0.05). Regarding antioxidant-related genes in the hemocytes, the relative expression levels of Nrf1, Nrf2, GPx, SOD, CAT, and Hippo were significantly higher in the RL0.5 and RL1 groups compared to the DL2 group (p < 0.05). Additionally, the relative expression levels of GPx and SOD were significantly elevated in the RL2 group compared to the DL2 group (p < 0.05). In the intestinal tract, the activities of trypsin and α-amylase (AMS) were significantly elevated in the RL0.1, RL0.5, and RL1 groups compared to the DL2 group (p < 0.05). Additionally, the RL0.1 group demonstrated significantly higher lipase (LPS) activity than the other groups supplemented with lysophospholipids (p < 0.05). Furthermore, the relative expression levels of the trypsin and α-amylase genes were significantly increased in the RL1 and RL1.5 groups in comparison to the DL2 group (p < 0.05). Sequencing analysis of the intestinal microbiota indicated that the incorporation of lysophospholipids resulted in an enhancement of the composition and structure of the intestinal microbiota. The functional abundance of the intestinal microbiome was primarily enriched in metabolic pathways. Overall, the incorporation of lysophospholipids into the diet exerted a beneficial effect on the antioxidant capacity, digestive performance, and intestinal microbiota of L. vannamei, especially with the supplementation of 0.1% lysophospholipids.

The nanocomposite of chitosan-vitamin C modulates the expression of immune and antioxidant-related genes in Nile tilapia stressed with lead (Pb)

Fish cultivated in a polluted environment usually face complicated disease cases. Pollution is an evitable event in aquaculture that weakens surface immunity, delaying and lowering the immune responses of aquatic animals. In an indoor experiment, Nile tilapia were reared in water polluted with lead (Pb) at a concentration of 51 µg/l for 8 weeks. A trial was conducted to mitigate the immunosuppression using pre-acclimatized Nile tilapia that were subdivided into six groups in which the exposed fish treated with nanocomposite (chitosan-vitamin C-protected nanoparticles (CVC-NPs)) consisted of 1 g of chitosan nanoparticles containing 400 mg vitamin C/kg fish and 200 mg vitamin C/kg fish feed for 1 week. Fish exposed to Pb pollution were immunocompromised as gene expression of immune-related cytokine and antioxidant enzymes significantly declined. Innate immunity was drastically impacted as OBA, phagocytosis and serum antibacterial activity (SAA) showed low values compared to the control fish; meanwhile, exposed fish was challenged against Streptococcus agalactiae and showed a high mortality rate (MR%). Dietary nanocomposite could restore normal immune status, and supplemented fish achieved low MR% with significantly high gene expression of proinflammatory cytokines. It was concluded that adding 200 mg of CVC-NPs/kg fish feed for 1 week could effectively protect Nile tilapia from S. agalactiae, having superiority over the high dose of 400 mg of CVC-NPs.

Ethyl Acetate Extract of Cichorium glandulosum Activates the P21/Nrf2/HO-1 Pathway to Alleviate Oxidative Stress in a Mouse Model of Alcoholic Liver Disease.

Alcoholic liver disease (ALD) is a significant global health concern, primarily resulting from chronic alcohol consumption, with oxidative stress as a key driver. The ethyl acetate extract of Cichorium glandulosum (CGE) exhibits antioxidant and hepatoprotective properties, but its detailed mechanism of action against ALD remains unclear. This study investigates the effects and mechanisms of CGE in alleviating alcohol-induced oxidative stress and liver injury. Ultra-Performance Liquid Chromatography coupled with Quadrupole-Orbitrap Mass Spectrometry (UPLC-Q-Orbitrap-MS) was used to identify CGE components. A C57BL/6J mouse model of ALD was established via daily oral ethanol (56%) for six weeks, with CGE treatment at low (100 mg/kg) and high doses (200 mg/kg). Silibinin (100 mg/kg) served as a positive control. Liver function markers, oxidative stress indicators, and inflammatory markers were assessed. Transcriptomic and network pharmacology analyses identified key genes and pathways, validated by reverse transcription quantitative polymerase chain reaction (RT-qPCR) and Western blotting. UPLC-Q-Orbitrap-MS identified 81 CGE compounds, mainly including terpenoids, flavonoids, and phenylpropanoids. CGE significantly ameliorated liver injury by reducing alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) levels and enhancing antioxidative markers such as total antioxidant capacity (T-AOC) and total superoxide dismutase (T-SOD) while lowering hepatic malondialdehyde (MDA) levels. Inflammation was mitigated through reduced levels of Tumor Necrosis Factor Alpha (TNF-α), Interleukin-1 Beta (IL-1β), and C-X-C Motif Chemokine Ligand 10 (CXCL-10). Transcriptomic and network pharmacology analysis revealed seven key antioxidant-related genes, including HMOX1, RSAD2, BCL6, CDKN1A, THBD, SLC2A4, and TGFβ3, validated by RT-qPCR. CGE activated the P21/Nuclear Factor Erythroid 2-Related Factor 2 (Nrf2)/Heme Oxygenase-1 (HO-1) signaling axis, increasing P21, Nrf2, and HO-1 protein levels while suppressing Kelch-like ECH-associated Protein 1 (Keap1) expression. CGE mitigates oxidative stress and liver injury by activating the P21/Nrf2/HO-1 pathway and regulating antioxidant genes. Its hepatoprotective effects and multi-target mechanisms highlight CGE's potential as a promising therapeutic candidate for ALD treatment.

Putative effects of moringa oil or its nano-emulsion on the growth, physiological responses, blood health, semen quality, and the sperm antioxidant-related genes in ram

Phytochemicals have been effectively used to enhance the growth and productivity of farm animals, while the potential roles of essential oils and their nano-emulsions are limited. This plan was proposed to investigate the impacts of orally administered moringa oil (MO) or its nano-emulsion (NMO) on the growth, physiological response, blood health, semen attributes, and sperm antioxidant-related genes in rams. A total of 15 growing Rahmani rams were enrolled in this study and allotted into three groups. The 1st control group received a basal diet only and treated orally one mL of distilled water, while the 2nd, and 3rd groups received a basal diet and were orally treated with 1 mL of NMO or 2 mL of MO /head/day for 4 months, respectively. Growth, physiological response, blood health, semen quality, and antioxidant genes in sperm were assessed. The MO and NMO treatments had no significant effect on growth indices (final body weight and weight gain ) and physiological response (rectal temperature, pulse, and respiration rates) (P > 0.05). The NMO group had the lowest levels of MCV (mean corpuscular volume) (P < 0.05), while all treated groups produced higher levels of mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin concentration (MCHC) compared to those in the control group (P < 0.05). Aspartate transferase (AST) and total cholesterol were significantly reduced in the MO and NMO groups, while total protein and glucose levels were significantly improved in NMO group (P < 0.05). Serum and seminal interstitial-cell-stimulating hormone (ICSH) levels were significantly improved (P < 0.0001) in the NMO group. Testosterone in serum and seminal plasma was significantly improved (P < 0.0001) in the MO group. Total antioxidant capacity (TAC) levels showed a tendency to increase in both the MO and NMO groups, but this increase was not significant compared to the untreated group (P > 0.05). On the other hand, the MO group exhibited lower levels of AST and malondialdehyde (MDA), while the alanine aminotransferase (ALT) levels were the lowest in the NMO group (P > 0.05). Mass motility, viability, membrane integrity and sperm concentration were significantly improved in the MO group (P < 0.0001) compared to the other groups. The NMO group had worse expressions of superoxide dismutase 1 (SOD1) compared to the control and MO groups. MO group significantly upregulated the catalase gene compared to the other groups (P < 0.001). The expression of Caspase-3 was highest in the group that received NMO compared to the other groups (P < 0.001). This study suggests that MO may serve as a novel therapeutic agent for improving the reproductive health in Rahmani rams.

Preparation, structural property, and antioxidant activities of a novel pectin polysaccharide from the flowers of Hibiscus syriacus Linn.

Oxidative stress, triggered by an imbalance between reactive oxygen species (ROS) production and cellular antioxidant defense mechanisms, is implicated in various pathological conditions. Plant-derived polysaccharides have gained significant attention as potential natural antioxidants due to their biocompatibility, biodegradability, and structural versatility. This study focuses on the purification, structural characterization, and antioxidant activities of a novel pectin polysaccharide (HFPS) isolated from the flowers of Hibiscus syriacus Linn. HFPS was purified using anion-exchange chromatography. Its chemical composition, monosaccharide profile, molecular weight distribution, and structural properties were elucidated through various analytical techniques. HFPS exhibited a predominant acidic monosaccharide composition, with galacturonic acid as the major constituent, indicating its pectin nature. The free radical scavenging activity of HFPS against ABTS·, DPPḤ, and ·OH radicals was evaluated, demonstrating a positive correlation between its antioxidant capacity and concentration. Furthermore, HFPS effectively protected HepG2 cells against H2O2-induced oxidative stress by reducing ROS accumulation, modulating redox-related enzymes (Superoxide dismutase, Catalase, Glutathione peroxidase), and alleviating oxidative damage. Notably, HFPS upregulated the expression of antioxidant-related genes, including B-cell lymphoma-2 (Bcl-2), heme oxygenase 1 (HO-1), NAD(P)H quinone oxidoreductase 1 (NQO1), and nuclear factor erythroid 2-related factor 2 (Nrf2), while downregulating pro-apoptotic genes like Bcl-2-associated X protein (Bax) and Caspase-3. These findings suggest that HFPS exerts its antioxidant effects by modulating the Nrf2/HO-1 pathway and redox homeostasis. This study contributes to the understanding of the structure-function relationships and antioxidant mechanisms of HFPS, highlighting its potential applications as a natural antioxidant in various fields.

Effects of fulvic acid on zebrafish (Danio rerio) growth, immunity and antioxidant status.

This experiment aimed to determine the efficacy of fulvic acid (FLA) on growth performance, innate immune system, antioxidant parameters, and expression of immune and antioxidant-related genes in zebrafish (Danio rerio). To this end, 12 tanks (3 per group), each containing 50 zebrafish (with an average weight of 85.7 ± 10.05 mg) in 72 L, were assigned to diets containing FLA at four levels: 0 (control), 0.25 (FLA1), 0.5 (FLA2), and 1 (FLA3) g/kg diet. Following an eight-week culture period, no significant differences in growth performance were observed among the treatment groups (P > 0.05). However, lysozyme activity, total immunoglobulin (Ig), and total protein concentrations in whole-body extracts were significantly enhanced in the 0.5-1 g FLA/kg diet groups compared to the other treatments (P < 0.05). No significant differences were observed among the groups in catalase (CAT), glutathione peroxidase (GPx), or superoxide dismutase (SOD) activities (P > 0.05). The supplementation of FLA significantly upregulated the gene expression of interferon-α (IFN-α) and tumor necrosis factor-alpha (TNF-α), with the highest expression observed in the 0.5 g FLA/kg diet group (P < 0.05). Additionally, interleukin 1 (IL-1) expression was markedly elevated in this group in comparison to the other treatments (P < 0.05). While there was a significant increase in GPx gene expression with dietary FLA (P < 0.05), no notable differences were observed among FLA treatments (P > 0.05). CAT gene expression remained consistent across all groups (P > 0.05). In contrast, SOD gene expression significantly increased in response to all FLA-supplemented diets, with the highest level observed in the 0.5 g FLA/kg group (P < 0.05). These findings suggest that FLA may serve as an effective dietary supplement to enhance the immune response and antioxidant capacity in zebrafish.

Bisphenol A induces apoptosis and disrupts testosterone synthesis in TM3 cells via reactive oxygen species-mediated mitochondrial pathway and autophagic flux inhibition.

Bisphenol A (BPA) is a common endocrine disruptor chemical that is widely used in the production of food plastic packaging, and it has been shown to potentially harm the reproductive system. However, the specific mechanism by which BPA induces apoptosis of Leydig cells (LCs) and inhibits testosterone synthesis in these cells is unclear. In the present study, TM3 cells were used as an experimental model in combination with a reactive oxygen species (ROS) scavenger (N-acetylcysteine), Caspase-3 inhibitor (Ac-DEVD-CHO), autophagy activator (Torin2), and autophagy inhibitor (Chloroquine) to investigate the potential mechanisms by which BPA causes TM3 cell damage in vitro. BPA treatment increased ROS production, which led to a marked decrease in antioxidant enzyme activity and the expression levels of antioxidant-related genes and proteins in TM3 cells. Upregulated ROS cause excessive opening of the mitochondrial permeability transition pore and significantly decrease the expression levels of genes related to membrane potential and mitochondrial function in TM3 cells. The release of cytochrome C from damaged mitochondria into the cytoplasm activated a Caspase cascade reaction. In addition, excessive ROS levels impaired autophagic degradation by inhibiting the fusion of autophagosomes with lysosomes. These abnormalities eventually induced apoptosis and inhibited testosterone synthesis in TM3 cells. The collective findings suggest that BPA induces apoptosis and interferes with testosterone synthesis in TM3 cells by upregulating ROS production, thereby activating the mitochondrial apoptotic pathway and inhibiting autophagic flux. These findings provide novel mechanistic insights into male reproductive toxicity caused by BPA exposure.

Polyethylene terephthalate nanoplastics affect potassium accumulation in foxtail millet (Setaria italica) seedlings

BackgroundAs modern industrial activities have advanced, the prevalence of microplastics and nanoplastics in the environment has increased, thereby impacting plant growth. Potassium is one of the most crucial nutrient cations for plant biology. Understanding how polyethylene terephthalate (PET) treatment affects potassium uptake will deepen our understanding of plant response mechanisms to plastic pollution.ResultsIn this study, we examined the impact of PET micro- and nanoplastics on foxtail millet seedling growth and potassium accumulation. Additionally, we measured reactive oxygen species (ROS) production, antioxidant enzyme activities, and the expression levels of the corresponding enzyme-encoding genes. Our findings indicated that the germination and seedling growth of foxtail millet were not significantly affected by exposure to PET plastics. However, the ROS levels in foxtail millet increased under these conditions. This increase in ROS led to the upregulation of several genes involved in K+ uptake and transport (SiHAK1, SiHAK2, SiAKT2/3, SiHKT2;2, SiHKT1;1, SiGORK, and SiSKOR), thereby increasing K+ accumulation in foxtail millet leaves. Further research revealed that higher K+ concentrations in plant leaves were correlated with increased expression of the antioxidant-related genes SiCAT1, SiPOD1, and SiSOD3, as well as increased activities of the corresponding antioxidant enzymes. This response helps mitigate the excessive accumulation and damage caused by ROS in plant cells after PET nanoplastic treatment, suggesting a potential stress response mechanism in foxtail millet against nanoplastic pollution.ConclusionsOur research indicates that PET nanoplastic treatment induces the expression of genes related to K+ uptake in foxtail millet through ROS signaling, leading to increased K+ accumulation in the leaves. This process mitigates the ROS damage caused by PET nanoplastic treatment by increasing the expression and activity of genes encoding antioxidant enzymes. The present research has unveiled the K+ accumulation-related response mechanism of foxtail millet to PET nanoplastic treatment, contributing significantly to our understanding of both the potassium absorption regulation mechanism in plants and the broader impact of plastic pollution on agricultural crops. This discovery not only highlights the complexity of plant responses to environmental stressors but also underscores the importance of considering such responses when evaluating the ecological and agricultural implications of plastic pollution.

Regulatory Mechanism of Exogenous ABA on Gibberellin Signaling and Antioxidant Responses in Rhododendron chrysanthum Pall. Under UV-B Stress.

In the present work, we examined the effects of exogenous abscisic acid (ABA) under ultraviolet B (UV-B) exposure on gibberellin (GA) production, signaling, and antioxidant-related genes in Rhododendron chrysanthum Pall (R. chrysanthum). Using transcriptomics, acetylated proteomics, and widely targeted metabolomics, the effects of UV-B stress on R. chrysanthum and the regulatory effects of exogenous ABA on it were revealed from multiple perspectives. The findings revealed that R. chrysanthum's antioxidant enzyme genes were differentially expressed by UV-B radiation and were substantially enriched in the glutathione metabolic pathway. Exogenous ABA supplementation boosted plant resistance to UV-B damage and further enhanced the expression of antioxidant enzyme genes. Furthermore, under UV-B stress, glutathione reductase, glutathione peroxidase, and L-ascorbate peroxidase were found to be the primary antioxidant enzymes controlled by exogenous ABA. In addition, gibberellin content was altered due to UV-B and exogenous ABA treatments, with greater effects on GA3 and GA53. The acetylation proteomics study's outcomes disclosed that the three main oxidative enzymes' acetylation modifications were dramatically changed during UV-B exposure, which may have an impact on the antioxidant enzymes' functions and activities. The protective impact of exogenous ABA and gibberellin on R. chrysanthum's photosynthetic system was further established by measuring the parameters of chlorophyll fluorescence. This research offers a theoretical foundation for the development of breeding highly resistant plant varieties as well as fresh insights into how hormone levels and antioxidant systems are regulated by plants in response to UV-B damage.

Caffeic acid improves biocontrol effect of Pantoea jilinensis D25 against tomato gray mold.

Gray mold in tomato caused by Botrytis cinerea is a destructive disease, which can be treated using biocontrol agents. Pretreatment of biocontrol strains with oxidative-stress-ameliorating compounds can enhance their tolerance to oxidative microenvironment in infected fruit wounds. In this study, we aimed to determine the effect of caffeic acid (CA) on the biocontrol efficacy of Pantoea jilinensis D25 in gray mold in cherry tomato. D25 strain pretreated with CA exhibited enhanced oxidative stress response in cherry tomato wounds. CA-treated D25 cells recovered from cherry tomato wounds had lower ROS level and cellular oxidative damage than D25 cells not treated with CA. The antioxidation-related genes (CAT and GPX) were upregulated and colonization ability of D25 strain was improved in cherry tomato wounds after CA application. Furthermore, the biocontrol effects of CA-treated D25 strain were improved. CA pretreatment to D25 strain could significantly improve the expression of defense-related genes (SlMYC-2, SlLoxD, SlEIN2, and SlEIN3) and activity of defense-related enzymes in cherry tomato wounds. Application of CA to D25 strain could improve its ability to combat antioxidant stress and biocontrol efficacy against postharvest tomato gray mold. © 2024 Society of Chemical Industry.

Obesity induced by a high-fat diet changes p62 protein levels in mouse reproductive organs.

Obesity is one of the major risk factor for infertility since it causes decreased quality and quantity of gametes and a disrupted uterine environment which might result in miscarriage, stillbirth, and fetal abnormal growth. Obesity induces oxidative stress which is strongly associated with infertility. The clearing of oxidative stress by autophagy is maintained through the p62/ Keap1/Nrf2 pathway. In this pathway, oxidative stress induces p62 for binding to Keap1, thereby Keap1 cannot bind to the Nrf2 transcription factor. Then, Nrf2 translocates into the nucleus and initiates antioxidant-related gene expression. While p62, bound to Keap1, acts as an adaptor protein between autophagosome and damaged substrates which needs to be degraded for homeostasis. Up to date, obesity is strongly linked to abnormal autophagy activity. However, p62 protein expression has not been investigated in the obese ovary, testis, and uterus in detail. Thus, in the present study, we aimed to evaluate the effects of a high-fat diet (HFD)-induced obesity on p62 protein levels of the ovary, testis, and uterus in mice. Our results demonstrated that the p62 expression level was significantly altered by HFD in uterine glands, epithelium, myometrium, and stroma, and in the ovarian corpus luteum, testicular spermatogonium and spermatocytes.

Stimulatory effects of dietary savory (Satureja hortensis L.) ethanolic extract on growth, digestive enzymes, immune parameters, antioxidant defense, and immune and antioxidant-related genes in zebrafish (Danio rerio)

The current investigation focused on examining the growth performance, immune and antioxidative factors, and mRNA levels of immune and antioxidant-related genes in zebrafish (Danio rerio) that were fed with different levels of savory (Satureja hortensis L.) ethanolic extract (SEE) for 8 weeks. To achieve this objective, a total of 240 zebrafish with a mean weight of 65.37 ± 5.9 mg were fed on 0.0 (the control; T0), 0.5 % (T0.5), 1 % (T1), and 2 % (T2) of SEE for a period of 8 weeks. The results for the growth performance of zebrafish showed that the final weight (165.20±1.92 mg), Weight gain (147.71±1.15 mg), specific growth rate (1.62±0.03) was significantly (P < 0.05) enhanced with the dietary SEE levels and the best performance was noted in T1 and T2. highest activity levels of α-amylase (53.56±1.21), lipase (3.56±0.16), proteases (13.78±0.21), pepsin (0.31±0.01), chymotrypsin (0.44±0.01), and trypsin (0.68±0.01) were observed especially T2 (P < 0.05). The results of tissue and mucus immune factors revealed that feeding the fish on SEE diets significantly increased the immune activity represented by lysozyme, total Immunoglobulin (Ig), Immunoglobulin M (IgM), total protein, and ACH50 (P < 0.05). The malondialdehyde value was significantly (P < 0.05) affected by experimental diets and its lowest value was notably observed in T1 and T2 than those in T0 and T0.5. The tissue and mucus activity of catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), and total antioxidant activity (TAC) increased considerably (P < 0.05) in the treatments fed with SEE, and their highest levels were detected in T1 and T2. The relative mRNA expression of CAT, SOD, GPx, and glutathione reductase (GSR) genes in treatments fed with different SEE levels was higher than those in the control group. The relative expression of Lysozyme was notably higher, meanwhile the expression of genes including Interleukin 1β (IL.1B), Interleukin 8 (IL8), and Tumor necrosis factor (TNF-α), significantly decreased in fish fed with SEE; especially at T1 and T2. The present study, 1–2 % savory ethanolic extract of SEE improved the performance, immune, and antioxidant levels.

Exogenous Calcium Enhances Castor Tolerance to Saline-Alkaline Stress by Regulating Antioxidant Enzyme Activity and Activating Ca2+ and ROS Signaling Crosstalk.

Saline-alkaline stress is a major factor limiting agricultural development, with calcium (Ca2+) playing a role in regulating plant tolerance through multiple signaling pathways. However, the specific mechanisms by which Ca2+ mediates saline-alkaline stress tolerance at the molecular level remain incompletely understood. This study investigates the effects of exogenous Ca2+ application on enhancing plant tolerance to saline-alkaline stress, focusing on its impact on the antioxidant system and Ca2+ and reactive oxygen species (ROS) signaling pathways. Through physiological assays and transcriptomic analyses, we evaluated oxidative damage markers, antioxidant enzyme activities, and the expression of key Ca2+ and ROS signaling genes. The results showed that saline-alkaline stress significantly elevated ROS levels, which led to increased membrane lipid peroxidation and induced upregulation of antioxidant response elements in castor roots. Exogenous calcium treatment reduced ROS accumulation by increasing superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT) activities and decreasing malondialdehyde (MDA) levels, demonstrating a marked improvement in the antioxidant system. Transcriptomic analysis identified CAT2 (LOC107261240) as the primary target gene associated with increased CAT activity in response to exogenous calcium. Additionally, the upregulation of specific Ca2+ channels, Ca2+ sensors, ROS receptors, and antioxidant-related genes with calcium treatment highlights the critical role of Ca2+-ROS signaling crosstalk in enhancing stress tolerance. Protein-protein interaction analysis identified APX3 and other hub genes involved in Ca2+-ROS signaling transduction and the regulation of antioxidant activity. These findings enhance our understanding of calcium's complex regulatory roles in plant abiotic stress responses, offering new theoretical insights for improving crop resilience in agriculture.

Tobacco production under global climate change: combined effects of heat and drought stress and coping strategies.

With the intensification of global climate change, high-temperature and drought stress have emerged as critical environmental stressors affecting tobacco plants' growth, development, and yield. This study provides a comprehensive review of tobacco's physiological and biochemical responses to optimal temperature conditions and limited irrigation across various growth stages. It assesses the effects of these conditions on yield and quality, along with the synergistic interactions and molecular mechanisms associated with these stressors. High-temperature and drought stress induces alterations in both enzymatic and non-enzymatic antioxidant activities, lead to the accumulation of reactive oxygen species (ROS), and promote lipid peroxidation, all of which adversely impact physiological processes such as photosynthetic gas exchange, respiration, and nitrogen metabolism, ultimately resulting in reduced biomass, productivity, and quality. The interaction of these stressors activates novel plant defense mechanisms, contributing to exacerbated synergistic damage. Optimal temperature conditions enhance the activation of heat shock proteins (HSPs) and antioxidant-related genes at the molecular level. At the same time, water stress triggers the expression of genes regulated by both abscisic acid-dependent and independent signaling pathways. This review also discusses contemporary agricultural management strategies, applications of genetic engineering, and biotechnological and molecular breeding methods designed to mitigate adverse agroclimatic responses, focusing on enhancing tobacco production under heat and drought stress conditions.

Optimizing selenium-enriched yeast supplementation in laying hens: Enhancing egg quality, selenium concentration in eggs, antioxidant defense, and liver health

This study evaluated the effects of selenium-enriched yeast (SY) supplementation at various levels on health and production parameters in laying hens, including egg production, egg quality, selenium (Se) concentrations in eggs, liver health, serum biochemical markers, antioxidant function, and immune responses. A total of 360 Hy-Line Brown hens (28 weeks old) were randomly assigned to four dietary groups with six replicates of 15 birds each, monitored over a 12-week feeding trial after a two-week acclimatization period. The dietary groups included a control (basal diet without selenium) and three SY-supplemented groups with Se levels of 0.3 mg/kg (SY03), 1.5 mg/kg (SY15), and 6.0 mg/kg (SY60). The results showed no significant effects of dietary SY on laying performance or feed efficiency (P > 0.05). However, the SY15 group showed significant improvements in egg quality, particularly in albumen height, Haugh Unit and yolk color (P < 0.05). Selenium concentrations in eggs, albumen, and yolk increased dose-dependently, with significant differences in the SY-supplemented groups (P < 0.001). Increased activities of liver enzymes including alanine transaminase, alkaline phosphatase, and aspartate transaminase, alongside elevated levels of uric acid were notable in the SY60 group (P < 0.05). In addition, histological analysis revealed significant hepatocyte degeneration and a higher liver organ index (P < 0.05), in the SY60 group. All of which suggests potential liver toxicity at higher selenium levels. Antioxidant capacity of the birds were significantly enhanced due to dietary supplementation of SY as indicated by increased serum levels of total antioxidant capacity, and activities of catalase, glutathione peroxidase, and superoxide dismutase (P < 0.05). Analysis of hepatic genes expression revealed that SY15 supplementation significantly upregulated key antioxidant-related genes (Nrf2, HO-1, CAT, and NQO1) and downregulated Keap1 expression (P < 0.05), suggesting strong activation of the antioxidant defense system. In conclusion, SY supplementation at 1.5 mg/kg improved egg quality, increased Se concentrations in eggs, and enhanced antioxidant capacity without affecting laying performance or liver health. This makes it a balanced approach to improving egg quality and poultry health. However, higher supplementation levels (6.0 mg/kg) resulted in liver damage, underscoring the importance of careful dosage consideration.

VBNC Cronobacter sakazakii survives in macrophages by resisting oxidative stress and evading recognition by macrophages

Survival in host macrophages is an effective strategy for pathogenic bacterial transmission and pathogenesis. Our previous study found that viable but non-culturable (VBNC) Cronobacter Sakazakii (C. sakazakii) can survive in macrophages, but its survival mechanism is not clear. In this study, we investigated the possible mechanisms of VBNC C. sakazakii survival in macrophages in terms of environmental tolerance within macrophages and evasion of macrophages recognition. The results revealed that VBNC C. sakazakii survived under oxidative conditions at a higher rate than the culturable C. sakazakii. Moreover, the stringent response gene (relA and spoT) and the antioxidant-related genes (sodA, katG, and trxA) were up-regulated, indicating that VBNC C. sakazakii may regulate antioxidation through stringent response. On the other hand, compared with culturable C. sakazakii, VBNC C. sakazakii caused reduced response (Toll-like receptor 4) in macrophages, which was attributed to the suppression of biosynthesis of the lipopolysaccharides (LPS). Furthermore, we found that ellagic acid can reduce the survival rate of bacteria in macrophages by improving the immune TLR4 recognition ability of macrophages. In conclusion, VBNC C. sakazakii may survive in macrophages by regulating oxidative tolerance through stringent response and altering LPS synthesis to evade TLR4 recognition by macrophages, which suggests the pathogenic risk of VBNC C. sakazakii.

GmTRAB1, a Basic Leucine Zipper Transcription Factor, Positively Regulates Drought Tolerance in Soybean (Glycine max. L).

The basic leucine zipper (bZIP) transcription factors play crucial roles in plant resistance to environmental challenges, but the biological functions of soybean bZIP members are still unclear. In this study, a drought-related soybean bZIP gene, GmTRAB1, was analyzed. The transcript of GmTRAB1 was upregulated under drought, ABA, and oxidative stresses. Overexpression of GmTRAB1 improved the osmotic stress tolerance of transgenic Arabidopsis and soybean hairy roots associated with increased proline content and activity of antioxidant enzymes and reduced accumulations of malonaldehyde and reactive oxide species. However, RNA interference silencing of GmTRAB1 in the soybean hairy roots improved drought sensitivity. Furthermore, GmTRAB1 increased the sensitivity of transgenic plants to ABA and participated in modulating ABA-regulated stomatal closure upon drought stress. In addition, GmTRAB1 stimulated the transcript accumulation of drought-, ABA-, and antioxidant-related genes to respond to drought. Collectively, this research will contribute to understanding the molecular mechanisms of bZIP transcription factors in soybean's resistance to drought.