GSSG Content Research Articles

Effects of Selenium on Serotonin Synthesis and the Glutathione Redox Cycle in Plum Leaves

Selenium (Se), an essential micronutrient for humans, is also a beneficial nutrient for growth and development of many plants. The aim of the present study was to determine whether low-dose Se application could increase plum growth and serotonin synthesis, as well as upregulate the glutathione redox cycle. Two-year-old plum trees were treated with Se6+ (Na2SeO4) and Se2− (SeMet). Growth parameters, levels of serotonin synthesis precursors, compounds and enzymes of the glutathione (GSH) redox cycle, and the antioxidant capacity were analyzed. Results showed that plant height and stem diameter were increased by Se treatment. The leaf Se content was significantly increased; tryptophan was not affected by Se treatment, while the 5-hydroxytryptophan content was significantly higher than control. Although serotonin levels were also increased, the effect was not significant, and no tryptamine was detected in our study. On the 30th day, the MDA content in Se2− was highest followed by the control and Se6+ treatment, and the activities of T-AOT and CAT were increased, while GST was reduced by Se treatment. The two forms of Se treatments increased the activity of GPX and GR, and the total content of GSH + glutathione disulfide (GSSG) at the end of treatment. Furthermore, the level of GSH and GSH/GSSG was instable changed. GSSG content was similar during the treatment time except on the 20 days. Conclusively, the pathway of plum serotonin was clear, both Se6+ and Se2− could influence the serotonin synthesis. Additionally, the GSH redox cycle was sensitive to the Se application. Moreover, Se6+ performed better than Se2− on leaf Se content, plant growth parameters, and antioxidant capacity.

Effects of Antimony on Reactive Oxygen and Nitrogen Species (ROS and RNS) and Antioxidant Mechanisms in Tomato Plants.

This research studies the effects that Sb toxicity (0.0, 0.5, and 1.0 mM) has on the growth, reactive oxygen and nitrogen species, and antioxidant systems in tomato plants. Sb is accumulated preferentially in the roots, with little capacity for its translocation to the leaves where the concentration is much lower. The growth of the seedlings is reduced, with alteration in the content in other nutrients. There is a decrease in the content of Fe, Mg, and Mn, while Cu and Zn increase. The contents in chlorophyll a and b decrease, as does the photosynthetic efficiency. On the contrary the carotenoids increase, indicating a possible action as antioxidants and protectors against Sb. The phenolic compounds do not change, and seem not to be involved in the defense response of the tomato against the stress by Sb. The water content of the leaves decreases while that of proline increases in response to the Sb toxicity. Fluorescence microscopy images and spectrofluorometric detection showed increases in the production of O2.–, H2O2, NO, and ONOO–, but not of nitrosothiols. The Sb toxicity induces changes in the SOD, POX, APX, and GR antioxidant activities, which show a clear activation in the roots. In leaves, only the SOD and APX increase. The DHAR activity is inhibited in roots but undergoes no changes in the leaves, as is also the case for the POX and GR activities. Ascorbate increases while GSH decreases in the roots. The total AsA + DHA content increases in the roots, but the total GSH + GSSG content decreases, while neither is altered in the leaves. Under Sb toxicity increases the expression of the SOD, APX, and GR genes, while the expression of GST decreases dramatically in roots but increases in leaves. In addition, an alteration is observed in the pattern of the growth of the cells in the elongation zone, with smaller and disorganized cells. All these effects appear to be related to the ability of the Sb to form complexes with thiol groups, including GSH, altering both redox homeostasis and the levels of auxin in the roots and the quiescent center.

Effect of Polydatin on Neurological Function and the Nrf2 Pathway during Intracerebral Hemorrhage.

This study investigates the effect of polydatin on the neurological function of cerebral hemorrhage rats and on the Nrf2 pathway of the endogenous antioxidant system in tissues around cerebral hematoma. Further, the study also aims to provide solid insights for clinical diagnosis and treatment. A total of 54 SPF grade male Wistar rats were divided into three groups: the sham group, model group, and polydatin group. Various parameters such as neurological deficit score, brain water content, pathological morphology, oxidative stress index content, Nrf2, NQO1, HO-1 mRNA expression, and the expression of HO-1, Nrf2, and kelch-like epichlorohydrin-1 (Keap1) protein were observed. Compared with the sham group, the mNSS score and brain water content of rats in the model group increased significantly after dosing (P < 0.05). When compared with the model group, the mNSS score and brain water content of rats in the polydatin group decreased significantly after dosing (P < 0.05). Compared with the other group, the serum NSE content of rats in the polydatin group decreased (P < 0.05). An increase was observed in the contents of NO, SOD, MDA, GSSG, and GSH in the brain tissue of rats in the model group when compared with the sham group. Compared with the model group, the contents of NO and MDA in the brain tissue of rats in the polydatin group decreased, while the contents of SOD, GSSG, and GSH increased (P < 0.05). The relative expressions of Nrf2, NQO1, and HO-1mRNA in the brain tissue of rats in the polydatin group was relatively high compared with both groups (P < 0.05). Polydatin can improve the neurological function of ICH rats and reduce the oxidative stress response by regulating the Nrf2-ARE pathway and downstream gene expression. This study preliminarily discussed the relevant mechanism of polydatin in the treatment of ICH rats, thus providing a theoretical reference to ICH treatment.

Effects of dietary Cu and Zn on the accumulation, oxidative stress and the expressions of immune-related genes in the livers of Nile tilapia (Oreochromis niloticus)

Excess Cu and Zn can cause many adverse effects in fish. However, few studies have addressed the effects of dietary Cu and Zn on antioxidant physiology and immunity and the underlying mechanisms in fishes. In this study, accumulation of Cu and Zn, effects on the antioxidant enzymes and the transcriptional expressions of immune-related genes were examined in the Oreochromis niloticus fed the Cu and/or Zn enriched duckweed. The results showed that the liver and intestine had the highest accumulation of Cu2+ and Zn2+ while the muscle had the lowest accumulation of these two metals. The activities of SOD, CAT, GPx and the contents of GSH, GSSG in the liver of all treatment groups were significantly decreased compared to the control group. MDA content was significantly elevated in all treatment groups after feeding for 21 days, implying lipid peroxidation in the liver. In the Cu + Zn group, the activities of SOD, GPx and the GSSG content in the liver were significantly decreased. Compared with the Zn group, the LZM activity in the Cu + Zn group was reversed after feeding for 42 days (P < 0.05). The transcriptional expressions of immune-related genes (TNF-α, INF-γ and IL-1β) in Cu, Zn, Cu + Zn groups were significantly inhibited compared with the control group after treatment for 21 days. Compared with the Cu + Zn group, the level of INF-γ transcripts was significantly reduced in the Cu and Zn group, while the TNF-α expression was elevated after treatment for 42 days. Cu and Zn had synergistic effects on the antioxidant system. Cu has greater effects than Zn on the immunity of O. niloticus. This study demonstrates that dietary Cu and Zn may pose a potential threat to the tilapia populations.

Biochemical markers for prolongation of the acute stress of triclosan in the early life stages of four food fishes

In the present study, embryos of four food fishes viz. Cyprinus carpio, Ctenopharyngodon idella, Labeo rohita and Cirrhinus mrigala were given acute (96 h) exposure to their respective LC0, LC10 and LC30 (causing 0, 10 and 30% mortality, respectively) concentrations of triclosan [TCS, 5-chloro-2-(2,4-dichlorophenoxy) phenol], a broad spectrum biocide. Bioaccumulation, contents of protein, non-enzymatic antioxidants (GSH and GSSG), MDA (lipid peroxidation product) and organic acids (fumarate, succinate, malate and citrate) along with the activities of AChE (neurological enzyme), GST (detoxification enzyme) and three metabolic enzymes (LDH, AST and ALT) were estimated after 48 and 96 h exposure and 10 days post exposure. Around 1/10 of the TCS in water got accumulated in the hatchlings after 96 h, increase over 48 h values was maximum at LC0 (+195.30, +143.23 and + 140.75%) but minimum at LC30 (+89.62, +84.26 and + 126.72%) for C. idella, L. rohita and C. mrigala, respectively. In C. carpio, TCS got accumulated only at LC30 after 48 h but at all the concentrations after 96 h exposure. Contents of protein, GSH, GSSG and activity of AChE decreased but activities of GSH, LDH, AST and ALT and contents of MDA and organic acids increased concentration dependently in all the fishes. TCS declined by 85–90% but its toxic effects on biomolecules prolonged till the end of the recovery period. Such acute exposures are accidental but there is a need to evaluate biomarkers for prolongation of the stress of small concentrations especially LC0 and LC10 (causing negligible mortality) of lipophilic pollutants like TCS.

Allyl isothiocyanate treatment alleviates chronic obstructive pulmonary disease through the Nrf2-Notch1 signaling and upregulation of MRP1

AimsChronic obstructive pulmonary disease (COPD) is a disease with high morbidity and mortality worldwide, which can cause serious social and economic burdens. Allyl isothiocyanate (AITC) is one of the most common natural isothiocyanates and has been shown to have anti-inflammatory and antioxidant biological activities. The purpose of this study was to investigate whether AITC regulated Multidrug resistance-associated protein 1 (MRP1), reactive oxide species (ROS) and reduced glutathione (GSH) levels via Nrf2 and Notch1 signaling pathways to treat COPD and whether there was an interaction between these two pathways. Main methodsLung function indexes and histopathological changes in mice were determined by lung function instrument and HE staining, respectively. The protein expression was analyzed using immunohistochemistry and Western blotting. The mRNA expression was measured by RT-PCR in human bronchial epithelial cell line 16HBE. The contents of ROS, GSH and GSSG were detected by kits in 16HBE cells. Key findingsThe protein expression of Notch1, Hes1, MRP1, Nrf2, and HO-1 in lung tissues of WT mice and untransfected cells were significantly down-regulated in COPD, then significantly ameliorated in treatment groups. The protein expression of MRP1, Notch1 and Hes1 in lung tissues of Nrf2−/− mice were markedly reduced. There was a significant reduction in expression of Nrf2, HO-1 and MRP1 in si-Notch1 transfected cells. Pretreatment with AITC markedly improved oxidative stress and GSH-redox disorder in COPD. SignificanceOur study demonstrates that there is a potential interaction between Nrf2 and Notch1 signaling pathways during treatment of COPD.

Selenite antagonizes the phytotoxicity of Cd in the cattail Typha angustifolia.

The Phytotoxicity of and mechanism underlying selenite-mediated tolerance to Cd stress in Typha angustifolia were studied hydroponically with respect to metal uptake and translocation, photosynthesis-related parameters, contents of proline and O2•-, products of lipid peroxidation, cell viability, enzymatic and non-enzymatic antioxidants, glyoxalases and phytochelatins. T. angustifolia were exposed to 25, 50 and 100μM of Cd alone and in conjunction with 5mgL-1 of selenite in full-strength Hoagland's nutrient solution for 30 days. Results showed that Cd contents in T. angustifolia leaves and roots increased in a dose-dependent manner and were higher in roots, but those of BAC, BCF and TF changed in a contrary pattern. Addition of selenite to Cd-containing treatments further reduced Cd levels in T. angustifolia leaves and roots, as well as BAC, BCF and TF. A diphasic effect was found in T. angustifolia for the contents of total chlorophyll, GSH, PC and GSSG, as well as activities of CAT, POD, SOD and GR, in response to Cd stress alone and in conjunction with selenite supplementation, but the same effect was not observed for Pn, Cond, Tr, Ci, Fv/Fm and ϕPSII. In contrast, exogenous selenite supplementation enhanced the contents of total chlorophyll and the non-enzymatic antioxidants, as well as activities of enzymatic antioxidants, while the values of photosynthetic fluorescence parameters were rescued. Selenite addition decreased Cd-induced cell death. Proline contents and Gly I activities in T. angustifolia leaves kept increasing in a dose-dependent manner of Cd concentrations in the growth media and selenite addition further enhanced both parameters. Addition of selenite could quench Cd-mediated generation of MDA, O2•- and MG in T. angustifolia leaves and reduce Cd-induced Gly II activity. A U-shaped GSH/GSSG ratio in T. angustifolia leaves suggests a possible trade-off between PC synthesis and GR activity since both share the same substrate GSH. Therefore, confined BAC, BCF and TF were a mechanism that confers T. angustifolia tolerance to Cd stress, and that exogenous selenite supplementation could depress Cd-induced stress in T. angustifolia by rescuing the photosynthetic fluorescence, enhancing non-enzymatic and enzymatic antioxidants that scavenge O2•- and MG, and potentiating PC synthesis that chelates Cd.

Sterigmatocystin-induced cytotoxicity via oxidative stress induction in human neuroblastoma cells

Sterigmatocystin (STE) is a mycotoxin produced by fungi of the genus Aspergillus. Considering that the effect of STE on neuronal system has not been well studied, the aim of the present study consists to investigate the cytotoxic effects of STE in human neuroblastoma (SH-SY5Y) cells. Moreover, the role of oxidative stress and intracellular defense systems was assessed by evaluating reactive oxygen species (ROS) generation, lipid peroxidation (LPO) and antioxidant no-enzymatic (GSH) levels and enzymatic (GPx, GST, CAT and SOD) activity. Our results revealed that STE decreased cell viability in a dose and time-dependent manner. Furthermore, after 24 h of exposure, STE induced an increase in ROS generation and LPO at all concentrations tested (0.78, 1.56 and 3.12 μM), as well as a depletion of GSH levels, an increase in GSSG content and a decrease in GSH/GSSG ratio at the highest concentrations. The activity of all antioxidant enzymes resulted to be also decreased. Additionally, an enhance of the oxidative damage was caused by BSO, a GSH depletor, while NAC, a GSH precursor, showed a scavenger activity. Our findings suggest that STE could injure SH-SY5Y cells via oxidative stress and highlight the antioxidant role of the glutathione system.

Influence of polymorphism of the gene GCLC on antioxidant defense status in healthy children of Omsk region

Aim. To study the status of antioxidant defense in healthy children, living in Omsk Region, depending on polymorphism of the gene GCLC.&#x0D; Materials and methods. There were examined 50 healthy children aged 3 to 17 years, including 54 % of boys. Polymorphism of the gene GCLC 129С/C, 129C/Т, 129T/T and reduced (GSH) and oxidized (GSSG) glutathione concentrations were determined. Statistical analysis was implemented using the programs Statistica 6.0 and DoctorStat1.9.&#x0D; Results. Polymorphism of the gene GCLC was represented by the genotypes 129C/C (43 children, 86 %) and 129C/T (7 children, 14 %); GSH concentration was within 6.0 [4.4; 7.0] mcmol/l, GSSG concentration 3.0 [2.3; 3.5] mcmol/l, GSH:GSSG ratio was 2:1. Weak direct correlation between the child age and GSH (r = 0.31; р = 0.028) and GSSG (r = 0.31; р = 0.031) content was established; no gender differences were revealed. Among the subjects with the genotype 129C/T, the blood plasma GSH (р = 0.017) and GSSG (р = 0.016) concentrations decreased by 30 %.&#x0D; Conclusions. Glutathione concentration in children depends on polymorphism of the gene GCLC.

Does Exogenously Applied Gallic Acid Regulate the Enzymatic and Non-Enzymatic Antioxidants in Wheat Roots Exposed to Cadmium Stress?

The aim of the current study was to determine whether gallic acid (GLA) triggers the growth, osmoregulation and antioxidant system related to defense mechanisms in wheat roots to cadmium (Cd)-induced oxidative stress. For this purpose, wheat plants were hydroponically grown for 21 (d) and were treated with GLA (GLA1-2; 25 and 75 mM), Cd stress (Cd1-2; 100 and 200 mM) and their combination for 7 d. The significant reduction in growth (RGR) and osmotic potential (YP) was observed under stress. After GLA applications in response to stress, RGR, YP and proline (Pro) increased, except for 200 mM Cd plus 75 mM GLA. Under stress, hydrogen peroxide (H2O2) was induced by the activated superoxide dismutase (SOD) activity but, NADPH oxidase (NOX) had no contribution on the accumulation of H2O2. Despite of the increased catalase (CAT) and glutathione reductase (GR), H2O2 did not eliminate and then lipid peroxidation (TBARS content) was induced with the decreased scavenging capacity of hydroxyl radical (OH·) under stress. Besides, to remove of H2O2 content produced by SOD, H2O2 could effectively scavenge through CAT activity in combination form of GLA and Cd. On the other hand, GLA did not induce the enzymes and non-enzymes related to Asada-Halliwell cycle (ascorbate peroxidase (APX), GR, dehydroascorbate reductase (DHAR), monodehydroascorbate reductase (MDHAR), reduced and oxidized contents of glutathione (GSH and GSSG contents). Under high Cd concentration, GLA2 could not eliminate H2O2 content because of increased NOX activity and then in this group (Cd2+GLA2) the scavenging capacity of OH· did not change and TBARS content increased.

Effect of reduced glutathione on the quality characteristics of apple wine during alcoholic fermentation

To investigate the effect of reduced glutathione (GSH) on the quality characteristics of apple wine, 10, 20 and 30 mg/L of GSH were added to apple juice before alcoholic fermentation. Meanwhile, apple wine fermented by Saccharomyces cerevisiae which had been pre-incubated with GSH (100 mg/L) was another experimental group. Mono-phenols, GSH and oxidized glutathione (GSSG) were determined by HPLC. Aroma compounds were analysed by GC–MS. Further, E-nose was applied to monitor the odor. After fermentation, GSH content was the same in all of the samples. However, for the apple wine with GSH addition, GSSG content increased significantly. Notably, GSH could reduce the color index, protect chlorogenic acid and phloretin, decrease the content of epicatechin and catechin as well as change the profile of aroma compounds (higher levels of 2-methyl-1-propanol, 3-methyl-1-butanol, ethyl benzoate, linalool, etc.). GSH may be used for flavor enhancement and quality improvement of apple wine.

Experimental Overweight Impairs Mitochondrial Brown Adipose Tissue Bioenergetics: Positive Effect After Serotonin Modulation

Infant overweight/obesity has achieved epidemiologic proportions worldwide and several metabolic dysfunctions are present in such condition. Brown adipose tissue (BAT) plays a critical role in thermogenesis and metabolic efficiency through mitochondrial function and recruitment of their mitochondrial uncoupling protein (UCP1). Besides that, some hormones as leptin also regulates energy metabolism by peripheral action in BAT. Interesting, early modulation of central serotonergic system with SSRI (Fx) can induce higher metabolic activity in BAT; even though the effects of Fx exposure later in life in experimental overweight/obese model was never studied. To study these effects, seventy‐two hours after delivery, puppies were randomly assigned into two groups: Normofed (nine pups/mother; n=9) or Overfed (three pups/mother; n=9). SSRI (Fx, 10mg/kg b.w.) or vehicle solution (NaCl 0.9%) administration was carried out from 39th through 59th day of age, according to the groups: Normofed + Vehicle (NV), Normofed + Fx (NF), Overfed + Vehicle (OV) and Overfed + Fx (OF). At 60 days of age UCP 1 protein expression, mitochondrial oxygen consumption‐MOC (in the presence or absence of the UCP inhibitor GDP) and ROS production, lipid peroxidation, protein oxidation, GSH and GSSG content and leptin gene expression were evaluated in the interscapular BAT (iBAT). Fx increased UCP 1 expression only in NF group (p=0.0076). Related to MOC in the absence of GDP, the basal state increased in OF group (p=0.0366). With GDP addition, both FLX groups increased MOC compared to their controls (NF: p=0.0003 and OF: p=0.050). In the uncoupling state without GDP, both groups had a higher MOC compared to their controls (NF: p=0.0316 and OF: p=0.0242) and presented superior MOC with GDP addition (NF: p&lt;0.0001 and OF: p=0.0034). ROS production increased in NF group (p=0.0010) and in OV group (p=0.0143) and decreased in OF group (p=0.0036). Lipid peroxidation was higher in NF group (p=0.0177) and OV group (p=0.0001) and lower in OF group (p=0.0418). Protein oxidation increased in NF group (p=0.0072) and OV group (p=0.0247). GSSG content increased in NF group (p&lt;0.0001) and decreased in OF group (p&lt;0.0001). Redox state (GSH/GSSG) decreased in NF group (p=0.0092) and increased in OF group (p=0.0031). Leptin gene expression decreased in NF group (p=0.004) and increased in OF group (p=0.0434). Taken together our data suggest that Fx administration in early adult life was detrimental for mitochondrial oxidative balance in normofed conditions; on the other hand in overfed rats pharmacological intervention shows mitochondrial and oxidative improvements in iBAT and readjustment of peripheral metabolic efficiency.Support or Funding InformationCAPES, CNPq and FACEPEThis abstract is from the Experimental Biology 2019 Meeting. There is no full text article associated with this abstract published in The FASEB Journal.

Novel molecularly imprinted polymer (MIP) multiple sensors for endogenous redox couples determination and their applications in lung cancer diagnosis

Multiplex electrochemical sensors for amperometric detection of glutathione disulfide (GSSG), glutathione (GSH), cysteine (Cys), cystine (Cyss), β-nicotinamide adenine dinucleotide phosphate (NADP+) and coenzyme II reduced tetrasodium salt (NADPH) were developed, in which analysis of Cyss, NADP+ and NADPH are the first report using this sensing system. Specificity of these sensors were ensured by a layer of molecularly imprinted polymer (MIP) which was electropolymerized in situ with the analytes as template. All the sensors were tested with standard buffers and mouse blood samples, showing satisfactory performance towards the corresponding analytes. Dynamic concentration for the six analytes was in the range of 10−11–10−8 mol/L with the detection limit down to 20 pmol/L. In addition, artificially synthesized MIP film on the electrodes allowed for good selectivity and stability. Real blood sample measurement proved that the sensors owned decent accuracy with recovery value ranging from 92%~112%. More importantly, blood samples from lung cancer patients and healthy donors were assayed by using the proposed sensors. Redox potentials (Ehc) were calculated based on the contents of these endogenic substances, which were utilized to reflect the health status of human body and help diagnose lung cancer. The levels of GSH, NADPH and the absolute value of Ehc(GSH/GSSG) in patients with lung cancer are significantly lower (P < 0.01) than those in healthy people, while the contents of GSSG (P < 0.01) are higher. The blood test results suggested that the content of GSH, NADPH, NADP+ and Ehc(GSH/GSSG) might serve as biomarkers for lung cancer prediagnosis. These novel sensors for liquid biospy of cancer have cost–benefit and scalability advantage over current techniques, potentially enabling broader clinical access and efficient population screening.

Hydrogen gas promotes the adventitious rooting in cucumber under cadmium stress.

Hydrogen gas (H2) plays an important role in plant development and stress responses. Here, cucumber (Cucumis sativus L.) explants were used to investigate the roles of H2 in adventitious root development under cadmium (Cd) stress and its physiological mechanism. The results showed that hydrogen-rich water (HRW) promoted adventitious rooting under Cd stress and 50% HRW obtained the maximal biological response. Compared with Cd treatment, HRW + Cd treatment significantly reduced the content of malondialdehyde (MDA), hydrogen peroxide (H2O2), superoxide radical (O2-), thiobarbituric acid reactive substances (TBARS), ascorbic acid (AsA) and reduced glutathione (GSH), as well as relative electrical conductivity (REC), lipoxygenase (LOX) activity, AsA/docosahexaenoic acid (DHA) ratio, and GSH/oxidized glutathione (GSSG) ratio, while increasing DHA and GSSG content. HRW + Cd treatment also significantly increased in the activity and related gene expression of ascorbate peroxidase (APX), dehydroascorbate reductase (DHAR), monodehydroascorbate reductase (MDHAR) and glutathione reductase (GR). Additionally, HRW + Cd treatment increased the contents of osmotic adjustment substances, as well as the activities of peroxidase (POD) and polyphenol oxidase (PPO), while significantly decreasing indoleacetic acid oxidase (IAAO) activity. In summary, H2 could induce adventitious rooting under Cd stress by decreasing the oxidative damage, increasing osmotic adjustment substance content and regulating rooting-related enzyme activity.

Overexpression of three orthologous glutathione S-transferases from Populus increased salt and drought resistance in Arabidopsis

Glutathione S-transferases (GSTs) are multifunctional proteins and play a role in detoxification of xenobiotics as well as prevention of oxidative damage. This study exogenously overexpressed PtGSTF4 from Populus trichocarpa and its two orthologs from Populus yatungensis and Populus euphratica in Arabidopsis thaliana, respectively. To elucidate the function of three GSTF4 proteins in stress response, we compared germination and seedling growth in transgenic Arabidopsis with salt and drought treatments. All three Populus GSTF4 genes overexpressed Arabidopsis showed enhanced resistance to salt stress and drought. GSTF4 transgenic plants accumulated less hydrogen peroxide and more chlorophylls and decreased levels of lipid peroxidation under salt stress and drought comparing to the mock control plants. The difference observed by GSH and GSSG measurements indicated GSTF4 proteins may involve in glutathione-dependent peroxide scavenging which lead to reduced oxidative damage. The Arabidopsis transformed with the GSTF4 gene form P. euphratica showed higher germination rate and different performance of affecting GSSG contents comparing with the other two orthologous GST genes under NaCl treatment. These results suggested three Populus GSTF4 orthologs may have functional divergence in stress responding. This study provides insights into molecular mechanisms that underlie salt and drought stress tolerance of Phi GSTs and gives evidence for the functional divergence among orthologs in vivo.

The relationships between changes in main biochemical parameters in sperm cells of infertile men

Detection of the regularities of functions of male genital cells, playing a principal role in the reproductive realization (environmental and psychological stresses) is especially relevant. Thus, the definition of the biochemical parameters of sperm at patho­spermia is an actual problem of medical biochemistry and laboratory diagnostic. A cluster analysis was performed to determine the distribution of men (normozoospermic and with different semen abnormalities – oligo-, astheno-, oligoasthenzoospermia and leukocytospermia) by groups according to biochemical indices. To determine a degree of affinity between the individual biochemical indicators and distinguish the most important changes, the obtained results were analyzed by principal component analysis (PCA). Based on parameters of glutathion antioxidant system (GSG, GP, GR, GST), arginase/NO-synthase system (cNOS, iNOS, arginase), membrane-bound ion transporting enzymes (Na + ,K + - and Ca 2+ , Mg 2+ -ATPase) and prooxidant manifestations (TBARS, GSSG), a cluster analysis of studied infertile male groups was performed. Normozoospermic males were the most distant from infertility men with leucocytospermia. However, the latter were involved in the formation of a subcluster which consisted of oligo-, astheno- and oligoasthenozoospermic groups. It is worth noting that oligo- and oligo­ashtenozoospermic males were the most related and formed a clear cluster based on the analyzed parameters. A usage of principal component analysis allowed quantitative pro­ving a degree of affinity between changes of the individual investigated parameters under the conditions of pathospermia. By means of principal component analysis of the studied parameters a consistency of changes in oxidative manifestation (TBARS and GSSG content), and the activity of glutathione-S-transferase and ion-transporting systems of spermal membranes of asthenozoospermic samples were set up. In the oligozoospermic samples the closest relations between the activity of the ion-transporting systems of the spermal membranes and the content of the lipoperoxidation products were detected.

Determination of Ascorbic Acid, Rutin and Antioxidant Capacities of Wild &amp;lt;i/&amp;gt;Allium roseum&amp;lt;/i&amp;gt; from Italy

This study is designed to investigate the antioxidant status and the presence of biologically-active compounds in Allium roseum L. and to compare the results with those of Allium sativum L. The content of thiosulfinates (Thio) and the levels of flavonols (quercetin and rutin), ascorbic acid (AA), glutathione reduced (GSH), glutathione oxidized (GSSG) and the antioxidant enzymes activities of glutathione peroxidase (GPx), glutathione reductase (GR) and catalase (CAT), were evaluated in bulbs, bulblets, flowers bulblets, leaves and flowers. Our study shows that bulbs of Allium roseum contain levels significantly higher of GSH, GSSG, AA, Thio, rutin and the activity of GPx and GR significantly higher than bulbs of Allium sativum. Moreover, the bulbs of Allium roseum show a significantly higher content of GPx, GR, CAT, GSH and GSSG than bulblets, flowers bulblets, leaves and flowers of Allium roseum. In Allium roseum, the greatest content of Thio is present in the flowers bulblets, while the levels of AA, quercetin and rutin are greater in the flowers. In conclusion, our result shows how Allium roseum exhibits antioxidant capabilities in all its fresh organs. The bulbs, bulblets, flowers bulblets, leaves and flowers are a good source of important bioactive compounds. Allium roseum possesses properties comparable to garlic indicating its possible nutritional and medicinal value.

Blueberry anthocyanin alleviate perfluorooctanoic acid-induced toxicity in planarian (Dugesia japonica) by regulating oxidative stress biomarkers, ATP contents, DNA methylation and mRNA expression

Blueberry anthocyanin (BA) have strong health benefits as an active natural antioxidant and perfluorooctanoic acid (PFOA) can result in oxidative stress in animals. In our study, the protective effects of BA against stress induced by PFOA was investigated in the planarian Dugesia japonica using oxidative stress biomarkers, ATP contents, ATPase activity, DNA methylation and mRNA expression. PFOA exposure could resulted in malondialdehyde production. At the same time, treatment with BA decreased the production of malondialdehyde in BA-exposed and co-treatment planarians. PFOA caused activities increase in glutathione peroxidase (GPx), glutathione S-transferase (GST) and activities decrease in glutathione reductase (GR). PFOA exposure decreased the GSH and ATP contents. Additionally, it increased the GSSG contents and ATPase activity. BA administration increased the activities of GPx, GST and GR in BA and co-treatment planarians. Meanwhile BA maintained the contents of ATP, ATPase activity, GSH and GSSG by alleviating PFOA toxicity. Moreover, PFOA and BA increased the contents of 5-methylcytosine and decreased 5-hydroxymethylcytosine in all group. In addition, PFOA and BA treated planarians significantly altered the expression of genes associated with above biochemical parameters. The results showed that the mRNA expression of gpx, Djgst, gr, Djnak and dnmt1 were significantly elevated in all groups. Alterations in the mRNA expression levels indicated a stress response to PFOA exposure and anthocyanin protection. These alterations regulated biomarkers of oxidative stress, energy metabolism and DNA methylation levels in planarians. These results indicate that BA attenuated PFOA-induced oxidative stress, energy metabolism, DNA methylation and gene expression disorders.

The nephroprotective properties of taurine in colistin-treated mice is mediated through the regulation of mitochondrial function and mitigation of oxidative stress

Colistin (COL) belongs to the polymixin class of antibiotics used as the last line antibiotic against drug-resistant infections. However, nephrotoxicity is the major deleterious and dose-limiting side effect associated with COL therapy. Oxidative stress and mitochondrial impairment are suspected mechanisms involved in COL-induced nephrotoxicity. Taurine is one of the most abundant amino acids in the human body with antioxidant and mitochondria protecting properties. The current study was designed to evaluate the potential nephroprotective properties of taurine against COL-associated nephrotoxicity. Mice were treated with COL (15 mg/kg/day, i.v, for 7 consecutive days) alone or in combination with taurine (500 and 1000 mg/kg, i.p). Plasma biomarkers of nephrotoxicity in addition of kidney tissue markers of oxidative stress were evaluated. Additionally, kidney mitochondria were isolated, and several mitochondrial indices were assessed. The COL-associated renal injury was evident by a significant increase in plasma markers of renal injury including creatinine (Cr), and blood urine nitrogen (BUN). COL treatment also caused a significant increase in kidney reactive oxygen species (ROS) and lipid peroxidation (LPO). Renal GSH reservoirs and antioxidant capacity were also decreased in COL-treated animals. Mitochondrial parameters including mitochondrial dehydrogenase activity, membrane potential, GSH, and ATP were significantly decreased while mitochondrial LPO, permeabilization, and GSSG content were increased in the kidney of COL-treated mice. It was found that taurine (500 and 1000 mg/kg, i.p) treatment alleviated COL-induced oxidative stress and mitochondrial dysfunction in the kidney tissue. The data obtained from the current study suggest mitochondrial dysfunction and oxidative stress as fundamental mechanisms of renal injury induced by COL. On the other hand, taurine supplementation protected kidney through decreasing oxidative stress and regulating mitochondrial function.

RNase1 alleviates the Aeromonas hydrophila-induced oxidative stress in blunt snout bream

RNase1 is an enzyme important in host defense in vertebrates where it degrades the RNA of bacteria and viruses. We evaluated the effect of RNase1 on the resistance to Aeromonas hydrophila infection in Megalobrama amblycephala. The fish were randomly divided into four groups: a blank group (none-treated M. amblycephala), a control group (injected PBS), a challenge group (A. hydrophila-injected) and a treatment group (pre-treated with RNase1 24 h before the A. hydrophila injection), and we collected five tissues of each group. Then we recorded changes in the levels of glutathione (GSH), oxidized glutathione (GSSG), hepatic catalase (CAT), superoxide dismutase (SOD), malondialdehyde (MDA) and lysozyme; and the relative mRNA expression of catalase (CAT), selenium-dependent glutathione peroxidase (GPx), Cu/Superoxide dismutase (Cu/Zn-SOD), glutamate-cysteine ligase (GCLC), glutathione reductase (GR) and nuclear factor erythroid 2-related factor 2 (Nrf2) for four groups. The expression of six genes was highest in liver and blood of the blank group. It was significantly higher in the gut of the treatment group (compared to control and challenge groups) 12 h after the infection. The treatment group exhibited a significant increase in GSH, SOD and CAT activity, and a decrease in GSSG, MDA and lysozyme content (compared to the control and challenge groups) 6 and 12 h after infection. These results suggest that supplementation with RNase1 protein can enhance resistance against A. hydrophila infections in M. amblycephala.