Antioxidant Defense Response Research Articles

Burkholderia phytofirmans PsJN and tree twigs derived biochar together retrieved Pb-induced growth, physiological and biochemical disturbances by minimizing its uptake and translocation in mung bean (Vigna radiata L.)

Anthropogenic activities like industrial mining, refining and smelting release substantial amounts of lead (Pb) into the soil causing potential ecological menaces to environment, soil productivity and food security. Present pot scale study was undertaken to investigate the effects of tree twigs-derived biochar and a bacterium Burkholderia phytofirmans PsJN on Pb accumulation, growth, physiological, biochemical and antioxidative defense responses of mung bean grown in Pb spiked soil. The original soil was spiked with Pb (600 mg kg−1) and amended with biochar (1% w/w). Upon screening in laboratory, B. phytofirmans PsJN exhibited high Pb tolerance and was able to grow at high Pb concentrations. Surface-disinfected seeds of mung bean were inoculated with B. phytofirmans PsJN and sown in pots along with un-inoculated seeds. Data were collected for various growth, physiological and biochemical parameters from fully matured harvested plants. Application of biochar and B. phytofirmans PsJN ameliorated Pb induced negative impacts in mung bean both individually and in combination, but better growth, physiological and seed quality responses were observed with their combined use. Compared with respective controls, their combined use increased the following parameters in normal and Pb spiked soils, respectively: plant height (69% and 159%), root dry weight (97% and 130%), shoot dry weight (42% and 104%), number of pods (70% and 210%), grains weight (58% and 194%) and number of root nodules (71% and 255%). Moreover, combined use increased chlorophyll contents (27% and 37%), photosynthetic rate (93% and 204%), transpiration rate (42% and 132%), stomatal conductance (70% and 218%), sub-stomatal conductance (93% and 148%) and water use efficiency (35% and 43%). In addition, combined application of biochar and B. phytofirmans PsJN retarded Pb-induced oxidative stress by intensifying antioxidant enzyme activities and reducing activities of reactive oxygen species. Similarly, considerable reduction in Pb uptake, translocation and bioaccumulation in mung bean was noticed in Pb spiked soil due to applied amendments. Furthermore, their combined use resulted in considerable increase in grain quality parameters (protein, fat, ash) both in normal and Pb-spiked soils. Therefore, it can be inferred that interactive use of biochar and B. phytofirmans PsJN provides an efficient innovative strategy to repossess Pb induced growth, physiological, biochemical and oxidative disturbances in mung bean.

Changes in the antioxidant intensities of seven different soybean (Glycine max (L.) Merr.) cultivars during drought.

Drought stress-induced antioxidative defense responses were studied in seven soybean (Glycine max (L) Merr.) cultivars PUSA 9712, LSB 1, JS 335, ADB 22, NRC 37, DSB 20, and MAUS 61, respectively. Drought stress was imposed by withholding irrigation till the leaf water potentials reached -1.0, -1.5, and -2.0MPa. Lipid peroxidation and superoxide, H2 O2 , • OH, DPPH radical scavenging assays were performed. Antioxidants during drought stress were studied by quantifying the ascorbic acid, glutathione, α-tocopherol, phenolics, flavonoids, tannins, enzymes superoxide dismutase, catalase, ascorbate peroxidase, and glutathione reductase. Antioxidant levels were significantly high in soybean foliages exposed to drought with the increased concentrations of radicals and enhanced lipid peroxidation rates. Isoenzyme analysis of SOD has shown the upregulation of Cu/Zn and MnSODs. Our results demonstrate that cultivars PUSA 9712 and LSB1 have shown to possess a high rate of antioxidants and a very efficient antioxidative defense system when compared with other cultivars. PRACTICAL APPLICATIONS: Soybean (Glycine max (L.) Merr.) is an economically important cash crop, cultivated globally for its rich protein, oil, nutraceutical, and antioxidant constituents. It is also cultivated for its rich enriched food, animal feed as well as several other commercial products. In India, most of the soybean cultivation is being done under rainfed conditions. Hence, identification of superior soybean cultivars rich in antioxidants is very important. The work presented here is the output of the investigation carried out on cramming the changes in antioxidative defense mechanisms of seven popular soybean cultivars that are regularly cultivated in India. A study was performed by quantifying the radicals, H2 O2 concentrations, lipid peroxidation, determination of enzymatic, and nonenzymatic antioxidants in all selected soybean cultivars exposed to control and increased the duration of drought stress, for the identification of superior cultivars with a rich avenue of enzymatic and nonenzymatic antioxidants.

Hemin treatment protects neonatal rats from sevoflurane-induced neurotoxicity via the phosphoinositide 3-kinase/Akt pathway

AimsAnaesthesia-related neurotoxicity in the developing brain is a controversial issue that has recently attracted much attention. Hemin plays a protective role in hypoxic and ischemic brain damage; however, its effects on sevoflurane-induced neurotoxicity remain unclear. Our aim was to investigate the mechanisms of sevoflurane neurotoxicity and potential neuroprotective roles of hemin upon sevoflurane exposure. Main methodsHippocampi were harvested 18 h after sevoflurane exposure. Haem oxygenase 1 (HMOX1), superoxide dismutase 2 (SOD2), discs large MAGUK scaffold protein 4 (DLG4), phosphorylated Akt, Akt, cleaved caspase 3, and neuroglobin were detected by western blotting. A water maze test was used to assess learning and memory ability in P30 rats. Key findingsSevoflurane inhalation increased cleaved caspase 3 levels. Hemin treatment enhanced the antioxidant defence response, protecting rats from oxidative stress injury. Hemin plays its neuroprotective role via phosphoinositide 3-kinase (PI3K)/Akt signalling. A single inhalation of sevoflurane did not affect DLG4 expression, while hemin treatment did. Platform crossing increased in rats treated with hemin as well, which may be related to increased DLG4. Neuroglobin expression was not affected, suggesting that it may act upstream of PI3K/Akt signalling. SignificanceOur study demonstrates that hemin plays a protective role in anaesthesia-induced neurotoxicity by both inhibiting apoptosis via the PI3K/Akt pathway and increasing the expression of antioxidant enzymes, reducing oxidative damage. The results provide mechanistic insight into the effects of sevoflurane anaesthesia on the developing brain and suggest that hemin could help avoid these effects.

Comparative Assessment of PAHs Reduction in Soil by Growing Zea mays L. Augmented with Microbial Consortia and Fertilizer: Modulation in Uptake and Antioxidant Defense Response

Polyaromatic hydrocarbons (PAHs) are found ubiquitously in the environment and are carcinogenic and recalcitrant in nature, hence their fate in crops is imperative to quantify. In present study, the role of petroleum hydrocarbon (PH) degrading microbial consortium and organic fertilizer in the translocation and accumulation of PAHs in a crop plant i.e., Zea mays var. NMH-589 was determined under experimental simulated condition using spiked soil with PAHs mixture (300 µg g−1 phenantherene, 300 µg g−1 anthracene, 200 µg g−1 pyrene, and 200 µg g−1 fluoranthene). After 32 days of treatment, removal of 49.7% of PAHs mixture (k = 0.01552 d−1, t1/2 = 44.6 d) in soil was observed due to growth of maize plant, compared to only 31% removal in non-planted soil (k = 0.0097, t1/2 = 71.456). While growing maize plant amended with organic fertilizer and microbial consortium (Pseudomonas sp. BP10 and Penicillium oxalicum PS10), enhanced the degradation rate of PAHs in soil by 99.4% (k = 0.03107 d−1, t1/2 = 22.3 d). Maximum accumulation of total PAHs mixture in plant tissues (root, shoot, and leaves) was 99.5, 63.5, and 43.5 µg g−1, respectively without any amendment, while the accumulation was lowest i.e., 11.4 µg g−1, 1.2 µg g−1 and not detected, respectively when the soil was amended with microbes and cow-dung manure. Plants also stimulated the microbial count in soil by enhancing their CFU g−1 of soil up to 503%), while the addition of microbial consortium reduced the PAHs stress to plant concurrent with the decrease in antioxidant activities of the plant.

Accumulation, morpho-physiological and oxidative stress induction by single and binary treatments of fluoride and low molecular weight phthalates in Spirodela polyrhiza L. Schleiden

The present study examined the interactive effects of fluoride and phthalates on their uptake, generation of reactive oxygen species and activation of antioxidative defence responses in Spirodela polyrhiza L. Schleiden. A hydroponic study was conducted in which S. polyrhiza cultured in Hoagland’s nutrient medium, was exposed to fluoride (50 ppm) and different concentrations viz., 75, 150 300 ppm of diethyl phthalate (DEP) and diallyl phthalate (DAP) individually as well as in combination for the time period of 24, 72, 120 and 168 h respectively. A significant decline in fresh weight, dry to fresh weight ratio, total chlorophyll, carotenoid content and increased anthocyanin content was observed. Fluoride and phthalates was found to be readily accumulated by S. polyrhiza in all the exposure periods. Interestingly, when binary treatments were given in nutrient medium, uptake of both fluoride and phthalate was found to be influenced by each other. In combined treatments, DEP stimulated fluoride uptake, while its own uptake was restricted by fluoride. In contrary to this, fluoride stimulated DAP uptake. Moreover, combined stress further caused significant decrement in carbohydrate, protein content and increment in MDA levels, phenolic content and electrolyte leakage. Nevertheless, phthalates showed more pronounced oxidative stress and growth inhibition compared to fluoride. To cope up with the oxidative damage, enhanced level of antioxidant enzymatic activities was observed in S. polyrhiza under both fluoride and phthalate stress as compared to control. Scanning electron microscope imaging of leaf stomata revealed that combined stress of fluoride with phthalates caused distortion in the shape of guard cells. Confocal micrographs confirmed the generation of reactive oxygen species, cell damage, disruption in membrane integrity, and enhanced levels of glutathione in plant cells. This study focussed on ecotoxicological and interactive significance of fluoride led phthalate uptake or vice versa which was also assumed to confer tolerance attributes.

Insights into acetate-mediated copper homeostasis and antioxidant defense in lentil under excessive copper stress

Gradual contamination of agricultural land with copper (Cu), due to the indiscriminate uses of fungicides and pesticides, and the discharge of industrial waste to the environment, poses a high threat for soil degradation and consequently food crop production. In this study, we combined morphological, physiological and biochemical assays to investigate the mechanisms underlying acetate-mediated Cu toxicity tolerance in lentil. Results demonstrated that high dose of Cu (3.0 mM CuSO4. 5H2O) reduced seedling growth and chlorophyll content, while augmenting Cu contents in both roots and shoots, and increasing oxidative damage in lentil plants through disruption of the antioxidant defense. Principle component analysis clearly indicated that Cu accumulation and increased oxidative damage were the key factors for Cu toxicity in lentil seedlings. However, acetate pretreatment reduced Cu accumulation in roots and shoots, increased proline content and improved the responses of antioxidant defense (e.g. increased catalase and glutathione-S-transferase activities, and improved action of glutathione-ascorbate metabolic pathway). As a result, excess Cu-induced oxidative damage was reduced, and seedling growth was improved under Cu stress conditions, indicating the role of acetate in alleviating Cu toxicity in lentil seedlings. Taken together, exogenous acetate application reduced Cu accumulation in lentil roots and shoots and mitigated oxidative damage by activating the antioxidant defense, which were the major determinants for alleviating Cu toxicity in lentil seedlings. Our findings provide mechanistic insights into the protective roles of acetate in mitigating Cu toxicity in lentil, and suggest that application of acetate could be a novel and economical strategy for the management of heavy metal toxicity and accumulation in crops.

Cigarette smoke extract exacerbates hyperpermeability of cerebral endothelial cells after oxygen glucose deprivation and reoxygenation

Cigarette smoking is a risk factor for stroke and is linked to stroke severity. Previous studies have shown that cigarette smoke extract (CSE) triggers endothelial dysfunction in vitro by initiating oxidative stress and/or an inflammatory response. In addition, cerebral endothelial dysfunction (particularly at the level of the blood-brain barrier [BBB]) contributes to stroke pathogenesis. Therefore, we hypothesized that cigarette smoking may influence stroke, at least in part, by exacerbating ischaemia-induced BBB disruption. To test this, we examined the effect of CSE on the permeability of cerebral endothelial cells exposed to oxygen glucose deprivation and reoxygenation (OGD + RO). We found that the loss of BBB integrity following ischaemic/reperfusion-like conditions was significantly worsened by CSE. Despite this being associated with increased mRNA expression of Nox catalytic subunits, reactive oxygen species (ROS) levels were however markedly lower. Furthermore, this occurred in association with elevated expression of antioxidant enzymes (SOD1, SOD2, and Gpx-1), suggesting an antioxidant defence response. Lastly, we found that CSE significantly upregulated mRNA expression of cytokines (IL-6 and TGF-β). Collectively, these results show that acute exposure to CSE worsens BBB disruption caused by OGD + RO, however, this is not linked to elevated ROS levels but may involve inflammatory mechanisms.

Antioxidative defense response of Ulva prolifera under high or low-temperature stimulus

Because marine organisms have evolved to adapt to a wide variety of environmental factors on varying temporal and spatial scales, the antioxidative metabolic pathway are different. The aim of this study was to investigate the different antioxidative response of Ulva Prolifera (U. prolifera) that have been exposed to high temperature (UpHT) or low-temperature (UpLT) stresses. The results of our study suggested that mainly UpHT and not UpLT increased the expression of superoxide dismutase (SOD), catalase (CAT), and L-ascorbate peroxidase (APX) more than those in the medium-temperature (UpMT) controls. In addition, biological index analyses indicated that both SOD and CAT activities increased after culturing for 48h. The chlorophyll levels increased to the highest point after culturing for 4 d in the UpHT group but remained unchanged in the UpLT group. In addition, peroxide (H2O2) and malondialdehyde (MDA) levels increased under UpHT but remained unchanged under UpLT stimuli. We suggest that our findings have significantly improved our understanding of the different molecular mechanisms involved in the tolerance of algae to UpHT or UpLT stimulus, which might explain the seasonal blooms of U. prolifera.

The role of Mu-type glutathione S-transferase in the mud crab (Scylla paramamosain) during ammonia stress

Glutathione S-transferase (GST) plays important roles in cellular detoxification and antioxidant defense. A Mu-type glutathione S-transferase (designated as SpMu-GST) was obtained from the mud crab Scylla paramamosain. The open reading frame of SpMu-GST was comprised a 690 bp, which encoded a putative protein of 229 amino acids. Quantitative real-time PCR (qRT-PCR) revealed that the SpMu-GST mRNA was expressed in all examined tissues, with highest expression in hepatopancreas. During ammonia exposure, the SpMu-GST transcriptions in hepatopancreas and gill were significantly up-regulated at early exposure time. Moreover, RNA interference (RNAi) experiment was designed to understand the roles of SpMu-GST under ammonia exposure. Ammonia exposure reduced the levels of glutathione S-transferase (GST), superoxide dismutase (SOD), catalase (CAT) and total antioxidative capacity (T-AOC), and increased the formation of malondialdehyde (MDA). After knockdown of the SpMu-GST level, GST activity and T-AOC were significantly decreased at some exposure time after ammonia exposure. However, the mortality of mud crabs and malondialdehyde (MDA) contents significantly increased under ammonia exposure. These results further suggested that SpMu-GST played a critical role in mud crab antioxidant defenses in response to environmental stress.

Ellagic acid supports neuron by regulating astroglia Nrf2.

Astroglia support neuron by providing substrates for neuronal metabolism, glutamate clearance, and antioxidative protection. Nuclear factor erythroid 2-related factor 2 (Nrf2) participates in the antioxidative defense response. Also, Nrf2 signaling is recognized to activate the neurotrophic pathway to replace/protect damaged organelles. Ellagic acid (EA), an extraction component of fruits and nuts, presents many pharmacological activities such as anti-inflammation, antioxidation, and neuroprotection. However, few studies have been focused on the neurotrophic properties of EA. Our study investigated whether EA could increase neuronal survival and the target cells. Thus, primary neuron-enriched cultures and primary astroglia-enriched cultures were applied to detect whether EA-elicited neurotrophic effects were mediated by astroglia Nrf2. This study indicated that EA promoted neuronal survival. Further, astroglia Nrf2 participate in EA-elicited neuronal survival with the following scenarios. First, EA elicited astroglia proliferation, glial cell line-derived neurotrophic factor (GDNF) release, and Nrf2 activation. Second, after silencing astroglia Nrf2, EA-induced astrogliosis, GDNF release, and neuronal survival disappeared. Thus, EA-mediated astroglia Nrf2 activation is important to enhance neurotrophic effects on neurons, which might provide new insights for neurodegenerative disease.

Ozone phytotoxicity to Panicum maximum and Cenchrus ciliaris at Indo-Gangetic plains: an assessment of antioxidative defense and growth responses

Two common tropical grassland species, Panicum maximum Jacq. (Guinea grass) and Cenchrus ciliaris (Buffel grass) of Indo-Gangetic plains were assessed for their responses under future level of O3 (ambient +30 ppb) using open top chambers. Plants were assessed for foliar injuries, pigments, growth, biomass accumulation, histochemical localization of reactive oxygen species (ROS), antioxidant defense system and ROS scavenging activities at two stages. Foliar injuries were noticed at an early stage in P. maximum compared to C. ciliaris. Significant reductions were observed in total chlorophyll, growth and total biomass in both species. Significant increases in contents of melondialdehyde and ascorbic acid in P. maximum while total phenolics and thiols in C. ciliaris were found. Histochemical analysis showed more production of superoxide radicals and hydrogen peroxide in leaf tissues of P. maximum compared to C. ciliaris. It can be concluded that higher level of primary antioxidants (total phenolics and thiols) along with superoxide dismutase and ascorbate peroxidase scavenged O3 effectively in C. ciliaris causing less reduction of biomass which is used as a feed for cattles. In P. maximum, more photosynthates were allocated for defense, leading to higher reduction in total biomass compared to C. ciliaris. The leaf area ratio was higher in P. maximum compared to C. ciliaris under elevated O3. The study further suggests higher susceptibility of P. maximum compared to C. ciliaris under future level of O3 exposure.

Glucoindole alkaloid accumulation induced by yeast extract in Uncaria tomentosa root cultures is involved in defense response.

To evaluate the induction of monoterpenoid indole alkaloids (MIA) and phenolic compound production by yeast extract (YE) and its relationship with defense responses in Uncaria tomentosa (Rubiaceae) root cultures. Root cultures were elicited by YE at three concentrations. The 0.5mg YE ml-1 treatment did not affect cell viability but increased the hydrogen peroxide concentration by 5.7 times; guaiacol peroxidase activity by twofold; and the glucoindole alkaloid 3α-dihydrocadambine (DHC) content by 2.6 times (to 825.3 ± 27.3μgg-1). This treatment did not affect the contents of monoterpenoid oxindole alkaloids or chlorogenic acids. In response to 0.5mg YE ml-1 treatment, the transcript levels of MIA biosynthetic genes, TDC and LAMT, increased 5.4 and 1.9-fold, respectively, that of SGD decreased by 32%, and that of STR did not change. The transcript levels of genes related to phenolic compounds, PAL, CHS and HQT, increased by 1.7, 7.7, and 1.2-fold, respectively. Notably, the transcript levels of Prx1 and Prx encoding class III peroxidases increased by 1.4 and 2.5-fold. The YE elicitor induced an antioxidant defense response, increased the transcript levels of genes encoding enzymes related to strictosidine biosynthesis precursors and class III peroxidases, and decreased the transcript level of SGD. Thus, YE could stimulate antifungal DHC production in root cultures of U. tomentosa.

Coupled Application of Antioxidant Defense Response and Embryo Development in Amphipod Crustaceans in the Assessment of Sediment Toxicity.

Survival rate, frequency of malformed embryos, and antioxidant defense system responses in the benthic amphipod Gmelinoides fasciatus from the Baltic Sea were measured to examine the effects of toxic sediments, and to assess the usefulness of these endpoints in sediment toxicity biotesting. A highly contaminated sediment sample from the Baltic Sea was diluted with sediment from a clean site to come up with a series of 5 test sediments with dilutions from 1:32 to 1:1024, and the reference sediment. The 1:32 dilution of the test sediment was analyzed for organotins (2862 µg tin [Sn] kg dry wt -1 ), polycyclic aromatic hydrocarbons (6064 µg kg dry wt -1 ), and selected trace metals (e.g., copper 352 mg kg dry wt -1 ). The survival rate of G. fasciatus (10-d toxicity test) was 100% in the reference and 1:1024 treatments, and began to decline from the 1:256 dilution onward. In a 28-d experiment, various types of morphological malformations were observed in 11 to 80% of the amphipod embryos in the 1:64, 1:128, and 1:256 dilutions, with only <5% in the reference treatment. Also, elevated activities in the antioxidant defense system enzymes glutathione S-transferase and catalase were observed in amphipods exposed to the contaminated sediments compared with the reference treatment, with responses at lower contamination levels compared with the appearance of malformations in the embryos. The results obtained illustrate the effectiveness of the combined application of embryonic malformations and antioxidant defense system biomarkers in amphipods in the assessment of sediment toxicity, and potentially also of sublethal effects of chemical contamination in aquatic ecosystems. Environ Toxicol Chem 2019;38:2020-2031. © 2019 SETAC.

Particulate Matter Exposure History Affects Antioxidant Defense Response of Mouse Lung to Haze Episodes.

Few studies have focused on the association between previous particulate matter (PM) exposure and antioxidant defense response to a haze challenge. In this study, a combined exposure model was used to investigate whether and how PM exposure history affected the antioxidant defense response to haze episodes. At first, C57BL/6 male mice were randomly assigned to three groups and exposed for 5 weeks to whole ambient air, ambient air containing a low (≤75 μg/m3) PM concentration, and filtered air, which simulated different exposure history of high, relatively low, and almost zero PM concentrations. Thereafter, all mice underwent a 3-day haze exposure followed by a 7-day exposure to filtered air. The indexes involved in the primary and secondary antioxidant defense response were determined after pre-exposure and haze exposure, as well as 1 day, 3 days, and 7 days after haze exposure. Our research demonstrated repeated exposure to a high PM concentration compromised the antioxidant defense response and was accompanied by an increased susceptibility to a haze challenge. Conversely, mice with a lower PM exposure developed an oxidative stress adaption that protected them against haze challenge more efficiently and in a more timely manner than was the case in mice without PM exposure history.

Exposure time relevance of response to nitrite exposure: Insight from transcriptional responses of immune and antioxidant defense in the crayfish, Procambarus clarkii

To understand the toxic effects of nitrite exposure on crayfish, expression of genes involved in the immune system, the antioxidant defense, and the heat shock protein 70 (HSP70) was measured after 12, 24, and 48 h of different nitrite concentrations exposure in the hepatopancreas and hemocytes of Procambarus clarkii. Nitrite exposure up-regulated mRNA levels of cytoplasmic Mn superoxide dismutase (cMn-SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione-S-transferase (GST), after 24 h nitrite exposure. At 48 h, nitrite exposure decreased the mRNA levels of mitochondrial MnSOD (mMn-SOD), CAT, and GPx. High concentrations of nitrite at 48 h of exposure decreased expression of β-1,3-glucan-bingding protein in the hepatopancreas, and lysozyme expression in hemocytes. Nitrite exposure caused little effect on the heat shock protein 70 (HSP70) in hemocytes. Through overall clustering analysis, we found that 24 h of nitrite exposure caused stronger transcriptional responses. Our study indicated that the response of P. clarkii to acute nitrite exposure was exposure time-dependent. These results will help to understand the dynamic response pattern of crustaceans to nitrite pollution, and improve our understanding of the toxicological mechanisms of nitrite in crustaceans.

Growth, DNA damage and biochemical toxicity of cyantraniliprole in earthworms (Eisenia fetida)

Cyantraniliprole is a second-generation diamide insecticide that exhibited excellent biological efficacy against a variety of pests. To assess the toxic impact of cyantraniliprole on earthworms, the levels of reactive oxygen species (ROS) and malondialdehyde (MDA), activities of superoxide dismutase (SOD), catalase (CAT) and glutathione S-transferase (GST), as well as DNA damage were measured after exposed to five cyantraniliprole concentrations ranging from 0 to 10.00 mg/kg for 7, 14, 21 and 28 days. In most treatment groups, the ROS levels increased significantly before exposure time of 14 days and then returned to normal levels. However, the SOD and CAT activities showed different response with activities were first significantly decreased and subsequently increased. The peroxidase (POD) activity showed no significant differences between treatment and control groups at first and then significantly increased. However, the opposite pattern characterized the GST activity. Also, maybe being dose-dependent before 14 days. The MDA concentration was used as a measure of lipid peroxidation (LPO). During experiment period, the MDA concentrations significantly increased when treated by this pesticide. The olive tail moment (OTM) was used as a measure of DNA damage. At higher concentrations of cyantraniliprole and longer exposure times, the OTM gradually increased, and DNA damage in the earthworms gradually increased. The weight of the high-dose (i.e., 5 mg/kg, 10 mg/kg) earthworms showed a significant trend of decrease phenomenon. Overall, the results suggest that sub-chronic exposure to cyantraniliprole causes DNA damage and LPO, weight loss and growth inhibition, leading to antioxidant defence responses in earthworms.

Characterization of a catalase from red-lip mullet (Liza haematocheila): Demonstration of antioxidative activity and mRNA upregulation in response to immunostimulants

Reactive oxygen species, generated in all the aerobic organisms, can cause oxidative stress. Excessive ROS may become a source of carcinogen due to DNA damage, lipid peroxidation, cell injury, and cell death. In order to prevent these adverse effects of ROS, antioxidant enzymes have evolved in aerobic organisms. Catalase is a major antioxidant enzyme that breaks down excessive H2O2 and inhibits apoptotic cell death. Here we molecularly characterized catalase from red-lip mullet. The cDNA sequence of LhCAT consists of an ORF of 1545 bp, which encodes a 527 amino acid peptide (~60 kDa). Based on bioinformatics analysis, LhCAT possesses a domain architecture characteristic of catalases, including a catalase proximal active site signature and a catalase proximal heme-ligand signature. It also has heme and NADPH binding sites homologous to previously described catalases. Pairwise alignment with its homologs revealed that LhCAT shares 95.1% identity with Oplegnathus fasciatus catalase and 97.4% similarity with Sparus aurata catalase. An uprooted phylogenetic tree demonstrated that LhCAT resides in a clade with catalases from other teleosts and exhibits a close relationship with Oplegnathus fasciatus catalase. Among twelve tissue types, we observed the highest LhCAT mRNA expression in the liver, followed by blood. Immune challenge by Lactococcus garvieae, or Poly I:C in the blood or spleen resulted in up-regulation at 24 h post injection. We also tested the antioxidant activity of recombinant LhCAT against hydrogen peroxide and found its optimal concentration to be 12.5 μg/mL. Collectively, these data suggested that LhCAT play an important role in antioxidant defense and immune response of red-lip mullet.

Induced expression of NOX and SOD by gaseous sulfur dioxide and chlorine dioxide enhances antioxidant capacity and maintains fruit quality of ‘Daw’ longan fruit during storage through H2O2 signaling

Hydrogen peroxide (H2O2) is known to be a signaling molecule involved in the activation of plant defense against both biotic and abiotic stresses. The current study aimed to demonstrate that fumigation induces H2O2 production, which is believed to act as the upstream signaling molecule in the antioxidant defense responses. Longan (Dimocarpus longan Lour. cv. Daw) fruit were fumigated with either 1000 mg L−1 sulfur dioxide (SO2) or 10 mg L−1 chlorine dioxide (ClO2), or in combination, and stored for 8 d. Both types of fumigation reduced pericarp browning and maintained fruit quality for up to 3, 5 or 7 d, respectively, comparing with a 2 d shelf life for the non-fumigated control fruit. 2,2’-Azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) and 1,1-diphenyl-2-picrylhydrazy (DPPH) assays indicated that antioxidant capacity was enhanced in treated fruit. H2O2 concentrations increased immediately after the fumigation in treated fruit, reaching a maximum within 6–12 h. Treatments increased expression of the plasma membrane nicotinamide adenine dinucleotide phosphate oxidase (RbohD) and superoxide dismutase (SOD). Subsequent nicotinamide adenine dinucleotide phosphate oxidase (NOX) and superoxide dismutase activity surges coincided with the rise of H2O2. Compared with the fumigated samples, H2O2 concentrations did not increase in the control until day 1, reaching concentrations that were about three times higher than those of the fumigated samples at the end of the experiment, while that of the fumigated fruit remained lower. These results suggested that SO2 and/or ClO2 fumigation triggers the NOX-dependent H2O2 generation, which could activate the antioxidant response in longan aimed to overcome the subsequent H2O2 production, thereby reducing the pericarp browning and maintaining fruit quality.

Zinc sulphide nanoparticle (nZnS): A novel nano-modulator for plant growth

In spite of extraordinary properties of zinc sulphide nanoparticle (nZnS), its role on plant system is not well understood, yet. Therefore, this study was aimed to assess the uptake, translocation and effects of nZnS in mung bean (Vigna radiata) plant at 0, 0.1, 0.5 and 1 mg L−1 concentrations. In this study, nZnS was synthesized by modified reflux method and physicochemical characterizations were conducted. The effects of nZnS on mung bean plant were determined by seed germination, growth parameters, membrane integrity and ROS-antioxidant defense assays. Our results showed that nZnS treatment has significantly increased seed germination, root-shoot length, pigment content and decreased lipid peroxidation. There were increased total antioxidant activity (TAA), DPPH and flavonoid contents found in treated plants. Also, nZnS treatment did not activate oxidative stress determined by SOD, CAT, CPX, APOX and GR activities. The uptake and translocation of nZnS in mung bean plants were determined by Transmission Electron Microscope (TEM) and Scanning Electron Microscope (SEM), revelling that nZnS localized primarily in the vacuoles and chloroplasts. Besides, electron micrographs showed no alteration in cell structures between treated and control plants, further confirming that nZnS treatment has no phytotoxic effects. In vitro and in vivo studies on Zn release from nZnS were also determined using Inductively Coupled Plasma Mass Spectroscopy (ICPMS) and Energy Dispersive X-ray (EDX), which showed that the Zn release and particles uptake were concentration dependent. Overall, results of this study demonstrated the positive role of nZnS on growth and antioxidant defense responses in V. radiata at the experimental concentrations.

Exogenous hydrogen sulfide alleviates salt stress by improving antioxidant defenses and the salt overly sensitive pathway in wheat seedlings

Hydrogen sulfide (H2S) has the ability to strengthen plant stress tolerance; however, the effects of H2S on wheat seedlings under salt stress and the underlying molecular mechanism are still unclear. This study examined the effects of exogenous NaHS as H2S donor on photosynthesis, antioxidant system, and the expression profile of genes related to antioxidant defense responses, the salt overly sensitive (SOS) and mitogen-activated protein kinase (MAPK) pathways in wheat seedlings treated with NaCl stress. H2S application improved photosynthesis, and decreased H2O2 and malondialdehyde (MDA) contents in wheat seedling leaves under NaCl stress. In addition, antioxidant enzyme activity and the content of ascorbic acid and reduced glutathione increased with H2S application. Moreover, H2S pretreatment up-regulated expression levels of genes related to antioxidant system, SOS pathway and MAPK pathway as well as the transcription factor dehydration-responsive element binding gene. Overall, these findings suggest that H2S alleviates salt stress in wheat seedlings not only by strengthening antioxidant defense systems, but by coordinating signal transduction pathways related to the stress response at a transcriptional level.