OsbZIP53 Negatively Regulates Immunity Response by Involving in Reactive Oxygen Species and Salicylic Acid Metabolism in Rice

The basic region/leucine zipper(bZIP)transcription factors play important roles in plant development and responses to abiotic and biotic stresses.OsbZIP53 regulates resistance to Magnaporthe oryzae in rice by analyzing APIP5-RNAi transgenic plants.To further investigate the biological functions of OsbZIP53,we generated osbzip53 mutants using CRISPR/Cas9 editing and also constructed OsbZIP53 over-expression transgenic plants.Comprehensive analysis of phenotypical,physiological,and transcriptional data showed that knocking-out OsbZIP53 not only improved disease resistance by inducing a hypersensitivity response in plants,but also regulated the immune response through the salicylic acid pathway.Specifically,disrupting OsbZIP53 increased H2O2 accumulation by promoting reactive oxygen species generation through up-regulation of several respiratory burst oxidase homologs(Osrboh genes)and weakened H2O2 degradation by directly targeting OsMYBS1.In addition,the growth of osbzip53 mutants was seriously impaired,while OsbZIP53 over-expression lines displayed a similar phenotype to the wild type,suggesting that OsbZIP53 has a balancing effect on rice immune response and growth.

Effects of Nitric Oxide on the Germination of Wheat Seeds and Its Reactive Oxygen Species Metabolisms Under Osmotic Stress

Effects of sodium nitroprusside (SNP), a nitric oxide (NO) donor, on the germination and metabolism of reactive oxygen species were surveyed in wheat (Triticum aestivum L.) seeds. Germination of wheat seeds and even the elongation of radicle and plumule were dramatically promoted by SNP treatments during the germination under osmotic stress. Meanwhile, activities of amylase and EP were enhanced, thus leading to the degradation of storage reserve in seeds. After osmotic stress was removed, higher viability of wheat seeds was also maintained. In addition, the activities of CAT, APX and the content of proline were increased by SNP treatment simultaneously, but activities of LOX were inhibited, and both of which were beneficial for improving the antioxidant capacity during the germination of wheat seeds under osmotic stress. It was also shown that the increase of the activity of amylase induced by SNP in embryoless half-seeds of wheat in the beginning period of germination (6 h) might be indirectly related to GA(3).

Decreased osteogenesis of adult mesenchymal stem cel s by reactive oxygen species under cyclic stretch: a possible mechanism of age related osteoporosis

Age related defect of the osteogenic differentiation of mesenchymal stem cells（MSCs） plays a key role in osteoporosis. Mechanical loading is one of the most important physical stimuli for osteoblast differentiation.Here, we compared the osteogenic potential of MSCs from young and adult rats under three rounds of 2 h of cyclic stretch of 2.5% elongation at 1 Hz on 3 consecutive days. Cyclic stretch induced a significant osteogenic differentiation of MSCs from young rats, while a compromised osteogenesis in MSCs from the adult rats.Accordingly, there were much more reactive oxygen species（ROS） production in adult MSCs under cyclic stretch compared to young MSCs. Moreover, ROS scavenger N-acetylcysteine rescued the osteogenic differentiation of adult MSCs under cyclic stretch. Gene expression analysis revealed that superoxide dismutase 1（SOD1） was significantly downregulated in those MSCs from adult rats. In summary, our data suggest that reduced SOD1 may result in excessive ROS production in adult MSCs under cyclic stretch, and thus manipulation of the MSCs from the adult donors with antioxidant would improve their osteogenic ability.

Changes of Reactive Oxygen Species and Related Enzymes in Mitochondria Respiratory Metabolism During the Ripening of Peach Fruit

The fruits of peach cultivar Yuhua 3 were used as materials to investigate the changes of active oxygen and related enzymes in mitochondria respiratory metabolism during ripening of peach fruit, involving their influence on the proceeding of peach fruit senescence. The results showed that the large decrease in firmness occurred between maturity II and IV. The decrease in firmness coincided with an increase in respiratory intensity. Obvious peaks of respiratory intensity lagging to the rapid change of fruit firmness could be shown during peach ripening. Reactive oxygen species （ROS） had a cumulative process and positively correlated with respiratory intensity. During peach ripening, the content of Ca^2＋ increased, the activities of succinic dehydrogenase （SDH）, cytochrome C oxidase （CCO）, H＋-ATPase, and Ca^2＋-ATPase decreased varying in different degree at the later step of ripening. These suggested a close relationship existed between ROS metabolism and mitochondrial respiration, namely, both ROS metabolism and mitochondrial respiration probably played important roles in ripening and senescing of peach fruit.

Effect of dietary supplementation of vitamin C on growth, reactive oxygen species, and antioxidant enzyme activity of Apostichopus japonicus(Selenka) juveniles exposed to nitrite

Different amounts of vitamin C were added to diets fed to juveniles （2.5＋0.15 g） of sea cucumber Apostichopus japonicus （Selenka） in an attempt to reduce the stress response of specimens exposed to nitrite stress. A commercial feed was used as the control diet and three experimental diets were made by supplementing 1 000, 1 500, or 2 000 mg vitamin C/kg diet to control diet separately in a 45-day experiment. Sea cucumbers were exposed to three different levels （0.5, 1.0, and 1.5 mg/L） of nitrite stress for 4, 8, and 12 h at four time intervals （0, 15, 30, and 45 d）. Growth of the animals was recorded during the experiment. Reactive oxygen species （ROS） （i.e. hydroxyl free radical （-OH）, malondialdehyde （MDA） and total antioxidant capacity （T-AOC）） and antioxidant enzyme activities （i.e., superoxide dismutase （SOD） and eatalase （CAT）） were measured. Response surface methodology （RSM） was used to analyze the effect of multiple factors on ROS indices and enzyme activities. Weight gain （WG） and special growth rate （SGR） of vitamin C supplementation groups were significantly higher than those of control group （P〈0.05）. The levels of-OH and MDA increased under exposure time extending and nitrite concentration increasing, whereas T-AOC level decreased. SOD and CAT activities increased at 4 h and 8 h and decreased at 12 h. During the days in which the animal consumed experimental diets, the levels of-OH and MDA decreased and that of T-AOC increased. This result suggests that diets containing vitamin C could reduce the nitrite stress response in the animals and increase their antioxidant capacity. The multifactor regression equation of growth performance, ROS indices, and duration of feeding results suggest that vitamin C supplementation of 1 400-2 000 mg/kg diet for 29-35 days could reduce effectively the effects of nitrite exposure.

TaNF-YB11,a gene of NF-Y transcription factor family in Triticum aestivum,confers drought tolerance on plants via modulating osmolyte accumulation and reactive oxygen species homeostasis

Transcription factors(TFs)regulate diverse stress defensive-associated physiological processes and plant stress responses.We characterized TaNF-YB11,a gene of the NF-YB TF family in Triticum aestivum,in mediating plant drought tolerance.TaNF-YB11 harbors the conserved domains specified by its NF-YB partners and targets the nucleus after the endoplasmic reticulum(ER)assortment.Yeast two-hybrid assay indicated the interactions of TaNF-YB11 with TaNF-YA2 and TaNF-YC3,two proteins encoded by genes in the NF-YA and NF-YC families,respectively.These results suggested that the heterotrimer established among them further regulated downstream genes at the transcriptional level.The transcripts of TaNF-YB11 were promoted in roots and leaves under a 27-h drought regime.Moreover,its upregulated expression levels under drought were gradually restored following a recovery treatment,suggesting its involvement in plant drought response.TaNF-YB11 conferred improved drought tolerance on plants;the lines overexpressing target gene displayed improved phenotype and biomass compared with wild type(WT)under drought treatments due to enhancement of stomata closing,osmolyte accumulation,and cellular reactive oxygen species(ROS)homeostasis.Knockdown expression of TaP5CS2,a P5CS family gene modulating proline biosynthesis that showed upregulated expression in drought-challenged TaNF-YB11 lines,alleviated proline accumulation of plants treated by drought.Likewise,TaSOD2 and TaCAT3,two genes encoding superoxide dismutase(SOD)and catalase(CAT)that were upregulated underlying TaNF-YB11 regulation,played critical roles in ROS homeostasis via regulating SOD and CAT activities.RNA-seq analysis revealed that numerous genes associated with processes of‘cellular processes',‘environmental information processing',‘genetic information processing',‘metabolism',and‘organismal systems'modified transcription under drought underlying control of TaNF-YB11.These results suggested that the TaNF-YB11-mediated drought response is possibly accomplished through the target gene in modifying gene transcription at the global level,which modulates complicated biological processes related to drought response.TaNF-YB11 is essential in plant drought adaptation and a valuable target for molecular breeding of drought-tolerant cultivars in T.aestivum.

Overproduction of reactive oxygen species–obligatory or not for induction of apoptosis by anticancer drugs

Many studies demonstrate that conventional anticancer drugs elevate intracellular level of reactive oxygen species （ROS） and alter redox-homeostasis of cancer cells. It is widely accepted that anticancer effect of these chemotherapeutics is due to induction of oxidative stress and ROS-mediated apoptosis in cancer. On the other hand, the harmful side effects of conventional anticancer chemotherapy are also due to increased production of ROS and disruption of redox-homeostasis of normal cells and tissues. This article describes the mechanisms for triggering and modulation of apoptosis through ROS-dependent and ROS^independent pathways. We try to answer the question： ＂Is it possible to induce highly specific apoptosis only in cancer cells, without overproduction of ROS, as well as without harmful effects on normal cells and tissues？＂ The review also suggests a new therapeutic strategy for selective killing of cancer cells, without significant impact on viability of normal cells and tissues, by combining anticancer drugs with redox-modulators, affecting specific signaling pathways and avoiding oxidative stress.

Effects of Selenium Dioxide on Apoptosis, Bcl-2 and P53 Expression, Intracellular Reactive Oxygen Species and Calcium Level in Three Human Lung Cancer Cell Lines

Objective: To evaluate the anti-tumor effects of SeO2 and its mechanisms on three human lung cancer cell lines. Methods: Three lung cancer cells A549, GLC-82 and PG were treated with 3-30 μmol/L SeO2. Flow cytometry was used to detect apoptosis, and analyze the changes of expression of p53 and Bcl-2, as well as ROS and Ca2+ level within cells. Results:SeO2 markedly inhibited cell proliferation and viability, and prompted apoptosis after 48 h treatment. SeO2 at 10 μmol/L induced 47.8% apoptosis in A549 cells, 40.8% in GLC-82 cells, 18.2% in PG cells. SeO2 at 30 μmol/L induced 37.8% apoposis in PG cells,but did not increase apoptotic raes in other two cells. SeO2 could down-regulate the mean fluorescent intensity of Bcl-2 from 65.8 to 9.6 in A549, but not in GLC-82 and in PG cells, up-regulate wild type p53 level in all three cells. SeO2 decreased the ROS and Ca2+ level markedly within three tested cells. Conclusion: SeO2 showed anti-tumor effect via apoptosis pathway in three lung cancer cell lines. The decrease of ROS and Ca2+ level within cells as well as regulation of Bcl-2 and p53 expression may play important roles in above apoptotic procedure.

Reactive oxygen species mediates a metabolic memory of high glucose stress signaling in bovine retinal pericytes

AIM: To investigate the role of reactive oxygen species (ROS) and antioxidant mechanism underlying the metabolic memory of bovine retinal pericytes (BRPs) induced by high glucose.METHODS: Effects of high glucose levels and culture time on BRPs viability were evaluated by CCK-8. BRPs were grown in high-glucose media (30 mmol/L) for 4d followed by culture in normal glucose condition (5.6 mmol/L) for 4d in an experimental group. In contrast, in negative and positive control groups, BRPs were grown in either normal-glucose media or high-glucose media for 8d, respectively. The ROS levels, apoptosis, the expression and activity of manganese superoxide dismutase (MnSOD) in BRPs, as well as the protective effect of adeno-associated viral (AAV)-mediated over expression of MnSOD were determined separately by DCHFA, ELISA and Western blot.RESULTS: Comparing the result of cells apoptosis, activity and protein expression of MnSOD and caspase-3, the cell culture system that exposed in sequence in 30 mmol/L and normal glucose for 4d was demonstrated as a suitable model of metabolic memory. Furthermore, delivery of antioxidant gene MnSOD can decrease BRPs apoptosis, reduce activated caspase-3, and reverse hyperglycemic memory by reducing the ROS of mitochondria.CONCLUSION: Increased ROS levels and decreased MnSOD levels may play important roles in pericyte loss of diabetic retinopathy. BRPs cultured in high glucose for 4d followed by normal glucose for 4d could be an appropriate model of metabolic memory. rAAV-MnSOD gene therapy provides a promising strategy to inhibit this blinding disease.

Dichloroacetic Acid (DCA)-Induced Cytotoxicity in Human Breast Cancer Cells Accompanies Changes in Mitochondrial Membrane Permeability and Production of Reactive Oxygen Species

Cancer cells utilize cytosolic glycolysis for their energy production even in the presence of adequate levels of oxygen (Warbug effect) due to mitochondrial defects. Dichloroacetic acid (DCA) shifts cytosolic glucose metabolism to aerobic oxidation by inhibiting mitochondrial pyruvate dehydrogenase kinase (PDK) and increasing pyruvate uptake. Therefore, DCA has potential in reversing the glycolytic metabolism defect in cancerous cells. DCA is also known to induce apoptosis in a number of cancer cell lines, the mechanism of which is not well understood. In this study, an attempt has been made to investigate the effects of DCA on aggressive human breast cancer (MCF-7) cells as compared with less aggressive mouse osteoblastic (MC3T3) cells. Cell cytotoxicity was determined by MTT, crystal violet and Trypan blue exclusion assays. Western blot was used to detect any changes in the expression of apoptotic markers. Flow cytometry was used to measure apoptotic and necrotic effects of DCA. Mitochondrial integrity was determined by change in mitochondrial membrane potential (Δψm), whereas oxidative damage was determined by production of reactive oxygen species (ROS). DCA caused a concentration-dependent cytotoxicity both in MCF-7 and MC3T3 cell lines. MCF-7 cells were most affected. Flow cytometry results showed a significantly higher apoptosis in MCF-7 even at lower concentrations of DCA. However, higher concentrations of DCA were necrotic. Western blotting showed an increased expression of Mn-SOD-1 upon DCA treatment. Further, DCA decreased Δψm and increased ROS production. The effects of DCA were more pronounced on MCF-7 cells as compared to MC3T3 cells. Our results suggest that DCA-induced cytotoxicity in cancerous cells is mediated via changes in Δψm and production of ROS.

The cell cycle related apoptotic susceptibility to arsenic trioxide is associated with the level of reactive oxygen species

Double staining flow cytometry was performed using 7-amino actinomycin D and 6-carboxy-2',7'-dichlorodihydrofluorescein diacetate,to detect the level fluctuation of reactive oxygen species (ROS) during the cell cycle of normal NB4 cells. Our results showed that NB4 cells possessed higher level of ROS in G2/M phase than in G1 and S phases. Double staining flow cytometry,with TdT mediated dUTP nick end labeling (Tunel) and propidium iodide (PI),indicated that As2O3 (2 μM) could induce apoptosis in NB4 cells prevailingly from G2/M phase,and this efficacy was enhanced upon co-administration of 2,3-dimethoxy-1,4-naphthoquinone (DMNQ) (2.5 μM) which could produce the endogenous ROS. These results suggested that different ROS level in different cell cycle phases of NB4 cells might determin the selective induction of G2/M apoptosis and the cells' susceptibility to apoptosis by As2O3.

Disinfection Kinetics and Contribution of Reactive Oxygen Species When Eliminating Bacteria with TiO_(2) Induced Photocatalysis

Titania (TiO2) induced photocatalysis has been widely investigated and applied as a disinfection strategy in many industrial and clinical applications. Reactive oxygen species (ROS), including hydroxyl radicals (&8226OH), superoxide radicals () and hydrogen peroxide (H2O2), generated in the photocatalytic reaction process are considered to be the active components prompting the bactericidal effect. In the present work, the kinetics of photocatalytic inactivation of Staphylococcus epidermidis and specific contributions of &#8226OH, and H2O2 to the bactericidal process were studied using two disinfection settings sutilizing photocatalytic resin-TiO2 nanocomposite surfaces and suspended TiO2 nanoparticles, respectively. In antibacterial tests against S. epidermidis with a layer of bacterial suspension on the resin-TiO2 surfaces, H2O2 was found to be the most efficient ROS component contributing to the antibacterial effect. Disinfection kinetics showed a two-step behavior with an initial region having a lower disinfection rate followed by a higher rate region after 10 min of UV irradiation. By contrast, in antibacterial tests with suspended bacteria and photocatalytic TiO2 nanoparticles, &#8226OH and H2O2 showed equal significance in the bacterial inactivation having a typical Chick-Watson disinfection kinetics behavior with a steady disinfection rate. The results contribute to the understanding of the bactericidal mechanism and kinetics of photocatalytic disinfection that are essential for designing specific antibacterial applications of photocatalytic materials.

Cell metabolism pathways involved in the pathophysiological changes of diabetic peripheral neuropathy

Diabetic peripheral neuropathy is a common complication of diabetes mellitus.Elucidating the pathophysiological metabolic mechanism impels the generation of ideal therapies.However,existing limited treatments for diabetic peripheral neuropathy expose the urgent need for cell metabolism research.Given the lack of comprehensive understanding of energy metabolism changes and related signaling pathways in diabetic peripheral neuropathy,it is essential to explore energy changes and metabolic changes in diabetic peripheral neuropathy to develop suitable treatment methods.This review summarizes the pathophysiological mechanism of diabetic peripheral neuropathy from the perspective of cellular metabolism and the specific interventions for different metabolic pathways to develop effective treatment methods.Various metabolic mechanisms(e.g.,polyol,hexosamine,protein kinase C pathway)are associated with diabetic peripheral neuropathy,and researchers are looking for more effective treatments through these pathways.

ROS Balance Autoregulating Core-Shell CeO_(2)@ZIF-8/Au Nanoplatform for Wound Repair

Reactive oxygen species(ROS)plays important roles in living organisms.While ROS is a double-edged sword,which can eliminate drug-resistant bacteria,but excessive levels can cause oxidative damage to cells.A core–shell nanozyme,Ce O_(2)@ZIF-8/Au,has been crafted,spontaneously activating both ROS generating and scavenging functions,achieving the multifaceted functions of eliminating bacteria,reducing inflammation,and promoting wound healing.The Au Nanoparticles(NPs)on the shell exhibit high-efficiency peroxidase-like activity,producing ROS to kill bacteria.Meanwhile,the encapsulation of Ce O_(2) core within ZIF-8 provides a seal for temporarily limiting the superoxide dismutase and catalase-like activities of Ce O_(2) nanoparticles.Subsequently,as the ZIF-8 structure decomposes in the acidic microenvironment,the Ce O_(2) core is gradually released,exerting its ROS scavenging activity to eliminate excess ROS produced by the Au NPs.These two functions automatically and continuously regulate the balance of ROS levels,ultimately achieving the function of killing bacteria,reducing inflammation,and promoting wound healing.Such innovative ROS spontaneous regulators hold immense potential for revolutionizing the field of antibacterial agents and therapies.

亚硒酸钠通过增加ROS抑制PI3K/AKT通路改善肺癌PC-9/GR细胞对吉非替尼的耐药性

目的:探讨亚硒酸钠对肺癌耐药细胞PC-9/GR增殖、凋亡的影响,研究其是否能改善吉非替尼耐药及可能机制。方法:不同浓度(0、5、10、20、40μmol/L)亚硒酸钠处理细胞24、36、48 h后,CCK-8法检测亚硒酸钠对细胞增殖的影响并选择合适浓度用于后续实验。不同浓度(0、2.5、5、10、20、40μmol/L)吉非替尼单药及联合亚硒酸钠(6μmol/L)处理细胞48 h,分别计算半数抑制浓度(IC50),得出亚硒酸钠对PC-9/GR逆转倍数;流式细胞术检测各组细胞凋亡;DCFH-DA法检测细胞内ROS水平;Western blot实验检测各组细胞中p-PI3K、p-AKT、Bax、Bcl-2表达水平。结果:随亚硒酸钠浓度升高及作用时间延长,细胞增殖抑制率逐渐升高(P<0.05);单药吉非替尼组的IC50值为16.051μmol/L,联合亚硒酸钠后IC50值为5.406μmol/L,表明亚硒酸钠能够逆转吉非替尼的耐药,其逆转耐药倍数为2.969倍。与吉非替尼和亚硒酸钠单药组相比,联合治疗组的细胞凋亡率显著升高,ROS水平及Bax蛋白表达上调,p-PI3K、p-AKT、Bcl-2表达下调,经N-乙酰半胱氨酸(NAC)消除ROS后抵消了亚硒酸钠对PI3K/AKT通路的抑制作用(P<0.05)。结论:亚硒酸钠联合吉非替尼能提高肺腺癌耐药细胞的敏感性,抑制细胞的增殖,同时诱导细胞凋亡,这一过程可能通过ROS依赖性下调PI3K/AKT通路的表达实现。

High Fe‑Loading Single‑Atom Catalyst Boosts ROS Production by Density Effect for Efficient Antibacterial Therapy

The current single-atom catalysts(SACs)for medicine still suffer from the limited active site density.Here,we develop a synthetic method capable of increasing both the metal loading and mass-specific activity of SACs by exchanging zinc with iron.The constructed iron SACs(h^(3)-FNC)with a high metal loading of 6.27 wt%and an optimized adjacent Fe distance of~4 A exhibit excellent oxidase-like catalytic performance without significant activity decay after being stored for six months and promising antibacterial effects.Attractively,a“density effect”has been found at a high-enough metal doping amount,at which individual active sites become close enough to interact with each other and alter the electronic structure,resulting in significantly boosted intrinsic activity of single-atomic iron sites in h^(3)-FNCs by 2.3 times compared to low-and medium-loading SACs.Consequently,the overall catalytic activity of h^(3)-FNC is highly improved,with mass activity and metal mass-specific activity that are,respectively,66 and 315 times higher than those of commercial Pt/C.In addition,h^(3)-FNCs demonstrate efficiently enhanced capability in catalyzing oxygen reduction into superoxide anion(O_(2)·^(−))and glutathione(GSH)depletion.Both in vitro and in vivo assays demonstrate the superior antibacterial efficacy of h^(3)-FNCs in promoting wound healing.This work presents an intriguing activity-enhancement effect in catalysts and exhibits impressive therapeutic efficacy in combating bacterial infections.

Effect of Lanthanum (Ⅲ) on Reactive Oxygen Metabolism of Soybean Seedlings under Supplemental UV-B Irradiation

The effect of lanthanum （Ⅲ） on reactive oxygen metabolism of soybean seedlings under elevated ultraviolet-B radiation（UV-B：280~320 nm）at 0.15 and 0.45 W·cm-2 levels respectively was studied through hydroponics in the laboratory.Plasmolemma permeability and contents of malonadialdehyde（MDA）,hydrogen peroxide（H2O2）,and proline gradually increased during the imposition of UV-B radiation and subsequently decreased during recovery from UV-B stress.The dynamic tendency of catalase（CAT）activity was similar to that of the above four indices.The activity of peroxidase（POD）initially increased,then remained at a high level,and finally dropped steeply when soybean seedlings were exposed to a low dosage of UV-B radiation.However,POD activity rose throughout and declined slightly on the eleventh day when soybean seedlings were stressed by a high dosage.With the addition of La （Ⅲ） of 20 mg·L-1,the rising tendency of plasmolemma permeability and contents of MDA,H2O2,and proline were slowed down during the stress period,whereas the declining speed was accelerated during the recovery period.The activities of CAT and POD were higher than those without La （Ⅲ） in all experiments.It suggested that the regulative effect of La （Ⅲ） on antioxidant enzymes such as CAT and POD could strengthen their capacities to scavenge reactive oxygen species（ROS）,decrease contents of MDA and proline,and maintain normal plasmolemma permeability.Further more,the protective potential of La （Ⅲ） was better under low UV-B radiation than under a high one.

Effect of Foliar GA_(3) and ABA Applications on Reactive Oxygen Metabolism in Black Currants (Ribes nigrum L.) During Bud Para-dormancy and Secondary Bud Burst

The secondary bud burst can cause around 10%-20%yield losses in black currants,an economically important crop in parts of Europe,Asia and North America.The metabolism of reactive oxygen species(ROS)has been linked to bud dormancy and its early release(secondary bud burst)in several fruit crops.But the relationship between ROS metabolism and the secondary bud burst is still not well understood in black currants.In the present study,two black currant cultivars(Adelinia and Heifeng)with opposing tendency of exhibiting the secondary bud burst were sprayed with abscisic acid(ABA)and gibberellic acid(GA_(3))to either inhibit or induce the secondary bud burst.The results showed that ABA inhibited the secondary bud burst by reducing the contents of ROS(H_(2)O_(2),O_(2)-·)in buds;decreasing the activities of superoxide dismutase(SOD),peroxidase(POD)and catalase(CAT);and increasing the contents of oxidized glutathione(GSSG)and ascorbic acid(AsA).GA_(3) effectively induced the secondary bud burst by increasing ROS contents;increasing the activities of several antioxidant enzymes,such as SOD,POD,CAT,glutathione reductase(GR),ascorbate peroxidase(APX)and the contents of reduced glutathione(GSH);and decreasing the contents of AsA.The experimental results showed that GA_(3) treatment increased the content of ROS,accelerated the metabolism of reactive oxygen species,and promoted the second burst of black currants.However,ROS metabolism was at a low level under ABA treatment,and the buds remained dormant.These results suggested that ROS metabolism might play an important role in the two black currants of the secondary bud burst.

橙皮苷抑制ROS/NLRP3通路改善小鼠急性支气管炎的作用机制研究

目的从活性氧簇(ROS)/NOD样受体家族蛋白3(NLRP3)通路,探讨橙皮苷对急性支气管炎小鼠支气管组织损伤的影响及相关作用机制。方法取C57BL/6小鼠100只,用随机数字表法分为正常对照组、模型组、橙皮苷组(36 mg·kg^(-1),灌胃)、ROS/NLRP3通路激活剂(三甲胺N-氧化物)组、橙皮苷+三甲胺N-氧化物组,每组20只;用香烟暴露法制备模型,末次给药后观察小鼠一般行为,检测肺泡灌洗液中炎症细胞数量及炎症因子白细胞介素1β(IL-1β)、白细胞介素18(IL-18)水平,肺组织中氧化应激产物髓过氧化物酶(MPO)、丙二醛(MDA)水平;氨水引咳法测咳嗽潜伏期及咳嗽次数;取支气管肺组织,HE染色法测组织病理变化;流式细胞仪测ROS含量;免疫组化法测NLRP3阳性表达水平;Western Blot法测IL-1β、IL-18、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、硫氧还蛋白结合蛋白(TXNIP)、凋亡相关斑点样蛋白(ASC)、凋亡前体蛋白(pro-Caspase-1)、半胱天冬酶-1(Caspase-1)水平。结果与正常对照组比,模型组小鼠咳嗽症状加重,支气管肺泡灌洗液中炎症细胞数目及炎症因子水平升高,支气管肺组织炎症反应及氧化应激加重,ROS/NLRP3通路及其相关蛋白表达升高(P<0.05)。橙皮苷可抑制ROS/NLRP3通路及其相关蛋白表达,缓解小鼠咳嗽症状,减轻炎症及氧化应激反应(P<0.05)。ROS/NLRP3通路激活剂-三甲胺N-氧化物可逆转橙皮苷上述作用(P<0.05)。结论橙皮苷可能通过抑制ROS/NLRP3通路活化,改善急性支气管炎小鼠支气管肺组织炎症及氧化应激损伤,缓解咳嗽症状。

温阳益髓方对膝骨关节炎模型大鼠膝关节软骨、骨代谢及NOX2/ROS/NF-κB水平的影响

目的:探讨温阳益髓方对膝骨关节炎模型大鼠膝关节软骨、骨代谢及NOX2/ROS/NF-κB水平的影响。方法:选取40只SPF级SD雄性大鼠,随机分为正常组、模型组、低剂量温阳益髓方(低剂量)组、高剂量温阳益髓方(高剂量)组。除正常组外,其余3组均采用膝关节腔注射0.05 mL(20 mg/mL)碘乙酸钠,建立膝骨关节炎模型。建模成功后,低、高剂量组分别以6、24 mg/kg温阳益髓方汤剂灌胃,正常组、模型组以同体积生理盐水灌胃。采用H-E染色、光镜观察各组膝关节软骨组织的形态结构;ELISA法检测血清骨代谢相关指标水平;二氢乙锭荧光探针检测膝关节软骨组织活性氧(ROS)水平;免疫印迹检测膝关节软骨组织NADPH氧化酶2(NOX2)、核因子-κB(NF-κB)水平。结果:模型组膝关节软骨组织边缘的软骨基质减少、软骨囊结构不清、软骨细胞减少,且出现钙化灶。与模型组比较,低、高剂量组上述结构变化明显改善。与正常组比较,模型组Mankin评分显著升高;与模型组比较,低、高剂量组Mankin评分显著降低,且高剂量组低于低剂量组。与正常组比较,模型组血清骨钙素(OCN)、Ⅰ型胶原C末端肽(CTX-Ⅰ)水平显著降低,软骨寡聚基质蛋白(COMP)水平显著升高;与模型组比较,低、高剂量组血清OCN、CTX-Ⅰ水平显著升高,且高剂量组高于低剂量组,COMP水平显著降低,且高剂量组低于低剂量组。与正常组比较,模型组ROS水平显著升高;与模型组比较,低、高剂量组ROS水平显著降低,且高剂量组低于低剂量组。与正常组比较,模型组NOX2、NF-κB水平显著升高;与模型组比较,低、高剂量组NOX2、NF-κB水平显著降低,且高剂量组低于低剂量组。结论:温阳益髓方可改善膝骨关节炎模型大鼠膝关节软骨、骨代谢,其机制可能与其降低膝关节软骨组织NOX2/ROS/NF-κB水平有关。