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牛体外受精卵的二步法培养体系的研究 总被引:1,自引:0,他引:1
以CR1aa为基础培养液,采用二步法对牛体外受精卵进行体外培养,完善牛体外受精卵的培养体系.实验一:对照组连续7 d均为CR1aa 50 mL/L FBS培养,处理组前3 d为CR1aa 3 mg/mLBSA培养,后4 d换为CR1aa 50 mL/L FBS.处理组的囊胚率显著高于对照组,但卵裂率和囊胚孵化率无显著差异.实验二:对照组连续7 d均为CR1aa 50 mL/L FBS培养,处理组前3 d为CR1aa培养,后4 d换为CR1aa 50 mL/L FBS.处理组的卵裂率显著高于对照组,但囊胚率和囊胚孵化率差异不显著.实验三:对照组连续7 d均为CR1aa 50 mL/L FBS 0.1mmol/L GSH培养,处理组前3 d为CR1aa 0.1 mmol/L GSH培养,后4 d换为CR1aa 50 mL/L FBS 0.1 mmol/L GSH.处理组的卵裂率显著高于对照组,囊胚率极显著高于对照组,但囊胚孵化率差异不显著.结果表明,GSH与二步法培养系统结合相对于传统的一步法培养系统更适于牛体外受精卵的体外培养. 相似文献
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饮用天然高钼水诱发的钼中毒耕牛主要生物酶测定 总被引:7,自引:0,他引:7
本研究对高钼饮水诱导钼中毒的耕牛及对照牛的血浆及组织(肝脏、肺脏、肾脏、脾脏、心脏、肌肉)中超氧化物歧化酶(SOD)、黄嘌呤氧化酶(XOD)及谷胱甘肽过氧化物酶(GSH-PX)等3种生物酶活性进行了对比分析测定。结果表明,血浆和组织中SOD、XOD及GSH-PX均随着钼中毒的加重其活性显著下降。这3种生物酶是钼中毒比较灵敏且相关较大的生化指标,对钼中毒具有一定诊断价值;测定SOD。XOD、GSH-PX可作为钼中毒监测的重要手段。 相似文献
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为观察马尾藻多糖(SP)对鸡脾脏淋巴细胞内氧化还原状态的影响,无菌分离鸡脾脏淋巴细胞,采用终浓度为12.5、25、50、100、200μg/mL的马尾藻多糖分别刺激培养鸡脾脏淋巴细胞4、8、12、24h,测定细胞内还原型谷胱甘肽(GSH)和氧化型谷胱甘肽(GSSG)水平。结果表明,各浓度SP与鸡脾脏淋巴细胞共同培养4、8、12h均能不同程度地升高细胞内GSH水平,降低鸡脾脏淋巴细胞内GSSG水平,升高鸡脾脏淋巴细胞内GSH/GSSG比值,与空白对照组相比差异显著或极显著(P0.05或P0.01)。说明SP可以通过调节鸡脾脏淋巴细胞内GSH和GSSG的水平来调节细胞内的氧化还原状态,从而发挥其抗氧化作用。 相似文献
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采用模拟咪唑乙烟酸土壤残留,以油菜盆栽试验研究萘二甲酐对咪唑乙烟酸土壤残留的解毒效果和解毒机理。结果表明,咪唑乙烟酸25g ai/hm2用量下对油菜有较重药害,可使油菜苗的株高、鲜重等生长指标和谷胱甘肽(GSH)含量、谷胱甘肽-S-转移酶(GST)活力、氨基酸含量等生理指标明显降低。用种子重量0.5%萘二甲酐(NA)湿润拌种处理油菜种子能减轻咪唑乙烟酸对油菜苗的药害。萘二甲酐+咪唑乙烟酸处理的油菜苗株高和鲜重明显高于咪唑乙烟酸处理。萘二甲酐和咪唑乙烟酸都能导致油菜苗的氨基酸含量发生变化,并对GSH含量和GST活力有不同程度的影响。与咪唑乙烟酸25g ai/hm2处理相比,萘二甲酐加入咪唑乙烟酸后,使16种氨基酸含量升高,只有脯氨酸含量降低,氨基酸总量升高;GSH含量略有增加,但GST活力有显著提高。可以认为提高油菜苗氨基酸含量和GST的活力是萘二甲酐对咪唑乙烟酸解毒的重要途径。 相似文献
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The beneficial effect of compost, the final product of aerobic biodegradation of organic matter, on growth, lipid peroxidation [as malondialdehyde (MDA], hydrogen peroxide (H2O2) and superoxide anion (O2•−), activities of superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX) and glutathione reductase (GR), as well as reduced ascorbate (ASC) and glutathione (GSH) and their oxidized forms was investigated in squash (Cucurbita pepo L. cv. Eskandarany) plants exposed to normal and low temperature (LT) conditions. LT stress of 8 °C significantly reduced the plant growth of untreated plants, but compost alleviated the adverse effect of stress and significantly increased the fresh and dry weights under normal and stress conditions. LT also induced accumulation of H2O2 and O2•− and resulted in increased lipid peroxidation, pointing out to cellular oxidative stress. Under compost application, such reactive oxygen species (ROS) and peroxidized lipids were markedly reduced, but SOD, CAT, APX and GR activities, key enzymes of ROS-scavenging systems, were significantly increased. Data also indicated that there were general reductions in total ascorbate and glutathione pool in LT control plants, but compost-treated ones considerably have maintained higher levels of such redox metabolites. Significantly higher ratios of ASC/DHA (dehydroascorbate) and GSH/GSSG (glutathione disulfide) were generally found in compost-treated plants than in untreated-ones. It is evident that compost induced enhancement of LT tolerance was related to up-regulation of enzymatic and non-enzymatic antioxidant systems. Such enhancement would eventually protect plant cells from LT-induced oxidative stress reactions via scavenging ROS. 相似文献
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Jalal Pourahmad Mir-Jamal HosseiniSoudeh Bakan Mahmoud Ghazi-Khansari 《Pesticide biochemistry and physiology》2011,99(1):105-110
Paraquat is a highly toxic herbicide that is used in most countries without restriction. The cytotoxic action of paraquat is mediated by reactive radicals that are products of its metabolic reduction in cells. It has already been hypothesized that some angiotensin-converting enzyme inhibitors (e.g., captopril and enalapril) could show antioxidant and radical scavenging activity through their structural thiol groups, increasing antioxidant enzymes production or nitric oxide synthesis. In this study the hepatoprotective effect of captopril and enalapril against paraquat induced oxidative stress cytotoxicity was evaluated in isolated rat hepatocyte. Subtoxic concentrations of captopril (0.2 mM) and enalapril (0.2 mM) significantly (p < 0.05) protected the hepatocytes against paraquat (2 mM) induced oxidative stress cytotoxicity markers including: cell lysis, reactive oxygen species (ROS) generation, lipid peroxidation, glutathione depletion, mitochondrial membrane potential decrease, lysosomal membrane oxidative damage and cellular proteolysis. Moreover, we showed that non-thiol enalapril acts as well as thiol containing captopril at inhibiting oxidative stress cytotoxicity markers. Finally, our results support the hypothesis that it is the increase in nitric oxide synthesis and not the presence of the thiol group that accounts for the antioxidant activity of ACE inhibitors. 相似文献
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