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机构地区:[1]首都医科大学神经生物学系
出 处:《首都医科大学学报》2007年第3期337-340,共4页Journal of Capital Medical University
基 金:国家自然科学基金(39670271);北京市自然科学基金(7962009)资助项目~~
摘 要:目的检测氯化钴预处理后小鼠海马组织缺氧诱导因子-1α(HIF-1α)在急性重复氧过程中的变化及其可能的机制。方法用数字表法将Balb/C小鼠随机分为氯化钴实验组和生理盐水对照组,2组动物分别在实验前3 h注射氯化钴和生理盐水,进行0次(H0)、1次(H1)、4次(H4)缺氧暴露,随即分别取海马组织,用Western blot及EMSA法检测HIF-1α蛋白质含量及HIF-1 DNA结合活性。结果生理盐水预处理后,小鼠的缺氧耐受时间逐次显著递增;氯化钴预处理后缺氧耐受时间恒定增高。氯化钴预处理H0、H1、H4组海马组织的HIF-1α蛋白质含量差异未见统计学意义,但HIF-1 DNA结合活性在H1组升高、H4组降低。生理盐水预处理组海马组织的蛋白质含量及HIF-1 DNA结合活性在H0、H1、H4组均依次增加。结论氯化钴预处理能显著增强小鼠对缺氧的耐受能力、激活海马组织中的HIF-1,但其分子机制可能与急性重复缺氧暴露增强缺氧耐受力的机制不同。Objective To investigate the effect of CoCl2 pretreatment on expression of HIF-1α in the hippocampus of hypoxic preconditioned mice. Methods Balb/c mice were randomly divided into group of CoCl2 and normal saline (NS) , respectively injected with CoCl2 and NS 3 h before exposure to hypoxia for 0 run(H0) , 1 run( H1 ) and 4 runs(H4). The tissue of hippocampus was removed immediately after the exposure. Technique of Western blot and electrophoretic mobility shift assay(EMSA) were used to measure the HIF-1α protein level and HIF-1α DNA binding activity, respectively. Results The hypoxic tolerance time in group NS was significantly increased run by run but unchanged in group CoCl2. In group CoCl2 , the level of HIF-1α protein was unchanged whereas HIF-1α DNA binding activity was increased in H1 and decreased in H4. In group NS, both HIF-1α protein and DNA binding activity were increased. Conclusion Hypoxic-tolerance of mice to hypoxia and HIF-1α in their hippocampus are, respectively, increased and activated by CoCl2 while its underlying molecular mechanisms are thought to be different from those induced by acute repetitive hypoxic exposure.
分 类 号:R338.26[医药卫生—人体生理学]
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