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Preinduction of HSP70 promotes hypoxic tolerance and facilitates acclimatization to acute hypobaric hypoxia in mouse brain

机译:HSP70的预诱导促进缺氧耐受性并促进小鼠脑中急性低压缺氧的适应

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It has been shown that induction of HSP70 by administration of geranylgeranylacetone (GGA) leads to protection against ischemia/reperfusion injury. The present study was performed to determine the effect of GGA on the survival of mice and on brain damage under acute hypobaric hypoxia. The data showed that the mice injected with GGA survived significantly longer than control animals (survival time of 9.55?±?3.12?min, n?=?16 vs. controls at 4.28?±?4.29?min, n?=?15, P?
机译:已经显示,通过施用香叶基香叶基丙酮(GGA)诱导HSP70导致针对缺血/再灌注损伤的保护。进行本研究以确定在急性低压缺氧下GGA对小鼠存活和脑损伤的影响。数据显示,注射GGA的小鼠存活时间明显长于对照动物(存活时间为9.55±3.12min,n = 16,而对照组为4.28±4.29min,n = 15, P≤0.005)。因此,通过预先注射GGA可以减轻亚致死性缺氧持续6?h引起的海马的细胞坏死或变性,尤其是在海马的CA2和CA3区。此外,暴露于致死性缺氧6h后,海马和皮层的一氧化氮合酶(NOS)活性增加,但可能被GGA的预注射所抑制。此外,在GGA注射后1小时,HSP70的表达显着增加。这些结果表明,GGA的使用可以提高存活率并防止对大脑的急性缺氧损伤,其潜在机制涉及HSP70的诱导和NOS活性的抑制。

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