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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Proteomic analysis of CA1 and CA3 regions of rat hippocampus and differential susceptibility to intermittent hypoxia.
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Proteomic analysis of CA1 and CA3 regions of rat hippocampus and differential susceptibility to intermittent hypoxia.

机译:大鼠海马CA1和CA3区的蛋白质组学分析和间断性缺氧的易感性。

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摘要

The CA1 and CA3 regions of the hippocampus markedly differ in their susceptibility to hypoxia in general, and more particularly to the intermittent hypoxia that characterizes sleep apnea. Proteomic approaches were used to identify proteins differentially expressed in the CA1 and CA3 regions of the rat hippocampus and to assess changes in protein expression following a 6-h exposure to intermittent hypoxia (IH). Ninety-nine proteins were identified, and 15 were differentially expressed in the CA1 and the CA3 regions. Following IH, 32 proteins in the CA1 region and only 7 proteins in the more resistant CA3 area were up-regulated. Hypoxia-regulated proteins in the CA1 region included structural proteins, proteins related to apoptosis, primarily chaperone proteins, and proteins involved in cellular metabolic pathways. We conclude that IH-mediated CA1 injury results from complex interactions between pathways involving increased metabolism, induction of stress-induced proteins and apoptosis, and, ultimately, disruption of structural proteins and cell integrity. These findings provide initial insights into mechanisms underlying differences in susceptibility to hypoxia in neural tissue, and may allow for future delineation of interventional strategies aiming to enhance neuronal adaptation to IH.
机译:通常,海马的CA1和CA3区域对缺氧的敏感性明显不同,更具体地说,对表现为睡眠呼吸暂停的间歇性缺氧的敏感性不同。蛋白质组学方法用于鉴定大鼠海马CA1和CA3区差异表达的蛋白质,并评估在间歇性缺氧(IH)暴露6小时后蛋白质表达的变化。鉴定出九十九个蛋白,并且在CA1和CA3区域中差异表达了15个蛋白。 IH之后,CA1区的32种蛋白质和耐药性更高的CA3区的7种蛋白质被上调。 CA1区中的缺氧调节蛋白包括结构蛋白,与细胞凋亡相关的蛋白(主要是伴侣蛋白)和参与细胞代谢途径的蛋白。我们得出的结论是,IH介导的CA1损伤是由涉及新陈代谢增加,应激诱导的蛋白质诱导和细胞凋亡以及最终破坏结构蛋白和细胞完整性的途径之间的复杂相互作用导致的。这些发现提供了对神经组织对缺氧的敏感性差异的潜在机制的初步见解,并可能为将来旨在增强神经元对IH的适应性的干预策略划清界限。

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