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亚致死性缺血及3-硝基丙酸化学预处理对沙鼠海马蛋白质表达的差异影响。

Differential effects of sublethal ischemia and chemical preconditioning with 3-nitropropionic acid on protein expression in gerbil hippocampus.

作者信息

Kato Kengo, Shimazaki Kuniko, Kamiya Tatsushi, Amemiya Shimon, Inaba Toshiki, Oguro Keiji, Katayama Yasuo

机构信息

The Second Department of Internal Medicine, Nippon Medical School, 1-1-5 Bunkyo-ku, Sendagi, Tokyo, 113-8603, Japan.

出版信息

Life Sci. 2005 Oct 21;77(23):2867-78. doi: 10.1016/j.lfs.2005.01.037. Epub 2005 Jun 14.

Abstract

Pretreatment with a low dose of 3-nitropropionic acid (3-NPA) has been shown to induce ischemic tolerance in the gerbil hippocampus. It is well known that sublethal (2-min) ischemia also induces ischemic tolerance. To investigate the acquisition of ischemic tolerance with 3-NPA, we examined the protein expression after 3-NPA treatment in comparison with sublethal ischemia. Immunohistochemical studies revealed intense expression of Bcl-2 and Bcl-xL in the hippocampal CA1 area after 3-NPA treatment. Furthermore, the time course of the expression of Bcl-xL showed a similar pattern to the acquisition of ischemic tolerance by 3-NPA treatment. The induction of Bcl-xL occurred in the hippocampal CA1 area at 24 h after 3-NPA treatment, and significant induction was observed at 48 h. Western blot analysis of hippocampus harvested 48 h after the pretreatment, showed that the expression of Bcl-2 and Bcl-xL was significantly increased by either 3-NPA treatment or 2-min ischemia. However, PMCA1 and HSP70 protein expression increased only in the sublethal ischemia treated group. The difference between 3-NPA treated group and control group was not statistically significant. These results suggest that Bcl-2 and Bcl-xL are essential for acquisition of ischemic tolerance, while HSP70 and PMCA1 play important roles in the enhancement of ischemic tolerance.

摘要

低剂量3-硝基丙酸(3-NPA)预处理已被证明可诱导沙鼠海马体产生缺血耐受。众所周知,亚致死性(2分钟)缺血也可诱导缺血耐受。为了研究3-NPA诱导缺血耐受的机制,我们将3-NPA处理后的蛋白表达与亚致死性缺血进行了比较。免疫组织化学研究显示,3-NPA处理后海马CA1区Bcl-2和Bcl-xL表达增强。此外,Bcl-xL表达的时间进程与3-NPA处理诱导缺血耐受的模式相似。Bcl-xL的诱导在3-NPA处理后24小时出现在海马CA1区,48小时观察到显著诱导。对预处理48小时后采集的海马进行蛋白质印迹分析表明,3-NPA处理或2分钟缺血均可显著增加Bcl-2和Bcl-xL的表达。然而,PMCA1和HSP7蛋白表达仅在亚致死性缺血处理组中增加。3-NPA处理组与对照组之间的差异无统计学意义。这些结果表明,Bcl-2和Bcl-xL对缺血耐受的获得至关重要,而HSP70和PMCA1在增强缺血耐受中起重要作用。

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