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17β-雌二醇通过上调 ERα 和抑制 caspase-3 活化减轻创伤性脑损伤后皮质旁区程序性细胞死亡。

17beta-estradiol attenuates programmed cell death in cortical pericontusional zone following traumatic brain injury via upregulation of ERalpha and inhibition of caspase-3 activation.

机构信息

Emergency Department, Shengjing Hospital, China Medical University, Shenyang, Liaoning, China.

出版信息

Neurochem Int. 2011 Jan;58(1):126-33. doi: 10.1016/j.neuint.2010.11.006. Epub 2010 Nov 17.

Abstract

Pericontusional zone (PCZ) of traumatic cerebral contusion is a target of pharmacological intervention. It is well studied that 17beta-estradiol has a protective role in ischemic brain injury, but its role in brain protection of traumatic brain damage deserves further investigation, especially in pericontusional zone. Here we show that 17beta-estradiol enhances the protein expression and mRNA induction of estrogen alpha receptor (ERalpha) and prevents from programmed cell death in cortical pericontusional zone. ERalpha specific antagonist blocks this protective effect of 17beta-estradiol. Caspase-3 activation occurs in cortical pericontusional zone of the oil-treated injured rat brain and its activation is inhibited by 17beta-estradiol treatment. Additionally, ERalpha specific antagonist reverses this inhibition. Pan-caspase inhibitor also protect cortical pericontusional zone from programmed cell death. Our present study indicates 17beta-estradiol protects from programmed cell death in cortical pericontusional zone via enhancement of ERalpha and decrease of caspase-3 activation.

摘要

创伤性脑挫裂伤的周边区(PCZ)是药物干预的靶点。已有研究表明,17β-雌二醇在缺血性脑损伤中具有保护作用,但它在创伤性脑损伤的脑保护作用值得进一步研究,特别是在 PCZ 中。在这里,我们发现 17β-雌二醇增强了皮质 PCZ 中雌激素受体 α(ERα)的蛋白表达和 mRNA 诱导,并防止程序性细胞死亡。ERα 特异性拮抗剂阻断了 17β-雌二醇的这种保护作用。在油处理的受伤大鼠脑皮质 PCZ 中发生了半胱天冬酶-3 的激活,并且其激活被 17β-雌二醇处理抑制。此外,ERα 特异性拮抗剂逆转了这种抑制。泛半胱天冬酶抑制剂也可保护皮质 PCZ 免受程序性细胞死亡。我们的研究表明,17β-雌二醇通过增强 ERα 和减少半胱天冬酶-3 的激活来保护皮质 PCZ 免受程序性细胞死亡。

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