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[乳糖苷B对大鼠脑缺血再灌注损伤后大脑皮质bcl-2和bax mRNA及其蛋白表达的影响]

[Effect of lactuside B on the expression of bcl-2 and bax mRNA and their protein in rats' cerebral cortex after cerebral ischemia-reperfusion injury].

作者信息

Li Sheng-ying, Sun Juan, Niu Bing-xuan, Yan Fu-lin, Zhan He-qin

机构信息

School of Pharmacy, Xinxiang Medical University, Xinxiang 453003, China.

出版信息

Yao Xue Xue Bao. 2011 Nov;46(11):1314-20.

Abstract

This study is to investigate the effect of the major chemical composition in rhizome of Pterocypsela elata, lactuside B, on expression of bcl-2, bax mRNA and their protein in rats' cerebral cortex after cerebral ischemia-reperfusion injury. First, middle cerebral artery ischemia-reperfusion injury model was established, and each group was treated with the corresponding medicines. Animals were separately sacrificed at 24 h and 72 h. The brain infarct volumes were detected by TTC dye, bcl-2 and bax mRNA expression was checked by RT-PCR, and the proteins of bcl-2 and bax were explored by two-step immunohistochemistry in cerebral cortex of rats. Lactuside B can reduce brain infarct volume of cerebral cortex of rats, increase the expression of bcl-2 mRNA and decrease that of bax mRNA. Moreover, the ratio of bcl-2 to bax mRNA is higher in 12.5 and 25 mg kg(-1) dose group, respectively, which is significantly different from that of model group (P < 0.05 or P < 0.01). Generally, either 12.5 or 25 mg kg(-1) dose group is better than positive control medicine nimodipine (P < 0.05 or P < 0.01). In addition, the expression of bcl-2 and bax protein is consistent with their gene expression. Infarct volume and the ratio of bcl-2 to bax mRNA expression are significantly different (P < 0.05 or P < 0.01) between 72 h and 24 h group. The results demonstrated that lactuside B could play a good role in resisting cerebral ischemia by upregulating the expression of bcl-2 mRNA and protein and downregulating that of bax mRNA and protein.

摘要

本研究旨在探讨翼柄翅果菊根茎中的主要化学成分——异绿原酸B(lactuside B)对大鼠脑缺血再灌注损伤后大脑皮质中bcl-2、bax mRNA及其蛋白表达的影响。首先,建立大脑中动脉缺血再灌注损伤模型,各实验组给予相应药物处理。分别于24小时和72小时处死动物。采用TTC染色法检测脑梗死体积,运用RT-PCR检测bcl-2和bax mRNA表达,通过两步免疫组化法检测大鼠大脑皮质中bcl-2和bax蛋白。异绿原酸B可减小大鼠大脑皮质的脑梗死体积,增加bcl-2 mRNA表达,降低bax mRNA表达。此外,12.5和25 mg·kg⁻¹剂量组bcl-2与bax mRNA的比值较高,与模型组相比差异有统计学意义(P<0.05或P<0.01)。总体而言,12.5或25 mg·kg⁻¹剂量组均优于阳性对照药物尼莫地平(P<0.05或P<0.01)。另外,bcl-2和bax蛋白的表达与其基因表达一致。72小时组与24小时组的梗死体积以及bcl-2与bax mRNA表达比值差异有统计学意义(P<0.05或P<0.01)。结果表明,异绿原酸B可通过上调bcl-2 mRNA和蛋白表达、下调bax mRNA和蛋白表达,在抗脑缺血中发挥良好作用。

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