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活血养血汤对兔脊髓缺血再灌注损伤Bcl-2和Bax表达的影响

Observation of factor Bcl-2、Bax during rabbit spinal ischemia-reperfusion injury via HuoXue YangXue Decoction.

中文摘要英文摘要

目的:通过研究活血养血汤对兔脊髓缺血再灌注损伤脊髓组织Bcl-2和Bax表达的影响,探讨其作用机制。方法:新西兰大白兔随机分成手术假手术组、手术组和活血养血汤组,每组30只,术前1周分别灌服0.9%氯化钠溶液和活血养血汤,假手术组只分离出腰动脉,其余二组制作脊髓缺血再灌注损伤模型,三组分别于缺血再灌注后0.5、1、4、8、12h检测Bcl-2和Bax的表达。结果:(1)假手术组Bcl-2、Bax均呈轻度表达;(2)手术组和活血养血汤组Bcl-2、Bax在0.5h即开始增高,随再灌注的时间延长表达量逐渐升高;(3)活血养血汤组各时间点Bcl-2的表达与手术组各组相应时间点对比显著升高,差异显著(P<0.05或P<0.01);活血养血汤组各时间点Bax的表达与手术组各组相应时间点对比显著降低,差异显著(P<0.05或P<0.01)。结论:活血养血汤可以升高脊髓缺血再灌注损伤中脊髓组织Bcl-2的表达,降低Bax的表达,从而抑制细胞凋亡,减轻脊髓损伤。

Objective: To detect the expression of B cell lymphoma/lewkmia-2(Bcl-2)、Bcl-2 associated X protein(Bax) during Spinal Cord Ischemia-reperfusion injury via HuoXue YangXue Decoction in order for its involved mechanism. Methods: Ninety New Zealand rabbits were randomly divided into there groups: sham-operated, operated and HuoXue YangXue Decoction groups (n=30). They were given either saline、saline and HuoXue YangXue Decoction one week before opereation,Lumbar arter were seperated only in the sham operation group,Othere there groups were performed into models of spinal cord ischemia-referfusion injury. The expression of Bcl-2、Bax were observed at hour 0.5h, 1h, 4h, 8h, 12h following perfusion. Results: (1)In sham operation group the expression of Bcl-2、Bax,were lowest;(2)Compared with sham operation group, the expression of Bcl-2、Bax in the other two group were obviously increased at different time (P<0.05 or P<0.01) (3) Compared with model group, the expression of Bcl-2 in Huoxue Tongdu Decoction group were significantly increase (P<0.05 or P<0.01);Compared with model group, the expression of Bax in Huoxue Tongdu Decoction group were significantly reduce (P<0.05 or P<0.01).

刘宇、张俐

中医学基础医学神经病学、精神病学

活血养血汤脊髓缺血再灌注损伤Bcl-2Bax

HuoXue YangXue DecoctionSpinal ischemia-reperfusion injuryB cell lymphoma/lewkmia-2Bcl-2 associated X protein

刘宇,张俐.活血养血汤对兔脊髓缺血再灌注损伤Bcl-2和Bax表达的影响[EB/OL].(2014-08-04)[2025-08-02].http://www.paper.edu.cn/releasepaper/content/201408-11.点此复制

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