摘要
目的:研究人参二醇组皂甙(PDS)对大鼠脑缺血-再灌注海马超微结构、皮层和海马一氧化氮合酶(NOS)活性的影响。方法:双侧颈总动脉阻断和再灌注建立脑缺血-再灌流模型,电镜技术和NADPH-d组织化学技术。结果:电镜观察可见,缺血30min再灌注2h大鼠海马超微结构发生缺血性病理改变,PDS对缺血脑组织病理变化有显著保护作用。NADPH-d组织化学实验表明,脑缺血15min和再灌注24h后,皮层及海马NOS阳性细胞数目显著增多,PDS可显著抑制此增多。结论:PDS可通过降低脑内NOS的活性,减少脑缺血-再灌注过程中NO的产生。
AbstractAim: To study the effects of panaxadiol saponins (PDS) on ultrastructures in hippocampus and NOS in hippocampus and cortex of Wistar rats in ischemiareperfusion model. Methods: The cerebral ischemic molde was reproduced by bilateral common carotid arteries occlusion 30 or 15 min and reperfusion 2 or 24 h. Ultrastructures were observed by electromicroscope and NOS was detected by NADPHdiaphorase histochemistry technique. Results: PDS inhibited the morphological changes of hippocampus induced by ischemiareperfusion. The numbers of NOSpositive cells in cortex and hippocampus increased significantly in ischemiareperfusion rats, and PDS inhibited them. Conclusion: PDS protected ultrastructures morphological changes of cerebral from brain ischemiareperfusion injury by inhibited the increase of NOSpositive cells and decreased the NO content during cerebral ischemiareperfusion. KEY WORDS ischemiareperfusion; ultrastructures; NOS; ginseng; saponins; rat
出处
《中国应用生理学杂志》
CAS
CSCD
1998年第3期205-207,共3页
Chinese Journal of Applied Physiology