摘要
兴奋性氨基酸受体拮抗剂对大鼠缺血海马磷脂酰肌醇代谢的影响卢步峰,鲁友明,黄森(镇江医学院生物化学研究室,镇江212001;海军神经生物学研究中心分子药理学研究室,南京210049)代谢型兴奋性氨基酸受体偶联的第二信使肌醇1,4,5一三磷酸(inosi...
An increment of phosphatidyl- inositol(PI) hydrolysis was observed as directly studied inhippocampus of the adult Sprague-Dawley ratreceiving 10 min of cerebral ischemia. 2-Amino-3phosphonopropionic acid (16.9 ng, by intrahippo-campalinjection 5 min before isehemia) or daurisoline (1 mg· kg-1 ip 20 min before ischemia) markedlydecreased the activation of PI tumover (P<0.01).Ketamine(100 mg · kg-1, ip) and mmodipine (0.5 mg·kg-1, ip) only brought about a slight reduction in theischemia-induced PI hydrolysis. These results suggest thatthe activation of PI turnover in this isehemic model is ametabotropic excitatory anuno acid naptor-mediated re-sponse, which supports the idea that glutamaterelease indutal by cerebral isehenua plays a role inneurotoxiclty.
出处
《中国药理学与毒理学杂志》
CSCD
北大核心
1994年第2期155-156,共2页
Chinese Journal of Pharmacology and Toxicology
基金
江苏省自然科学基金
关键词
氨基酸受体
海马
缺血
磷脂酰肌醇
hippocainpiis
phosphatidylineeitols
calcium channel blockers
raxptoro
glutamate