摘要
用来自中国五步蛇毒(VenomofAgkistrodonacutus)的新ACEI(AI93)与卡托普利,在麻醉大鼠体内进行抑制AngI和对抗大鼠2K—IC型急性肾性高血压的作用效应比较。结果AI93在体外对ACE的抑制虽较弱(11.0μmol/L),但在体内效应却较强。80μg/kg的AI93和卡托普利在大鼠体内抑制AngI和抗急性肾性高血压已有显著意义。AI93在20~180μg/kg的范围内抑制AngI的量—效对数回归分析呈正比;在相同条件下用同一剂量的卡托普利作比较,它们的作用功能和反应程度却不一致,卡托普利对肾性高血压有更强的效应,且量一效对数回归不呈正比。
A new angiotensin-converting engyme inhibitors(AI93)from the venom of agk-istrodOn acutus and captopril were compared for their efficacy in hypertensive rats caused by in-jecting ang I and 2K- 1C medel.The activity of AI93 was higher in vivo than in vitro.The injec-tions of 80μg/kg of AI93 and captopril could antagonize the hypertension caused by 2.5μg/kgAng I and the hypertension 2K-1C model,P<0.05.With doses with in 20~180μg/ks AI93 hadpositive dose-effect relationship in analytic logarithmic regression,while captoprll did not showsuch relatiOnship.But captopril was more effective against the hypertension in 2K-1C model.
出处
《广西医科大学学报》
CAS
1996年第2期4-7,共4页
Journal of Guangxi Medical University
基金
国家自然科学基金
关键词
高血压
蛇毒
血管紧张素酶
抑制剂
卡托普利
angiotensin coverting~enzyme inhibitor from venom of agkistredon acutus
capto-pril
angiotensin I
acut renal hypertension