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机构地区:[1]暨南大学医学院药理学教研室
出 处:《暨南大学学报(自然科学与医学版)》1995年第4期22-25,共4页Journal of Jinan University(Natural Science & Medicine Edition)
基 金:国务院侨办基金;广东省科委自然科学基金资助项目
摘 要:20%的乌拉坦麻醉的大鼠静脉注射OL-W(红丝线草醇提水转溶物)分别为LD50的1/90,1/50、1/30和1/10后,平均血压分别下降15.1%±4.1%、19.7%±3.8%、26.8%±7.1%和67.1%±6.6%,清醒SD大鼠给予OL-W0.8g(生药)7/kg灌胃后,降压幅度为1.2±0.6kPa,与给药前相比,P<0.01.在降压机理研究中,OL-W脑室给药不引起血压下降,表明OL-W的降压部位不在中抠;普萘洛尔、苯海拉明、西米替丁、卡托普利等对其降压作用无明显影响;阿托品可显著减弱其降压作用(P<0.01),提示OL-W的降压作用机制可能与M一受体有关;此外,在整体麻醉开胸猫实验所见,TPvR显著降低,提示其降压机制与直接扩张血管等因素有关。The antihypertensive mechanism of alcoholic extract of water solube HSX(OL-W) werestudied in rats. Four dosage(1/90 of LD50、1/50 of LD50、1/30 of LD50、1/10 of LD50)of HSX(OL-W)were injected via jugular vein,The blood pressure fell downimmediatelly.as follows:(15.1±4.5)%、(19.7±3.8)%、(26.8±7.1)% and(67.1±6.6)%respectilly,The fell was short lived and dose-dependent,the diastolic pressure wasaffed more pronounced. Similar antihypertensive potency but much fonger dunttion(30min)was obeerved after oral adrminaistiation of 0.8g(crud drugs)/kg in the study of mechanism ofhypotensive effect,BP did not change when OL-W was given to cerebral ventricle in rats.Propranolol、dipen-hydraiamine、cintitidine、captoprill did nOt bfock its action,but atrDpine did.These results suggested one that the mechanism of hypotensive action OL-W is concernedwith M-receptor and was related directly with its vosodiating action.
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