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来自黄花稔的抗炎镇痛生物碱

Anti-inflammatory and analgesic alkaloid from Sida cordifolia linn.

作者信息

Sutradhar Ranajit Kumar, Rahman Akm Matior, Ahmad Mesbahuddin, Bachar Sitesh Chandra, Saha Achinto, Roy Tapashi Ghosh

机构信息

Department of Chemistry, Chittagong University of Engineering and Technology (CUET), Chittagong-4349, Bangladesh.

出版信息

Pak J Pharm Sci. 2007 Jul;20(3):185-8.

Abstract

The analgesic and anti-inflammatory activities of a new alkaloid, 1,2,3,9-tetrahydro-pyrrolo [2,1-b] quinazolin-3-ylamine (compound 1) isolated from Sida cordifolia Linn. were investigated in animal models. In the acetic acid induced writhing model, the compound 1 showed 25.4 (P<0.05) and 52.43% (P<0.01) inhibition of writhing response at doses of 25 and 50 mg/kg body weight respectively. The alkaloid also produced significant increase in the tail flick latency in radiant heat tail-flick method. In Carrageenan induced rat paw edema the compound 1 produced 16.93 and 24.43 % inhibition of paw edema at the doses of 25 and 50 mg/kg body weight respectively at the third hour of study.

摘要

对从心叶黄花稔中分离出的一种新生物碱1,2,3,9-四氢-吡咯并[2,1-b]喹唑啉-3-胺(化合物1)的镇痛和抗炎活性进行了动物模型研究。在醋酸诱导的扭体模型中,化合物1在体重剂量分别为25和50mg/kg时,对扭体反应的抑制率分别为25.4%(P<0.05)和52.43%(P<0.01)。该生物碱在辐射热甩尾法中还显著延长了甩尾潜伏期。在角叉菜胶诱导的大鼠足爪水肿模型中,在研究的第三小时,化合物1在体重剂量分别为25和50mg/kg时,对足爪水肿的抑制率分别为16.93%和24.43%。

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