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清香桂的心脏抑制、血管舒张及气管舒张作用研究。

Studies on cardio-suppressant, vasodilator and tracheal relaxant effects of Sarcococca saligna.

作者信息

Ghayur Muhammad Nabeel, Gilani Anwarul Hassan

机构信息

Department of Biological and Biomedical Sciences, The Aga Khan University Medical College, Karachi, Pakistan.

出版信息

Arch Pharm Res. 2006 Nov;29(11):990-7. doi: 10.1007/BF02969283.

Abstract

Sarcococca saligna is a shrub that is traditionally used for its medicinal properties in Pakistan. In this study we report the cardio-suppressant, vasodilator and tracheal relaxant activities of the aqueous-methanolic extract (Ss.Cr) of the plant. Ss.Cr, that tested positive for the presence of saponins, flavonoids, tannins, phenols, and alkaloids, exhibited a dose-dependent (0.3-5 mg/mL) negative inotropic and chronotropic effect on the isolated guinea-pig atrium which was resistant to atropine (1 microM) and aminophylline (10 microM) pretreatment. In rabbit thoracic aorta, Ss.Cr dose-dependently (0.1-3 mg/mL) relaxed the high K+ (80 mM) and phenylephrine (PE, 1 microM)-induced contractions, indicating a possible Ca++ channel blocking (CCB) effect. When tested against PE (1 microM) control peaks in normal Ca++ and Ca++-free Kreb's solution, Ss.Cr exhibited dose-dependent (0.1-3 mg/mL) inhibition, being more potent in relaxing the PE responses in Ca++-free Kreb's solution, thus indicating specific blockade of Ca++ release from the intracellular stores. Ss.Cr also relaxed the agonist-induced contractions in: a) rat aorta irrespective of the presence of endothelium or nitric oxide synthase inhibitor L-NAME and b) rabbit and guinea-pig tracheal strips. The data shows that Ss.Cr possesses possible Ca++ channel blocking activity which might be responsible for its observed cardio-suppressant, vasodilator and tracheal relaxant effects though more tests are required to confirm this Ca++ channel blocking effect.

摘要

水红木是一种灌木,在巴基斯坦传统上因其药用特性而被使用。在本研究中,我们报告了该植物水甲醇提取物(Ss.Cr)的心脏抑制、血管舒张和气管舒张活性。Ss.Cr经检测皂甙、黄酮类化合物、单宁、酚类和生物碱呈阳性,对离体豚鼠心房表现出剂量依赖性(0.3 - 5mg/mL)的负性变力和变时作用,该作用对阿托品(1μM)和氨茶碱(10μM)预处理具有抗性。在兔胸主动脉中,Ss.Cr剂量依赖性(0.1 - 3mg/mL)地舒张了高钾(80mM)和去氧肾上腺素(PE,1μM)诱导的收缩,表明可能具有钙通道阻滞(CCB)作用。当在正常钙和无钙的克雷布斯溶液中针对PE(1μM)对照峰值进行测试时,Ss.Cr表现出剂量依赖性(0.1 - 3mg/mL)抑制,在无钙的克雷布斯溶液中舒张PE反应更有效,从而表明对细胞内钙库释放钙的特异性阻滞。Ss.Cr还舒张了以下激动剂诱导的收缩:a)大鼠主动脉,无论有无内皮或一氧化氮合酶抑制剂L - NAME;b)兔和豚鼠气管条。数据表明,Ss.Cr具有可能的钙通道阻滞活性,这可能是其观察到的心脏抑制、血管舒张和气管舒张作用的原因,不过需要更多测试来证实这种钙通道阻滞作用。

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