Ghayur Muhammad Nabeel, Gilani Anwarul Hassan
Department of Biological and Biomedical Sciences, The Aga Khan University Medical College, Karachi, Pakistan.
Arch Pharm Res. 2006 Nov;29(11):990-7. doi: 10.1007/BF02969283.
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.
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。