Gilani Anwar Ul Hassan, Shah Abdul Jabbar, Ahmad Manzoor, Shaheen Farzana
Department of Biological and Biomedical Sciences, The Aga Khan University Medical College, Karachi-74800, Pakistan.
Phytother Res. 2006 Dec;20(12):1080-4. doi: 10.1002/ptr.2000.
Acorus calamus Linn. (Araceae) is a native of Central Asia and Eastern Europe and has widespread use in the traditional system of medicine for gastrointestinal disorders such as colic pain and diarrhoea. This study was aimed at providing a possible pharmacological basis to the use of this plant as an antispasmodic and antidiarrhoeal. In the isolated rabbit jejunum preparation the crude extract (Ac.Cr), which tested positive for the presence of alkaloid, saponins and tannins, caused inhibition of spontaneous and high K(+) (80 mm)-induced contractions, with respective EC(50) values of 0.42 +/- 0.06 and 0.13 +/- 0.04 mg/mL (mean +/- SEM; n = 6-8), thus showing spasmolytic activity, mediated possibly through calcium channel blockade (CCB). The CCB activity was confirmed when pre-treatment of the tissue with Ac.Cr (0.3-1.0 mg/mL) caused a rightward shift in the Ca(++) dose-response curves similar to that caused by verapamil, a standard calcium channel blocker. Activity-directed fractionation revealed that the CCB activity was concentrated in the n-hexane fraction while the ethylacetate fraction was less potent. These results suggest that the spasmolytic effect of the plant extract is mediated through the presence of CCB-like constituent(s) which is concentrated in the n-hexane fraction and this study provides a strong mechanistic base for its traditional use in gastrointestinal disorders such as colic pain and diarrhoea.
菖蒲(天南星科)原产于中亚和东欧,在传统医学体系中广泛用于治疗胃肠道疾病,如绞痛和腹泻。本研究旨在为该植物作为解痉剂和止泻剂的应用提供可能的药理学依据。在离体兔空肠标本中,粗提取物(Ac.Cr)对生物碱、皂苷和单宁呈阳性反应,可抑制自发性收缩和高钾(80 mM)诱导的收缩,其EC50值分别为0.42±0.06和0.13±0.04 mg/mL(平均值±标准误;n = 6 - 8),从而显示出解痉活性,可能是通过钙通道阻滞(CCB)介导的。当用Ac.Cr(0.3 - 1.0 mg/mL)预处理组织时,Ca(++)剂量反应曲线向右移动,类似于标准钙通道阻滞剂维拉帕米引起的移动,CCB活性得到证实。活性导向分级分离显示,CCB活性集中在正己烷馏分中,而乙酸乙酯馏分的活性较弱。这些结果表明,植物提取物的解痉作用是通过存在类似CCB的成分介导的,该成分集中在正己烷馏分中,本研究为其在绞痛和腹泻等胃肠道疾病中的传统应用提供了有力的机制基础。