Inhibitory effects of potassium channel blockers on tetramethylpyrazine-induced relaxation of rat aortic strip in vitro

被引:56
作者
Tsai, CC
Lai, TY
Huang, WC
Liu, IM
Cheng, JT [1 ]
机构
[1] Natl Cheng Kung Univ, Coll Med, Dept Pharmacol, Tainan 70101, Taiwan
[2] China Med Coll, Sch Post Baccalaureate Chinese Med, Dept Tradit Med, Taichung 40401, Taiwan
[3] Tajen Inst Technol, Dept Pharm, Yen Pou 90701, Ping Tung Shien, Taiwan
关键词
tetramethylpyrazine; Chuang-chung; antihypertension; calcium influx; potassium channel blockers;
D O I
10.1016/S0024-3205(02)01852-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Tetramethylpyrazine (TMP) is one of the active principles contained in Ligusticum chuanxiong Hort. (Umbelliferae), a herb that has been widely used to treat vascular disorders in China. In the present study, role of potassium channel in the vasodilatation of TMP was investigated using the effect of potassium channel blocker on TMP induced relaxation in isolated aortic rings from Wistar rats. TMP produced a concentration-dependent relaxation in the aortic rings precontracted with vasopressin or phenylephrine. Similar effect of TMP on vasoconstrictions by phenylephrine and vasopressin, induced through two different receptors, indicating the direct vasodilatation of TMP. Specific inhibitors for potassium channel were used to characterize the role of potassium channel in this action of TMP. Only the inhibitors specific to small conductance calcium-activated potassium (SKca) channel or ATP-sensitive potassium (K-ATP) channel inhibited the action of TMP. Also, the TMP-induced relaxation was reversed by the inhibitor of soluble guanylyl cyclase in a way similar to that of K-ATP channel blockade. The obtained results indicated that vasodilatation induced by TMP is related to the opening of SKCa and K-ATP channels. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1321 / 1330
页数:10
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