Endothelium-independent vasorelaxation by leonurine, a plant alkaloid purified from Chinese motherwort

被引:70
作者
Chen, CX [1 ]
Kwan, CY [1 ]
机构
[1] McMaster Univ, Fac Hlth Sci, Dept Med, Hamilton, ON L8N 3Z5, Canada
关键词
leonurine; rat aorta; carotid artery; portal vein; relaxation; calcium channel; alpha-adrenoceptor;
D O I
10.1016/S0024-3205(00)00987-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Leonurine, a plant alkaloid present in Chinese motherwort, induced concentration- dependent and endothelium-independent relaxation of phenylephrine (PE)- pretreated rat aortic arterial rings. The IC,, values for leonurine were 86.4 +/- 10.4 and 85.9 +/- 17.2 muM in the presence and absence of endothelium respectively. It inhibited the responses of aortic smooth muscle to PE in Ca2+ free medium containing 100 muM EGTA, suggesting a possible action on the release of intracellular Ca2+. Leonurine is not a specific ol-adrenoceptor blocker, since it also caused a concentration-dependent inhibition of vascular contractile responses to KCl with an IC50 value of 96.4 +/- 13.4 muM, suggesting that leonurine also blocks the L-type Ca2+-channel. In addition, leonurine relaxed the aortic contraction induced by prostaglandin F-2 alpha (PGF(2 alpha)). These inhibitory effects of leonurine were reversible and did not affect the resting tension. In conclusion, these findings suggest that leonurine is an effective inhibitor of vascular smooth tone, probably acting by inhibiting the Ca2+ influx and the release of intracellular Ca2+. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:953 / 960
页数:8
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