Involvements of calcium channel and potassium channel in Danshen and Gegen decoction induced vasodilation in porcine coronary LAD artery

被引:20
作者
Hu, Fan [1 ,2 ,3 ]
Koon, Chi Man [1 ,3 ]
Chan, Judy Yuet Wa [1 ,3 ]
Lau, Kit Man [1 ,3 ]
Kwan, Y. W. [3 ]
Fung, Kwok Pui [1 ,3 ,4 ]
机构
[1] Chinese Univ Hong Kong, Inst Chinese Med, Shatin, Hong Kong, Peoples R China
[2] Hefei Univ Technol, Sch Biotechnol & Food Engn, Hefei, Anhui, Peoples R China
[3] Chinese Univ Hong Kong, Sch Biomed Sci, Shatin, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, State Key Lab Phytochem & Plant Resources W China, Shatin, Hong Kong, Peoples R China
关键词
Danshen and Gegen decoction (DG); Vasodilation; Endothelium; Potassium; Calcium; Myosin light chain; SALVIANOLIC ACID-B; PUERARIA-LOBATA; NITRIC-OXIDE; MILTIORRHIZA; RAT; INHIBITION; EXTRACT; HYPERTENSION; CONTRACTION; MECHANISMS;
D O I
10.1016/j.phymed.2012.07.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Danshen (Salviae Miltiorrhizae Radix) and Gegen (Puerariae Lobatae Radix) have been widely used in treating cardiovascular diseases for thousands of years in China. The present study was carried out to evaluate the effects of a Danshen and Gegen decoction (DG) on the vascular reactivity of a porcine isolated coronary artery and the underlying mechanisms involved. Porcine coronary rings were precontracted with 15 nM U46619. The involvement of endothelium-dependent mechanisms was explored by removing the endothelium; the involvement of potassium channels was investigated by the pretreatment of the artery rings with various blockers, and the involvement of the calcium channels was investigated by incubating the artery rings with Ca2+-free buffer and priming them with high [K+] prior to adding CaCl2 to elicit contraction. The involvement of Ca2+ sensitization was explored by evaluating the Rho-activity expression. The results revealed that DG elicited a concentration-dependent relaxation on a U46619-precontracted coronary artery ring. These relaxation responses were not altered by the pretreatment of inhibitors of endothelium-related dilator synthases, cGMP and cAMP pathway inhibitors, potassium channel (BKCa, SKCa, K-V and K-ATP) blockers and endothelium removal. The K-IR channel blocker BaCl2 only slightly attenuated the DG-induced relaxation. However, the Ca2+-induced artery contraction was inhibited by DG. Additionally, the expression of the phosphorylated myosin light chain was inhibited by DG whereas the activity of RhoA was not affected. Therefore, DG could be a useful cardioprotective agent for vasodilation in patients who have hypertension. (C) 2012 Elsevier GmbH. All rights reserved.
引用
收藏
页码:1051 / 1058
页数:8
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