Involvement of CA2+-activated K+ channels in ginsenosides-induced aortic relaxation in rats

Z. Li, X. Chen, Y. Niwa, S. Sakamoto, Y. Nakaya

研究成果: ジャーナルへの寄稿学術論文査読

43 被引用数 (Scopus)

抄録

Ginsenosides (GS), an extract of Panax ginseng, have been reported to be effective in inducing vascular relaxation mediated by nitric oxide (NO) release. The present experiments were designed to determine whether this GS-induced vasorelaxation also involves Ca2+-activated K+ (KCa) channels in vascular smooth muscle cells (VSMC) in addition to endothelium-derived NO. GS induced vasorelaxation in rat aortic rings, which had been precontracted with phenylephrine, in a concentration-dependent manner. This GS-induced relaxation was partially reversed by tetraethylammonium (TEA), an inhibitor of KCa channels; methylene blue (MB), an inhibitor of soluble guanylate cyclase; as well as Nω-nitro-L-arginine (L-NNA), but not by glybenclamide. In cultured VSMC and endothelial cells, KCa channels were activated by GS. This action was abolished by TEA, but was not blocked by glybenclamide. In addition, the GS-induced activity of KCa channels was partially inhibited by MB or H-8. These results indicate that the activation of KCa channels involved, at least in part, the GS-induced vasorelaxation of rat aorta.

本文言語英語
ページ(範囲)41-47
ページ数7
ジャーナルJournal of Cardiovascular Pharmacology
37
1
DOI
出版ステータス出版済み - 2001

All Science Journal Classification (ASJC) codes

  • 薬理学
  • 循環器および心血管医学

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