Vascular relaxation by ethanol extract of Xanthoceras sorbifolia via Akt- and SOCE-eNOS-cGMP pathways

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• 作者：Song Nan Jin ; Jin Fu Wen ; Hye Yoom Kim ; Dae Gill Kang ; Ho Sub Lee ; Kyung Woo Cho
• 关键词：Xanthoceras sorbifolia ; Akt ; ENOS ; Nitric oxide ; Guanosine 3′ ; 5′ ; -cyclic monophosphate ; Store-operated Ca²⁺ entry (SOCE)
• 刊名：Journal of Ethnopharmacology
• 出版年：2010
• 出版时间：28 October 2010
• 年：2010
• 卷：132
• 期：1
• 页码：240-245
• 全文大小：530 K

文摘

Aim of the study

The aim of the present study was to define the effect of Xanthoceras sorbifolia extracts (XS) on vascular tension and responsible mechanisms in rat thoracic aortic rings.

Materials and methods

Ethanol extract of the leaves of XS (EXS) was examined for their vascular relaxant effects in isolated phenylephrine-precontracted rat thoracic aorta.

Results

EXS (0.1–100 μg/ml) induced relaxation of the phenylephrine-precontracted aortic rings in a concentration-dependent manner. Endothelium-denudation abolished EXS-induced vasorelaxation. Pretreatment of the endothelium-intact aortic rings with N^G-nitro-l-arginine methylester (l-NAME) and 1H-[1,2,4]-oxadiazolo-[4,3-α]-quinoxalin-1-one (ODQ) inhibited EXS-induced vasorelaxation. Inhibition of Ca²⁺ entry via l-type Ca²⁺ channels failed to block the EXS-induced vasorelaxation. Extracellular Ca²⁺ depletion significantly attenuated EXS-induced vasorelaxation. Modulators of the store-operated Ca²⁺ entry (SOCE), thapsigargin, 2-aminoethyl diphenylborinate (2-APB) and Gd³⁺, and an inhibitor of Akt, wortmannin, markedly attenuated the EXS-induced vasorelaxation. EXS increased cGMP levels of the aortic rings in a concentration-dependent manner and the effect was blocked by l-NAME, ODQ, thapsigargin, Gd³⁺, 2-APB, and wortmannin. Further, EXS-induced vasorelaxation was significantly attenuated by tetraethylammonium, a non-selective K_ca channels blocker, but not by glibenclamide, an ATP-sensitive K⁺ channels inhibitor. Inhibition of cyclooxygenase with indomethacin, and adrenergic and muscarinic receptors blockade had no effects on EXS-induced vasorelaxation.

Conclusions

The present study suggests that EXS relaxes vascular smooth muscle via endothelium-dependent NO-cGMP signaling through activation of the Akt- and SOCE-eNOS-sGC pathways, which may, at least in part, be related to the function of K⁺ channels.