College of Oriental Medicine and Hanbang Body-fluid Research Center, Wonkwang University, Iksan, Jeonbuk 570-749, Republic of Korea.
J Nat Med. 2012 Jan;66(1):17-24. doi: 10.1007/s11418-011-0546-6. Epub 2011 May 24.
The aqueous extract of Lespedeza cuneata G. Don. (ALC) induced vasorelaxation of phenylephrine precontracted aorta in a dose-dependent manner. This effect disappeared in the absence of functional endothelium. Pretreatment of the aortic tissues with N(G)-nitro-L-arginine methyl ester (L-NAME), or 1H-[1,2,4]-oxadiazole-[4,3-α]-quinoxalin-1-one (ODQ) blocked ALC-induced vascular relaxation. Incubation of endothelium-intact thoracic aortic rings with ALC increased cGMP production. ALC-induced cGMP production was blocked by pretreatment with L-NAME or ODQ. ALC-induced vascular relaxation was also markedly attenuated by addition of verapamil or diltiazem, but was not blocked by pretreatment with indomethacine, glibenclamide, tetraethylammonium, atropine, or propranolol. The results suggest that ALC dilates vascular smooth muscle via endothelium-dependent NO-cGMP signaling.
胡枝子的水提物(ALC)可剂量依赖性地诱导预先收缩的胸主动脉对苯肾上腺素的血管舒张反应。这种作用在没有功能内皮的情况下消失。用 N(G)-硝基-L-精氨酸甲酯(L-NAME)或 1H-[1,2,4]-恶二唑-[4,3-α]-喹喔啉-1-酮(ODQ)预处理主动脉组织可阻断 ALC 诱导的血管舒张。与 ALC 孵育完整内皮的胸主动脉环可增加 cGMP 的产生。用 L-NAME 或 ODQ 预处理可阻断 ALC 诱导的 cGMP 产生。维拉帕米或地尔硫卓的加入也明显减弱了 ALC 诱导的血管舒张,但预先用吲哚美辛、格列本脲、四乙铵、阿托品或普萘洛尔处理并不阻断。结果表明,ALC 通过内皮依赖性 NO-cGMP 信号转导舒张血管平滑肌。