Bornia Elaine Campana Sanches, do Amaral Valéria, Bazotte Roberto Barbosa, Alves-Do-Prado Wilson
Department of Pharmacy and Pharmacology, State University of Maringa, Maringa-PR, Brazil.
J Smooth Muscle Res. 2008 Feb;44(1):1-8. doi: 10.1540/jsmr.44.1.
In endothelium-intact rat aortic ring preparations pre-contracted with norepinephrine or KCl, NG-nitro L-arginine (L-NOARG, 0.1 mM) and 1H-[1,2,4] oxidiazolo [4,3-a] quinoxalin-1-one (ODQ, 10 microM) antagonized the reduction of the vascular tone induced by stevioside, but this antagonism did not occur when the experiment was performed with endothelium-denuded aortic rings. The data indicates that the vasodilatation produced by stevioside is dependent on nitric oxide synthase and guanylate cyclase activities when the endothelium is not damaged.
在预先用去甲肾上腺素或氯化钾预收缩的内皮完整的大鼠主动脉环标本中,NG-硝基-L-精氨酸(L-NOARG,0.1 mM)和1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ,10 microM)拮抗甜菊糖苷诱导的血管张力降低,但当用去内皮的主动脉环进行实验时,这种拮抗作用未发生。数据表明,当内皮未受损时,甜菊糖苷产生的血管舒张依赖于一氧化氮合酶和鸟苷酸环化酶的活性。