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作 者:姚兴海[1] 王晓红 王雯[1] 符民桂 张立克[1] 唐朝枢
机构地区:[1]首都医科大学病理生理教研室,北京100054 [2]北京医科大学第一临床医学院,北京100034
出 处:《基础医学与临床》2000年第6期530-533,共4页Basic and Clinical Medicine
摘 要:本文观察了RGDS肽对兔离体股动脉舒张反应、主动脉一氧化氮(NO)生成、一氧化氮合酶(NOS)活性及左旋精氨酸(L-Arg)转运的影响。结果发现,RGDS肽呈剂量依赖性地引起内皮依赖和非依赖性的血管扩张;增加NOS活性及NO的产生,可被L-NNA所逆转。RGDS肽亦可增加血管组织高和低亲和性L-Arg的最大转运速率(与对照组相比分别增加126%和64%,P<0.05和P<0.01)。表明RGDS肽可显著增加L-Arg转运及NOS的活性,对内皮衍化舒张因子(EDRF)/NO系统具有重要调节作用。The present study investigated the effects of Arg-G ly-Asp-Ser(RGDS) Peptide on femoralis relaxation, aortic nitric oxide (NO) pro duction, activity of NO synthase and L-arginine transport of rabbit in vitro . Results showed that RGDS peptide could cause vasorelaxation in the pre sence and absence of a functional endothelium in dose-dependence. When incubat ed With RGDS peptide, aortic slices NOS activity and NO production were obviousl y enhanced, and could be countered after using L-NNA. Furthermore, the maximal velocity of high and low affinity L-Arg transport were promoted about 126% and 64% more than that of control group ( P<0.05 and P< 0.01) by RGDS pep tide. The results suggested RGDS peptide might affect several point of L-Arg/N O system to different extents.
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