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作 者:崔玉英[1] 潘春水[1] 齐永芬[1] 唐朝枢[1] 耿彬[1]
机构地区:[1]北京大学第一医院心血管研究所,北京100034
出 处:《中国药理学通报》2005年第11期1335-1339,共5页Chinese Pharmacological Bulletin
基 金:国家自然科学基金资助项目(No30400151)
摘 要:目的 观察H2S对血管L-精氨酸/一氧化氮(L-Arg/NO)通路的影响以探讨H2S和NO这两种气体信号分子间的相互作用。方法 离体孵育大鼠主动脉薄片, 加入H2S供体NaHS(10^-7~10^-4 mol·L^-1)孵育4 h,及50 μmol·L^-1NaHS分别孵育2、4和6 h.采用Greiss法测定血管亚硝酸盐含量;同位素示踪法检测血管组织一氧化氮合酶(NOS)活性及L-Arg转运, RT-PCR检测eNOS、CAT1基因表达。结果 一次性给予50 μmol·L^-1NaHS,孵育2 h,孵育液中NO2-含量比对照组低62%,血管NOS活性下降48%,L-Arg转运减少50%(P〈0.01);孵育6 h,NO2-含量比对照组低19%(P〈0.05),而NOS活性和L-Arg转运已基本恢复(P〉0.05).NaHS(10^-7~10^-4 mol·L^-1),呈浓度依赖的抑制了L-Arg/NOS/NO通路,IC50分别为0.499、3.198及3.927 μmol·L-1(P〈0.01);而给予50 μmol·L^-1NaHS后,eNOS和CAT-1A的mRNA表达分别减少34.3%和55.1%(P〈0.01)。结论 H2S通过抑制血管组织L-Arg转运和NOS活性和基因表达,下调L-Arg/NOS/NO通路,从而减少血管NO生成。Abstract: Aim To observe the influence of hydrogen sulfide on L-arginine/nitric oxide synthase (NOS)/NO pathway,explore the interaction between H2S and NO as cardiovascular regulatory gasotransmitters. Methods Aortic thin slices in vitro were administrated with NariS( 10^-7 mol · L^-1 - 10^-4 mol · L^-1 ) , a donor of H2S, and incubated for 4 hours, or 50 μmol · L^-1 Naris and incubated for 2 h, 4 h and 6 h, respectively. The nitrite production Was measured with greiss assay; NOS activity and L-arginine transportation,with isotope tracer method; the eNOS and CAT1-A gene expression, with RT-PCR. Results After being given with NariS(50 μmol · L^-1 ) one time, and incubating for 2 h, the nitrite production decreased by 62% , NOS activity reduced by 48% and L-arginine transport decreased by 50%. After incubation for 6 h, the nitrite production further was inhibited by 19% ( P 〈 0. 05 ) , but NOS activity and L-arginine transporta were recovered to a large extert (P 〉0.05). NariS( 10^-7 mol· L^-1 - 10^-4 mol · L^-1 ) inhibited the L-arginine/NOS/ NO pathway in a dose-dependent manner, and IC50 was 0.499,3. 198 and 3.927 μmol · L^-1(p〈0.01), respectively. The amount of eNOS and CAT-1 mRNA reduced by 34.3% and 55.1% (P〈0.01) after admistration of 50 μmol · L^-1 NariS. Conclusion H2S inhibits NO release by inhibiting L-arginine transport, NOS activity, CAT-1 and eNOS gene expression, and down-regulating L-arginine/NOS/NO pathway in aortic vessels of rat.
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