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In vitro induction of nitric oxide by fructose-1,6-diphosphate in the cardiovascular system of rats

机译:1,6-二磷酸果糖在大鼠心血管系统中体外诱导一氧化氮

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Nitric oxide (NO) functions as a cellular messenger in a number of organs and cell systems in the cardiovascular system (CVS); it is a significant determinant of basal vascular tone and regulates myocardial contractility and platelet aggregation. The present study focused upon understanding the in vitro effects of fructose-1,6-diphosphate (FDP) on the rat cellular NO pathway. The iNOS activity was measured by monitoring the formation of (~3H)-citrulline in 50,000 g soluble fractions of crude homogenates of endothelial (ET) and smooth muscle cells (SMC) from the arteries of rats, and macrophages (MAC) and lymphocytes (LYM) from rat blood. FDP in concentrations of 10-1000 μM stimulated rat cellular iNOS activity in a concentration-dependent manner. FDP-stimulated rat cellular iNOS was found to be completely reversed by 5 μM concentration of NG-monomethyl-L-arginine (L- NMMA), the potent mammalian NOS inhibitor. These studies demonstrated that FDP may induce the formation of NO by stimulating rat cardiovascular iNOS activity.
机译:一氧化氮(NO)在心血管系统(CVS)的许多器官和细胞系统中充当细胞信使;它是基础血管张力的重要决定因素,并调节心肌收缩力和血小板聚集。本研究集中于了解果糖-1,6-二磷酸(FDP)对大鼠细胞NO途径的体外作用。 iNOS活性是通过监测50,000 g大鼠动脉内皮细胞(ET)和平滑肌细胞(SMC)的粗匀浆中的(〜3H)-瓜氨酸的形成以及巨噬细胞(MAC)和淋巴细胞( LYM)。浓度为10-1000μM的FDP以浓度依赖性方式刺激大鼠细胞iNOS活性。发现FDP刺激的大鼠细胞iNOS被浓度为5μM的有效的哺乳动物NOS抑制剂NG-单甲基-L-精氨酸(L-NMMA)完全逆转。这些研究表明,FDP可能通过刺激大鼠心血管iNOS活性来诱导NO的形成。

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