首页> 外文期刊>Neuroscience research communications >7-NITROINDAZOLE REDUCES ISCHEMIA-INDUCED INCREMENT OF APOPTOSIS AND CELL PROLIFERATION IN THE DENTATE GYRUS OF RATS
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7-NITROINDAZOLE REDUCES ISCHEMIA-INDUCED INCREMENT OF APOPTOSIS AND CELL PROLIFERATION IN THE DENTATE GYRUS OF RATS

机译:7-硝基吲哚减轻大鼠齿状回缺血再灌注诱导的细胞凋亡和细胞增殖

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摘要

Nitric oxide is synthesized from L-arginine by nitric oxide synthase (NOS), and it is a free radical with signaling functions. Neuronal nitric oxide synthase (nNOS) is mainly expressed in the central nervous system, and it has been implicated in the pathogenesis of brain injury such as ischemia,. In the present study, the effects of 7-nitroindazole, which specifically inhibits nNOS, on apoptosis and cell proliferation in the dentate gyms after transient global ischemia in gerbils were investigated. Enhanced apoptotic neuronal cell death and cell proliferation were observed in the dentate gyms of ischemic gerbils. However, 7-nitroindazole suppressed the ischemia-induced apoptosis and cell proliferation. These results suggest that 7-nitroindazole has an inhibitive effect on apoptosis and cell proliferation following transient global ischemia. The present study shows that nitric oxide, the synthesis of which is augmented by ischemia, plays an important role in the regulation of apoptosis and cell proliferation following ischemic injury.
机译:一氧化氮是由L-精氨酸通过一氧化氮合酶(NOS)合成的,是具有信号传导功能的自由基。神经元型一氧化氮合酶(nNOS)主要在中枢神经系统中表达,并且与脑损伤(例如缺血)的发病机制有关。在本研究中,研究了特异性抑制nNOS的7-硝基吲唑对沙土鼠短暂性整体缺血后牙本质细胞凋亡和细胞增殖的影响。在齿状沙鼠的齿状体育馆中观察到凋亡神经元细胞死亡和细胞增殖增强。然而,7-硝基吲唑抑制了缺血诱导的细胞凋亡和细胞增殖。这些结果表明7-硝基吲唑对短暂性全局缺血后的细胞凋亡和细胞增殖具有抑制作用。本研究表明,一氧化氮的合成通过缺血增加,在缺血性损伤后细胞凋亡和细胞增殖的调节中起重要作用。

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