首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Kaempferol protects against rat striatal degeneration induced by 3-nitropropionic acid.
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Kaempferol protects against rat striatal degeneration induced by 3-nitropropionic acid.

机译:山emp酚可防止3-硝基丙酸引起的大鼠纹状体变性。

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摘要

3-Nitropropionic acid (NPA) produces degeneration of striatum and some neurological disturbances characteristic of Huntington's disease in rodents and primates. We have shown that the flavonoid kaempferol largely reduced striatal damage induced by cerebral ischaemia-reperfusion in rats (Lopez-Sanchez et al. 2007). In this work, we report that intraperitoneal (i.p.) administration of kaempferol affords an efficient protection against NPA-induced neurodegeneration in Wistar rats. We studied the effects of daily i.p. injections of 7, 14 and 21 mg of kaempferol/kg body weight during the NPA-treatment (25 mg/kg body weight/12 h i.p., for 5 days) on the neurological deficits, degeneration of rat striatum and oxidative stress markers. Intraperitoneal injections of 14-21 mg of kaempferol/kg body weight largely attenuated motor deficit and delayed mortality. The higher dose of kaempferol prevented the appearance of NPA-induced striatal lesions up to the end of treatment, as revealed by haematoxylin-eosin and TUNEL staining, and also NPA-induced oxidative stress, because it blocked the fall of reduced glutathione and the increase of protein nitrotyrosines in NPA-treated rats. It was found that striatal degeneration was associated with calpains activation and a large inactivation of creatine kinase, which were also prevented when the higher doses of kaempferol were administered.
机译:3-硝基丙酸(NPA)在啮齿动物和灵长类动物中产生纹状体变性和亨廷顿氏病特征的某些神经系统疾病。我们已经表明,类黄酮山emp酚在很大程度上减少了大鼠脑缺血再灌注所致的纹状体损伤(Lopez-Sanchez等,2007)。在这项工作中,我们报告腹膜内(i.p.)施用山ka酚可有效抵抗Wistar大鼠中NPA诱导的神经变性。我们研究了每日i.p.在NPA治疗期间(每7天25 mg / kg体重/ 12 h腹膜内注射,持续5天)注射7、14和21 mg的山ka酚/ kg体重,可改善神经纹状体,大鼠纹状体的变性和氧化应激标志物。腹膜内注射14-21毫克山mg酚/千克体重可大大减轻运动功能障碍并延迟死亡率。如苏木精-曙红和TUNEL染色所揭示的,高剂量的山emp酚可防止NPA诱导的纹状体病变的出现直至治疗结束,以及NPA诱导的氧化应激,因为它阻止了还原型谷胱甘肽的下降和增加。 NPA处理的大鼠中蛋白质硝基酪氨酸的含量发现纹状体变性与钙蛋白酶的活化和肌酸激酶的大量失活有关,当给予更高剂量的山奈酚时,这也可以防止。

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