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山奈酚可预防3-硝基丙酸诱导的大鼠纹状体变性。

Kaempferol protects against rat striatal degeneration induced by 3-nitropropionic acid.

作者信息

Lagoa Ricardo, Lopez-Sanchez Carmen, Samhan-Arias Alejandro K, Gañan Carlos M, Garcia-Martinez Virginio, Gutierrez-Merino Carlos

机构信息

Human Anatomy and Embryology, Faculty of Medicine, University of Extremadura, Badajoz, Spain.

出版信息

J Neurochem. 2009 Oct;111(2):473-87. doi: 10.1111/j.1471-4159.2009.06331.x. Epub 2009 Aug 13.

DOI:10.1111/j.1471-4159.2009.06331.x
PMID:19682208
Abstract

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.

摘要

3-硝基丙酸(NPA)可导致啮齿动物和灵长类动物纹状体变性以及一些具有亨廷顿舞蹈病特征的神经功能紊乱。我们已经表明,黄酮类化合物山奈酚可在很大程度上减轻大鼠脑缺血再灌注诱导的纹状体损伤(Lopez-Sanchez等人,2007年)。在这项研究中,我们报告腹腔注射山奈酚可为Wistar大鼠提供针对NPA诱导的神经变性的有效保护。我们研究了在NPA治疗期间(25mg/kg体重/12小时腹腔注射,共5天)每天腹腔注射7、14和21mg/kg体重的山奈酚对神经功能缺损、大鼠纹状体变性和氧化应激标志物的影响。腹腔注射14-21mg/kg体重的山奈酚可在很大程度上减轻运动功能缺损并延迟死亡。苏木精-伊红染色和TUNEL染色显示,较高剂量的山奈酚在治疗结束前可预防NPA诱导的纹状体损伤,并且还可预防NPA诱导的氧化应激,因为它可阻止NPA处理大鼠中还原型谷胱甘肽的下降和蛋白质硝基酪氨酸的增加。研究发现,纹状体变性与钙蛋白酶激活以及肌酸激酶的大量失活有关,当给予较高剂量的山奈酚时,这些情况也可得到预防。

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