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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Effects of allopurinol on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurochemical changes in the striatum and in the brainstem of the rat.
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Effects of allopurinol on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurochemical changes in the striatum and in the brainstem of the rat.

机译:别嘌醇对大鼠纹状体和脑干中1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的神经化学变化的影响。

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摘要

Levels of uric acid, xanthine, hypoxanthine, ascorbic acid (AA), dehydroascorbic acid (DHAA), glutathione (GSH), noradrenaline (NA), dopamine (DA), dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and 1-methyl-4-phenylpyridinium ion (MPP+) were determined in the striatum and/or in the brainstem of 3-month-old male Wistar rats, given allopurinol (500 mg/kg day by gavage) for 3 days before a single MPTP 52 mg/kg dose i.p. Allopurinol alone decreased uric acid and hypoxanthine levels in the striatum and in the brainstem; moreover, allopurinol increased AA oxidation and decreased striatal DA metabolites. Allopurinol affected neither regional MPTP and MPP+ levels nor the MPTP-induced inhibition of striatal DA oxidative metabolism. On the contrary, the MPTP-induced increase in uric acid levels and decrease in xanthine, hypoxanthine and NA levels were fully antagonised. Such findings demonstrate that the claimed MPP(+)-induced oxidative stress mediated by xanthine oxidase may be involved at least in the NA depletion; moreover, uric acid may have a physiological role as an active component of the neuronal antioxidant pool.
机译:尿酸,黄嘌呤,次黄嘌呤,抗坏血酸(AA),脱氢抗坏血酸(DHAA),谷胱甘肽(GSH),去甲肾上腺素(NA),多巴胺(DA),二羟苯乙酸(DOPAC),高香草酸(HVA),1-在3个月大的雄性Wistar大鼠的纹状体和/或脑干中测定了甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)和1-甲基-4-苯基吡啶鎓离子(MPP +) ,在每次单剂量MPTP 52 mg / kg腹膜内给予别嘌醇(每天500 mg / kg灌胃)3天单独使用别嘌醇会降低纹状体和脑干中的尿酸和次黄嘌呤水平;此外,别嘌呤醇增加了AA的氧化,减少了纹状体DA的代谢产物。别嘌呤醇既不影响区域MPTP和MPP +水平,也不影响MPTP诱导的对纹状体DA氧化代谢的抑制。相反,MPTP诱导的尿酸水平升高以及黄嘌呤,次黄嘌呤和NA水平的降低被完全拮抗。这些发现表明,由黄嘌呤氧化酶介导的MPP(+)诱导的氧化应激可能至少与NA耗竭有关。此外,尿酸可作为神经元抗氧化剂池的活性成分具有生理作用。

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