首页> 外文期刊>International journal of developmental neuroscience: the official journal of the International Society for Developmental Neuroscience >Intrastriatal hypoxanthine administration affects Na+,K+-ATPase, acetylcholinesterase and catalase activities in striatum, hippocampus and cerebral cortex of rats.
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Intrastriatal hypoxanthine administration affects Na+,K+-ATPase, acetylcholinesterase and catalase activities in striatum, hippocampus and cerebral cortex of rats.

机译:纹状体次黄嘌呤的给药会影响大鼠纹状体,海马和大脑皮层中的Na +,K + -ATPase,乙酰胆碱酯酶和过氧化氢酶活性。

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The aim of this study was to investigate the effects of a single intrastriatal injection of hypoxanthine, the major metabolite accumulating in Lesch-Nyhan disease, on Na(+),K(+)-ATPase, acetylcholinesterase and catalase activities in striatum, cerebral cortex and hippocampus of rats at different post-infusion periods. Adult Wistar rats were divided in two groups: (1) vehicle-injected group (control) and (2) hypoxanthine-injected group. For Na(+),K(+)-ATPase activity determination, the animals were sacrificed 3h, 24h and 7 days after drug infusion. For the evaluation of acetylcholinesterase and catalase activities, the animals were sacrificed 30min, 3h, 24h and 7 days after hypoxanthine infusion. Results show regional and time dependent effects of hypoxanthine on Na(+),K(+)-ATPase, acetylcholinesterase and catalase activities. The in vitro effect of hypoxanthine on the same enzymes in striatum was also investigated. Results showed that hypoxanthine inhibited Na(+),K(+)-ATPase, but not the activities of acetylcholinesterase and catalase in rat striatum. We suggest that these modification on cerebral biochemical parameters (Na(+),K(+)-ATPase, acetylcholinesterase and catalase activities) induced by intrastriatal administration of hypoxanthine in all cerebral structures studied, striatum, hippocampus and cerebral cortex, could be involved in the pathophysiology of Lesch-Nyhan disease.
机译:这项研究的目的是调查纹状体内注射次黄嘌呤(Lesch-Nyhan病中积累的主要代谢产物)对纹状体,大脑皮层中Na(+),K(+)-ATPase,乙酰胆碱酯酶和过氧化氢酶活性的影响输注后不同时期大鼠的海马和海马。将成年Wistar大鼠分成两组:(1)媒介物注射组(对照组)和(2)次黄嘌呤注射组。为了测定Na(+),K(+)-ATPase活性,在输注药物后3h,24h和7天处死动物。为了评估乙酰胆碱酯酶和过氧化氢酶的活性,在次黄嘌呤输注后30分钟,3小时,24小时和7天处死动物。结果显示次黄嘌呤对Na(+),K(+)-ATPase,乙酰胆碱酯酶和过氧化氢酶活性的区域和时间依赖性影响。还研究了次黄嘌呤对纹状体内相同酶的体外作用。结果表明次黄嘌呤抑制大鼠纹状体中的Na(+),K(+)-ATPase,但不抑制乙酰胆碱酯酶和过氧化氢酶的活性。我们建议在研究的所有大脑结构,纹状体,海马和大脑皮层中纹状体内注射次黄嘌呤引起的脑生化参数(Na(+),K(+)-ATPase,乙酰胆碱酯酶和过氧化氢酶活性)的这些修饰Lesch-Nyhan病的病理生理学。

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