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Energy Metabolism of Synaptosomes from Different Neuronal Systems of Rat Cerebellum During Aging: A Functional Proteomic Characterization

机译:衰老过程中大鼠小脑不同神经元系统突触体的能量代谢:功能蛋白质组学表征

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摘要

Functional proteomics was used to characterize age-related changes in energy metabolism of different neuronal pathways within the cerebellar cortex of Wistar rats aged 2, 6, 12, 18, and 24 months. The "large" synaptosomes, derived from the glutamatergic mossy fibre endings which make synaptic contact with the granule cells of the granular layer, and the "small" synaptosomes, derived from the pre-synaptic terminals of granule cells making synaptic contact with the dendrites of Purkinje cells, were isolated by a combined differential/gradient centrifugation technique. Because most brain disorders are associated with bioenergetic changes, the maximum rate (V-max) of selected enzymes of glycolysis, Krebs' cycle, glutamate and amino acids metabolism, and acetylcholine catabolism were evaluated. The results show that "large" and "small" synaptosomes possess specific and independent metabolic features. This study represents a reliable model to study in vivo (1) the physiopathological molecular mechanisms of some brain diseases dependent on energy metabolism, (2) the responsiveness to noxious stimuli, and (3) the effects of drugs, discriminating their action sites at subcellular level on specific neuronal pathways.
机译:功能蛋白质组学用于表征 2、6、12、18 和 24 个月大的 Wistar 大鼠小脑皮层内不同神经元通路能量代谢的年龄相关变化。通过差分/梯度联合离心技术分离出“大”突触体,来源于与颗粒层颗粒细胞发生突触接触的谷氨酸能苔藓纤维末端,以及来源于颗粒细胞突触前末端的“小”突触体与浦肯野细胞的树突接触。由于大多数脑部疾病与生物能量变化有关,因此评估了糖酵解、克雷布斯循环、谷氨酸和氨基酸代谢以及乙酰胆碱分解代谢等选定酶的最大速率 (V-max)。结果表明,“大”和“小”突触体具有特异性和独立的代谢特征。这项研究代表了一个可靠的模型,可以在体内研究 (1) 一些依赖于能量代谢的脑部疾病的生理病理分子机制,(2) 对有害刺激的反应,以及 (3) 药物的影响,区分它们在亚细胞水平上的作用位点对特定神经元通路。

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