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大鼠脑中多胺的摄取、结合与释放

Polyamine uptake, binding and release in rat brain.

作者信息

Gilad G M, Gilad V H

机构信息

Neuropsychiatry Branch, NIMH Neuroscience Center, Saint Elizabeths Hospital, Washington, DC 20032.

出版信息

Eur J Pharmacol. 1991 Jan 25;193(1):41-6. doi: 10.1016/0014-2999(91)90198-y.

Abstract

The uptake, binding and release of the polyamines, spermidine and spermine, and of their diamine precursor, putrescine, were examined in synaptosomal preparations from rat hippocampus. The specific and relatively high-affinity uptake by synaptosomes was found only with putrescine (Vmax = 21.6 pmol/mg protein per h; Km = 28.6 nM) and not with the other polyamines. In contrast, specific binding to membranes was found for spermidine (Bmax = 28.6 pmol/mg protein; Kd = 42.9 nM) and for spermine (Bmax = 156.3 pmol/mg protein; Kd = 83.3 nM), but not for putrescine. High potassium concentrations (35 mM) both induced the release of accumulated polyamines from synaptosomes and inhibited their binding. Specific polyamine binding evidently occurs selectively on the inner but not on the outer synaptosomal membranes.

摘要

在大鼠海马体的突触体制剂中,研究了多胺、亚精胺和精胺及其二胺前体腐胺的摄取、结合和释放情况。仅发现突触体对腐胺有特异性且相对高亲和力的摄取(Vmax = 21.6 pmol/mg蛋白质每小时;Km = 28.6 nM),而对其他多胺则没有。相反,发现亚精胺(Bmax = 28.6 pmol/mg蛋白质;Kd = 42.9 nM)和精胺(Bmax = 156.3 pmol/mg蛋白质;Kd = 83.3 nM)能与膜特异性结合,而腐胺则不能。高钾浓度(35 mM)既诱导突触体中积累的多胺释放,又抑制它们的结合。特异性多胺结合显然选择性地发生在突触体内膜而非外膜上。

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