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大鼠脑突触体中快速腺苷摄取系统的一些生化特性。

Some biochemical properties of the rapid adenosine uptake system in rat brain synaptosomes.

作者信息

Bender A S, Wu P H, Phillis J W

出版信息

J Neurochem. 1981 Nov;37(5):1282-90. doi: 10.1111/j.1471-4159.1981.tb04679.x.

Abstract

The rapid uptake of adenosine into rat brain cortical synaptosomes is mediated by a facilitated diffusion process. The carrier mediated uptake is sensitive to pH and temperature. The average Q10 value for the system is approximately 1.77 and the necessary activation energy (Ea) is estimated to be 8870 cal/mol. These values are essentially in agreement with values reported for adenosine uptake carriers of other tissues. Substrate specificity of the uptake system in the CNS demonstrates that nucleotides do not interact with the carrier until they have been hydrolyzed to nucleosides. Structural modification of the purine moiety at the "2" position did not have a profound effect on the ability of the molecule to serve as a substrate for the uptake system. Competitive inhibition by sulfhydryl reagents, p-chloromercuribenzoate, and N-ethylmaleimide on adenosine uptake suggests a direct involvement of sulfhydryl group(s) in the uptake mechanism. Other purines and pyrimidines also inhibit adenosine uptake, suggesting that a variety of nucleosides can interact with a common carrier system.

摘要

腺苷快速进入大鼠脑皮质突触体是由易化扩散过程介导的。载体介导的摄取对pH值和温度敏感。该系统的平均Q10值约为1.77,所需的活化能(Ea)估计为8870卡/摩尔。这些值与其他组织中腺苷摄取载体报道的值基本一致。中枢神经系统摄取系统的底物特异性表明,核苷酸在水解为核苷之前不会与载体相互作用。嘌呤部分在“2”位的结构修饰对该分子作为摄取系统底物的能力没有深远影响。巯基试剂、对氯汞苯甲酸和N-乙基马来酰亚胺对腺苷摄取的竞争性抑制表明巯基直接参与摄取机制。其他嘌呤和嘧啶也抑制腺苷摄取,这表明多种核苷可与共同的载体系统相互作用。

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