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胆碱能传递中的腺嘌呤核苷酸:突触前方面。

Adenine nucleotides in cholinergic transmission: presynaptic aspects.

作者信息

Dowdall M J

出版信息

J Physiol (Paris). 1978;74(5):497-501.

PMID:217998
Abstract
  1. Isolated nerve terminals (T-sacs and synaptosomes) prepared from the purely cholinergic Torpedo electric organ have been studied for their ability to incorporate and metabolise [2-3H] adenosine and to degrade 5'-AMP to adenosine. 2. A temperature-dependent, saturable uptake system for adenosine was found with kinetic properties similar to nucleoside transport systems in other cells. The uptake system in Torpedo nerve terminals was inhibited by 2'-deoxyadenosine, a known inhibitor of adenosine transport. 3. Intraterminal adenosine is rapidly metabolised to a number of products including AMP, ADP and ATP. 4. Isolated nerve terminals contain considerable 5'-nucleotidase activity, most of which resides on the outer face of the external membrane. The Km of the enzyme is congruent to 5 micron and it is inhibited by a phosphonate analogue of ADP, alpha-beta-methylene-ADP. It is suggested that this 5'-nucleotidase plays an important role in the production of adenosine from a nucleotide pool in the synaptic cleft.
摘要
  1. 已对从纯胆碱能的电鳐电器官制备的分离神经末梢(T囊泡和突触体)摄取和代谢[2-³H]腺苷以及将5'-AMP降解为腺苷的能力进行了研究。2. 发现了一种对温度敏感的、可饱和的腺苷摄取系统,其动力学特性与其他细胞中的核苷转运系统相似。电鳐神经末梢中的摄取系统受到2'-脱氧腺苷(一种已知的腺苷转运抑制剂)的抑制。3. 末梢内的腺苷迅速代谢为多种产物,包括AMP、ADP和ATP。4. 分离的神经末梢含有相当数量的5'-核苷酸酶活性,其中大部分位于外膜的外表面。该酶的Km约为5微米,并且受到ADP的膦酸类似物α-β-亚甲基-ADP的抑制。有人提出,这种5'-核苷酸酶在从突触间隙中的核苷酸库产生腺苷的过程中起重要作用。

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