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海马切片中的长时程增强:丙酮酸脱氢酶的可能作用

Long-term potentiation in the hippocampal slice: possible involvement of pyruvate dehydrogenase.

作者信息

Hoch D B, Dingledine R J, Wilson J E

出版信息

Brain Res. 1984 Jun 4;302(1):125-34. doi: 10.1016/0006-8993(84)91292-7.

Abstract

Tetanic stimulation of fibers in the hippocampal slice preparation produces long-term potentiation (LTP) and also decreases the in vitro incorporation of phosphate into the alpha subunit of pyruvate dehydrogenase (alpha PDH). This paper describes 6 experiments that were undertaken to replicate this observation. Hippocampal slices were incubated in a specially designed chamber and stimulated with a tungsten wire electrode in the stratum radiatum for 1 s at 100 Hz. Two minutes after the tetanus, the stimulated slices were removed alternately with control (not tetanized) slices and each group was pooled for subcellular fractionation and labeling of the fractions with [32P]ATP. Proteins were separated by electrophoresis and relative 32P contents of 41K and 50K protein bands were studied. Tetanic stimulation of the stratum radiatum did not affect subsequent phosphorylation of a 50K Mr protein that has been reported to be altered by perforant path activation. Stimulation also had no effect on pyruvate dehydrogenase enzyme activity or on the ratio of active (dephosphorylated) to inactive enzyme. In most cases tetanic stimulation produced no significant change in the in vitro phosphorylation of this enzyme. Only under one set of conditions, labeling with 250 microM [gamma-32P]ATP for 10 s, was a decrease in the in vitro labeling of alpha PDH shown to be statistically significant. These findings suggest that LTP is not necessarily accompanied by an initial change in PDH phosphorylation level or activity but may be associated with a decrease in the kinase activity directed toward this protein.

摘要

对海马脑片制备中的纤维进行强直刺激可产生长时程增强(LTP),并且还会降低体外磷酸盐掺入丙酮酸脱氢酶α亚基(αPDH)的量。本文描述了为重复这一观察结果而进行的6项实验。将海马脑片置于一个特别设计的小室中,并用钨丝电极在辐射层以100Hz的频率刺激1秒。强直刺激后两分钟,交替取出受刺激的脑片和对照(未进行强直刺激)脑片,将每组脑片合并进行亚细胞分级分离,并用[32P]ATP对各组分进行标记。通过电泳分离蛋白质,并研究41K和50K蛋白条带的相对32P含量。对辐射层的强直刺激并不影响一种据报道会因穿通通路激活而发生改变的50K Mr蛋白的后续磷酸化。刺激对丙酮酸脱氢酶的酶活性或活性(去磷酸化)与无活性酶的比例也没有影响。在大多数情况下,强直刺激并未使该酶的体外磷酸化产生显著变化。只有在一组条件下,即使用250μM[γ-32P]ATP标记10秒时,αPDH的体外标记减少才具有统计学意义。这些发现表明,LTP不一定伴随着PDH磷酸化水平或活性的初始变化,但可能与针对该蛋白的激酶活性降低有关。

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