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自由活动大鼠海马亚区蛋白质合成的长时程增强诱导变化:时间进程

Long-term potentiation induced changes in protein synthesis of hippocampal subfields of freely moving rats: time-course.

作者信息

Frey S, Schwiegert C, Krug M, Lössner B

机构信息

Institute of Pharmacology and Toxicology, Medical Academy Magdeburg, FRG.

出版信息

Biomed Biochim Acta. 1991;50(12):1231-40.

PMID:1824541
Abstract

The incorporation of L-[U-14C]leucine into proteins of cytosolic (soluble proteins) and of the 100,000 x g pellet fraction from ipsilateral hippocampal subfields (CA1, CA3, CA4/area dentata) of rats was studied during and at various times after electrical tetanisation of the right perforant pathway using topical precursor applications and 1 h incorporation periods. Rates of protein synthesis were estimated calculating the relative specific radioactivity of proteins (RSA). The RSA-values of both protein fractions estimated in the ipsilateral CA4/area dentata were found to be about two times higher in tetanised rats compared to either passive or stimulated controls (p less than 0.05) when leucine was administered 5 min after tetanisation. Under these conditions, no differences between tetanised and control animals were observed in all other hippocampal subfields studied. No differences in RSA-values evaluated in CA4/area dentata between tetanised and passive controls were detected when leucine was administered immediately prior to tetanisation. From 2 h to 8 h after induction of LTP, protein synthesis in CA4/area dentata of tetanised rats appeared to be decreased (p less than 0.05) compared to passive controls. These results provide evidence for a transient LTP-induced augmentation of protein synthesis in the targets which might be an essential prerequisite for those structural changes realising the long-lasting enhanced efficacy of synaptic transmission at perforant path/granular cells connections.

摘要

利用局部前体应用和1小时的掺入期,研究了在右侧穿通通路电强直刺激期间及之后的不同时间,L-[U-¹⁴C]亮氨酸掺入大鼠同侧海马亚区(CA1、CA3、CA4/齿状回)胞质(可溶性蛋白)和100,000×g沉淀部分蛋白质中的情况。通过计算蛋白质的相对比放射性(RSA)来估计蛋白质合成速率。当强直刺激后5分钟给予亮氨酸时,发现在强直刺激的大鼠中,同侧CA4/齿状回中估计的两种蛋白质组分的RSA值比被动或刺激对照组大约高两倍(p<0.05)。在这些条件下,在所研究的所有其他海马亚区中,未观察到强直刺激动物与对照动物之间的差异。当在强直刺激前立即给予亮氨酸时,在CA4/齿状回中评估的RSA值在强直刺激组和被动对照组之间未检测到差异。在诱导长时程增强(LTP)后2小时至8小时,与被动对照组相比,强直刺激大鼠的CA4/齿状回中的蛋白质合成似乎减少(p<0.05)。这些结果为LTP诱导的靶标蛋白质合成的短暂增强提供了证据,这可能是实现穿通通路/颗粒细胞连接处突触传递长期增强效能的那些结构变化的必要前提。

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