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蛋白激酶 A 的 RIβ 亚基缺失导致大鼠出现震颤和恐惧条件反射记忆受损。

Deficiency of the RIβ subunit of protein kinase A causes body tremor and impaired fear conditioning memory in rats.

机构信息

Laboratory of Animal Nutrition, Department of Animal Science, Faculty of Agriculture, Tokyo University of Agriculture, 1737 Funako, Atsugi, Kanagawa, 243-0034, Japan.

Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan.

出版信息

Sci Rep. 2021 Jan 21;11(1):2039. doi: 10.1038/s41598-021-81515-x.

Abstract

The RIβ subunit of cAMP-dependent protein kinase (PKA), encoded by Prkar1b, is a neuronal isoform of the type I regulatory subunit of PKA. Mice lacking the RIβ subunit exhibit normal long-term potentiation (LTP) in the Schaffer collateral pathway of the hippocampus and normal behavior in the open-field and fear conditioning tests. Here, we combined genetic, electrophysiological, and behavioral approaches to demonstrate that the RIβ subunit was involved in body tremor, LTP in the Schaffer collateral pathway, and fear conditioning memory in rats. Genetic analysis of WTC-furue, a mutant strain with spontaneous tremors, revealed a deletion in the Prkar1b gene of the WTC-furue genome. Prkar1b-deficient rats created by the CRISPR/Cas9 system exhibited body tremor. Hippocampal slices from mutant rats showed deficient LTP in the Schaffer collateral-CA1 synapse. Mutant rats also exhibited decreased freezing time following contextual and cued fear conditioning, as well as increased exploratory behavior in the open field. These findings indicate the roles of the RIβ subunit in tremor pathogenesis and contextual and cued fear memory, and suggest that the hippocampal and amygdala roles of this subunit differ between mice and rats and that rats are therefore beneficial for exploring RIβ function.

摘要

环腺苷酸依赖蛋白激酶(PKA)的 RIβ 亚基(由 Prkar1b 编码)是 PKA 的 I 型调节亚基的神经元同工型。缺乏 RIβ 亚基的小鼠在海马体 Schaffer 侧支通路中表现出正常的长时程增强(LTP),并且在旷场和恐惧条件反射测试中表现出正常的行为。在这里,我们结合遗传、电生理和行为方法,证明 RIβ 亚基参与了大鼠的躯体震颤、Schaffer 侧支通路中的 LTP 和恐惧条件反射记忆。对具有自发性震颤的突变株 WTC-furue 的遗传分析显示,WTC-furue 基因组中的 Prkar1b 基因缺失。通过 CRISPR/Cas9 系统创建的 Prkar1b 缺陷型大鼠表现出躯体震颤。来自突变大鼠的海马切片显示 Schaffer 侧支-CA1 突触中的 LTP 不足。突变大鼠在情境和线索恐惧条件反射后也表现出冻结时间减少,以及在旷场中探索行为增加。这些发现表明 RIβ 亚基在震颤发病机制以及情境和线索恐惧记忆中起作用,并表明该亚基在小鼠和大鼠中的海马和杏仁核作用不同,因此大鼠有利于探索 RIβ 功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc1e/7820254/c292ce6f3cc8/41598_2021_81515_Fig1_HTML.jpg

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