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缰核 G 蛋白 γ8 通过调节中枢乙酰胆碱系统对学习记忆的调控。

Regulation of habenular G-protein gamma 8 on learning and memory via modulation of the central acetylcholine system.

机构信息

Department of Physiology, College of Medicine, Kyung Hee University, Seoul, 02435, Republic of Korea.

Department of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu, 41068, Republic of Korea.

出版信息

Mol Psychiatry. 2021 Aug;26(8):3737-3750. doi: 10.1038/s41380-020-00893-2. Epub 2020 Sep 28.

DOI:10.1038/s41380-020-00893-2
PMID:32989244
Abstract

Guanine nucleotide binding protein (G protein) gamma 8 (Gng8) is a subunit of G proteins and expressed in the medial habenula (MHb) and interpeduncular nucleus (IPN). Recent studies have demonstrated that Gng8 is involved in brain development; however, the roles of Gng8 on cognitive function have not yet been addressed. In the present study, we investigated the expression of Gng8 in the brain and found that Gng8 was predominantly expressed in the MHb-IPN circuit of the mouse brain. We generated Gng8 knockout (KO) mice by CRISPR/Cas9 system in order to assess the role of Gng8 on cognitive function. Gng8 KO mice exhibited deficiency in learning and memory in passive avoidance and Morris water maze tests. In addition, Gng8 KO mice significantly reduced long-term potentiation (LTP) in the hippocampus compared to that of wild-type (WT) mice. Furthermore, we observed that levels of acetylcholine (ACh) and choline acetyltransferase (ChAT) in the MHb and IPN of Gng8 KO mice were significantly decreased, compared to WT mice. The administration of nAChR α4β2 agonist A85380 rescued memory impairment in the Gng8 KO mice, suggesting that Gng8 regulates cognitive function via modulation of cholinergic activity. Taken together, Gng8 is a potential therapeutic target for memory-related diseases and/or neurodevelopmental diseases.

摘要

鸟嘌呤核苷酸结合蛋白(G 蛋白)γ 8(Gng8)是 G 蛋白的一个亚基,在中脑缰核(MHb)和脚间核(IPN)中表达。最近的研究表明,Gng8 参与了大脑发育;然而,Gng8 对认知功能的作用尚未得到解决。在本研究中,我们研究了 Gng8 在大脑中的表达,发现 Gng8 主要在小鼠大脑的 MHb-IPN 回路中表达。我们通过 CRISPR/Cas9 系统生成了 Gng8 敲除(KO)小鼠,以评估 Gng8 对认知功能的作用。Gng8 KO 小鼠在被动回避和 Morris 水迷宫测试中表现出学习和记忆缺陷。此外,与野生型(WT)小鼠相比,Gng8 KO 小鼠的海马体长时程增强(LTP)显著减少。此外,我们观察到 Gng8 KO 小鼠 MHb 和 IPN 中的乙酰胆碱(ACh)和胆碱乙酰转移酶(ChAT)水平明显低于 WT 小鼠。nAChR α4β2 激动剂 A85380 的给药挽救了 Gng8 KO 小鼠的记忆障碍,表明 Gng8 通过调节胆碱能活性来调节认知功能。综上所述,Gng8 是与记忆相关疾病和/或神经发育疾病的潜在治疗靶点。

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