| Literature DB >> 32989244 |
Hyun-Ju Lee1,2, Tae-Ik Choi3, Yong-Min Kim4,5, Soonje Lee4,5, Bing Han3,6, In Seon Bak6, Sun Ae Moon7,8, Dae-Yeul Yu6, Ki Soon Shin4,5, Yunhee Kim Kwon4,5, Cheil Moon7,8, Jae Hwan Ryu1, Hyang-Sook Hoe2, Cheol-Hee Kim9, Insop Shim10.
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.Entities:
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Year: 2020 PMID: 32989244 DOI: 10.1038/s41380-020-00893-2
Source DB: PubMed Journal: Mol Psychiatry ISSN: 1359-4184 Impact factor: 13.437