Therapeutic role of long non-coding RNA TCONS_00019174 in depressive disorders is dependent on Wnt/β-catenin signaling pathway

Chronic stress is one of the major causes that lead to major depressive disorder (MDD), which is a prevalent mood disorder worldwide. Lots of MDD patients could not benefit from available medication due to the complex etiology of MDD. Recently, long non-coding RNAs (lncRNAs), molecular switches of d...

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Veröffentlicht in:Journal of integrative neuroscience 2018, Vol.17 (2), p.203-215
Hauptverfasser: Ni, Xinqiang, Liao, Yingzhao, Li, Limin, Zhang, Xiaoli, Wu, Zhengzhi
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Sprache:eng
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Zusammenfassung:Chronic stress is one of the major causes that lead to major depressive disorder (MDD), which is a prevalent mood disorder worldwide. Lots of MDD patients could not benefit from available medication due to the complex etiology of MDD. Recently, long non-coding RNAs (lncRNAs), molecular switches of downstream genes expression, have been reported to be involved in the pathogenesis of MDD. LncRNA TCONS_00019174 has been implicated in MDD risk and antidepressant effects, However, the effect of lncRNA TCONS_00019174 on antidepressant responses has not been investigated. This study is designed to determine whether altered expression of lncRNA TCONS_00019174 contributes to the depression-like behaviors associated with chronic stress. We found that mice exposed to chronic ultra-mild stress (CUMS) displayed apparent depression-like behaviors and decreased expression of lncRNA TCONS_00019174 in hippocampus. Both changed behaviors and lncRNA TCONS_00019174 expression level were rescued by chronic treatment of imipramine (IMI). Viral-mediated lncRNA TCONS_00019174 overexpression in hippocampal neurons improved behaviors of mice exposed to CUMS. Further, we found lncRNA TCONS_00019174 overexpression upregulated phosphorylated-GSK3β (p-GSK3β) protein and β-catenin in the hippocampus. These findings suggest that lncRNA TCONS_00019174 exerts antidepressant-like effect in mice by activating Wnt/β-catenin pathway, proposing that lncRNAs may serve as a potential therapeutic target for MDD in the clinical application.
ISSN:0219-6352
1757-448X
DOI:10.3233/JIN-170052