| Literature DB >> 28764913 |
Shuang-Shuang Wang1, Rong-Hao Mu1, Cheng-Fu Li2, Shu-Qi Dong1, Di Geng3, Qing Liu3, Li-Tao Yi4.
Abstract
Dysregulation of microRNA (miRNA) has been shown to be involved in early observations of depression. MicroRNA-124-3p (miR-124) is the most abundant microRNA in the brain. Previous studies have shown that miR-124 plays a major role in depression. Here we showed that miR-124 directly targeted glucocorticoid receptor (GR) in HEK 293 cells. In addition, inhibition of miR-124 by its antagomir (2nmol/every two days) could reverse the decrease of sucrose preference and the increase of immobility time in mice exposed to chronic corticosterone (CORT, 40mg/kg) injection. Moreover, these effects on behavioral improvement were coupled to the activation of brain-derived neurotrophic factor (BDNF), TrkB, ERK, and CREB, as well as the induction of synaptogenesis and neuronal proliferation. Altogether, our study suggests that miR-124 can be served as a biomarker for depression and a novel target for drug development, and demonstrates that inhibition of miR-124 may be a strategy for treating depression by activating BDNF-TrkB signaling pathway in the hippocampus.Entities:
Keywords: Brain-derived neurotrophic factor (BDNF); Depression; Glucocorticoid receptor (GR); Hippocampus; microRNA (miRNA)
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Year: 2017 PMID: 28764913 DOI: 10.1016/j.pnpbp.2017.07.024
Source DB: PubMed Journal: Prog Neuropsychopharmacol Biol Psychiatry ISSN: 0278-5846 Impact factor: 5.067