Department of Chemical and Pharmaceutical Engineering, College of Chemical Engineering, Huaqiao University, Xiamen 361021, Fujian Province, PR China; Institute of Pharmaceutical Engineering, Huaqiao University, Xiamen 361021, Fujian Province, PR China.
Xiamen Hospital of Traditional Chinese Medicine, Xiamen 361009, Fujian Province, PR China.
Prog Neuropsychopharmacol Biol Psychiatry. 2017 Oct 3;79(Pt B):417-425. doi: 10.1016/j.pnpbp.2017.07.024. Epub 2017 Jul 29.
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.
MicroRNA (miRNA) 失调已被证明与抑郁症的早期观察结果有关。miR-124 是大脑中最丰富的 microRNA。先前的研究表明,miR-124 在抑郁症中发挥着重要作用。在这里,我们在 HEK 293 细胞中显示 miR-124 直接靶向糖皮质激素受体 (GR)。此外,用其反义寡核苷酸 (2nmol/每两天) 抑制 miR-124 可以逆转慢性皮质酮 (CORT,40mg/kg) 注射暴露的小鼠中蔗糖偏好的降低和不动时间的增加。此外,这些行为改善的效果与脑源性神经营养因子 (BDNF)、TrkB、ERK 和 CREB 的激活以及突触形成和神经元增殖的诱导有关。总之,我们的研究表明,miR-124 可以作为抑郁症的生物标志物和药物开发的新靶点,并表明抑制 miR-124 可能通过激活海马中的 BDNF-TrkB 信号通路成为治疗抑郁症的一种策略。