Department of Chemical and Pharmaceutical Engineering, College of Chemical Engineering, Huaqiao University, Xiamen 361021, Fujian Province, PR China.
Research Center of Natural Resources of Chinese Medicinal Materials and Ethnic Medicine, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, Jiangxi Province, PR China.
Steroids. 2019 Sep;149:108419. doi: 10.1016/j.steroids.2019.05.011. Epub 2019 May 30.
Our previous study has demonstrated that oleanolic acid produced an antidepressant-like effect in mice exposed to chronic stress. Considering that serine/threonine-protein kinase 1 (SGK1) is involved in stress response, the present study aimed to evaluate the involvement of SGK1 in the antidepressant-like effects of oleanolic acid in depression-like mice induced by long term corticosterone (CORT) injection. Behaviors, SGK1, brain-derived neurotrophic factor (BDNF) and its downstream targets were assessed after administration with oleanolic for three weeks. The results indicated that oleanolic acid increased the sucrose preference and decreased the immobility time. In addition, oleanolic acid decreased SGK1 and activated BDNF-AKT/mTOR signaling in the hippocampus of CORT-induced animals. However, we found that GSK650394, an inhibitor of SGK1 did not exert any effects on the behaviors, GR levels and BDNF signaling. The number of spines in hippocampal neurons was not changed by GSK650394 as well. Taken together, this study demonstrated that oleanolic acid produced the antidepressant-like effects, which might be related to the down-regulation of SGK1. However, inhibition of SGK1 directly lacks the effects in the treatment of depression.
我们之前的研究表明,齐墩果酸可在慢性应激的小鼠中产生抗抑郁样作用。鉴于丝氨酸/苏氨酸蛋白激酶 1(SGK1)参与应激反应,本研究旨在评估 SGK1 在长期皮质酮(CORT)注射诱导的抑郁样小鼠中齐墩果酸抗抑郁样作用中的作用。在给予齐墩果酸三周后,评估行为、SGK1、脑源性神经营养因子(BDNF)及其下游靶标。结果表明,齐墩果酸增加了蔗糖偏好,减少了不动时间。此外,齐墩果酸降低了 CORT 诱导动物海马中的 SGK1 并激活了 BDNF-AKT/mTOR 信号。然而,我们发现 SGK1 的抑制剂 GSK650394 对行为、GR 水平和 BDNF 信号没有任何影响。GSK650394 也没有改变海马神经元中的棘突数量。总之,这项研究表明,齐墩果酸产生了抗抑郁样作用,这可能与 SGK1 的下调有关。然而,直接抑制 SGK1 缺乏治疗抑郁症的作用。