Department of Pharmacology, School of Pharmacy, Nantong University, Nantong, 226001, Jiangsu, China; Provincial Key Laboratory of Inflammation and Molecular Drug Target, Nantong, 226001, Jiangsu, China.
Department of Pharmacy, The Sixth People's Hospital of Nantong, Nantong, 226011, Jiangsu, China.
Behav Brain Res. 2021 Feb 5;399:113038. doi: 10.1016/j.bbr.2020.113038. Epub 2020 Dec 1.
Antidepressants currently used in clinical practice have limitations such as low efficacy, slow onset and various adverse reactions. It has become necessary to develop novel antidepressants beyond monoaminergic drugs. L-701,324 is a potent NMDA receptor antagonist, and the purpose of this study was to investigate the possible antidepressant effects of L-701,324 in mice. Here, various methods including the forced swim test (FST), tail suspension test (TST), chronic unpredictable mild stress (CUMS) model of depression, western blotting and immunofluorescence, were used together. A single injection of L-701,324 exhibited antidepressant-like potential in the FST and TST without affecting the locomotor activity of mice. Repeated injection of L-701,324 not only prevented CUMS-induced depressive-like behaviors in mice, but also ameliorated the downregulating effects of CUMS on the hippocampal BDNF signaling cascade and neurogenesis. Furthermore, K252a, a potent inhibitor of the BDNF system, fully blocked the antidepressant-like activity of L-701,324 in mice. K252a administration also abolished the activating actions of L-701,324 on the hippocampal BDNF signaling cascade and neurogenesis in CUMS-treated mice. Collectively, these data indicated that L-701,324 possesses antidepressant-like activity in mice, which was mediated, at least in part, by promoting the hippocampal BDNF system.
目前临床上使用的抗抑郁药存在疗效低、起效慢、不良反应多等局限性。因此,有必要开发新型抗抑郁药,超越单胺能药物。L-701,324 是一种有效的 NMDA 受体拮抗剂,本研究旨在探讨 L-701,324 对小鼠的潜在抗抑郁作用。在此,我们采用了强迫游泳试验(FST)、悬尾试验(TST)、慢性不可预测轻度应激(CUMS)抑郁模型、Western blot 和免疫荧光等多种方法。单次注射 L-701,324 可在 FST 和 TST 中表现出抗抑郁样作用,而不影响小鼠的运动活性。重复注射 L-701,324 不仅可以预防 CUMS 诱导的小鼠抑郁样行为,还可以改善 CUMS 对海马 BDNF 信号级联和神经发生的下调作用。此外,BDNF 系统的强效抑制剂 K252a 完全阻断了 L-701,324 在小鼠中的抗抑郁样作用。K252a 给药也消除了 L-701,324 在 CUMS 处理的小鼠中海马 BDNF 信号级联和神经发生中的激活作用。综上所述,这些数据表明 L-701,324 对小鼠具有抗抑郁样作用,至少部分是通过促进海马 BDNF 系统介导的。