Department of Psychiatry, University of Maryland School of Medicine , Baltimore, MD 21201.
Department of Physiology, University of Maryland School of Medicine , Baltimore, MD 21201.
eNeuro. 2017 Mar 7;4(1). doi: 10.1523/ENEURO.0285-16.2017. eCollection 2017 Jan-Feb.
New antidepressant pharmacotherapies that provide rapid relief of depressive symptoms are needed. The NMDA receptor antagonist ketamine exerts rapid antidepressant actions in depressed patients but also side effects that complicate its clinical utility. Ketamine promotes excitatory synaptic strength, likely by producing highfrequency correlated activity in mood-relevant regions of the forebrain. Negative allosteric modulators of GABA-A receptors containing α5 subunits (α5 GABA-NAMs) should also promote highfrequency correlated electroencephalogram EEG) activity and should therefore exert rapid antidepressant responses. Because α5 subunits display a restricted expression in the forebrain, we predicted that α5 GABA-NAMs would produce activation of principle neurons but exert fewer side effects than ketamine. We tested this hypothesis in male mice and observed that the α5 GABA-NAM MRK-016 exerted an antidepressant-like response in the forced swim test at 1 and 24 h after administration and an anti-anhedonic response after chronic stress in the female urine sniffing test (FUST). Like ketamine, MRK-016 produced a transient increase in EEG γ power, and both the increase in γ power and its antidepressant effects in the forced swim test were blocked by prior administration of the AMPA-type glutamate receptor antagonist 2,3-dioxo-6-nitro-1,2,3,4-tetrahydrobenzo[]quinoxaline-7-sulfonamide (NBQX). Unlike ketamine, however, MRK-016 produced no impairment of rota-rod performance, no reduction of prepulse inhibition (PPI), no conditionedplace preference (CPP), and no change in locomotion. α5 GABA-NAMs, thus reproduce the rapid antidepressant-like actions of ketamine, perhaps via an AMPA receptor (AMPAR)-dependent increase in coherent neuronal activity, but display fewer potential negative side effects. These compounds thus demonstrate promise as clinically useful fast-acting antidepressants.
需要新的抗抑郁药治疗方法,以快速缓解抑郁症状。NMDA 受体拮抗剂氯胺酮在抑郁患者中迅速发挥抗抑郁作用,但也有一些副作用,使其临床应用复杂化。氯胺酮增强兴奋性突触强度,可能通过在前脑与情绪相关的区域产生高频相关活动。包含 α5 亚基的 GABA-A 受体的负变构调节剂(α5 GABA-NAMs)也应该促进高频相关脑电图(EEG)活动,因此应该产生快速的抗抑郁反应。由于 α5 亚基在前脑中有受限表达,我们预测 α5 GABA-NAMs 将激活主要神经元,但产生的副作用比氯胺酮少。我们在雄性小鼠中测试了这一假设,观察到 α5 GABA-NAM MRK-016 在给药后 1 小时和 24 小时的强迫游泳试验中表现出抗抑郁样反应,在慢性应激后的雌性尿液嗅探试验(FUST)中表现出抗快感缺失反应。与氯胺酮一样,MRK-016 导致 EEG γ 功率短暂增加,γ 功率增加及其在强迫游泳试验中的抗抑郁作用均被 AMPA 型谷氨酸受体拮抗剂 2,3-二氧代-6-硝基-1,2,3,4-四氢苯并喹喔啉-7-磺酰胺(NBQX)预先给药阻断。然而,与氯胺酮不同,MRK-016 不会损害转棒性能,不会降低前脉冲抑制(PPI),不会产生条件性位置偏爱(CPP),也不会改变运动。α5 GABA-NAMs 因此复制了氯胺酮的快速抗抑郁样作用,可能通过 AMPA 受体(AMPAR)依赖性增加相干神经元活动,但显示出较少的潜在负面副作用。这些化合物因此有望成为具有临床应用价值的快速作用抗抑郁药。