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Lanicemine: a low-trapping NMDA channel blocker produces sustained antidepressant efficacy with minimal psychotomimetic adverse effects

机译:Lanicemine:一种低捕集性NMDA通道阻滞剂,可产生持续的抗抑郁药功效,同时最小化拟精神病药物的不良反应

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摘要

Ketamine, an N-methyl-D-aspartate receptor (NMDAR) channel blocker, has been found to induce rapid and robust antidepressant-like effects in rodent models and in treatment-refractory depressed patients. However, the marked acute psychological side effects of ketamine complicate the interpretation of both preclinical and clinical data. Moreover, the lack of controlled data demonstrating the ability of ketamine to sustain the antidepressant response with repeated administration leaves the potential clinical utility of this class of drugs in question. Using quantitative electroencephalography (qEEG) to objectively align doses of a low-trapping NMDA channel blocker, AZD6765 (lanicemine), to that of ketamine, we demonstrate the potential for NMDA channel blockers to produce antidepressant efficacy without psychotomimetic and dissociative side effects. Furthermore, using placebo-controlled data, we show that the antidepressant response to NMDA channel blockers can be maintained with repeated and intermittent drug administration. Together, these data provide a path for the development of novel glutamatergic-based therapeutics for treatment-refractory mood disorders.
机译:氯胺酮是一种N-甲基-D-天冬氨酸受体(NMDAR)通道阻滞剂,已在啮齿动物模型和难治性抑郁症患者中诱导出快速而稳定的抗抑郁药样作用。然而,氯胺酮的明显的急性心理副作用使临床前和临床数据的解释变得复杂。而且,缺乏证明氯胺酮通过反复给药维持抗抑郁反应能力的受控数据的缺乏,使得这类药物具有潜在的临床应用价值。使用定量脑电图(qEEG)客观地将低捕集性NMDA通道阻滞剂AZD6765(lanicemine)的剂量与氯胺酮对齐,我们证明了NMDA通道阻滞剂具有产生抗抑郁功效而不产生拟精神分裂和解离副作用的潜力。此外,使用安慰剂对照的数据,我们表明可以通过重复和间歇给药来维持对NMDA通道阻滞剂的抗抑郁反应。总之,这些数据为开发用于治疗难治性情绪障碍的新型基于谷氨酸能的疗法提供了途径。

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