低冲击安帕金 CX1739 在啮齿动物中发挥促进认知的作用并逆转鸦片制剂引起的呼吸抑制

Daniel Pierce Radin, S. Zhong, Rok Cerne, Mohammed Shoaib, Jeffrey M Witkin, A. Lippa
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摘要

AMPA 谷氨酸受体(AMPARs)在整个中枢神经系统中都有表达,并介导了大部分快速兴奋性突触传递。安帕金是一种口服小分子药物,能与 AMPARs 异源结合,增强内源性激动剂谷氨酸诱发的兴奋电流。在临床前研究中,安非他酮能有效改善一系列神经退行性疾病和神经精神疾病的症状,在这些疾病中,兴奋传递会受到损害。然而,由于某些安帕金类药物在啮齿类动物中出现神经毒性和癫痫发作,导致安帕金类药物作为药物的发展缓慢。在这里,我们描述了一种新型安帕金--N-甲基-N-(四氢-2H-吡喃-4-基)苯并[c][1,2,5]恶二唑-5-甲酰胺(CX1739)的临床前药理学。CX1739 可剂量依赖性地增强大鼠体内的长期电位,这一过程被认为是学习和记忆的分子基质。相应地,CX1739 还能提高大鼠在新物体识别测试、赢移径向臂迷宫和五选一连续反应时间任务等多种认知测试中的表现。CX1739 还能减弱苯丙胺诱导的运动活动,这表明它可以与兴奋剂一起使用,以提高认知能力,同时减轻基于兴奋剂的多动症药物的副作用。CX1739 还能迅速逆转阿片类药物引起的呼吸抑制。虽然这些测试中的疗效发生在 0.03-18 毫克/千克的剂量下,但在对大鼠进行的安全性研究(最高达 2000 毫克/千克)中未发现任何不良事件。这些临床前研究结果表明,CX1739 可以安全地应用于临床,用于治疗痴呆症、神经精神障碍以及鸦片制剂引起的内源性吸气呼吸节律抑制这一危及生命的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-Impact Ampakine CX1739 Exerts Pro-Cognitive Effects and Reverses Opiate-Induced Respiratory Depression in Rodents
AMPA-glutamate receptors (AMPARs) are expressed throughout the CNS and mediate the majority of fast excitatory synaptic transmission. Ampakines are orally available small molecules that bind allosterically to AMPARs and enhance excitatory currents elicited by the endogenous agonist glutamate. In preclinical studies, ampakines are effective in ameliorating symptoms in a battery of neurodegenerative and neuropsychiatric diseases in which excitatory transmission is compromised. However, the development of ampakines as medicines was slowed by the emergence of neurotoxicity and seizures in rodents due to some ampakines. Here, we describe the preclinical pharmacology of a novel ampakine, N-methyl-N-(tetrahydro-2H-pyran-4-yl)benzo[c][1,2,5] oxadiazole-5-carboxamide (CX1739), that does not induce seizures in animals or humans at efficacious doses. CX1739 dose-dependently enhanced long-term potentiation in vivo in rats, a process thought to be a molecular substrate of learning and memory. Correspondingly, CX1739 dose-dependently enhanced performance in assays that probed multiple aspects of cognition—the novel object recognition test, the win shift radial arm maze, and the five-choice serial reaction time task in rats. CX1739 also abrogated amphetamine-induced locomotor activity, demonstrating that it may be given in conjunction with stimulants for pro-cognitive gains while mitigating the side effects of stimulant-based ADHD medications. CX1739 also rapidly reversed opioid-induced respiratory depression. While efficacy in these tests occurred at doses of 0.03–18 mg/kg, there were no adverse events detected in safety studies in rats up to 2000 mg/kg. These preclinical findings suggest that CX1739 can be translated safely into the clinical setting to potentially treat dementia, neuropsychiatric disorders, and the life-threatening complication of opiate-induced suppression of endogenous inspiratory breathing rhythms.
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