Departments of Chemistry and Molecular Biosciences, Chemistry of Life Processes Institute, Center for Molecular Innovation and Drug Discovery, and Center for Developmental Therapeutics, Northwestern University , Evanston, Illinois 60208, United States.
Department of Chemistry and Biochemistry, Loyola University Chicago , Chicago, Illinois 60660, United States.
J Am Chem Soc. 2018 Feb 14;140(6):2151-2164. doi: 10.1021/jacs.7b10965. Epub 2018 Jan 30.
γ-Aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the central nervous system. Inhibition of GABA aminotransferase (GABA-AT), a pyridoxal 5'-phosphate (PLP)-dependent enzyme that degrades GABA, has been established as a possible strategy for the treatment of substance abuse. The raised GABA levels that occur as a consequence of this inhibition have been found to antagonize the rapid release of dopamine in the ventral striatum (nucleus accumbens) that follows an acute challenge by an addictive substance. In addition, increased GABA levels are also known to elicit an anticonvulsant effect in patients with epilepsy. We previously designed the mechanism-based inactivator (1S,3S)-3-amino-4-difluoromethylenyl-1-cyclopentanoic acid (2), now called CPP-115, that is 186 times more efficient in inactivating GABA-AT than vigabatrin, the only FDA-approved drug that is an inactivator of GABA-AT. CPP-115 was found to have high therapeutic potential for the treatment of cocaine addiction and for a variety of epilepsies, has successfully completed a Phase I safety clinical trial, and was found to be effective in the treatment of infantile spasms (West syndrome). Herein we report the design, using molecular dynamics simulations, synthesis, and biological evaluation of a new mechanism-based inactivator, (S)-3-amino-4-(difluoromethylenyl)cyclopent-1-ene-1-carboxylic acid (5), which was found to be almost 10 times more efficient as an inactivator of GABA-AT than CPP-115. We also present the unexpected crystal structure of 5 bound to GABA-AT, as well as computational analyses used to assist the structure elucidation process. Furthermore, 5 was found to have favorable pharmacokinetic properties and low off-target activities. In vivo studies in freely moving rats showed that 5 was dramatically superior to CPP-115 in suppressing the release of dopamine in the corpus striatum, which occurs subsequent to either an acute cocaine or nicotine challenge. Compound 5 also attenuated increased metabolic demands (neuronal glucose metabolism) in the hippocampus, a brain region that encodes spatial information concerning the environment in which an animal receives a reinforcing or aversive drug. This multidisciplinary computational design to preclinical efficacy approach should be applicable to the design and improvement of mechanism-based inhibitors of other enzymes whose crystal structures and inactivation mechanisms are known.
γ-氨基丁酸(GABA)是中枢神经系统中主要的抑制性神经递质。抑制 GABA 氨基转移酶(GABA-AT),一种依赖吡哆醛 5'-磷酸(PLP)的酶,可降解 GABA,已被确定为治疗物质滥用的一种可能策略。由于这种抑制作用,GABA 水平升高,已发现其拮抗腹侧纹状体(伏隔核)中多巴胺的快速释放,这种释放是由成瘾物质的急性挑战引起的。此外,增加 GABA 水平也已知在癫痫患者中产生抗惊厥作用。我们之前设计了基于机制的失活剂(1S,3S)-3-氨基-4-二氟亚甲基-1-环戊烷羧酸(2),现在称为 CPP-115,比唯一被 FDA 批准的 GABA-AT 失活剂 vigabatrin 对 GABA-AT 的失活效率高 186 倍。CPP-115 被发现具有治疗可卡因成瘾和各种癫痫的高治疗潜力,已成功完成 I 期安全性临床试验,并被发现对婴儿痉挛症(West 综合征)有效。本文报告了使用分子动力学模拟、合成和生物学评估一种新的基于机制的失活剂(S)-3-氨基-4-(二氟亚甲基)环戊-1-烯-1-羧酸(5)的设计,发现其对 GABA-AT 的失活效率比 CPP-115 高近 10 倍。我们还介绍了 5 与 GABA-AT 结合的出乎意料的晶体结构,以及用于辅助结构阐明过程的计算分析。此外,5 具有良好的药代动力学特性和低脱靶活性。在自由活动大鼠的体内研究表明,5 在抑制纹状体多巴胺释放方面明显优于 CPP-115,纹状体多巴胺释放是急性可卡因或尼古丁挑战后的结果。化合物 5 还减弱了海马中代谢需求的增加(神经元葡萄糖代谢),海马是一个编码关于动物接受强化或厌恶药物的环境的空间信息的大脑区域。这种多学科计算设计到临床前疗效的方法应该适用于其他已知晶体结构和失活机制的基于机制的抑制剂的设计和改进。