Morain Philippe, Lestage Pierre, De Nanteuil Guillaume, Jochemsen Roeline, Robin Jean-Loïc, Guez David, Boyer Pierre-Alain
Institut de Recherches Internationales Servier, 6 Place des pleïades, 92415 Courbevoie, France.
CNS Drug Rev. 2002 Spring;8(1):31-52. doi: 10.1111/j.1527-3458.2002.tb00214.x.
Any treatment that could positively modulate central neuropeptides levels would provide a promising therapeutic approach to the treatment of cognitive deficits associated with aging and/or neurodegenerative diseases. Therefore, based on the activity in rodents, S 17092 (2S,3aS,7aS)-1][(R,R)-2-phenylcyclopropyl]carbonyl]-2-[(thiazolidin-3-yl)carbonyl]octahydro-1H-indole) has been selected as a potent inhibitor of cerebral prolyl-endopeptidase (PEP). By retarding the degradation of neuroactive peptides, S 17092 was successfully used in a variety of memory tasks. These tasks explored short-term, long-term, reference and working memory in aged mice, as well as in rodents and monkeys with chemically induced amnesia or spontaneous memory deficits. S 17092 has also been safely administered to humans, and showed a clear peripheral expression of its mechanism of action through its inhibitory effect upon PEP activity in plasma. S 17092 exhibited central effects, as evidenced by EEG recording in healthy volunteers, and could improve a delayed verbal memory task. Collectively, the preclinical and clinical effects of S 17092 have suggested a promising role for this compound as an agent for the treatment of cognitive disorders associated with cerebral aging.
任何能够正向调节中枢神经肽水平的治疗方法,都将为治疗与衰老和/或神经退行性疾病相关的认知缺陷提供一种有前景的治疗途径。因此,基于在啮齿动物身上的活性表现,S 17092((2S,3aS,7aS)-1][(R,R)-2-苯基环丙基]羰基]-2-[(噻唑烷-3-基)羰基]八氢-1H-吲哚)已被选为一种有效的脑脯氨酰内肽酶(PEP)抑制剂。通过延缓神经活性肽的降解,S 17092成功应用于各种记忆任务中。这些任务研究了老年小鼠以及患有化学诱导失忆或自发记忆缺陷的啮齿动物和猴子的短期、长期、参考和工作记忆。S 17092也已安全地应用于人体,并通过其对血浆中PEP活性的抑制作用,显示出其作用机制在外周的明显表现。S 17092表现出中枢效应,健康志愿者的脑电图记录证明了这一点,并且它可以改善一项延迟言语记忆任务。总体而言,S 17092的临床前和临床效果表明,该化合物作为一种治疗与脑老化相关的认知障碍的药物具有广阔前景。