Price Raymond D, Milne Stuart A, Sharkey John, Matsuoka Nobuya
Pharmacology Research Laboratories, Astellas Pharma Inc., 21 Miyukigaoka, Tsukuba 305-8585, Japan.
Pharmacol Ther. 2007 Aug;115(2):292-306. doi: 10.1016/j.pharmthera.2007.03.005. Epub 2007 Apr 20.
Nerve growth factor (NGF) and other members of the neurotrophin family are critical for the survival and differentiation of neurons and have been implicated in the pathophysiology of numerous disease states. Although the therapeutic potential of neurotrophins has generated much excitement over the past decade, inconvenient pharmacokinetics and adverse side-effect profiles have limited the clinical usefulness of neurotrophic factors themselves. Compounds that mimic neurotrophin signaling and overcome the pharmacokinetic and side-effect barriers may have greater therapeutic potential. Here, we review the progress to date of clinical trials with direct neurotrophin modulators and describe alternative strategies to target (modulate) neurotrophin production and/or their signal transduction pathways. Particular emphasis is placed on small molecules that are able to modulate neurotrophin function in diseases of the nervous system. These alternative strategies show promise in preclinical studies, with some advancing into clinical development. Moreover, the recognition that clinically effective therapeutics, such as antidepressants and immunophilin ligands, can modulate neurotrophin function suggests that the concept of small molecule therapeutics that promote neurotrophic function may still be viable.
神经生长因子(NGF)和神经营养因子家族的其他成员对神经元的存活和分化至关重要,并与多种疾病状态的病理生理学有关。尽管在过去十年中,神经营养因子的治疗潜力引起了广泛关注,但不便的药代动力学和不良副作用限制了神经营养因子本身的临床应用。模拟神经营养因子信号传导并克服药代动力学和副作用障碍的化合物可能具有更大的治疗潜力。在这里,我们回顾了直接神经营养因子调节剂的临床试验进展,并描述了靶向(调节)神经营养因子产生和/或其信号转导途径的替代策略。特别强调了能够调节神经系统疾病中神经营养因子功能的小分子。这些替代策略在临床前研究中显示出前景,一些已进入临床开发阶段。此外,认识到临床上有效的治疗药物,如抗抑郁药和免疫亲和素配体,可以调节神经营养因子功能,这表明促进神经营养功能的小分子治疗概念可能仍然可行。