Lindsay R M, Altar C A, Cedarbaum J M, Hyman C, Wiegand S J
Regeneron Pharmaceuticals Inc., Tarrytown, New York 10591-6707.
Exp Neurol. 1993 Nov;124(1):103-18. doi: 10.1006/exnr.1993.1181.
Partial symptomatic relief from Parkinson's disease with levodopa has proven to be one of the rare success stories in the development of drugs to combat neurodegenerative diseases. However, no therapeutic agent has yet conclusively been shown to slow, halt, or reverse the underlying progression of neuronal loss in Parkinson's disease or any other human neurodegenerative disorder. This article reviews recent developments in the biology of neurotrophic growth factors, especially members of the nerve growth factor-related neurotrophin family, which may point to their potential as therapeutic agents for the treatment of Parkinson's disease. Parkinson's disease, characterized by the progressive loss of dopaminergic neurons of the substantia nigra, is one of the most well-characterized neurodegenerative disorders from both an anatomical and biochemical standpoint, but as yet the etiology of this disease remains poorly understood. Epidemiological, neurochemical, and pathological studies have provided a wealth of data that have spawned many theories of the underlying cause of Parkinson's disease, including environmental and genetic origins. Future elucidation of the disease process in Parkinson's disease may yield obvious therapeutic strategies, but even in the absence of such knowledge there are several general approaches that can be taken as strategies for the treatment of a "focal" neurodegenerative disease. These include: (a) mimetics, activation of the postsynaptic target(s) of the missing neurons through mimetics of the missing neurotransmitter, e.g., use of a dopamine precursor or dopamine receptor agonist in Parkinson's disease; (b) transplants, replenishment of the missing neurons via transplantation of neurons or nonneuronal cells secreting the appropriate neurotransmitter, e.g., fetal nigral grafts in Parkinson's disease; (c) neurotrophic factors or neuroprotectants, intervention with neurotrophic factors/neuroprotective agents which slow, halt, or reverse the progression of neuronal degeneration, e.g., a dopamine neurotrophic factor in Parkinson's disease. The scope of the present article is limited to a review of recent progress in the biology of neurotrophic factors that relates to their potential clinical use in treating the loss of dopamine neurons in Parkinson's disease.
左旋多巴对帕金森病的部分症状缓解已被证明是神经退行性疾病药物研发中罕见的成功案例之一。然而,尚无治疗药物能确凿地显示可减缓、阻止或逆转帕金森病或任何其他人类神经退行性疾病中神经元丢失的潜在进程。本文综述了神经营养生长因子生物学的最新进展,尤其是与神经生长因子相关的神经营养素家族成员,这些进展可能表明它们作为治疗帕金森病药物的潜力。帕金森病的特征是黑质多巴胺能神经元进行性丧失,从解剖学和生物化学角度来看,它是特征最明确的神经退行性疾病之一,但该病的病因至今仍知之甚少。流行病学、神经化学和病理学研究提供了大量数据,催生了许多关于帕金森病潜在病因的理论,包括环境和遗传起源。未来对帕金森病发病过程的阐明可能会产生明显的治疗策略,但即便缺乏此类知识,对于一种“局灶性”神经退行性疾病的治疗仍有几种通用方法可作为策略。这些方法包括:(a)模拟物,通过模拟缺失的神经递质激活缺失神经元的突触后靶点,例如在帕金森病中使用多巴胺前体或多巴胺受体激动剂;(b)移植,通过移植分泌适当神经递质的神经元或非神经元细胞来补充缺失的神经元,例如在帕金森病中进行胎儿黑质移植;(c)神经营养因子或神经保护剂,用能减缓、阻止或逆转神经元变性进程的神经营养因子/神经保护剂进行干预,例如在帕金森病中使用多巴胺神经营养因子。本文的范围限于综述神经营养因子生物学的最新进展,这些进展涉及其在治疗帕金森病中多巴胺能神经元丢失方面的潜在临床应用。