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[神经毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶在特发性帕金森病病因学及治疗中的意义]

[Significance of the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine for the etiology and therapy of idiopathic Parkinson disease].

作者信息

Lange K W

机构信息

University Department of Neurology, Institute of Psychiatry, London.

出版信息

Fortschr Neurol Psychiatr. 1989 Apr;57(4):142-8. doi: 10.1055/s-2007-1000755.

Abstract

Exposure of drug addicts to MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) has caused a Parkinsonian syndrome accompanied by a selective destruction of dopamine containing neurones in the pars compacta of the substantia nigra. MPTP in the human causes a severe irreversible state that very closely resembles idiopathic Parkinson's disease both in its clinical features and response to pharmacological treatment. Interest in potential environmental agents that might play a role in the aetiology of idiopathic Parkinson's disease is likely to increase as the result of the discovery of the relatively simple molecule MPTP which is highly toxic to the substantia nigra. Until the discovery of the neurotoxicity of MPTP there was no effective animal model of Parkinson's disease. Administration of PTP to monkeys induces persistent parkinsonism which responds to classical antiparkinsonian therapy. The morphological and biochemical changes in the brains of the animals are more limited and selective than those seen in idiopathic Parkinson's disease. The model of MPTP-treated monkeys appears to provide a useful testbed for the evaluation of future treatments for the disease. The precise mechanism of MPTP toxicity has yet to be determined and may provide the clue to the mechanism of neuronal death in Parkinson's disease. After entering the brain MPTP is oxidized to MPP+ (1-methyl-4-phenylpyridine) at an extraneuronal site.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

吸毒者接触1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)会引发帕金森综合征,并伴有黑质致密部含多巴胺神经元的选择性破坏。MPTP在人体中会导致一种严重的不可逆状态,其临床特征和对药物治疗的反应与特发性帕金森病极为相似。由于发现了对黑质具有高毒性的相对简单的分子MPTP,人们对可能在特发性帕金森病病因中起作用的潜在环境因素的兴趣可能会增加。在发现MPTP的神经毒性之前,没有有效的帕金森病动物模型。给猴子注射MPTP会诱发持续性帕金森症,对经典抗帕金森病疗法有反应。动物大脑中的形态学和生化变化比特发性帕金森病中所见的变化更有限且更具选择性。MPTP处理的猴子模型似乎为评估该疾病的未来治疗方法提供了一个有用的试验平台。MPTP毒性的确切机制尚未确定,可能为帕金森病神经元死亡机制提供线索。进入大脑后,MPTP在神经元外部位被氧化为MPP +(1-甲基-4-苯基吡啶)。(摘要截短于250字)

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