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1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)不会破坏坏血病豚鼠的黑质纹状体神经元。

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) does not destroy nigrostriatal neurons in the scorbutic guinea pig.

作者信息

Perry T L, Yong V W, Ito M, Jones K, Wall R A, Foulks J G, Wright J M, Kish S J

出版信息

Life Sci. 1985 Apr 1;36(13):1233-8. doi: 10.1016/0024-3205(85)90267-x.

Abstract

Guinea pigs were injected subcutaneously with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) in maximal tolerated doses (8 mg/kg, once daily) for 10 or 15 days. No neurological effects were noted, other than sedation and hypotonia lasting a few hours after each injection, either in animals maintained on normal diet or in animals fed an ascorbate-deficient diet and rendered severely scorbutic. Subsequent chemical analyses of the striatum showed no evidence of lasting damage to nigrostriatal dopaminergic neurons in MPTP treated guinea pigs on normal diet, and minimal evidence of permanent damage to these neurons in scorbutic animals. MPTP was undetectable in the urine of MPTP-treated animals, although a metabolite, presumably 1-methyl-4-phenylpyridinium ion (MPP+) was regularly present in urine. The relative lack of neurotoxicity of MPTP in the guinea pig remains unexplained. This species clearly is not a suitable small animal for MPTP-induced parkinsonism.

摘要

豚鼠皮下注射最大耐受剂量(8毫克/千克,每日一次)的1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP),持续10或15天。无论是正常饮食的动物,还是喂食缺乏抗坏血酸饮食并导致严重坏血病的动物,除了每次注射后持续数小时的镇静和肌张力减退外,未观察到神经学效应。随后对纹状体的化学分析表明,正常饮食的MPTP处理豚鼠中,没有证据表明黑质纹状体多巴胺能神经元受到持久损伤,而在坏血病动物中,这些神经元有轻微的永久损伤迹象。MPTP处理动物的尿液中未检测到MPTP,尽管尿液中经常存在一种代谢物,推测为1-甲基-4-苯基吡啶离子(MPP+)。MPTP在豚鼠中相对缺乏神经毒性的原因尚不清楚。该物种显然不是MPTP诱导帕金森病的合适小动物模型。

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