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通过鼻腔途径持续注射MPTP可诱发小鼠帕金森病。

Persistent penetration of MPTP through the nasal route induces Parkinson's disease in mice.

作者信息

Rojo Ana I, Montero Celia, Salazar María, Close Ryan M, Fernández-Ruiz Javier, Sánchez-González Miguel A, de Sagarra María Rosa, Jackson-Lewis Vernice, Cavada Carmen, Cuadrado Antonio

机构信息

Instituto de Investigaciones Biomédicas and Departamento de Bioquímica, Facultad de Medicina, Universidad Autónoma de Madrid, Arzobispo Morcillo 4, 28029 Madrid, Spain.

出版信息

Eur J Neurosci. 2006 Oct;24(7):1874-84. doi: 10.1111/j.1460-9568.2006.05060.x.

Abstract

The aetiology of idiopathic Parkinson's disease (PD) is poorly defined but environmental aggression may be relevant. Here, we report a new model of PD in mice, based on chronic inoculation with neurotoxins in the nasal cavity, which is a natural route of contact with the environment. C57BL/6 mice, submitted to daily intranasal inoculation with MPTP for 30 days, developed motor deficits that correlated with a progressive and severe depletion of striatal dopamine levels, and loss of tyrosine hydroxylase and dopamine transporter staining in substantia nigra and striatum. Moreover, mice intranasally inoculated with MPTP developed strong astrogliosis and microgliosis in substantia nigra and striatum. Consistent with these observations, a role for oxidant aggression was demonstrated by increased levels of Mn-superoxide dismutase. However, alpha-synuclein aggregation was not observed. This new animal model provides a new tool for studying PD symptoms that develop slowly over time, and it may be used to asses risk from environmental neurotoxins.

摘要

特发性帕金森病(PD)的病因尚不明确,但环境侵害可能与之相关。在此,我们报告一种小鼠PD新模型,该模型基于在鼻腔内长期接种神经毒素构建,鼻腔是与环境接触的天然途径。C57BL/6小鼠每日经鼻接种MPTP,持续30天,出现运动功能障碍,这与纹状体多巴胺水平的进行性严重耗竭以及黑质和纹状体中酪氨酸羟化酶和多巴胺转运体染色缺失相关。此外,经鼻接种MPTP的小鼠在黑质和纹状体中出现强烈的星形胶质细胞增生和小胶质细胞增生。与这些观察结果一致,锰超氧化物歧化酶水平升高证明了氧化应激的作用。然而,未观察到α-突触核蛋白聚集。这种新的动物模型为研究随时间缓慢发展的PD症状提供了新工具,可用于评估环境神经毒素的风险。

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