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运动改善MPTP处理小鼠的认知障碍和多巴胺代谢。

Exercise Improves Cognitive Impairment and Dopamine Metabolism in MPTP-Treated Mice.

作者信息

Aguiar Aderbal S, Lopes Samantha C, Tristão Fabrine S M, Rial Daniel, de Oliveira Gisele, da Cunha Cláudio, Raisman-Vozari Rita, Prediger Rui D

出版信息

Neurotox Res. 2016 Jan;29(1):118-25. doi: 10.1007/s12640-015-9566-4.

Abstract

The classical motor symptoms of Parkinson’s disease (PD) are preceded by non-motor symptoms in preclinical stages, including cognition impairment. The current drug treatment for PD is palliative and does not meet the clinical challenges of the disease, such as levodopa-induced dyskinesia, non-motor symptoms, and neuroprotection. We investigated the neuroprotective and disease-modifying potential of physical exercise in a preclinical animal model of PD. C57BL/6 mice (adult males) ran on a horizontal treadmill for 6 weeks (moderate intensity, 5 times/week) and were treated intranasally with 65 mg/kg of the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). Exercise did not protect against MPTP-induced nigrostriatal neurodegeneration or frontostriatal dopamine depletion but decreased striatal dopamine turnover. Exercise also attenuated procedural and working memory impairment and D2 receptor hypersensitivity in MPTP-treated mice. In summary, exercise improved dopaminergic neurotransmission and enhanced cognition in a preclinical animal model of PD.

摘要

帕金森病(PD)的典型运动症状在临床前期阶段之前就会出现非运动症状,包括认知障碍。目前针对PD的药物治疗只是姑息性的,无法应对该疾病的临床挑战,如左旋多巴诱发的运动障碍、非运动症状和神经保护问题。我们在PD的临床前动物模型中研究了体育锻炼的神经保护和疾病修饰潜力。C57BL/6小鼠(成年雄性)在水平跑步机上跑步6周(中等强度,每周5次),并经鼻给予65mg/kg神经毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)。运动并不能预防MPTP诱导的黑质纹状体神经变性或额叶纹状体多巴胺耗竭,但可降低纹状体多巴胺周转率。运动还减轻了MPTP处理小鼠的程序性和工作记忆损害以及D2受体超敏反应。总之,在PD的临床前动物模型中,运动改善了多巴胺能神经传递并增强了认知能力。

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