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

被引:30
作者
Aguiar, Aderbal S., Jr. [1 ,2 ]
Lopes, Samantha C. [1 ]
Tristo, Fabrine S. M. [3 ]
Rial, Daniel [1 ]
de Oliveira, Gisele [4 ]
da Cunha, Claudio [4 ]
Raisman-Vozari, Rita [3 ]
Prediger, Rui D. [2 ]
机构
[1] Univ Fed Santa Catarina, Dept Farmacol, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Fed Santa Catarina, Dept Bioquim, Ctr Cincias Biol, BR-88040900 Florianopolis, SC, Brazil
[3] Univ Paris 06, INSERM UMR 975, Ctr Rech Inst Cerveau & Moelle Epiniere, CNRS UMR 7225, F-75651 Paris, France
[4] Univ Fed Parana, Dept Farmacol, Ctr Politecn, BR-81531980 Curitiba, Parana, Brazil
关键词
Exercise; MPTP; Parkinson's disease; Cognition; Dopamine D2 receptor; CHRONIC MOUSE MODEL; PARKINSONS-DISEASE; TREADMILL EXERCISE; ENDURANCE EXERCISE; RECEPTOR-BINDING; 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE MPTP; BEHAVIORAL RECOVERY; BASAL GANGLIA; D2; RECEPTOR; DEFICITS;
D O I
10.1007/s12640-015-9566-4
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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 D-2 receptor hypersensitivity in MPTP-treated mice. In summary, exercise improved dopaminergic neurotransmission and enhanced cognition in a preclinical animal model of PD.
引用
收藏
页码:118 / 125
页数:8
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