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Exp Neurol ; 231(1): 171-80, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21703262

RESUMEN

Clinical studies have indicated a link between Parkinson's disease (PD) and Type 2 Diabetes. Although preclinical studies have examined the effect of high-fat feeding on dopamine function in brain reward pathways, the effect of diet on neurotransmission in the nigrostriatal pathway, which is affected in PD and parkinsonism, is less clear. We hypothesized that a high-fat diet, which models early-stage Type 2 Diabetes, would disrupt nigrostriatal dopamine function in young adult Fischer 344 rats. Rats were fed a high fat diet (60% calories from fat) or a normal chow diet for 12 weeks. High fat-fed animals were insulin resistant compared to chow-fed controls. Potassium-evoked dopamine release and dopamine clearance were measured in the striatum using in vivo electrochemistry. Dopamine release was attenuated and dopamine clearance was diminished in the high-fat diet group compared to chow-fed rats. Magnetic resonance imaging indicated increased iron deposition in the substantia nigra of the high fat group. This finding was supported by alterations in the expression of several proteins involved in iron metabolism in the substantia nigra in this group compared to chow-fed animals. The diet-induced systemic and basal ganglia-specific changes may play a role in the observed impairment of nigrostriatal dopamine function.


Asunto(s)
Cuerpo Estriado/fisiopatología , Complicaciones de la Diabetes/metabolismo , Dopamina/fisiología , Resistencia a la Insulina/fisiología , Enfermedad de Parkinson/metabolismo , Sustancia Negra/metabolismo , Animales , Cuerpo Estriado/metabolismo , Diabetes Mellitus Tipo 2/complicaciones , Diabetes Mellitus Tipo 2/metabolismo , Grasas de la Dieta/efectos adversos , Grasas de la Dieta/metabolismo , Modelos Animales de Enfermedad , Dopamina/metabolismo , Hierro/metabolismo , Trastornos del Metabolismo del Hierro/complicaciones , Trastornos del Metabolismo del Hierro/metabolismo , Masculino , Vías Nerviosas/metabolismo , Enfermedad de Parkinson/etiología , Ratas , Ratas Endogámicas F344 , Sustancia Negra/patología
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