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Publication : Dietary energy intake modifies brainstem autonomic dysfunction caused by mutant α-synuclein.

First Author  Griffioen KJ Year  2013
Journal  Neurobiol Aging Volume  34
Issue  3 Pages  928-35
PubMed ID  22883907 Mgi Jnum  J:194429
Mgi Id  MGI:5473758 Doi  10.1016/j.neurobiolaging.2012.07.008
Citation  Griffioen KJ, et al. (2013) Dietary energy intake modifies brainstem autonomic dysfunction caused by mutant alpha-synuclein. Neurobiol Aging 34(3):928-35
abstractText  Parkinson's disease (PD) patients often exhibit impaired regulation of heart rate by the autonomic nervous system (ANS) that may precede motor symptoms in many cases. Results of autopsy studies suggest that brainstem pathology, including the accumulation of alpha-synuclein, precedes damage to dopaminergic neurons in the substantia nigra in PD. However, the molecular and cellular mechanisms responsible for the early dysfunction of brainstem autonomic neurons are unknown. Here we report that mice expressing a mutant form of alpha-synuclein that causes familial PD exhibit aberrant autonomic control of the heart characterized by elevated resting heart rate and an impaired cardiovascular stress response, associated with reduced parasympathetic activity and accumulation of alpha-synuclein in the brainstem. These ANS abnormalities occur early in the disease process. Adverse effects of alpha-synuclein on the control of heart rate are exacerbated by a high energy diet and ameliorated by intermittent energy restriction. Our findings establish a mouse model of early dysregulation of brainstem control of the cardiovascular system in PD, and further suggest the potential for energy restriction to attenuate ANS dysfunction, particularly in overweight individuals.
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