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Title: Reduced vesicular storage of catecholamines causes progressive degeneration in the locus ceruleus.

Authors: Taylor, Tonya N; Alter, Shawn P; Wang, Minzheng; Goldstein, David S; Miller, Gary W

Published In Neuropharmacology, (2014 Jan)

Abstract: Parkinson's disease (PD) is the most common neurodegenerative motor disease. Pathologically, PD is characterized by Lewy body deposition and subsequent death of dopamine neurons in the substantia nigra pars compacta. PD also consistently features degeneration of the locus ceruleus, the main source of norepinephrine in the central nervous system. We have previously reported a mouse model of dopaminergic neurodegeneration based on reduced expression of the vesicular monoamine transporter (VMAT2 LO). To determine if reduced vesicular storage can also cause noradrenergic degeneration, we examined indices of damage to the catecholaminergic systems in brain and cardiac tissue of VMAT2 LO mice. At two months of age, neurochemical analyses revealed substantial reductions in striatal dopamine (94%), cortical dopamine (57%) and norepinephrine (54%), as well as cardiac norepinephrine (97%). These losses were accompanied by increased conversion of dopamine and norepinephrine to their deaminated metabolites. VMAT2 LO mice exhibited loss of noradrenergic innervation in the cortex, as determined by norepinephrine transporter immunoreactivity and (3)H-nisoxetine binding. Using unbiased stereological techniques, we observed progressive degeneration in the locus ceruleus that preceded degeneration of the substantia nigra pars compacta. In contrast, the ventral tegmental area, which is spared in human PD, remained unaffected. The coordinate loss of dopamine and norepinephrine neurons in VMAT2 LO mice parallels the pattern of neurodegeneration that occurs in human PD, and demonstrates that insufficient catecholamine storage can cause spontaneous degeneration in susceptible neurons, underscoring cytosolic catecholamine catabolism as a determinant of neuronal susceptibility in PD. This article is part of the Special Issue entitled 'The Synaptic Basis of Neurodegenerative Disorders'.

PubMed ID: 24025942 Exiting the NIEHS site

MeSH Terms: Animals; Catecholamines/metabolism*; Cerebral Cortex/metabolism; Cerebral Cortex/pathology; Corpus Striatum/metabolism; Dopamine/metabolism; Female; Locus Coeruleus/metabolism*; Locus Coeruleus/pathology*; Male; Mice; Mice, Neurologic Mutants; Myocardium/metabolism; Nerve Degeneration/genetics; Nerve Degeneration/metabolism*; Nerve Degeneration/pathology; Norepinephrine Plasma Membrane Transport Proteins/metabolism; Norepinephrine/metabolism; Parkinson Disease/metabolism; Parkinson Disease/pathology; Vesicular Monoamine Transport Proteins/genetics; Vesicular Monoamine Transport Proteins/metabolism*

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