4.5 Article

Alpha-synuclein-immunopositive myenteric neurons and vagal preganglionic terminals: Autonomic pathway implicated in Parkinson's disease?

Journal

NEUROSCIENCE
Volume 153, Issue 3, Pages 733-750

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2008.02.074

Keywords

calbindin; calretinin; enteric nervous system; Fischer 344; Lewy neurites/bodies; nitric oxide synthase

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Funding

  1. NIDDK NIH HHS [DK61317, R01 DK027627, R01 DK061317-06A1, R01 DK061317-05, DK27627, R01 DK061317, R37 DK027627-29, R37 DK027627] Funding Source: Medline

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The protein alpha-synuclein is implicated in the development of Parkinson's disease. The molecule forms Lewy body aggregates that are hallmarks of the disease, has been associated with the spread of neuropathology from the peripheral to the CNS, and appears to be involved with the autonomic disorders responsible for the gastrointestinal (GI) symptoms of individuals afflicted with Parkinson's. To characterize the normative expression of alpha-synuclein in the innervation of the GI tract, we examined both the postganglionic neurons and the preganglionic projections by which the disease is postulated to retrogradely invade the CNS. Specifically, in Fischer 344 and Sprague-Dawley rats, immunohistochemistry in conjunction with injections of the tracer Dextran-Texas Red was used to determine, respectively, the expression of alpha-synuclein in the myenteric plexus and in the vagal terminals. Alpha-synuclein is expressed in a sub-population of myenteric neurons, with the proportion of positive somata increasing from the stomach (similar to 3%) through duodenum (proximal, similar to 6%; distal, similar to 13%) to jejunum (similar to 22%). Alpha-synuclein is co-expressed with the nitrergic enzyme nitric oxide synthase (NOS) or the cholinergic markers calbindin and calretinin in regionally specific patterns: similar to 90% of forestomach neurons positive for alpha-synuclein express NOS, whereas similar to 92% of corpus-antrum neurons positive for alpha-synuclein express cholinergic markers. Vagal afferent endings in the myenteric plexus and the GI smooth muscle do not express alpha-synuclein, whereas, virtually all vagal preganglionic projections to the gut express alpha-synuclein, both in axons and in terminal varicosities in apposition with myenteric neurons. Vagotomy eliminates most, but not all, alpha-synuclein-positive neurites in the plexus. Some vagal preganglionic efferents expressing alpha-synuclein form varicose terminal rings around myenteric plexus neurons that are also positive for the protein, thus providing a candidate alpha-synuclein-expressing pathway for the retrograde transport of putative Parkinson's pathogens or toxins from the ENS to the CNS. (c) 2008 IBRO. Published by Elsevier Ltd. All rights reserved.

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