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Involvement of medullary regions controlling sympathetic output in Lewy body disease
Author(s) -
Eduardo E. Benarroch,
Ann M. Schmeichel,
Phillip A. Low,
Bradley F. Boeve,
Paola Sandroni,
Joseph E. Parisi
Publication year - 2004
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awh376
Subject(s) - raphe , lewy body , rostral ventrolateral medulla , medulla , raphe nuclei , medulla oblongata , serotonergic , tyrosine hydroxylase , neuroscience , catecholaminergic cell groups , alpha synuclein , catecholaminergic , pathology , biology , anatomy , medicine , parkinson's disease , central nervous system , catecholamine , serotonin , dopamine , disease , receptor
We sought to determine the involvement of medullary regions controlling sympathetic output in pathologically confirmed diffuse Lewy body disease (LBD). We studied eight limbic or neocortical stage LBD and eight multiple system atrophy (MSA) cases, confirmed neuropathologically, and eight age-matched controls. Five of the LBD cases and all MSA cases had orthostatic hypotension. Serial 50-mum sections obtained from the medulla rostral to the obex were immunostained for tyrosine hydroxylase, tryptophan hydroxylase and alpha-synuclein. Analysis was focused on the ventrolateral medulla and medullary raphe nuclei. In LBD cases, there were Lewy bodies and neurites, as well as dystrophic neurons in the ventrolateral medulla, but the number of catecholaminergic and serotonergic neurons was not significantly reduced. All these groups were depleted in MSA. There were Lewy body pathology and dystrophic neurons in the raphe in all LBD cases. Cell numbers were reduced in both the raphe obscurus and raphe pallidus. Our findings suggest that, although LBD affects medullary autonomic areas, it does so less severely than MSA, particularly in the case of the VLM, which controls sympathetic outputs maintaining arterial pressure. In LBD, orthostatic hypotension may be due primarily to involvement of sympathetic ganglion neurons rather than ventrolateral medulla neurons.

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