Literature DB >> 3676771

Neuronal versus endothelial origin of vasoactive acetylcholine in pial vessels.

E Hamel1, C Assumel-Lurdin, L Edvinsson, D Fage, E T MacKenzie.   

Abstract

Functional pial vessels denuded in situ of the endothelial cell layer exhibit a markedly decreased choline uptake capacity (-53%) but integrally preserved choline acetyltransferase (ChAT) activity and acetylcholine (ACh) release mechanisms. These studies demonstrate that endothelial cells possess a specific choline uptake system. However, the unimpaired ChAT activity in denuded pial vessels implies that the endothelial pool of choline is not significantly metabolized into ACh. In spite of possible differences in the mechanisms that govern release processes in endothelial and neuronal elements, taken together the findings of the present study suggest that the ACh released following depolarization of pial blood vessels originates predominantly from cholinergic perivascular nerve terminals.

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Year:  1987        PMID: 3676771     DOI: 10.1016/0006-8993(87)91263-7

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  3 in total

1.  BIBN4096BS is a potent competitive antagonist of the relaxant effects of alpha-CGRP on human temporal artery: comparison with CGRP(8-37).

Authors:  Raphaela Verheggen; Katja Bumann; Alberto J Kaumann
Journal:  Br J Pharmacol       Date:  2002-05       Impact factor: 8.739

2.  An immunohistochemical study of endothelial cell heterogeneity in the rat: observations in "en face" Häutchen preparations.

Authors:  A Tomlinson; H Van Vlijmen; A Loesch; G Burnstock
Journal:  Cell Tissue Res       Date:  1991-01       Impact factor: 5.249

3.  Potent P2Y6 receptor mediated contractions in human cerebral arteries.

Authors:  Malin Malmsjö; Mingyan Hou; William Pendergast; David Erlinge; Lars Edvinsson
Journal:  BMC Pharmacol       Date:  2003-05-09
  3 in total

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