Document Detail


What can current stimulation tell us about the vascular function of endogenous prostacyclin in healthy rat skin in vivo?
MedLine Citation:
PMID:  20827283     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In endothelial function, prostacyclin (PGI(2)) is as important as nitric oxide (NO); however, no test assesses specifically the vascular function of endogenous PGI(2). We hypothesized that PGI(2) has a dominant role in cathodal current-induced vasodilation (CIV) described in human skin. We thus aimed to study, in physiological conditions, the PGI(2) involvement in cathodal CIV in rats in order to use pharmacological blockers that could not be used in humans. CIV was reduced by cyclooxygenase (COX)-1 and PGI(2) synthase (PGIS) and PGI(2) receptor (IP) blockers, but was unchanged by COX-2 and NO synthase (NOS) blockers. The level of 6-ketoPGF(1)(α) present in skin biopsies, measured as endogenous PGI(2), was increased by cathodal current stimulation, except under COX-1 and PGIS inhibition. This study provides evidence that cathodal CIV mainly relies on the release of PGI(2) endogenously produced through the COX-1/PGIS pathway, and then acts on IP receptors to relax the cutaneous microvessels in healthy rats. In contrast, neither COX-2 nor NOS is involved in CIV and the endogenous PGI(2) release by current stimulation. This finding shows that cathodal current stimulation could be a valuable method to assess the vascular function of endogenous PGI(2) in healthy skin.
Authors:
Stéphanie Gohin; Dominique Sigaudo-Roussel; Agnès Conjard-Duplany; Laurence Dubourg; Jean Louis Saumet; Bérengère Fromy
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Publication Detail:
Type:  Journal Article     Date:  2010-09-09
Journal Detail:
Title:  The Journal of investigative dermatology     Volume:  131     ISSN:  1523-1747     ISO Abbreviation:  J. Invest. Dermatol.     Publication Date:  2011 Jan 
Date Detail:
Created Date:  2010-12-15     Completed Date:  2011-01-24     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0426720     Medline TA:  J Invest Dermatol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  237-44     Citation Subset:  IM    
Affiliation:
Neurovascular Interactions, FRE CNRS 3075, Institut des Sciences Biologiques et Pharmaceutiques, Université Claude Bernard Lyon 1, Lyon, France.
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MeSH Terms
Descriptor/Qualifier:
6-Ketoprostaglandin F1 alpha / metabolism
Acetylcholine / pharmacology
Animals
Biopsy
Cyclooxygenase 1 / metabolism
Cyclooxygenase 2 / metabolism
Cyclooxygenase Inhibitors / pharmacology
Electric Stimulation*
Epoprostenol / physiology*
Galvanic Skin Response / physiology
Male
Nitric Oxide Synthase / metabolism
Rats
Rats, Wistar
Skin / blood supply*,  drug effects,  radiation effects
Skin Physiological Processes*
Vasodilation / physiology*,  radiation effects
Vasodilator Agents / pharmacology
Chemical
Reg. No./Substance:
0/Cyclooxygenase Inhibitors; 0/Vasodilator Agents; 35121-78-9/Epoprostenol; 51-84-3/Acetylcholine; 58962-34-8/6-Ketoprostaglandin F1 alpha; EC 1.14.13.39/Nitric Oxide Synthase; EC 1.14.99.1/Cyclooxygenase 1; EC 1.14.99.1/Cyclooxygenase 2

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