Document Detail


Dehydroepiandrosterone reverses systemic vascular remodeling through the inhibition of the Akt/GSK3-{beta}/NFAT axis.
MedLine Citation:
PMID:  19752325     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: The remodeled vessel wall in many vascular diseases such as restenosis after injury is characterized by proliferative and apoptosis-resistant vascular smooth muscle cells. There is evidence that proproliferative and antiapoptotic states are characterized by a metabolic (glycolytic phenotype and hyperpolarized mitochondria) and electric (downregulation and inhibition of plasmalemmal K(+) channels) remodeling that involves activation of the Akt pathway. Dehydroepiandrosterone (DHEA) is a naturally occurring and clinically used steroid known to inhibit the Akt axis in cancer. We hypothesized that DHEA will prevent and reverse the remodeling that follows vascular injury.
METHODS AND RESULTS: We used cultured human carotid vascular smooth muscle cell and saphenous vein grafts in tissue culture, stimulated by platelet-derived growth factor to induce proliferation in vitro and the rat carotid injury model in vivo. DHEA decreased proliferation and increased vascular smooth muscle cell apoptosis in vitro and in vivo, reducing vascular remodeling while sparing healthy tissues after oral intake. Using pharmacological (agonists and antagonists of Akt and its downstream target glycogen-synthase-kinase-3beta [GSK-3beta]) and molecular (forced expression of constitutively active Akt1) approaches, we showed that the effects of DHEA were mediated by inhibition of Akt and subsequent activation of GSK-3beta, leading to mitochondrial depolarization, increased reactive oxygen species, activation of redox-sensitive plasmalemmal voltage-gated K(+) channels, and decreased [Ca(2+)](i). These functional changes were accompanied by sustained molecular effects toward the same direction; by decreasing [Ca(2+)](i) and inhibiting GSK-3beta, DHEA inhibited the nuclear factor of activated T cells transcription factor, thus increasing expression of Kv channels (Kv1.5) and contributing to sustained mitochondrial depolarization. These results were independent of any steroid-related effects because they were not altered by androgen and estrogen inhibitors but involved a membrane G protein-coupled receptor.
CONCLUSIONS: We suggest that the orally available DHEA might be an attractive candidate for the treatment of systemic vascular remodeling, including restenosis, and we propose a novel mechanism of action for this important hormone and drug.
Authors:
Sébastien Bonnet; Roxane Paulin; Gopinath Sutendra; Peter Dromparis; Melanie Roy; Kristalee O Watson; Jayan Nagendran; Alois Haromy; Jason R B Dyck; Evangelos D Michelakis
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-09-14
Journal Detail:
Title:  Circulation     Volume:  120     ISSN:  1524-4539     ISO Abbreviation:  Circulation     Publication Date:  2009 Sep 
Date Detail:
Created Date:  2009-09-29     Completed Date:  2009-10-29     Revised Date:  2011-11-02    
Medline Journal Info:
Nlm Unique ID:  0147763     Medline TA:  Circulation     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1231-40     Citation Subset:  AIM; IM    
Affiliation:
Centre de Recherche de L'Hôtel-Dieu de Québec, 9 Rue McMahon, Québec, Qc, G1R 2J6, Canada. sebastien.bonnet@crhdq.ulaval.ca
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MeSH Terms
Descriptor/Qualifier:
Adjuvants, Immunologic / pharmacology
Angioplasty, Balloon / adverse effects
Animals
Apoptosis / drug effects,  physiology
Calcium / metabolism
Carotid Arteries / cytology
Carotid Artery Injuries / drug therapy,  metabolism,  pathology
Cell Division / drug effects,  physiology
Cell Membrane / metabolism
Cells, Cultured
Cytochromes c / metabolism
Dehydroepiandrosterone / pharmacology*
Disease Models, Animal
Glycogen Synthase Kinase 3 / antagonists & inhibitors,  metabolism
Hexokinase / metabolism
Humans
Kv1.5 Potassium Channel / metabolism
Male
Muscle, Smooth, Vascular / cytology,  drug effects,  metabolism
NFATC Transcription Factors / metabolism*
Peripheral Vascular Diseases / drug therapy*,  metabolism*,  pathology
Proto-Oncogene Proteins c-akt / metabolism*
Rats
Rats, Sprague-Dawley
Voltage-Dependent Anion Channel 1 / metabolism
Chemical
Reg. No./Substance:
0/Adjuvants, Immunologic; 0/KCNA5 protein, human; 0/Kv1.5 Potassium Channel; 0/NFATC Transcription Factors; 0/VDAC1 protein, human; 0/Vdac1 protein, rat; 53-43-0/Dehydroepiandrosterone; 7440-70-2/Calcium; 9007-43-6/Cytochromes c; EC 1.6.-/Voltage-Dependent Anion Channel 1; EC 2.7.1.1/Hexokinase; EC 2.7.11.1/Proto-Oncogene Proteins c-akt; EC 2.7.11.1/glycogen synthase kinase 3 beta; EC 2.7.11.26/Glycogen Synthase Kinase 3

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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