Document Detail


Thromboxane A2 and vascular smooth muscle cell proliferation.
MedLine Citation:
PMID:  7591017     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In the present study we describe the intracellular pathways for the transmission of growth signals by the potent vasoconstricting eicosanoids prostaglandin H2 and thromboxane A2 in smooth muscle cells from rat aorta. Carbocyclic thromboxane A2 and U46619 are stable thromboxane A2 mimetics acting at the common thromboxane A2/prostaglandin H2 receptor. Carbocyclic thromboxane A2 (10(-6) mol/L) induced an approximately 2.5-fold increase in [Ca2+]i above the basal value at 25 seconds. Maximal stimulation of the 42-kD mitogen-activated protein kinase isoform by both thromboxane A2 mimetics occurred at 5 minutes. Both thromboxane A2 mimetics at a concentration of 10(-6) mol/L induced the expression of c-fos and early growth response gene-1 (egr-1) mRNA, with a maximum at 30 minutes. Carbocyclic thromboxane A2 (10(-6) mol/L) induced a 3.3-fold increase in [3H]thymidine incorporation into cell DNA above the basal value and produced a 3.5-fold elevation of platelet-derived growth factor-BB-dependent [3H]thymidine incorporation into cell DNA. Similar effects of U46619 (10(-6) to 10(-5) mol/L) alone did in combination with platelet-derived growth factor-BB on cell DNA synthesis were obtained. The thromboxane A2/prostaglandin H2 receptor antagonist SQ29548 (10(-6) mol/L) completely suppressed the mitogenic effect of both thromboxane A2 mimetics (10(-6) mol/L). Pertussis toxin (10 to 100 ng/mL) did not influence the mitogenic effects of the thromboxane A2 mimetics. Carbocyclic thromboxane A2 (10(-6) mol/L) and platelet-derived growth factor-BB (20 ng/mL) per ser caused a 44% and 100% increase in cell number, respectively. In the presence of carbocyclic thromboxane A2 (10(-6) mol/L), platelet-derived growth factor-BB induced a 152% increase in cell number. Similar results were obtained with U46619 alone or in combination with platelet-derived growth factor-BB.
Authors:
A Sachinidis; M Flesch; Y Ko; K Schrör; M Böhm; R Düsing; H Vetter
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Hypertension     Volume:  26     ISSN:  0194-911X     ISO Abbreviation:  Hypertension     Publication Date:  1995 Nov 
Date Detail:
Created Date:  1995-12-07     Completed Date:  1995-12-07     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  7906255     Medline TA:  Hypertension     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  771-80     Citation Subset:  IM    
Affiliation:
Medizinische Universitäts-Poliklinik, Bonn, Germany.
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MeSH Terms
Descriptor/Qualifier:
15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid
Animals
Aorta / metabolism*
Calcium / metabolism
Calcium-Calmodulin-Dependent Protein Kinases / metabolism
Cell Division / drug effects
Cells, Cultured
DNA Replication / drug effects
Muscle, Smooth, Vascular / metabolism*
Platelet-Derived Growth Factor / pharmacology
Prostaglandin Endoperoxides, Synthetic / pharmacology*
Rats
Rats, Inbred WKY
Receptors, Thromboxane / metabolism*
Signal Transduction
Thromboxane A2 / analogs & derivatives*,  pharmacology
Vasoconstrictor Agents / pharmacology*
Chemical
Reg. No./Substance:
0/Platelet-Derived Growth Factor; 0/Prostaglandin Endoperoxides, Synthetic; 0/Receptors, Thromboxane; 0/Vasoconstrictor Agents; 0/platelet-derived growth factor BB; 57576-52-0/Thromboxane A2; 73543-47-2/thromboxane A2, carbocyclic; 7440-70-2/Calcium; 76898-47-0/15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid; EC 2.7.11.17/Calcium-Calmodulin-Dependent Protein Kinases

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


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