Abstract
Endothelin (ET)-1 is a potent vasoconstrictor peptide involved in the derangement of respiratory mechanics during endotoxic shock. We measured the kinetics of pulmonary mRNA expression of the key components of the ET system [i.e., ET-1, ET-converting enzyme (ECE), and ETA and ETB receptors] by quantitative real-time reverse transcriptase-polymerase chain reaction in a swine model of endotoxic shock (0, 1, 2, 3, and 4 h of continuous LPS infusion at 40 microg/kg/hour; sham group, 4 hour saline infusion). A significant increase in mRNA expression levels was observed for ET-1 in LPS-treated piglets; the increase began as early as 1 hour. In contrast, no significant variations were observed for the ECE, ETA, or ETB genes. Small gene expression differences observed with respect to our previous results suggest a possible effect of the anesthesia or surgical protocol on ET system regulation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Aspartic Acid Endopeptidases / genetics
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Aspartic Acid Endopeptidases / metabolism
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Dose-Response Relationship, Drug
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Endothelin-Converting Enzymes
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Endothelins / genetics
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Endothelins / metabolism
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Female
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Gene Expression Regulation
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Lipopolysaccharides / administration & dosage
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Lipopolysaccharides / toxicity*
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Lung / metabolism*
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Male
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Metalloendopeptidases / genetics
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Metalloendopeptidases / metabolism
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Receptor, Endothelin A / genetics
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Receptor, Endothelin A / metabolism
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Receptor, Endothelin B / genetics
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Receptor, Endothelin B / metabolism
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Shock, Septic / metabolism
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Shock, Septic / veterinary*
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Swine
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Swine Diseases / chemically induced*
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Swine Diseases / metabolism
Substances
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Endothelins
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Lipopolysaccharides
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Receptor, Endothelin A
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Receptor, Endothelin B
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Aspartic Acid Endopeptidases
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Metalloendopeptidases
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Endothelin-Converting Enzymes