Endothelin-1 induces endothelial barrier failure in the cat hindlimb

• Published in: Shock (Augusta, Ga.) Ga.), 1999-02, Vol.11 (2), p.111-114
• Main Authors: PORTER, L. P, MCNAMEE, J. E, WOLFS, M. B
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Cats; Cell Membrane Permeability - drug effects; Cell Membrane Permeability - physiology; Dose-Response Relationship, Drug; Endothelin-1 - metabolism; Endothelin-1 - pharmacology; Endothelium - drug effects; Endothelium - metabolism; Fundamental and applied biological sciences. Psychology; Hindlimb; Inflammation; Molecular and cellular biology; Muscle, Skeletal - drug effects; Muscle, Skeletal - physiology
• ISSN: 1073-2322; 1540-0514
• DOI: 10.1097/00024382-199902000-00007

Our purpose was to see whether endothelin- (ET) 1 could produce a change in the endothelial membrane barrier to protein in skeletal muscle. Previous studies in other tissues have suggested that ET-1 affects this barrier, but the measurement methods used could not exclude vascular protein extravasation due to microvascular pressure changes or the effects of changes in perfused capillary surface area. We measured the protein sieving coefficient, a specific measure of the permeability of the membrane to protein, in the isolated, perfused cat hindlimb preparation. The integral-mass balance method determined this coefficient from the changes in hematocrit and plasma protein concentration induced by a period of transvascular fluid filtration. The data clearly indicate that ET-1 produces a dose (1-20 nM) dependent increase in permeability indicative of barrier dysfunction. Hence, elevated ET levels may contribute to the perivascular edema, hemoconcentration, and impaired tissue perfusion found in systemic inflammatory response syndromes and related diseases.