Evaluation of activation of protein kinase C during agonist-induced constriction of veins isolated from the laminar dermis of horses
Date
2007
Authors
Robertson, T.
Moore, J.
Noschka, E.
Lewis, T.
Lewis, S.
Peroni, J.
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Journal article
Citation
American Journal of Veterinary Research, 2007; 68(6):664-669
Statement of Responsibility
Tom P. Robertson, James N. Moore, Erik Noschka, Tristan H. Lewis, Stephen J. Lewis, John F. Peroni
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Abstract
Objective—To determine the effects of the protein kinase C (PKC) inhibitor, Ro-31-8220, on agonist-induced constriction of laminar arteries and veins obtained from horses. Sample Population—Laminar arteries and veins obtained from 8 adult mixed-breed horses. Procedures—Laminar arteries and veins were isolated and mounted on small vessel myographs for the measurement of isometric tension. Concentration-response curves were then obtained for the vasoconstrictor agonists phenylephrine, 5-hydroxytryptamine, prostaglandin F2α, and endothelin-1. All responses were measured with or without the addition of Ro-31-8220 (3μM). Results—Laminar veins were more sensitive to vasoconstrictor agonists than laminar arteries, and incubation of laminar veins with Ro-31-8220 resulted in significantly smaller agonist-induced contractile responses for all agonists tested. In contrast, Ro-31-8220 had no effect on agonist-induced contractile responses of laminar arteries. Conclusions and Clinical Relevance—Results of the study were consistent with activation of PKC being confined to agonist-induced contraction of laminar veins isolated from the laminar dermis of horses. Consequently, the possible involvement of PKC in the venoconstriction observed during the development of laminitis is worthy of further investigation.
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