Article date: July 2011
By: Zsolt Bagi, Attila Feher, James Cassuto, Komala Akula, Nazar Labinskyy, Gabor Kaley, Akos Koller in Volume 163, Issue 5, pages 1059-1068
BACKGROUND AND PURPOSE Antagonists of angiotensin AT1 receptors elicit beneficial vascular effects in diabetes mellitus. We hypothesized that diabetes induces sustained availability of AT1 receptors, causing enhanced arterial constriction to angiotensin II.
EXPERIMENTAL APPROACH To assess functional availability of AT1 receptors, constrictions to successive applications of angiotensin II were measured in isolated skeletal muscle resistance arteries (∼150 µm) of Zucker diabetic fatty (ZDF) rats and of their controls (+/Fa), exposed acutely to high glucose concentrations (HG, 25 mM, 1 h). AT1 receptors on cell membrane surface were measured by immunofluorescence.
KEY RESULTS Angiotensin II‐induced constrictions to first applications were greater in arteries of ZDF rats (maximum: 82 ± 3% original diameter) than in those from +/Fa rats (61 ± 5%). Constrictions to repeated angiotensin II administration were decreased in +/Fa arteries (20 ± 6%), but were maintained in ZDF arteries (67 ± 4%) and in +/Fa arteries vessels exposed to HG (65 ± 6%). In ZDF arteries and in HG‐exposed +/Fa arteries, Rho‐kinase activities were enhanced. The Rho‐kinase inhibitor, Y27632 inhibited sustained constrictions to angiotensin II in ZDF arteries and in +/Fa arteries exposed to HG. Levels of surface AT1 receptors on cultured vascular smooth muscle cells (VSMCs) were decreased by angiotensin II but were maintained in VSMCs exposed to HG. In VSMCs exposed to HG and treated with Y27632, angiotensin II decreased surface AT1 receptors.
CONCLUSIONS AND IMPLICATIONS In diabetes, elevated glucose concentrations activate Rho‐kinase which inhibits internalization or facilitates recycling of AT1 receptors, leading to increased functional availability of AT1 receptors and sustained angiotensin II‐induced arterial constriction.
DOI: 10.1111/j.1476-5381.2011.01307.x
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