| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Hypertension. 1996;27:955-961.)
© 1996 American Heart Association, Inc.
Articles |
From the Hypertension Unit, Department of Internal Medicine, University of Udine (Italy) (L.A.S., L.Z., C.C., E.B.); Clinica di Endocrinologia, Universitá di Ancona (Italy) (G.G.); and Division of Endocrinology, San Francisco General Hospital, University of California (L.A.S., C.A.G., G.G., M.S.).
Abstract Insulin resistance is present in some strains of rats with genetic hypertension. To determine whether this abnormality is present at the level of the insulin receptor, we compared insulin sensitivity, insulin receptor binding, and mRNA levels in tissues of 10-week-old spontaneously hypertensive rats (SHR) and their normotensive Wistar-Kyoto (WKY) controls. Because we have previously demonstrated an inverse relationship between dietary sodium intake and renal insulin receptor density and mRNA levels in normal Sprague-Dawley rats, the two rat strains in the current experiment were fed either low salt (0.07% NaCl) or high salt (7.5% NaCl) chow until the SHR became hypertensive. Fasting plasma glucose and plasma insulin levels did not differ between SHR and WKY and were not affected by salt intake. When the rats were maintained on the low salt diet, the rate of glucose infusion required to maintain euglycemia during a hyperinsulinemic clamp was significantly lower in SHR than WKY. High salt diet decreased the rate of glucose utilization during the hyperinsulinemic clamp in WKY but not SHR. During the low salt diet, insulin infusion decreased sodium excretion in both WKY and SHR. When the rats were maintained on the high salt diet, the antinatriuretic response to insulin was blunted in WKY but not SHR. Both the density and mRNA levels of insulin receptor were comparable in the kidney of WKY and SHR, but only WKY had the previously demonstrated decrease in receptor number and mRNA levels when fed the high salt chow. Hepatic insulin receptor mRNA levels were significantly lower in SHR than WKY fed the low salt diet. High salt diet decreased significantly insulin receptor mRNA levels in the liver of WKY but not of SHR. Thus, SHR appear to have lost the feedback mechanism that normally limits insulin-induced sodium retention when extracellular volume is expanded. A decreased expression of insulin receptor in the liver of SHR provides a possible explanation for the insulin resistance and decreased insulin clearance present in this strain.
Key Words: insulin receptors RNA liver kidney hypertension, genetic
This article has been cited by other articles:
![]() |
F. A. DeLano and G. W. Schmid-Schonbein Proteinase Activity and Receptor Cleavage: Mechanism for Insulin Resistance in the Spontaneously Hypertensive Rat Hypertension, August 1, 2008; 52(2): 415 - 423. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Tiwari, N. Sharma, P. S. Gill, P. Igarashi, C. R. Kahn, J. B. Wade, and C. M. A. Ecelbarger Impaired sodium excretion and increased blood pressure in mice with targeted deletion of renal epithelial insulin receptor PNAS, April 29, 2008; 105(17): 6469 - 6474. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Tiwari, S. Riazi, and C. A. Ecelbarger Insulin's impact on renal sodium transport and blood pressure in health, obesity, and diabetes Am J Physiol Renal Physiol, October 1, 2007; 293(4): F974 - F984. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Farjah, B. P. Roxas, D. L. Geenen, and R. S. Danziger Dietary Salt Regulates Renal SGK1 Abundance: Relevance to Salt Sensitivity in the Dahl Rat Hypertension, April 1, 2003; 41(4): 874 - 878. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Vecchione, C. Morisco, L. Fratta, L. Argenziano, B. Trimarco, and G. Lembo Dietary Sodium Restriction Impairs Endothelial Effect of Insulin Hypertension, June 1, 1998; 31(6): 1261 - 1265. [Abstract] [Full Text] [PDF] |
||||
|
Hypertension Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1996 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |