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Renal and systemic effects of endothelin-1 in diabetic-hypertensive rats.

Authors :
Hofman C
Rosenthal T
Winaver J
Rubinstein I
Ramadan R
Stern N
Limor R
Awad H
Abassi Z
Source :
Clinical and experimental hypertension (New York, N.Y. : 1993) [Clin Exp Hypertens] 2011; Vol. 33 (7), pp. 444-54. Date of Electronic Publication: 2011 Sep 20.
Publication Year :
2011

Abstract

The Cohen-Rosenthal Diabetic Hypertensive rat (CRDH) is a unique animal model in which genetic hypertension and diabetes developed after crossbreeding of Cohen diabetic rats sensitive substrain (CDR) and spontaneously hypertensive rats (SHR). The present study examined: 1) The acute effects of ET-1 on the systemic and renal hemodynamics in CRDH rats, CDR, and SHR; 2) The expression of ET-1 and its receptors in the renal tissue of CRDH rats. Intravenous injection of ET-1 (1.0 nmol/kg) into anesthetized SHR rats resulted in a significant immediate depressor response (mean arterial pressure (MAP) decreased from 165 ± 3 to 124 ± 12 mmHg, p < 0.0001) followed by a minor hypertensive phase (MAP increased to 170 ± 2 mmHg). Simultaneously, the administration of ET-1 caused a significant decrease in renal blood flow (RBF) from 5.8 ± 0.9 ml/min to 3.2 ± 0.5 ml/min (p = 0.026). These responses were blunted in CRDH rats and CDR. Analysis of intra-renal blood flow by laser-Doppler in CRDH rats revealed that ET-1 injection caused a decrease in cortical blood flow (Δ = -12 ± 2.9%). However, in contrast to its well-known renal medullary vasodilatory effect, ET-1 produced a significant decline in the medulla blood flow (Δ = -17.5 ± 3.4%) (p = 0.0125). These findings suggest that CDR and CRDH rats have reduced sensitivity to vascular and renal action of ET-1. Furthermore, in the CRDH rats, the expected ET-1-induced medullary vasodilatation was abolished and even reversed into prolonged vasoconstriction.

Details

Language :
English
ISSN :
1525-6006
Volume :
33
Issue :
7
Database :
MEDLINE
Journal :
Clinical and experimental hypertension (New York, N.Y. : 1993)
Publication Type :
Academic Journal
Accession number :
21932990
Full Text :
https://doi.org/10.3109/10641963.2010.549270