Related Experiment Video
Updated: May 29, 2026

Improved Renal Denervation Mitigated Hypertension Induced by Angiotensin II Infusion
Published on: May 26, 2022
Renal and systemic effects of endothelin-1 in diabetic-hypertensive rats
Cipy Hofman1, Talma Rosenthal, Joseph Winaver
1Hypertension Research Unit, Department of Physiology and Pharmacology, Sackler School of Medicine, Tel Aviv University, Israel.
Insights
The Cohen-Rosenthal Diabetic Hypertensive (CRDH) rat model shows reduced sensitivity to endothelin-1 (ET-1). Unlike in SHR rats, ET-1 caused vasoconstriction in CRDH rat kidneys, not vasodilation.
Area of Science:
- Cardiovascular Physiology
- Renal Physiology
- Endocrinology
Background:
- The Cohen-Rosenthal Diabetic Hypertensive (CRDH) rat is a hybrid model exhibiting both genetic hypertension and diabetes.
- Endothelin-1 (ET-1) is a potent vasoconstrictor with complex effects on renal hemodynamics.
Purpose of the Study:
- To investigate the acute effects of ET-1 on systemic and renal hemodynamics in CRDH rats, Cohen diabetic rats (CDR), and spontaneously hypertensive rats (SHR).
- To examine the expression of ET-1 and its receptors in the renal tissue of CRDH rats.
Main Methods:
- Intravenous administration of ET-1 to anesthetized rats (SHR, CDR, CRDH).
- Measurement of mean arterial pressure (MAP) and renal blood flow (RBF).
- Laser-Doppler analysis of intra-renal cortical and medullary blood flow in CRDH rats.
Main Results:
- ET-1 induced a transient depressor response followed by hypertension and reduced RBF in SHR rats.
- These vascular and renal responses to ET-1 were blunted in CRDH and CDR rats.
- In CRDH rats, ET-1 caused vasoconstriction in both renal cortex and medulla, reversing the expected medullary vasodilation.
Conclusions:
- CRDH and CDR rats exhibit diminished sensitivity to the vascular and renal actions of ET-1.
- The typical ET-1-mediated renal medullary vasodilation is abolished and reversed to vasoconstriction in CRDH rats.
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.
Related Concept Videos
Diabetic Nephropathy
Hypertension II: Pathophysiology
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
Antihypertensive Drugs: Direct Renin Inhibitors
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme (ECE). Of...
Antihypertensive Drugs: Action of β1 Blockers
