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.

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