Why the study?
Does intravenous ET-1 alter systemic and renal hemodynamics differently in diabetic-hypertensive rats compared to spontaneously hypertensive rats?
Does intravenous ET-1 alter systemic and renal hemodynamics differently in diabetic-hypertensive rats compared to spontaneously hypertensive rats?
Diabetic-hypertensive rats exhibit reduced sensitivity to the systemic and renal actions of ET-1, with a reversal of its typical medullary vasodilatory effect into prolonged vasoconstriction.
Answers are grounded in this paper and cite their sources.
Altered ET-1 responses in diabetic-hypertensive models warrant caution in extrapolation; leaves open endothelin targeting in combined human hypertension and diabetes.
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.
No takes yet. Share an insight, caveat, or question.
Hofman et al. (2011) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: