Effects of the endothelin A receptor antagonist darusentan on blood pressure and vascular contractility in type 2 diabetic Goto-Kakizaki rats

The present study evaluated the effects of long-term treatment with the endothelin A (ETA) receptor antagonist darusentan (LU135252) on blood pressure (BP) and vascular target-organ damage in spontaneously type 2 diabetic Goto-Kakizaki (GK) rats. BP was monitored by radiotelemetry in untreated and d...

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Hauptverfasser: Witte, Klaus (VerfasserIn) , Reitenbach, Ina (VerfasserIn) , Stolpe, Kerstin (VerfasserIn) , Schilling, Lothar (VerfasserIn) , Kirchengast, Michael (VerfasserIn) , Lemmer, Björn (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: June 2003
In: Journal of cardiovascular pharmacology
Year: 2003, Jahrgang: 41, Heft: 6, Pages: 890-896
ISSN:1533-4023
DOI:10.1097/00005344-200306000-00009
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1097/00005344-200306000-00009
Verlag, lizenzpflichtig, Volltext: https://journals.lww.com/cardiovascularpharm/Fulltext/2003/06000/Effects_of_the_Endothelin_A_Receptor_Antagonist.9.aspx
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Verfasserangaben:Klaus Witte, Ina Reitenbach, Kerstin Stolpe, Lothar Schilling, Michael Kirchengast, and Björn Lemmer
Beschreibung
Zusammenfassung:The present study evaluated the effects of long-term treatment with the endothelin A (ETA) receptor antagonist darusentan (LU135252) on blood pressure (BP) and vascular target-organ damage in spontaneously type 2 diabetic Goto-Kakizaki (GK) rats. BP was monitored by radiotelemetry in untreated and darusentan-treated GK rats from 10-24 weeks of age. Relaxation of mesenteric artery segments by acetylcholine (ACh) and sodium nitroprusside (SNP) was measured to assess endothelium-dependent and -independent vasorelaxation. Aortic soluble guanylyl cyclase (sGC) activity was studied in vitro after stimulation by the nitric oxide (NO) donor diethylamine-NONOate. Untreated GKs were mildly hypertensive and showed a blunted vascular relaxation by ACh and SNP and a reduction in NO-stimulated sGC activity in comparison with Wistar control rats. Darusentan led to a small but sustained reduction in 24-h BP but did not restore the endothelium-dependent vasorelaxation nor the NO-stimulated cGMP formation in GK rats. The present findings suggest that an activated endothelin pathway may contribute to elevated BP but is not involved in vascular dysfunction in this animal model of type II diabetes.
Beschreibung:Gesehen am 28.03.2022
Beschreibung:Online Resource
ISSN:1533-4023
DOI:10.1097/00005344-200306000-00009