HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Late-onset endothelin-A receptor blockade reduces podocyte injury in homozygous Ren-2 rats despite severe hypertension.

Abstract
We have recently found in male homozygous hypertensive Ren-2 transgenic rats (TGRs) fed a high-salt diet that early onset selective endothelin (ET) A (ET(A)) or nonselective ET(A)/ET B (ET(B)) receptor blockade improved survival rate and reduced proteinuria, glomerulosclerosis, and cardiac hypertrophy, whereas selective ET(A) receptor blockade also significantly attenuated the rise in blood pressure. Because antihypertensive therapy in general is known to be more efficient when started at early age, our study was performed to determine whether onset of ET receptor blockade at a later age in animals with established hypertension will have similar protective effects as does early-onset therapy. Male homozygous TGRs and age-matched normotensive Hannover Sprague-Dawley rats were fed a high-salt diet between days 51 and 90 of age. TGRs received vehicle (untreated), the selective ET(A) receptor blocker atrasentan (ABT-627), or the nonselective ET(A)/ET(B) receptor blocker bosentan. Survival rates in untreated and bosentan-treated TGRs were 50% and 64%, respectively, whereas with atrasentan, survival rate of TGR was 96%, thus, similar to 93% in Hannover Sprague-Dawley rats. From day 60 on, systolic blood pressure in atrasentan-treated TGRs was transiently lower (P<0.05) than in untreated or bosentan-treated TGRs. Glomerular podocyte injury was substantially reduced with atrasentan treatment independent of severe hypertension and strongly correlated with survival (P<0.001). Our data indicate that in homozygous TGR ET receptors play an important role also in established hypertension. Selective ET(A) receptor blockade not only reduces podocyte injury and end-organ damage but also improves growth and survival independently of hypertension.
AuthorsMartin Opocenský, Herbert J Kramer, Angela Bäcker, Zdenka Vernerová, Václav Eis, Ludek Cervenka, Vera Certíková Chábová, Vladimír Tesar, Ivana Vanecková
JournalHypertension (Dallas, Tex. : 1979) (Hypertension) Vol. 48 Issue 5 Pg. 965-71 (Nov 2006) ISSN: 1524-4563 [Electronic] United States
PMID17015777 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Endothelin A Receptor Antagonists
  • Endothelin B Receptor Antagonists
  • Receptor, Endothelin A
  • Receptor, Endothelin B
Topics
  • Animals
  • Animals, Genetically Modified
  • Endothelin A Receptor Antagonists
  • Endothelin B Receptor Antagonists
  • Hypertension (genetics, mortality, physiopathology, prevention & control)
  • Male
  • Mice
  • Podocytes (metabolism, pathology)
  • Rats
  • Rats, Mutant Strains
  • Rats, Sprague-Dawley
  • Receptor, Endothelin A (physiology)
  • Receptor, Endothelin B (physiology)
  • Survival Rate
  • Systole (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: