Characterization of a stable, hypertensive rat model suitable for the consecutive evaluation of human renin inhibitors

J Renin Angiotensin Aldosterone Syst. 2011 Sep;12(3):133-45. doi: 10.1177/1470320310392618. Epub 2011 Mar 10.

Abstract

Introduction: The hypertensive double-transgenic (dTG) rat strain, expressing human renin and angiotensinogen, develops severe hypertension and organ damage and 50% of individuals die by 7 weeks of age. Here, we characterise a variation of this model in which animals present stable hypertension.

Materials and methods: The effect of renin-angiotensin system blockers on blood pressure was determined with adult dTG rats treated with enalapril from 3 to 12 weeks of age. Tissue expression levels of renin and angiotensinogen were determined in dTG rats and rhesus monkeys by quantitative PCR.

Results: Upon withdrawal from enalapril, mean arterial pressure (MAP) rose to 160-180 mmHg, with 95% of the female dTG rats surviving for 6 to 12 months, In Sprague-Dawley (SD) rats and rhesus monkeys, renin mRNA was absent or weakly expressed in most tissues, except for the kidneys and adrenals. In dTG rats, human renin expression was high in many additional tissues. The expression of human angiotensinogen in dTG rats followed a similar tissue pattern to SD and rhesus monkey angiotensinogen. Oral dosing of aliskiren, enalapril or losartan provided a similar maximal reduction in MAP and duration of efficacy in telemetrised dTG rats.

Conclusions: Enalapril-pretreated dTG rats are suitable for long-term MAP monitoring and sequential evaluation of human renin inhibitors.

MeSH terms

  • Amides / administration & dosage
  • Amides / pharmacology
  • Amides / therapeutic use
  • Angiotensinogen / genetics
  • Angiotensinogen / metabolism
  • Animals
  • Blood Pressure / drug effects
  • Disease Models, Animal
  • Enalapril / administration & dosage
  • Enalapril / pharmacology*
  • Enalapril / therapeutic use*
  • Female
  • Fumarates / administration & dosage
  • Fumarates / pharmacology
  • Fumarates / therapeutic use
  • Gene Expression Regulation / drug effects
  • Heart Rate / drug effects
  • Humans
  • Hypertension / drug therapy*
  • Hypertension / physiopathology
  • Macaca mulatta
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Transgenic
  • Renin / antagonists & inhibitors*
  • Renin / blood
  • Renin / genetics
  • Tissue Distribution / drug effects

Substances

  • Amides
  • Fumarates
  • RNA, Messenger
  • Angiotensinogen
  • aliskiren
  • Enalapril
  • Renin