Diuretic effects on cardiac hypertrophy in the stroke prone spontaneously hypertensive rat

Cardiovasc Res. 1993 Mar;27(3):429-34. doi: 10.1093/cvr/27.3.429.

Abstract

Objective: The aim was to compare the effects of two diuretics, indapamide and hydrochlorothiazide, on cardiac hypertrophy in stroke prone spontaneously hypertensive rats (SHR-SP).

Methods: Six week old SHR-SP, on a 1% sodium chloride water intake, were treated with oral indapamide (3 mg.kg-1 x d-1) or hydrochlorothiazide (20 mg.kg-1 x d-1) over a 44 d period. The hypertrophic process was evaluated by classical indices and by the morphological analysis of myocyte cross sectional area, coronary artery thickness, and immunohistochemical analysis of interstitial fibrosis.

Results: In the untreated SHR-SP on 1% sodium chloride, all animals developed severe hypertension and cardiac hypertrophy when compared to normotensive salt loaded WKY by 13 weeks of age. In salt loaded SHR-SP treated with indapamide or hydrochlorothiazide, systolic blood pressure was moderately decreased by the end of the treatment when compared with untreated SHR-SP, at 259(7) and 245(7) mm Hg respectively, v 300(11) mm Hg, p < or = 0.05. Myocyte enlargement appears to be the main feature involved in the development of cardiac hypertrophy in the SHR-SP. By the end of treatment both indapamide and hydrochlorothiazide prevented the development of cardiac hypertrophy evaluated by heart weight to body weight ratio [4.69(0.07) and 4.61(0.08) respectively, v 5.39(0.13), p < or = 0.001] and myocyte hypertrophy (-33% and -21% of the SHR-SP values, p < or = 0.001). Myocardial interstitial fibrosis and perivascular fibrosis were practically absent in the two treated groups.

Conclusions: Our results allow the characterisation of SHR-SP cardiac hypertrophy and indicate that the two types of chronic diuretic treatment prevent SHR-SP cardiac hypertrophy with a drug specific efficiency.

MeSH terms

  • Animals
  • Blood Pressure / drug effects
  • Cardiomegaly / pathology
  • Cardiomegaly / prevention & control*
  • Coronary Vessels / pathology
  • Drug Evaluation, Preclinical
  • Fibrosis
  • Hydrochlorothiazide / therapeutic use*
  • Hypertension / complications*
  • Indapamide / therapeutic use*
  • Myocardium / pathology
  • Organ Size
  • Random Allocation
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred Strains
  • Urination / drug effects

Substances

  • Hydrochlorothiazide
  • Indapamide