Tempol attenuates the development of hypertensive renal injury in Dahl salt-sensitive rats

Am J Hypertens. 2005 May;18(5 Pt 1):707-13. doi: 10.1016/j.amjhyper.2004.11.045.

Abstract

Background: Dahl salt-sensitive (DS) rats given a high-salt diet develop renal lesions that are virtually identical to those in human hypertensive nephrosclerosis and are associated with increased oxidative stress. This study looks at the effects of a superoxide scavenger in preventing of hypertensive renal damage in high-salt-treated DS rats.

Methods: The DS rats (n = 5 per group) were treated with 0.3% NaCl diets (LS), 8% NaCl diets (HS), and 8% NaCl diets plus 10 mmol/L tempol in drinking water (HS+T) for 5 weeks. Systolic blood pressure (SBP) was measured by the tail-cuff method. As markers of renal damage, we measured serum creatinine, creatinine clearance, histopathologic indices, and transforming growth factor-beta1 (TGF-beta1; a mediator for renal fibrosis) expression. In addition, 8-hydroxy-2'-deoxyguanosine (8-OHdG)-positive cells and expression of heme oxygenase-1 (HO-1) were quantified as markers of oxidative stress.

Results: We found that a high-salt diet (8% NaCl) led to the development of hypertension, increased oxidative stress in the renal tissue (8-OHdG immunoreactive staining and HO-1 protein expression), increased renal histopathologic damage (arteriosclerosis index, matrix score, and interstitial volume) accompanied by accumulation of TGF-beta1, and decreased creatinine clearance in the DS rats. These adverse effects of salt were prevented by the tempol supplementation.

Conclusions: Histopathologic and biochemical findings indicate that, in the DS rat, salt-induced hypertensive nephropathy is associated with increased oxidative stress. Superoxide mimetic tempol can reduce this detrimental effect of salt feeding through TGF-beta1 suppression and consequently prevent the development of hypertension and hypertensive nephropathy.

MeSH terms

  • Animals
  • Heat-Shock Proteins / analysis
  • Heme Oxygenase (Decyclizing)
  • Hypertension / metabolism
  • Hypertension / pathology*
  • Immunohistochemistry
  • Kidney / enzymology
  • Kidney / pathology*
  • Male
  • Oxidative Stress
  • Oxygenases / analysis
  • Rats
  • Rats, Inbred Dahl
  • Sodium Chloride / pharmacology*
  • Superoxides / metabolism
  • Systole
  • Transforming Growth Factor beta / physiology

Substances

  • Heat-Shock Proteins
  • Transforming Growth Factor beta
  • Superoxides
  • Sodium Chloride
  • Oxygenases
  • Heme Oxygenase (Decyclizing)
  • Hmox1 protein, rat