Short-term hypercaloric diet induces blunted aortic vasoconstriction and enhanced vasorelaxation via increased nitric oxide synthase 3 activity and expression in Dahl salt-sensitive rats

Academic Article


  • Aim: To elucidate the role of the O2-, H2O2 or NO pathways in aortic angiotensin (Ang)II-induced vasoconstriction in Dahl salt-sensitive (SS) rats compared with control SS-13BN rats on a normal or hypercaloric diet. Methods: Aortic function was assessed using wire myography in 16-week-old rats maintained on a normal diet or a 4-week hypercaloric diet. Nitric oxide synthase (NOS) activity and expression was determined by the conversion of radio-labelled arginine to citrulline and Western blot analysis respectively. Results: On normal diet, AngII-induced vasoconstriction was greater in SS than SS-13BN rats. Polyethylene glycol superoxide dismutase (PEG-SOD) reduced the aortic AngII response similarly in both strains on normal diet. Catalase blunted, whereas Nω-Nitro-L-arginine methyl ester (L-NAME) did not affect the AngII response in SS rats. In SS-13BN rats, catalase had no effect and L-NAME enhanced AngII response. On hypercaloric diet, aortic AngII responsiveness was reduced in SS but unaltered in SS-13BN rats compared with their normal diet counterparts. PEG-SOD reduced the AngII response in both rats on hypercaloric diet. Catalase treatment did not alter aortic AngII response, while L-NAME increased the response in SS rats on hypercaloric diet. In SS-13BN rats on hypercaloric diet, catalase reduced and L-NAME did not alter the AngII response. Furthermore, aortic endothelial-dependent vasorelaxation was increased in SS rats on hypercaloric diet compared with normal diet and aortic NOS3 activity and expression was increased. Conclusion: A short-term hypercaloric diet induces a blunted vasoconstrictive and enhanced vasodilatory phenotype in SS rats, but not in SS-13BN rats, via reduced H2O2 and increased NOS3 function. © 2012 The Authors Acta Physiologica © 2012 Scandinavian Physiological Society.
  • Published In

  • Acta Physiologica  Journal
  • Digital Object Identifier (doi)

    Pubmed Id

  • 26111063
  • Author List

  • Spradley FT; Kang KT; Pollock JS
  • Start Page

  • 358
  • End Page

  • 368
  • Volume

  • 207
  • Issue

  • 2