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Iron restriction inhibits renal injury in aldosterone/salt-induced hypertensive mice

  • Hisashi Sawada
  • , Yoshiro Naito
  • , Makiko Oboshi
  • , Toshihiro Iwasaku
  • , Yoshitaka Okuhara
  • , Daisuke Morisawa
  • , Akiyo Eguchi
  • , Shinichi Hirotani
  • , Tohru Masuyama

Producción científica: Articlerevisión exhaustiva

20 Citas (Scopus)

Resumen

Excess iron is associated with the pathogenesis of several renal diseases. Aldosterone is reported to have deleterious effects on the kidney, but there have been no reports of the role of iron in aldosterone/salt-induced renal injury. Therefore, we investigated the effects of dietary iron restriction on the development of hypertension and renal injury in aldosterone/salt-induced hypertensive mice. Ten-week-old male C57BL/6J mice were uninephrectomized and infused with aldosterone for four weeks. These were divided into two groups: one fed a high-salt diet (Aldo) and the other fed a high-salt with iron-restricted diet (Aldo-IR). Vehicle-infused mice without a uninephrectomy were also divided into two groups: one fed a normal diet (control) and the other fed an iron-restricted diet (IR) for 4 weeks. As compared with control and IR mice, Aldo mice showed an increase in both systolic blood pressure and urinary albumin/creatinine ratio, but these increases were reduced in the Aldo-IR group. In addition, renal histology revealed that Aldo mice exhibited glomerulosclerosis and tubulointerstitial fibrosis, whereas these changes were attenuated in Aldo-IR mice. Expression of intracellular iron transport protein transferrin receptor 1 was increased in the renal tubules of Aldo mice compared with control mice. Dietary iron restriction attenuated the development of hypertension and renal injury in aldosterone/salt-induced hypertensive mice.

Idioma originalEnglish
Páginas (desde-hasta)317-322
Número de páginas6
PublicaciónHypertension Research
Volumen38
N.º5
DOI
EstadoPublished - may 11 2015

Nota bibliográfica

Publisher Copyright:
© 2015 The Japanese Society of Hypertension.

Financiación

FinanciadoresNúmero del financiador
Japan Society for the Promotion of Science25460919

    ASJC Scopus subject areas

    • Internal Medicine
    • Physiology
    • Cardiology and Cardiovascular Medicine

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