• Title of article

    Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference

  • Author/Authors

    Moslemi, Fatemeh Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Taheri, Pegah Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Azimipoor, Mahdis Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Ramtin, Sina Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Hashemianfar, Mostafa Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Momeni- Ashjerdi, Ali Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Eshraghi-Jazi, Fatemeh Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Talebi, Ardeshir Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Nasri, Hamid Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Nematbakhsh, Mehdi Water & Electrolytes Research Center - Isfahan University of Medical Sciences, Isfahan, Iran

  • Pages
    4
  • From page
    140
  • To page
    143
  • Abstract
    Background: Renal ischemia/reperfusion (I/R) injury may be related to activity of renin-angiotensin system (RAS), which is gender-related. In this study, it was attempted to compare the effect of angiotensin II (Ang II) receptor type 1 (AT1R) blockade; losartan in I/R injury in male and female rats. Materials and Methods: Male and female Wistar rats were assigned as sham surgery, control I/R groups treated with vehicle, and case I/R groups treated with losartan (30 mg/kg). Vehicle and losartan were given 2 hours before bilateral kidney ischemia induced by clamping renal arteries for 45 minutes followed by 24 hours of renal reperfusion. Results: The I/R injury significantly increased the serum levels of blood urea nitrogen (BUN) and creatinine (Cr), and kidney tissue damage score in both genders. However, losartan decreased these values in female rats significantly (P < 0.05). This was not observed in male rats. Conclusion: Losartan protects the kidney from I/R injury in female but not in male rats possibly because of gender-related difference of RAS.
  • Keywords
    Ischemia reperfusion injury , Losartan , Gender , Acute kidney injury
  • Journal title
    Journal of Renal Injury Prevention
  • Serial Year
    2016
  • Journal title
    Journal of Renal Injury Prevention
  • Record number

    2432003