Key result
Losartan pretreatment significantly attenuated ischemia/reperfusion-induced increases in BUN, creatinine, and kidney tissue damage in female rats (P < 0.05), but accelerated kidney injury in male rats.
Why the study?
Does losartan improve renal ischemia/reperfusion injury in male and female rats?
Does losartan improve renal ischemia/reperfusion injury in male and female rats?
p-value: p=<0.05
Losartan protects against renal ischemia/reperfusion injury in female rats but exacerbates it in male rats, highlighting a significant gender-related difference in the renin-angiotensin system.
May suggest gender-specific losartan effects in rat renal I/R; leaves open translation to human AKI.
BACKGROUND: Renal ischemia/reperfusion (I/R) injury may be related to activity of reninangiotensin 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.
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Moslemi et al. (2016) studied Renal ischemia/reperfusion injury (n=34). Losartan vs. Vehicle (saline) was evaluated on Serum levels of BUN and creatinine, and kidney tissue damage score (p=<0.05). Losartan pretreatment significantly attenuated ischemia/reperfusion-induced increases in BUN, creatinine, and kidney tissue damage in female rats (P < 0.05), but accelerated kidney injury in male rats.
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