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

被引:9
|
作者
Moslemi, Fatemeh [1 ]
Taheri, Pegah [1 ]
Azimipoor, Mahdis [1 ]
Ramtin, Sina [1 ]
Hashemianfar, Mostafa [1 ]
Momeni-Ashjerdi, Ali [1 ]
Eshraghi-Jazi, Fatemeh [1 ]
Talebi, Ardeshir [1 ]
Nasri, Hamid [1 ]
Nematbakhsh, Mehdi [1 ,2 ,3 ]
机构
[1] Isfahan Univ Med Sci, Water Electrolytes Res Ctr, Esfahan, Iran
[2] Isfahan Univ Med Sci, Dept Physiol, Esfahan, Iran
[3] IsfahanMN Inst Basic & Appl Sci Res, Esfahan, Iran
来源
JOURNAL OF RENAL INJURY PREVENTION | 2016年 / 5卷 / 03期
关键词
Ischemia reperfusion injury; Losartan; Gender; Acute kidney injury;
D O I
10.15171/jrip.2016.29
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:140 / 143
页数:4
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