Angiotensin Type-1 Receptor Blockade May Not Protect Kidney against Cisplatin-Induced Nephrotoxicity in Rats.

ISRN nephrology Pub Date : 2014-03-16 eCollection Date: 2014-01-01 DOI:10.1155/2014/479645
Roya Rastghalam, Mehdi Nematbakhsh, Mehrnoosh Bahadorani, Fatemeh Eshraghi-Jazi, Ardeshir Talebi, Maryam Moeini, Farzaneh Ashrafi, Soheila Shirdavani
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引用次数: 8

Abstract

Background. Cisplatin (CDDP) is an anticancer drug, which is accompanied with major side effects including nephrotoxicity. We tested two doses of losartan (10 and 20 mg/kg/day) against nephrotoxicity in a rat model treated with daily administration of CDDP (2.5 mg/kg/day). Methods. Five groups of rats were examined. Groups 1 and 2 received losartan 10 and 20 mg/kg/day, i.p, for a period of 10 days. Group 3 received saline for 10 days, but from day 3 the animals received CDDP (2.5 mg/kg/day, i.p) for the next seven days. Groups 4 and 5 received treatment regimen the same as groups 1 and 2, but from day 3 they also received CDDP for the next seven days. At the end of the experiment, blood samples were obtained and the kidneys were removed to undergo pathological investigation and to obtain supernatant from homogenized tissue. Results. CDDP induced nephrotoxicity, but the serum levels of creatinine and blood urea nitrogen were not attenuated by losartan. The pathological findings confirmed that losartan did not have nephroprotective effect in this experimental model. Conclusion. According to the findings, losartan could not improve renal function impaired by toxicity induced by continuous doses of CDDP, and also it worsened the renal failure.

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血管紧张素1型受体阻断可能不能保护大鼠免受顺铂诱导的肾毒性。
背景。顺铂(CDDP)是一种抗癌药物,其主要副作用包括肾毒性。我们测试了两种剂量的氯沙坦(10和20 mg/kg/天)对每天给药(2.5 mg/kg/天)的CDDP大鼠模型的肾毒性。方法。对五组大鼠进行检查。1、2组患者给予氯沙坦10、20 mg/kg/d, ig,疗程10 d。第3组连续10天给予生理盐水,第3天开始连续7天给予CDDP (2.5 mg/kg/d, i.p)。第4组和第5组接受与第1组和第2组相同的治疗方案,但从第3天开始,他们在接下来的7天内也接受CDDP治疗。实验结束时取血,取肾进行病理检查,取匀浆组织上清。结果。氯沙坦对大鼠血清肌酐和尿素氮水平无显著影响。病理结果证实氯沙坦在本实验模型中不具有肾保护作用。结论。结果表明,氯沙坦不仅不能改善连续剂量CDDP毒性所致的肾功能损害,而且加重了肾功能衰竭。
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Urinary biomarkers of acute kidney injury in patients with liver cirrhosis. Angiotensin Type-1 Receptor Blockade May Not Protect Kidney against Cisplatin-Induced Nephrotoxicity in Rats. The Utility of Serial Allograft Biopsies during Delayed Graft Function in Renal Transplantation under Current Immunosuppressive Regimens. Effect of α -Lipoic Acid on Oxidative Stress in End-Stage Renal Disease Patients Receiving Intravenous Iron. Proteinuria, (99m) Tc-DTPA Scintigraphy, Creatinine-, Cystatin- and Combined-Based Equations in the Assessment of Chronic Kidney Disease.
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