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血管紧张素1型受体阻断可能无法保护大鼠肾脏免受顺铂诱导的肾毒性。

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

作者信息

Rastghalam Roya, Nematbakhsh Mehdi, Bahadorani Mehrnoosh, Eshraghi-Jazi Fatemeh, Talebi Ardeshir, Moeini Maryam, Ashrafi Farzaneh, Shirdavani Soheila

机构信息

Water and Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan 81745, Iran ; Department of Biology, Falavarjan Branch, Islamic Azad University, Isfahan 84515, Iran.

Water and Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan 81745, Iran ; Department of Physiology, Isfahan University of Medical Sciences, Isfahan 81745, Iran ; Isfahan MN Institute of Basic and Applied Sciences Research, Isfahan 81546, Iran.

出版信息

ISRN Nephrol. 2014 Mar 16;2014:479645. doi: 10.1155/2014/479645. eCollection 2014.

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.

摘要

背景。顺铂(CDDP)是一种抗癌药物,伴有包括肾毒性在内的主要副作用。我们在每日给予CDDP(2.5毫克/千克/天)的大鼠模型中测试了两种剂量的氯沙坦(10和20毫克/千克/天)对肾毒性的影响。方法。检查了五组大鼠。第1组和第2组腹腔注射氯沙坦10和20毫克/千克/天,持续10天。第3组连续10天给予生理盐水,但从第3天起,动物在接下来的7天内接受CDDP(2.5毫克/千克/天,腹腔注射)。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天起,它们在接下来的7天内也接受CDDP。实验结束时,采集血样并取出肾脏进行病理检查,并从匀浆组织中获得上清液。结果。CDDP诱导了肾毒性,但氯沙坦并未降低血清肌酐和血尿素氮水平。病理结果证实,氯沙坦在该实验模型中没有肾保护作用。结论。根据研究结果,氯沙坦不能改善连续剂量CDDP诱导的毒性所损害的肾功能,而且还会加重肾衰竭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d450/4045571/0293b9c4c0f4/ISRN.NEPHROLOGY2014-479645.001.jpg

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