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肌苷在犬和大鼠肾脏模型中未能预防缺血性损伤。

Failure of inosine to prevent ischemic damage in the canine and rat kidney models.

作者信息

Okiye S E, Zincke H, Aydin G, Zinsmeister A R

出版信息

Urol Res. 1984;12(2):121-4. doi: 10.1007/BF00257177.

Abstract

Intravenous, renal artery, and intraperitoneal administration of inosine at dosages of 100 to 200 mg/kg, 160 mg/kg, and 200 mg/kg, respectively, in the dog and rat was used to test its efficacy in preventing ischemic damage after 60 min of warm ischemia in an in situ solitary renal model. No improvement of renal function as compared with a control and a conventional mannitol/furosemide treatment group was detected. Rather, inosine at dosages of greater than or equal to 160 mg/kg resulted in significantly impaired renal function in the experimental groups of the dog model; no improvement was observed in the rat model. These results suggest that the use of inosine in human renal surgery and preservation should be approached cautiously.

摘要

在犬和大鼠中,分别以100至200mg/kg、160mg/kg和200mg/kg的剂量静脉内、肾动脉内和腹膜内给予肌苷,用于测试其在原位孤立肾模型中预防60分钟热缺血后缺血性损伤的功效。与对照组和传统甘露醇/速尿治疗组相比,未检测到肾功能改善。相反,在犬模型的实验组中,剂量大于或等于160mg/kg的肌苷导致肾功能显著受损;在大鼠模型中未观察到改善。这些结果表明,在人类肾脏手术和肾脏保存中使用肌苷应谨慎。

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