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抗氧化剂可减轻内毒素-庆大霉素诱导的大鼠急性肾衰竭。

Antioxidants attenuate endotoxin-gentamicin induced acute renal failure in rats.

作者信息

Zurovsky Y, Haber C

机构信息

Department of Life Sciences, Bar-Ilan University, Ramat Gan, Israel.

出版信息

Scand J Urol Nephrol. 1995 Jun;29(2):147-54. doi: 10.3109/00365599509180555.

Abstract

The synergistic mechanism by which endotoxin enhances the nephrotoxic potential of gentamicin is unknown. In this study, we attempted to shed light on this mechanism by injecting rats with endotoxin plus gentamicin. Renal injury was assessed by measuring creatinine, inulin and PAH clearance, NADH levels and electrolyte reabsorption, for 24 hr following this injection. Gentamicin alone (20 mg/100 g) induced no renal injury, while endotoxin without gentamicin (0.075 mg/100 g) induced mild injury. However, endotoxin plus gentamicin resulted in acute renal failure. In an attempt to halt the progressive renal dysfunction, the antioxidants NAO (5 mg/100 g), Vitamin E (0.2 mg/100 g per day) and dimethylthiourea (DMTU-50 mg/100 g) were administered, or early endotoxin tolerance was induced before injecting the rats with endotoxin plus gentamicin. The reduction in renal function was markedly slower in rats administered with antioxidants compared with untreated rats. Similar results were obtained with endotoxin tolerance. These data suggest that NAO, vitamin E, DMTU and endotoxin tolerance are potentially beneficial in arresting progressive renal damage associated with endotoxin plus gentamicin.

摘要

内毒素增强庆大霉素肾毒性潜能的协同机制尚不清楚。在本研究中,我们试图通过给大鼠注射内毒素加庆大霉素来阐明这一机制。在注射后24小时内,通过测量肌酐、菊粉和对氨基马尿酸清除率、NADH水平以及电解质重吸收来评估肾损伤。单独使用庆大霉素(20mg/100g)未引起肾损伤,而未加庆大霉素的内毒素(0.075mg/100g)引起轻度损伤。然而,内毒素加庆大霉素导致急性肾衰竭。为了阻止进行性肾功能障碍,给予抗氧化剂NAO(5mg/100g)、维生素E(每天0.2mg/100g)和二甲基硫脲(DMTU - 50mg/100g),或者在给大鼠注射内毒素加庆大霉素之前诱导早期内毒素耐受。与未治疗的大鼠相比,给予抗氧化剂的大鼠肾功能下降明显较慢。内毒素耐受也得到了类似的结果。这些数据表明,NAO、维生素E、DMTU和内毒素耐受可能有助于阻止与内毒素加庆大霉素相关的进行性肾损伤。

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