Abu-Spetan K A, Abdel-Gayoum A A
Department of Biochemistry, Faculty of Medicine, Garyounis University, Benghazi, Libya.
Arch Toxicol. 2001 Jul;75(5):284-90. doi: 10.1007/s002040100233.
Administration of gentamicin to rabbits intramuscularly at a dose of 80 mg/kg per day for 5 days induced nephrotoxicity exhibited by significantly (P < 0.001) elevated serum urea and creatinine levels and a significant (P < 0.001) decrease in renal cortical alkaline phosphatase (ALP) activity, in addition to tubular necrosis revealed by the histopathological examination of the kidney cortices. The deranged parameters returned to normal within 1 week of drug withdrawal, except the cortical ALP activity, which was still significantly lower compared to control. In contrast, feeding of 2% cholesterol-supplemented diet (CSD) to the rabbits for 15 days did not produce any nephrotoxic effects. However, the concurrent feeding of CSD for 15 days and gentamicin treatment at a dose of 80 mg/kg per day for 5 days, starting from day 10 of feeding, resulted in extensive nephrotoxic effects which were more severe than those observed with the gentamicin alone, with delayed recovery of the injured kidney following drug withdrawal. Gentamicin treatment produced significant elevation in serum total cholesterol, which was greater in animals fed with CSD. The serum triglyceride levels in the groups injected with gentamicin were also significantly greater than their respective controls. However, the serum phosphlipids were significantly reduced with gentamicin treatment and this reduction was greater in animals fed with cholesterol and treated with the drug. The liver cholesterol contents in animals fed with the CSD were significantly higher than those fed with the plain diet. However, the kidney cortices of the animals injected with the gentamicin showed significantly increased total phospholipid contents compared to their respective controls. On the other hand, the liver function was not altered in any of the experimental groups. In summary, the present results suggest that cholesterol feeding exacerbated the gentamicin-induced nephrotoxicity. Moreover, it delayed the period required by the injured kidney to recover back to normal. However, neither gentamicin treatment nor cholesterol feeding, or both together, had any injurious effects on the liver.
以每天80毫克/千克的剂量给兔子肌肉注射庆大霉素,持续5天,可诱发肾毒性,表现为血清尿素和肌酐水平显著升高(P < 0.001),肾皮质碱性磷酸酶(ALP)活性显著降低(P < 0.001),此外,通过肾皮质的组织病理学检查还发现肾小管坏死。除皮质ALP活性外,这些紊乱的参数在停药1周内恢复正常,与对照组相比,皮质ALP活性仍显著较低。相比之下,给兔子喂食含2%胆固醇的饲料(CSD)15天未产生任何肾毒性作用。然而,从喂食第10天开始,同时喂食CSD 15天并以每天80毫克/千克的剂量注射庆大霉素5天,会导致广泛的肾毒性作用,比单独使用庆大霉素时观察到的更严重,停药后受损肾脏的恢复延迟。庆大霉素治疗使血清总胆固醇显著升高,在喂食CSD的动物中升高幅度更大。注射庆大霉素组的血清甘油三酯水平也显著高于各自的对照组。然而,庆大霉素治疗使血清磷脂显著降低,在喂食胆固醇并接受药物治疗的动物中这种降低更为明显。喂食CSD的动物肝脏胆固醇含量显著高于喂食普通饲料的动物。然而,注射庆大霉素的动物肾皮质总磷脂含量与各自对照组相比显著增加。另一方面,任何实验组的肝功能均未改变。总之,目前的结果表明,喂食胆固醇会加剧庆大霉素诱导的肾毒性。此外,它还延长了受损肾脏恢复正常所需的时间。然而,单独的庆大霉素治疗、胆固醇喂食或两者同时进行,对肝脏均无任何损害作用。