Corcoran G B, Salazar D E
Department of Pharmaceutics, School of Pharmacy, State University of New York, Buffalo.
J Pharmacol Exp Ther. 1989 Jan;248(1):17-22.
Obese humans suffer from excessive organ dysfunction, altered drug pharmacokinetics and may be at increased risk of various drug toxicities. A recent report shows that gentamicin nephrotoxicity in critically ill patients is more frequent and more severe than usual in individuals who are substantially overweight. The present study utilizes an overfed rat model to examine the influence of obesity on the nephrotoxic potential of gentamicin. After 52 weeks on an energy-dense diet, obese animals outweighed pellet controls by more than 80% (913 +/- 86 vs. 507 +/- 52 g; X +/- S.D., n = 7). When animals were treated twice daily for 6 days with 30 mg/kg of gentamicin i.p. based on total body mass, obese rats sustained more cortical necrosis than control (median score 3+ vs. 0), higher serum creatinine (4.36 +/- 2.72 vs. 0.71 +/- 0.17) and greater creatinine adjusted N-acetyl hexosaminidase excretion. The impact of obesity on intrinsic susceptibility to gentamicin nephrotoxicity was assessed by dosing animals for 5 days to ideal body mass plus 40% of excess body mass, the current clinical practice for achieving normal gentamicin concentrations in obese patients. Obese rats again sustained more frequent and severe cortical necrosis (2+ vs. 0) and excreted more N-acetyl hexosaminidase than control animals. Urine pH averaged 1.7 U below normal in obese animals, but restoration to normal values by 2 weeks on the pellet diet did not diminish the toxicity increase. Results from the overfed rat closely resemble the recent clinical observation that obese patients sustain more frequent and severe kidney damage from aminoglycoside antibiotics.(ABSTRACT TRUNCATED AT 250 WORDS)
肥胖人群存在多种器官功能异常、药物药代动力学改变的问题,并且可能面临各种药物毒性增加的风险。最近一份报告显示,在重症患者中,庆大霉素肾毒性在严重超重个体中比在正常个体中更频繁且更严重。本研究利用过度喂养的大鼠模型来研究肥胖对庆大霉素肾毒性潜力的影响。在给予高能量饮食52周后,肥胖动物比对照组体重超出80%以上(913±86克对507±52克;平均值±标准差,n = 7)。当根据动物总体重以每天30毫克/千克的剂量腹腔注射庆大霉素,连续注射6天,肥胖大鼠出现的皮质坏死比对照组更多(中位数评分3+对0),血清肌酐水平更高(4.36±2.72对0.71±0.17),肌酐调整后的N - 乙酰己糖胺酶排泄量也更大。通过按照理想体重加40%超重体重给动物给药5天来评估肥胖对庆大霉素肾毒性内在易感性的影响,这是目前在肥胖患者中实现正常庆大霉素浓度的临床实践方法。肥胖大鼠再次出现更频繁且更严重的皮质坏死(2+对0),并且比对照动物排泄更多的N - 乙酰己糖胺酶。肥胖动物的尿液pH平均比正常低1.7个单位,但在给予普通饮食2周后恢复到正常水平并没有减轻毒性增加的情况。过度喂养大鼠的实验结果与最近的临床观察结果非常相似,即肥胖患者更容易因氨基糖苷类抗生素而遭受更频繁且更严重的肾损伤。(摘要截断于250字)