Wood C A, Finkbeiner H C, Kohlhepp S J, Kohnen P W, Gilbert D N
Chiles Research Institute, Providence Medical Center, Portland, Oregon 97213.
Antimicrob Agents Chemother. 1989 Aug;33(8):1280-5. doi: 10.1128/AAC.33.8.1280.
The antibacterial efficacies of daptomycin and vancomycin were compared in male Fischer rats with subcutaneous abscesses caused by either methicillin-susceptible Staphylococcus aureus (MSSA) or methicillin-resistant S. aureus (MRSA). The influence of daptomycin on tobramycin nephrotoxicity was also assessed. MSSA or MRSA abscesses were treated with subcutaneous daptomycin (10 mg/kg every 12 h), vancomycin (125 mg/kg every 12 h), or diluent (every 12 h) for 5 to 10 days. Rats in both antibiotic treatment groups had lower abscess bacterial counts than did controls at days 5 and 10 (P less than 0.0025). The daptomycin treatment groups had lower abscess bacterial counts than did the vancomycin treatment groups for MSSA at day 5 (P less than 0.0025) and day 10 (P less than 0.025) and for MRSA at day 10 (P less than 0.0025). Nephrotoxicity treatment groups included animals treated for 3, 7, 10, 14, and 17 days with subcutaneous diluent (every 12 h), daptomycin (20 mg/kg every 12 h), tobramycin (40 mg/kg every 12 h), and the combination of daptomycin and tobramycin. Compared with controls, animals treated with daptomycin alone exhibited no detectable nephrotoxicity. Rats given tobramycin alone developed functional and histopathologic abnormalities from days 7 through 17. Animals treated with daptomycin and tobramycin for 14 days had a lower mean concentration of creatinine in serum (P less than 0.005), higher mean creatinine clearance values (P less than 0.05), and less cortical tubular cell regeneration (P less than 0.05) than did rats treated with tobramycin alone. In rats with staphylococcal subcutaneous abscesses, daptomycin was superior to vancomycin in treating both MSSA and MRSA. Daptomycin alone caused no detectable renal injury, and in rats given daptomycin combined with tombramycin, there was less histologic and functional renal injury than in animals given tobramycin alone.
在患有由甲氧西林敏感金黄色葡萄球菌(MSSA)或耐甲氧西林金黄色葡萄球菌(MRSA)引起的皮下脓肿的雄性Fischer大鼠中,比较了达托霉素和万古霉素的抗菌效果。还评估了达托霉素对妥布霉素肾毒性的影响。MSSA或MRSA脓肿分别用皮下注射达托霉素(每12小时10mg/kg)、万古霉素(每12小时125mg/kg)或稀释剂(每12小时)治疗5至10天。在第5天和第10天,两个抗生素治疗组的大鼠脓肿细菌计数均低于对照组(P<0.0025)。对于MSSA,在第5天(P<0.0025)和第10天(P<0.025),达托霉素治疗组的脓肿细菌计数低于万古霉素治疗组;对于MRSA,在第10天(P<0.0025)也是如此。肾毒性治疗组包括分别用皮下稀释剂(每12小时)、达托霉素(每12小时20mg/kg)、妥布霉素(每12小时40mg/kg)以及达托霉素和妥布霉素联合治疗3、7、10、14和17天的动物。与对照组相比,单独使用达托霉素治疗的动物未表现出可检测到的肾毒性。单独给予妥布霉素的大鼠在第7天至第17天出现功能和组织病理学异常。联合使用达托霉素和妥布霉素治疗14天的动物,其血清肌酐平均浓度较低(P<0.005),肌酐清除率平均数值较高(P<0.05),并且皮质肾小管细胞再生较少(P<0.05),优于单独给予妥布霉素治疗的大鼠。在患有葡萄球菌皮下脓肿的大鼠中,达托霉素在治疗MSSA和MRSA方面均优于万古霉素。单独使用达托霉素不会引起可检测到的肾损伤,并且在联合使用达托霉素和妥布霉素的大鼠中,与单独给予妥布霉素的动物相比,肾组织学和功能损伤较轻。