Oshima Kazuhiro, Nakamura Shigeki, Iwanaga Naoki, Takemoto Koji, Miyazaki Taiga, Yanagihara Kastunori, Miyazaki Yoshitsugu, Mukae Hiroshi, Kohno Shigeru, Izumikawa Koichi
Leading Program, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Unit of Molecular Microbiology and Immunology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Antimicrob Agents Chemother. 2016 Dec 27;61(1). doi: 10.1128/AAC.02056-16. Print 2017 Jan.
High-dose meropenem (MEPM; 6 g/day) has been approved as a treatment for purulent meningitis; however, little is known regarding its in vivo efficacy in refractory lower respiratory tract infections. The purpose of this study was to evaluate the efficacy of MEPM at 6 g/day in a murine model of severe pneumonia caused by MEPM-resistant Pseudomonas aeruginosa Experimental pneumonia induced by MEPM-resistant P. aeruginosa was treated with normal-dose MEPM (150 mg/kg of body weight, simulating a 3-g/day regimen in humans) or high-dose MEPM (500 mg/kg, simulating a 6-g/day regimen in humans). Mice treated with high-dose MEPM showed significantly restored survival relative to that of untreated mice and tended to show a survival rate higher than that of mice treated with normal-dose MEPM. The viable bacterial counts (of two clinical isolates) in the lungs decreased significantly in mice treated with high-dose MEPM from those for untreated mice (P < 0.001) or mice treated with normal-dose MEPM (P, <0.01 and <0.05). The number of inflammatory cells in the bronchoalveolar lavage fluid (BALF) was also significantly lower in mice treated with high-dose MEPM than in untreated mice. The free MEPM concentration in the epithelial lining fluid (ELF) exceeded 16 μg/ml for 85 min in mice treated with high-dose MEPM, but not for mice treated with normal-dose MEPM. Our results demonstrate that high-dose MEPM (6 g/day) might provide better protection against pneumonia caused by MEPM-resistant strains of P. aeruginosa than the dose normally administered (less than 3 g/day).
大剂量美罗培南(MEPM;6克/天)已被批准用于治疗化脓性脑膜炎;然而,关于其在难治性下呼吸道感染中的体内疗效知之甚少。本研究的目的是评估每天6克美罗培南在耐MEPM铜绿假单胞菌引起的重症肺炎小鼠模型中的疗效。用耐MEPM铜绿假单胞菌诱导的实验性肺炎,分别用正常剂量美罗培南(150毫克/千克体重,模拟人类3克/天的给药方案)或大剂量美罗培南(500毫克/千克,模拟人类6克/天的给药方案)进行治疗。与未治疗的小鼠相比,接受大剂量美罗培南治疗的小鼠存活率显著恢复,且存活率往往高于接受正常剂量美罗培南治疗的小鼠。接受大剂量美罗培南治疗的小鼠肺部(两种临床分离株的)活菌计数与未治疗小鼠相比显著降低(P<0.001),与接受正常剂量美罗培南治疗的小鼠相比也显著降低(P<0.01和<0.05)。接受大剂量美罗培南治疗的小鼠支气管肺泡灌洗液(BALF)中的炎性细胞数量也显著低于未治疗的小鼠。接受大剂量美罗培南治疗的小鼠上皮衬液(ELF)中的游离美罗培南浓度在85分钟内超过16微克/毫升,而接受正常剂量美罗培南治疗的小鼠则未达到。我们的结果表明,大剂量美罗培南(6克/天)可能比通常给药剂量(小于3克/天)能更好地预防耐MEPM铜绿假单胞菌菌株引起的肺炎。