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罗莫肽与头孢甲肟对小鼠实验性肺炎克雷伯菌感染的协同作用。

Synergistic effects of romurtide and cefmenoxime against experimental Klebsiella pneumonia in mice.

作者信息

Tatara O, Nakahama C, Niki Y

机构信息

Department of Medicine, Kawasaki Medical School, Kurashiki, Japan.

出版信息

Antimicrob Agents Chemother. 1992 Jan;36(1):167-71. doi: 10.1128/AAC.36.1.167.

Abstract

We investigated the synergistic effects of romurtide (MDP-Lys [L18]) and cefmenoxime (CMX) in the treatment of experimental Klebsiella pneumonia in mice. Mice were infected with 1 x 10(4) CFU of Klebsiella pneumoniae by inhalation of aerosol bacterial suspension. About 90% of untreated animals died within a week; however, the mortality rate of animals treated with CMX alone at a dose of 40 mg/kg/day was 60% at 7 days after the infection. When one or two doses of L18 were administered before or after the infection concomitantly with CMX, a remarkable improvement in the survival rate was observed. There was no significant improvement in the survival rate of animals treated with L18 alone before or after infection. Histopathological sections of the lungs of mice treated with CMX and L18 showed slower progression of infection than those of mice treated with CMX alone. Significant differences were also found in quantitative cultures of viable bacteria in the lungs 1 to 4 days after the infection. Although viable bacterial counts in the lungs of the control and CMX-treated groups showed a rapid increase 24 to 48 h after the infection, they remained lower than the initial counts (x 10(4)) in the lungs of mice treated with combination regimens. From these results, it can be concluded that L18 is a useful biological response modifier in the treatment of acute pulmonary bacterial infections.

摘要

我们研究了罗莫肽(MDP-Lys [L18])和头孢甲肟(CMX)在治疗小鼠实验性克雷伯菌肺炎中的协同作用。通过吸入气溶胶细菌悬液,用1×10⁴CFU的肺炎克雷伯菌感染小鼠。约90%未经治疗的动物在一周内死亡;然而,以40mg/kg/天的剂量单独用CMX治疗的动物在感染后7天的死亡率为60%。当在感染前或感染后与CMX同时给予一剂或两剂L18时,观察到存活率有显著提高。单独用L18治疗的动物在感染前或感染后的存活率没有显著提高。用CMX和L18治疗的小鼠肺部组织病理学切片显示,感染进展比单独用CMX治疗的小鼠慢。在感染后1至4天肺部活菌的定量培养中也发现了显著差异。尽管对照组和CMX治疗组小鼠肺部的活菌数在感染后24至48小时迅速增加,但它们仍低于联合治疗方案组小鼠肺部的初始菌数(×10⁴)。从这些结果可以得出结论,L18在治疗急性肺部细菌感染中是一种有用的生物反应调节剂。

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