Chusid M J, Davis S D, Sarff L D
J Lab Clin Med. 1983 Mar;101(3):441-9.
An in vivo model of Pseudomonas aeruginosa sepsis was developed with normal and neutropenic guinea pigs injected intravenously with a strain of Pseudomonas demonstrated in vitro to be synergistically susceptible to ticarcillin and tobramycin. Therapy with ticarcillin, tobramycin, or a combination of the two starting 4 hr after intravenous injection of microorganisms was administered every 2 hr for periods up to 40 hr. Each therapy was associated with significant reductions in bacterial counts in blood, liver, spleen, and kidney compared with untreated animals. In no tissue in either normal or granulocytopenic animals did therapy with a combination of ticarcillin and tobramycin reduce bacterial counts significantly more effectively than did the better single antibiotic agent alone. These findings suggest that when ticarcillin and tobramycin are administered to animals at doses equivalent to therapeutic doses given in humans, a synergistic effect in reduction of bacterial counts in parenchymal organs and blood is not observed. These studies may help explain clinical reports in humans describing a lack of synergistic activity of combination antibiotic therapy in patients with Pseudomonas sepsis.
利用正常和中性粒细胞减少的豚鼠建立了铜绿假单胞菌败血症的体内模型,通过静脉注射在体外已证明对替卡西林和妥布霉素协同敏感的一株铜绿假单胞菌。在静脉注射微生物4小时后开始用替卡西林、妥布霉素或两者联合进行治疗,每2小时给药一次,持续长达40小时。与未治疗的动物相比,每种治疗方法都使血液、肝脏、脾脏和肾脏中的细菌数量显著减少。在正常或粒细胞减少的动物的任何组织中,替卡西林和妥布霉素联合治疗在降低细菌数量方面都没有比单独使用更好的单一抗生素更有效。这些发现表明,当以等同于人类治疗剂量的剂量给动物使用替卡西林和妥布霉素时,未观察到在减少实质器官和血液中细菌数量方面的协同作用。这些研究可能有助于解释人类临床报告中描述的联合抗生素治疗对铜绿假单胞菌败血症患者缺乏协同活性的情况。