Smith G M, Slocombe B, Abbott K H, Mizen L W
Wells Medical, Surrey, United Kingdom.
Antimicrob Agents Chemother. 1998 Apr;42(4):813-7. doi: 10.1128/AAC.42.4.813.
High doses of amoxicillin, equivalent to those produced by 500- and 750-mg oral doses in humans (area under the plasma concentration-time curve), were effective against a penicillin-resistant strain of Streptococcus pneumoniae in an experimental respiratory tract infection in immunocompromised rats; this superior activity confirms the results of previous studies. An unexpected enhancement of amoxicillin's antibacterial activity in vivo against penicillin-resistant and -susceptible S. pneumoniae strains was observed when subtherapeutic doses of amoxicillin were coadministered with the beta-lactamase inhibitor potassium clavulanate. The reason for this enhancement was unclear since these organisms do not produce beta-lactamase. The differential binding of clavulanic acid and amoxicillin to penicillin-binding proteins may have contributed to the observed effects.
高剂量阿莫西林,相当于人类口服500毫克和750毫克剂量所产生的血浆浓度-时间曲线下面积,在免疫受损大鼠的实验性呼吸道感染中对青霉素耐药的肺炎链球菌菌株有效;这种优越活性证实了先前研究的结果。当亚治疗剂量的阿莫西林与β-内酰胺酶抑制剂克拉维酸钾共同给药时,观察到阿莫西林在体内对青霉素耐药和敏感的肺炎链球菌菌株的抗菌活性意外增强。由于这些菌株不产生β-内酰胺酶,这种增强的原因尚不清楚。克拉维酸和阿莫西林与青霉素结合蛋白的差异结合可能导致了观察到的效果。