Weinberg D S, Fernandes P B, Kao C C, Clark J M, Bonner D P, Sykes R B
J Antimicrob Chemother. 1986 Dec;18(6):729-45. doi: 10.1093/jac/18.6.729.
Aztreonam, ceftazidime, cefoperazone and latamoxef (moxalactam) were evaluated in a hamster model for antibiotic-associated colitis. Aztreonam, a novel monocyclic beta-lactam antibiotic specifically directed against aerobic Gram-negative bacteria with limited activity against Gram-positive and anaerobic bacteria did not cause haemorrhagic caecitis and death in hamsters when administered intraperitioneally or orally. Quantitative caecal cultures showed no changes in the anaerobic caecal microflora of hamsters treated intraperitoneally with aztreonam and only a temporary decrease in anaerobic Gram-negative bacilli in hamsters treated orally. Clostridium difficile and its cytotoxin were not present in these animals. Parenteral administration of ceftazidime also did not affect the anaerobic caecal microflora or cause caecitis. However, when given orally, ceftazidime suppressed the anaerobic caecal microflora and a lethal C. difficile-induced caecitis developed. Latamoxef or cefoperazone given parenterally resulted in caecitis and death in five days with marked changes in the anaerobic caecal microflora and C. difficile present in the caecal contents of these animals. The lethal haemorrhagic caecitis observed in this study was indistinguishable from that seen in the clindamycin-induced colitis model in the hamster. The possible correlation of these findings to gastrointestinal disturbances as a complication of antibiotic therapy in humans is discussed.
在仓鼠模型中对氨曲南、头孢他啶、头孢哌酮和拉氧头孢(羟羧氧酰胺菌素)进行了抗生素相关性结肠炎的评估。氨曲南是一种新型单环β-内酰胺抗生素,专门针对需氧革兰氏阴性菌,对革兰氏阳性菌和厌氧菌活性有限,经腹腔内或口服给药后,在仓鼠中不会引起出血性盲肠炎和死亡。定量盲肠培养显示,腹腔内给予氨曲南的仓鼠盲肠厌氧微生物群没有变化,口服给药的仓鼠中厌氧革兰氏阴性杆菌仅暂时减少。这些动物中不存在艰难梭菌及其细胞毒素。静脉注射头孢他啶也不会影响盲肠厌氧微生物群或引起盲肠炎。然而,口服时,头孢他啶会抑制盲肠厌氧微生物群,并引发致命的艰难梭菌诱导的盲肠炎。静脉注射拉氧头孢或头孢哌酮会在五天内导致盲肠炎和死亡,这些动物的盲肠内容物中厌氧盲肠微生物群有明显变化,且存在艰难梭菌。本研究中观察到的致命性出血性盲肠炎与仓鼠克林霉素诱导的结肠炎模型中所见的无法区分。讨论了这些发现与人类抗生素治疗并发症胃肠道紊乱的可能相关性。