Tanigawa M, Sawada T
Department of Veterinary Microbiology, Nippon Veterinary and Animal Science University, 1-7-1 Kyonan-cho, Musashino, Tokyo 180-8602, Japan.
J Vet Med B Infect Dis Vet Public Health. 2003 Nov;50(9):436-42. doi: 10.1046/j.0931-1793.2003.00703.x.
The pharmacodynamic effects of amoxicillin against Actinobacillus pleuropneumoniae at exposure concentration above and below minimum inhibitory concentration (MIC) were evaluated in both in vitro and in vivo. In vitro, the growth and morphological change of A. pleuropneumoniae in culture medium was observed. In vivo, the efficacy of amoxicillin on experimentally induced A. pleuropneumoniae infection in disease-free pigs was evaluated. Fifteen pigs were divided into three groups (n = 5 per group). After the onset of clinical respiratory disease symptoms, 6 h post-infection, amoxicillin sustained-release injectable formulation was injected intramuscularly at 7.5 mg/kg/day (group I) and 15 mg/kg/day (group II). Then the serum concentration of amoxicillin was measured. An untreated infected group served as controls. In each amoxicillin administration group, if symptoms were not absent after 48 h, the pig was injected with the amoxicillin sustained-release injectable formulation again using the same dosage. In vitro, the growth of A. pleuropneumoniae inhibited by amoxicillin exposure at the concentration above the MIC (1.28 x MIC), and the inhibition time was in directly proportion to the time of amoxicillin exposure. Moreover, all the cells were lysed. Whereas the bacterial growth inhibition at the amoxicillin exposure concentration below the MIC (0.25 x MIC) was not done, and the shape of cells were normal or long filamentous. In vivo, the group I clinical and pathological score was higher than the group II, and the group I weight gain was significantly less than the group II. Performance with respect to weight gain corresponded with clinical signs. The infected control group was severely affected with an 80% (4/5) mortality rate 24-96 h post-challenge. The duration of time above MIC (T > MIC) of serum amoxicillin concentration in the group I was less than group II. The present studies suggest that amoxicillin has exposure time-dependent bactericidal activity against A. pleuropneumoniae.
在体外和体内评估了阿莫西林在高于和低于最低抑菌浓度(MIC)的暴露浓度下对胸膜肺炎放线杆菌的药效学作用。在体外,观察了胸膜肺炎放线杆菌在培养基中的生长和形态变化。在体内,评估了阿莫西林对无病仔猪实验性诱导的胸膜肺炎放线杆菌感染的疗效。将15头猪分为三组(每组n = 5)。在临床呼吸道疾病症状出现后,感染后6小时,以7.5 mg/kg/天(I组)和15 mg/kg/天(II组)肌肉注射阿莫西林缓释注射剂。然后测量阿莫西林的血清浓度。未治疗的感染组作为对照。在每个阿莫西林给药组中,如果48小时后症状未消失,则以相同剂量再次给猪注射阿莫西林缓释注射剂。在体外,高于MIC(1.28×MIC)浓度的阿莫西林暴露可抑制胸膜肺炎放线杆菌的生长,且抑制时间与阿莫西林暴露时间成正比。此外,所有细胞均被裂解。而在低于MIC(0.25×MIC)的阿莫西林暴露浓度下,细菌生长未受到抑制,细胞形态正常或呈长丝状。在体内方面,I组的临床和病理评分高于II组,I组的体重增加明显低于II组。体重增加情况与临床症状相符。感染对照组受到严重影响,攻毒后24 - 96小时死亡率为80%(4/5)。I组血清阿莫西林浓度高于MIC的持续时间(T > MIC)低于II组。本研究表明,阿莫西林对胸膜肺炎放线杆菌具有暴露时间依赖性杀菌活性。