Pijpers A, Schoevers E J, van Gogh H, van Leengoed L A, Visser I J, van Miert A S, Verheijden J H
Department of Herd Health and Reproduction, Faculty of Veterinary Medicine, State University of Utrecht, The Netherlands.
J Vet Pharmacol Ther. 1990 Sep;13(3):320-6. doi: 10.1111/j.1365-2885.1990.tb00783.x.
The pharmacokinetics of oxytetracycline (OTC) were studied in healthy pigs and in pigs endobronchially inoculated with Actinobacillus pleuropneumoniae toxins. In two groups of seven pigs OTC was administered intravenously in a single dose of 10 or 50 mg/kg, respectively. OTC was administered to clinically healthy pigs and 7 days later at 3 h after a challenge with A. pleuropneumoniae toxins. Pneumonia developed in toxin-treated pigs. In the challenged pigs there was a decreased distribution-rate constant (alpha) and a significantly increased elimination-rate constant (beta) (P less than 0.05). Moreover, the apparent volume of distribution (Vd beta) was decreased. The elimination half-lives (t1/2 beta) were approximately 6 h in the healthy pigs and 5 h in the diseased animals. There was no difference in the pharmacokinetic profile of OTC following administration of 50 mg/kg compared to 10 mg/kg.
对土霉素(OTC)在健康猪以及经支气管内接种胸膜肺炎放线杆菌毒素的猪体内的药代动力学进行了研究。在两组各7头猪中,分别静脉注射单剂量10或50mg/kg的OTC。将OTC给予临床健康的猪,7天后在接种胸膜肺炎放线杆菌毒素3小时后给药。毒素处理的猪发生了肺炎。在受到攻击的猪中,分布速率常数(α)降低,消除速率常数(β)显著增加(P<0.05)。此外,表观分布容积(Vdβ)减小。健康猪的消除半衰期(t1/2β)约为6小时,患病动物为5小时。给予50mg/kg与10mg/kg的OTC后,其药代动力学特征没有差异。