Peck K, Mealey K L, Matthews N S, Taylor T S
Department of Small Animal Medicine and Surgery, College of Veterinary Medicine, Texas A&M University, College Station 77840, USA.
Am J Vet Res. 1997 Aug;58(8):881-4.
To determine whether clearance of capacity-limited drugs in horses differs from that in donkeys by comparing the serum disposition of caffeine and its metabolites, theophylline, theobromine, and paraxanthine after i.v. administration of caffeine to horses and donkeys.
4 healthy horses and 5 healthy donkeys.
Blood samples were collected from each animal at time 0 (before) and 5, 10, 15, 20, 30, and 45 minutes, and 1, 2, 3, 4, 6, 8, 12, 24, 30, 36, 48, 54, 60, 72, and 96 hours after IV administration of a bolus of caffeine. Serum was analyzed in triplicate by high-performance liquid chromatography to determine caffeine, theophylline, theobromine, and paraxanthine concentrations. The serum concentration-time curves for each animal were analyzed separately to estimate model-independent pharmacokinetic variables.
Mean pharmacokinetic values for caffeine, theophylline, and paraxanthine did not differ significantly in horses, compared with donkeys. Mean peak serum concentration of theobromine was significantly higher in donkeys, compared with horses.
Clearance of the capacity-limited drug caffeine does not appear to differ in horses, compared with donkeys.
For some drugs that undergo hepatic metabolism, the dose and dose interval used for horses may be appropriate for use in donkeys.
通过比较静脉注射咖啡因后马和驴体内咖啡因及其代谢产物茶碱、可可碱和副黄嘌呤的血清处置情况,确定马体内容量限制型药物的清除率是否与驴不同。
4匹健康马和5头健康驴。
在静脉推注咖啡因后的0(给药前)、5、10、15、20、30和45分钟以及1、2、3、4、6、8、12、24、30、36、48、54、60、72和96小时,从每只动物采集血样。血清通过高效液相色谱法进行三次分析,以测定咖啡因、茶碱、可可碱和副黄嘌呤的浓度。分别分析每只动物的血清浓度-时间曲线,以估计与模型无关的药代动力学变量。
与驴相比,马体内咖啡因、茶碱和副黄嘌呤的平均药代动力学值无显著差异。与马相比,驴体内可可碱的平均血清峰值浓度显著更高。
与驴相比,容量限制型药物咖啡因在马体内的清除率似乎没有差异。
对于一些经过肝脏代谢的药物,用于马的剂量和给药间隔可能适用于驴。