Mamman M, Aliu Y O, Peregrine A S
International Laboratory for Research on Animal Diseases (ILRAD), Nairobi, Kenya.
Antimicrob Agents Chemother. 1993 May;37(5):1050-5. doi: 10.1128/AAC.37.5.1050.
The pharmacokinetics of diminazene in five female Boran (Bos indicus) cattle before and then during acute and chronic phases of experimental infections with Trypanosoma congolense were investigated. A 7.0% (wt/vol) solution of diminazene aceturate (Berenil) was used in all three phases of the study and administered as a single intramuscular dose of 3.5 mg of diminazene base per kg of body weight. There were no significant differences between the values of pharmacokinetic parameters for the noninfected cattle and the values for cattle with a chronic T. congolense infection. However, the maximum concentration of the drug in plasma during the acute phase of infection (8.25 +/- 1.72 micrograms/ml) was significantly (P < 0.01) greater than that during chronic infection (5.04 +/- 0.26 micrograms/ml) and that in the noninfected state (4.76 +/- 0.76 micrograms/ml). Similarly, the time to maximum concentration of the drug in plasma when diminazene was administered during the acute phase of infection (18.00 +/- 6.71 min) was significantly (P < 0.02) shorter than that for noninfected cattle (36.00 +/- 8.22 min) and that during chronic infection (33.75 +/- 7.50 min). The volume of distribution at steady state during acute infection (1.01 +/- 0.31 liter/kg) was significantly (P < 0.01) smaller than that in the noninfected state (1.37 +/- 0.17 liter/kg) and that in chronic infection (1.51 +/- 0.24 liter/kg). Eight hours after the drug had been administered, the concentration-time data profiles for each of the three study phases were very similar. Mean concentrations of diminazene in plasma 48 h after administration of the drug were 0.43 +/- 0.07 microgram/ml in noninfected cattle, 0.43 +/- 0.11 microgram/ml during the acute phase of trypanosome infection, and 0.44 +/- 0.09 microgram/ml during the chronic phase of the infection. Results of the present study indicate that the area under the concentration-time curve for diminazene in trypanosome-infected cattle did not differ significantly for noninfected cattle. It, therefore, appears that the total amount of diminazene attained and maintained in the plasma of cattle is not significantly altered during infection with T. congolense.
研究了锥虫感染实验中,五只雌性博拉安格斯牛(瘤牛)在急性和慢性阶段感染刚果锥虫之前及期间,双脒苯脲的药代动力学。在研究的三个阶段均使用7.0%(重量/体积)的乙酰氨基苯脒(贝尼尔)溶液,以每千克体重3.5毫克双脒苯脲碱的剂量单次肌肉注射给药。未感染牛的药代动力学参数值与慢性感染刚果锥虫的牛的参数值之间没有显著差异。然而,感染急性期血浆中药物的最大浓度(8.25±1.72微克/毫升)显著高于慢性感染期(5.04±0.26微克/毫升)和未感染状态(4.76±0.76微克/毫升)(P<0.01)。同样,在感染急性期注射双脒苯脲后,血浆中药物达到最大浓度的时间(18.00±6.71分钟)显著短于未感染牛(36.00±8.22分钟)和慢性感染期(33.75±7.50分钟)(P<0.02)。急性感染期间稳态分布容积(1.01±0.31升/千克)显著小于未感染状态(1.37±0.17升/千克)和慢性感染期(1.51±0.24升/千克)(P<0.01)。给药8小时后,三个研究阶段各自的浓度-时间数据曲线非常相似。给药48小时后,未感染牛血浆中双脒苯脲的平均浓度为0.43±0.07微克/毫升,锥虫感染急性期为0.43±0.11微克/毫升,感染慢性期为0.44±0.09微克/毫升。本研究结果表明,锥虫感染牛的双脒苯脲浓度-时间曲线下面积与未感染牛没有显著差异。因此,似乎在感染刚果锥虫期间,牛血浆中达到并维持的双脒苯脲总量没有显著改变。