Broome Ted A, Brown Murray P, Gronwall Ronald R, Casey Matthew F, Meritt Kelly A
Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, Florida 32610-0136, USA.
Can J Vet Res. 2003 Oct;67(4):297-302.
Six healthy adult horses (5 mares and 1 stallion) were given a single dose of acetylsalicylic acid (ASA), 20 mg/kg of body weight, by intravenous (IV), rectal, and intragastric (IG) routes. Serial blood samples were collected via jugular venipuncture over a 36-h period, and plasma ASA and salicylic acid (SA) concentrations were determined by high-performance liquid chromatography. After IV administration, the mean elimination rate constant of ASA (+/- the standard error of the mean) was 1.32 +/- 0.09 h(-1), the mean elimination half-life was 0.53 +/- 0.04 h, the area under the plasma concentration-versus-time curve (AUC) was 2555 +/- 98 microg x min/mL, the plasma clearance was 472 +/- 18.9 mL/h/kg, and the volume of distribution at steady state was 0.22 +/- 0.01 L/kg. After rectal administration, the plasma concentration of ASA peaked at 5.05 +/- 0.80 microg/mL at 0.33 h, then decreased to undetectable levels by 4 h; the plasma concentration of SA peaked at 17.39 +/- 5.46 microg/mL at 2 h, then decreased to 1.92 +/- 0.25 microg/mL by 36 h. After rectal administration, the AUC for ASA was 439.4 +/- 94.55 microg x min/mL and the bioavailability was 0.17 +/- 0.037. After IG administration, the plasma concentration of ASA peaked at 1.26 +/- 0.10 microg/mL at 0.67 h, then declined to 0.37 +/- 0.37 microg/mL by 36 h; the plasma concentration of SA peaked at 23.90 +/- 4.94 microg/mL at 4 h and decreased to 0.85 +/- 0.31 microg/mL by 36 h. After IG administration, the AUC for ASA was 146.70 +/- 24.90 microg x min/mL and the bioavailability was 0.059 +/- 0.013. Administration of a single rectal dose of ASA of 20 mg/kg to horses results in higher peak plasma ASA concentrations and greater bioavailability than the same dose given IG. Plasma ASA concentrations after rectal administration should be sufficient to inhibit platelet thromboxane production, and doses lower than those suggested for IG administration may be adequate.
六匹健康成年马(5匹母马和1匹种马)通过静脉注射(IV)、直肠给药和胃内给药(IG)途径,给予单剂量20mg/kg体重的乙酰水杨酸(ASA)。在36小时内通过颈静脉穿刺采集系列血样,采用高效液相色谱法测定血浆中ASA和水杨酸(SA)的浓度。静脉注射后,ASA的平均消除速率常数(±均值标准误)为1.32±0.09h⁻¹,平均消除半衰期为0.53±0.04h,血浆浓度-时间曲线下面积(AUC)为2555±98μg·min/mL,血浆清除率为472±18.9mL/h/kg,稳态分布容积为0.22±0.01L/kg。直肠给药后,ASA血浆浓度在0.33小时达到峰值5.05±0.80μg/mL,然后在4小时降至检测不到的水平;SA血浆浓度在2小时达到峰值17.39±5.46μg/mL,然后在36小时降至1.