Veilleux-Lemieux Daphnée, Castel Aude, Carrier Denise, Beaudry Francis, Vachon Pascal
Laval University, Direction of Veterinary Services, Québec, Québec, Canada.
J Am Assoc Lab Anim Sci. 2013 Sep;52(5):567-70.
To compare the pharmacokinetics of coadministered intraperitoneal ketamine and xylazine in young (8 to 10 wk; n = 6) and old rats (2 to 2.4 y; n = 6), blood samples obtained at 15 and 30 min and 1, 2, and 4 h after drug administration were analyzed by HPLC-tandem mass spectrometry. In both groups, the withdrawal reflex was absent during anesthesia and was present at 1.1 (± 0.2) and 2.6 (± 0.7) h after drug administration in young and old rats, respectively, with the first voluntary movement at 1.5 ± 0.2 and 4.9 ± 1.0 h. Drug availability of ketamine and xylazine was 6.0 and 6.7 times greater, respectively, in old than young rats. The rate constant of elimination of both drugs was greatly decreased and the elimination half-life was significantly greater in old compared with young rats. In conclusion, age and associated factors affect the availability of ketamine and xylazine when coadministered to attain clinical anesthesia, changing the pharmacokinetics of these drugs and prolonging anesthesia duration and recovery times with aging. Compared with their young counterparts, aged rats required much higher doses to attain a similar level of anesthesia. Finally, the long half-life of both ketamine and xylazine, when coadministered to old rats, may be a factor in research protocols because residual plasma concentrations could still be present for as long as 3 and 5 d, respectively, after administration.
为比较腹腔注射氯胺酮和赛拉嗪在年轻大鼠(8至10周龄;n = 6)和老年大鼠(2至2.4岁;n = 6)体内的药代动力学,在给药后15分钟、30分钟、1小时、2小时和4小时采集血样,采用高效液相色谱-串联质谱法进行分析。在两组中,麻醉期间均无退缩反射,年轻和老年大鼠分别在给药后1.1(± 0.2)小时和2.6(± 0.7)小时出现退缩反射,首次自主活动分别在1.5 ± 0.2小时和4.9 ± 1.0小时。老年大鼠中氯胺酮和赛拉嗪的药物利用率分别比年轻大鼠高6.0倍和6.7倍。与年轻大鼠相比,两种药物的消除速率常数均大幅降低,老年大鼠的消除半衰期显著延长。总之,年龄及相关因素会影响联合使用氯胺酮和赛拉嗪以达到临床麻醉时的药物利用率,改变这些药物的药代动力学,随着年龄增长延长麻醉持续时间和恢复时间。与年轻大鼠相比,老年大鼠需要更高剂量才能达到相似的麻醉水平。最后,联合给老年大鼠使用氯胺酮和赛拉嗪时,二者的半衰期较长,这可能是研究方案中的一个因素,因为给药后血浆残留浓度可能分别长达3天和5天仍可检测到。