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Stereoselective pharmacokinetics of ketamine and norketamine after racemic ketamine or S-ketamine administration during isoflurane anaesthesia in Shetland ponies

机译:设得兰群岛小马异氟烷麻醉期间,外消旋氯胺酮或S-氯胺酮给药后,氯胺酮和去甲氯胺酮的立体选择性药代动力学

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摘要

Background The arterial pharmacokinetics of ketamine and norketamine enantiomers after racemic ketamine or S-ketamine i.v. administration were evaluated in seven gelding ponies in a crossover study (2-month interval). Methods Anaesthesia was induced with isoflurane in oxygen via a face-mask and then maintained at each pony's individual MAC. Racemic ketamine (2.2mgkg−1) or S-ketamine (1.1mgkg−1) was injected in the right jugular vein. Blood samples were collected from the right carotid artery before and at 1, 2, 4, 8, 16, 32, 64, and 128min after ketamine administration. Ketamine and norketamine enantiomer plasma concentrations were determined by capillary electrophoresis. Individual R-ketamine and S-ketamine concentration vs time curves were analysed by non-linear least square regression two-compartment model analysis using PCNonlin. Plasma disposition curves for R-norketamine and S-norketamine were described by estimating AUC, Cmax, and Tmax. Pulse rate (PR), respiratory rate (Rf), tidal volume (VT), minute volume ventilation (VE), end-tidal partial pressure of carbon dioxide (Pe′CO2), and mean arterial blood pressure (MAP) were also evaluated. Results The pharmacokinetic parameters of S- and R-ketamine administered in the racemic mixture or S-ketamine administered separately did not differ significantly. Statistically significant higher AUC and Cmax were found for S-norketamine compared with R-norketamine in the racemic group. Overall, Rf, VE, Pe′CO2, and MAP were significantly higher in the racemic group, whereas PR was higher in the S-ketamine group. Conclusions Norketamine enantiomers showed different pharmacokinetic profiles after single i.v. administration of racemic ketamine in ponies anaesthetised with isoflurane in oxygen (1 MAC). Cardiopulmonary variables require further investigation
机译:背景外消旋氯胺酮或S-氯胺酮静脉内注射后,氯胺酮和去甲氯胺酮对映异构体的动脉药代动力学。在一项交叉研究(2个月间隔)中,在七个胶凝小马中评估了给药。方法:通过面罩在氧气中用异氟烷诱导麻醉,然后在每个小马的单独MAC处维持麻醉。在右颈静脉注射消旋氯胺酮(2.2mgkg-1)或S-氯胺酮(1.1mgkg-1)。氯胺酮给药之前,1、2、4、8、16、32、64和128min时,从右颈动脉采集血样。氯胺酮和去甲胺酮对映体的血浆浓度通过毛细管电泳测定。使用PCNonlin通过非线性最小二乘回归两室模型分析来分析各个R-氯胺酮和S-氯胺酮的浓度-时间曲线。通过估计AUC,Cmax和Tmax来描述R-去甲酚胺和S-去甲酚胺的血浆处置曲线。还评估了脉搏率(PR),呼吸频率(Rf),潮气量(VT),分钟通气量(VE),潮气中二氧化碳的分压(Pe'CO2)和平均动脉血压(MAP) 。结果外消旋混合物中分别施用S-和R-氯胺酮或分别施用S-氯胺酮的药代动力学参数无显着差异。在外消旋组中,与R-去甲胺相比,S-去甲胺的统计学上显着较高的AUC和Cmax。总体而言,外消旋组的Rf,VE,Pe'CO2和MAP显着较高,而S-氯胺酮组的PR较高。结论Norketamine对映异构体在单次静脉注射后显示出不同的药代动力学特征。在氧中异氟醚麻醉的小马中使用外消旋氯胺酮(1 MAC)。心肺变量需要进一步调查

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