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硫喷妥钠对映体在离体灌注大鼠心脏中的心肌摄取。

Myocardial uptake of thiopental enantiomers by the isolated perfused rat heart.

作者信息

Nguyen K T, Morgan D J

机构信息

Victorian College of Pharmacy, Monash University, Melbourne, Australia.

出版信息

Chirality. 1996;8(7):477-80. doi: 10.1002/(SICI)1520-636X(1996)8:7<477::AID-CHIR3>3.0.CO;2-8.

Abstract

Myocardial uptake of thiopental enantiomers by an isolated perfused rat heart preparation was examined after perfusion with protein-free perfusate. Outflow perfusate samples were collected at frequent intervals for 20 min during single-pass perfusion with 10 micrograms/ml racemic thiopental (washin phase) and for another 45 min during perfusion with drug-free perfusate (washout phase). (+)- and (-)-thiopental concentrations were assayed by chiral high-performance liquid chromatography. Heart rate, perfusion pressure, and electro-cardiogram were also monitored. During the washin phase, there was no significant difference between the mean values of the equilibration rate constants of (+)- and (-)-thiopental enantiomers (0.44 +/- 0.07 min-1 and 0.43 +/- 0.09 min-1, respectively, P > 0.05). Mean volumes of distribution of (+)- and (-)-thiopental enantiomers were similar (6.34 +/- 1.20 and 6.45 +/- 1.29 ml/g for the washin phase and 7.22 +/- 0.71 and 7.47 +/- 0.81 ml/g for the washout phase, respectively, P > 0.05). This indicates that tissue accumulation of thiopental enantiomers in the isolated perfused rat heart was not stereoselective. Uptake of thiopental by the heart was perfusion flow rate-limited and independent of capillary permeability. These findings suggest that myocardial tissue concentration of racemic thiopental should be an accurate predictor of myocardial drug effect.

摘要

在用无蛋白灌注液灌注后,使用离体灌注大鼠心脏标本研究硫喷妥钠对映体的心肌摄取情况。在以10微克/毫升外消旋硫喷妥钠进行单程灌注的20分钟内(洗脱期),每隔一段时间收集流出灌注液样本,在随后用无药灌注液灌注的45分钟内(清除期)同样如此。通过手性高效液相色谱法测定(+)-和(-)-硫喷妥钠的浓度。同时监测心率、灌注压和心电图。在洗脱期,(+)-和(-)-硫喷妥钠对映体的平衡速率常数平均值之间无显著差异(分别为0.44±0.07分钟⁻¹和0.43±0.09分钟⁻¹,P>0.05)。(+)-和(-)-硫喷妥钠对映体的平均分布容积相似(洗脱期分别为6.34±1.20和6.45±1.29毫升/克,清除期分别为7.22±0.71和7.47±0.81毫升/克,P>0.05)。这表明在离体灌注大鼠心脏中硫喷妥钠对映体的组织蓄积无立体选择性。心脏对硫喷妥钠的摄取受灌注流速限制,且与毛细血管通透性无关。这些发现提示外消旋硫喷妥钠的心肌组织浓度应是心肌药物效应的准确预测指标。

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