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大鼠肺对(±)-美沙酮的摄取特性

Characterization of (+/-)-methadone uptake by rat lung.

作者信息

Chi C H, Dixit B N

出版信息

Br J Pharmacol. 1977 Apr;59(4):539-49. doi: 10.1111/j.1476-5381.1977.tb07719.x.

Abstract
  1. By use of a sensitive and specific fluorescence assay procedure it was shown that after subcutaneous administration to rats, (+/-)-methadone was concentrated in the lung. Lung to serum ratios ranging from 25 to 60 were obtained indicating that the rat lung tissue was capable of extracting (+/-)-methadone against a concentration gradient. 2. This phenomenon was investigated in vitro with rat lung slices incubated in Krebs-Ringer phosphate buffer (pH 7.4). The uptake was expressed in terms of tissue to medium concentration ratios (T/M ratio). 3. The principal observations were: (i) Studies on the time-course of the uptake showed that the T/M ratios of (+/-)-methadone increased rapidly during the first 60 min of incubation and then more slowly, with a plateau occurring at 180 min; (ii) The T/M ratio of (+/-)-methadone progressively increased from 9.5 to 17 as the pH of the incubation medium was varied from 6.2 to 7.5; (iii) When the concentration of (+/-)-methadone in the incubation medium was varied from 0.005 to 0.5 mM, the T/M ratio decreased rapidly suggesting self-saturation of the transport process. Beyond the medium concentration of 0.5 mM, the T/M ratio declined very slowly. 4. These results suggested that at low concentrations, (+/-)-methadone was transported predominantly by a self-saturable process while at higher concentrations it was transported by a process of simple diffusion. 5. At low concentrations (0.01 mM) the uptake of (+)-methadone was higher than that of (-)-isomer indicating stereo-specificity of the uptake process. The uptake of (+/-)-methadone at low concentration (0.01 mM) was significantly inhibited by low temperature, lack of O2, lack of glucose, lack of Na+ in the incubation medium, and by exposure of the tissue to high temperature (approximately 100 degrees C). The uptake was also inhibited by relatively high concentration of iodoacetate (1.0 mM) and of naloxone (1.0 mM). 6. Kinetic analysis of data showed that the diffusion constant for (+/-)-methadone was 5.0 (h-1) and the Vmax of the active transport process was 6.5 micronmol g-1h-1.
摘要
  1. 通过使用灵敏且特异的荧光检测程序表明,给大鼠皮下注射(±)-美沙酮后,其在肺中蓄积。肺与血清的比值在25至60之间,这表明大鼠肺组织能够逆浓度梯度摄取(±)-美沙酮。2. 利用在磷酸缓冲液(pH 7.4)中孵育的大鼠肺切片进行体外研究。摄取量用组织与培养基浓度比(T/M比)表示。3. 主要观察结果如下:(i)摄取时间进程研究表明,(±)-美沙酮的T/M比在孵育的前60分钟迅速增加,然后增加得更慢,在180分钟时达到平台期;(ii)随着孵育培养基的pH从6.2变化到7.5,(±)-美沙酮的T/M比从9.5逐渐增加到17;(iii)当孵育培养基中(±)-美沙酮的浓度从0.005 mM变化到0.5 mM时,T/M比迅速下降,表明转运过程存在自我饱和。培养基浓度超过0.5 mM时,T/M比下降非常缓慢。4. 这些结果表明,在低浓度下,(±)-美沙酮主要通过自我饱和过程转运,而在高浓度下则通过简单扩散过程转运。5. 在低浓度(0.01 mM)时,(+)-美沙酮的摄取高于(-)-异构体,表明摄取过程具有立体特异性。低浓度(0.01 mM)下(±)-美沙酮的摄取受到低温、缺氧、无糖、孵育培养基中无钠以及组织暴露于高温(约100℃)的显著抑制。摄取也受到相对高浓度的碘乙酸盐(1.0 mM)和纳洛酮(1.0 mM)的抑制。6. 数据的动力学分析表明,(±)-美沙酮的扩散常数为5.0(h-1),主动转运过程的Vmax为6.5微摩尔·克-1·小时-1。

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