Post C, Andersson R G, Ryrfeldt A, Nilsson E
Acta Pharmacol Toxicol (Copenh). 1978 Aug;43(2):156-63. doi: 10.1111/j.1600-0773.1978.tb02249.x.
The accumulation of radioisotopically labelled lidocaine was investigated in lung slices and perfused lungs of rats. Lidocaine was taken up by rat lung slices incubated in an oxygenated physiological solution (pH 7.4) at 37 degrees. 14C-lidocaine accumulated in lung slices to a much greater extent than did 3H-sucrose, and the lidocaine space was approximately 7 times that of the extracellular space. No metabolism of lidocaine took place during the incubation period. The accumulation of lidocaine was inhibited by low temperature, while anaerobic conditions had no inhibitor effect. The uptake of lidocaine (0.028 mM) was slightly antagonized by high concentrations of Ca2+ (10 mM). The isolated perfused lung model was used for studying the pulmonary absorption of lidocaine from the vascular bed. Lidocaine was rapidly extracted from the perfusion solution and the drug appeared to accumulate in at least two compartments. It seems that in the rat lung a portion of the lidocaine taken up had accumulated within the cells, while some of it may be fixed to the cell surfaces.
研究了放射性同位素标记的利多卡因在大鼠肺切片和灌注肺中的蓄积情况。利多卡因可被置于37℃充氧生理溶液(pH 7.4)中孵育的大鼠肺切片摄取。14C - 利多卡因在肺切片中的蓄积程度远高于3H - 蔗糖,且利多卡因空间约为细胞外空间的7倍。孵育期间未发生利多卡因的代谢。低温抑制利多卡因的蓄积,而厌氧条件无抑制作用。高浓度的Ca2 +(10 mM)对利多卡因(0.028 mM)的摄取有轻微拮抗作用。采用离体灌注肺模型研究利多卡因从血管床的肺部吸收情况。利多卡因迅速从灌注液中被提取出来,且该药物似乎蓄积于至少两个区室。在大鼠肺中,摄取的一部分利多卡因似乎蓄积在细胞内,而其中一些可能固定于细胞表面。