Yoshida H, Okumura K, Hori R
Department of Transfusion Medicine, Kyoto University Hospital, Faculty of Medicine, Japan.
Pharm Res. 1990 Apr;7(4):398-401. doi: 10.1023/a:1015879608367.
The effect of tertiary basic drugs on mitochondrial MAO activity and the effect of MAO inhibitors (MAOIs) on basic drug accumulation in the isolated perfused rat lung were studied to clarify the role of MAO in drug binding to lung tissue. In the perfused lung preparation, the inhibition of MAO by basic drugs correlated well with their lipid solubilities and followed competitive kinetics. The inhibitory rank order (imipramine not equal to diphenhydramine greater than quinine greater than metoclopramide greater than procainamide) also correlated with their accumulation in the perfused lung. Moreover, MAOI treatment decreased the accumulation of basic drugs in the lung, and the potency of MAOIs to inhibit drug accumulation in the lung correlated with their MAO inhibitory activity. These results indicate that lung MAO has specific binding sites for basic drugs and may function as a drug reservoir.
研究了叔胺类碱性药物对线粒体单胺氧化酶(MAO)活性的影响以及单胺氧化酶抑制剂(MAOIs)对分离的灌注大鼠肺中碱性药物蓄积的影响,以阐明MAO在药物与肺组织结合中的作用。在灌注肺制备中,碱性药物对MAO的抑制作用与其脂溶性密切相关,并遵循竞争性动力学。抑制顺序(丙咪嗪不等于苯海拉明大于奎宁大于甲氧氯普胺大于普鲁卡因胺)也与其在灌注肺中的蓄积相关。此外,MAOI处理可降低碱性药物在肺中的蓄积,且MAOIs抑制肺中药物蓄积的效力与其MAO抑制活性相关。这些结果表明,肺MAO对碱性药物具有特异性结合位点,可能起到药物储存库的作用。