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消化道上皮中麻醉药品及麻醉药品拮抗剂的转运机制。

Transport mechanisms for narcotics and narcotic antagonists in alimentary epithelia.

作者信息

Jackson M J

出版信息

J Pharmacol Exp Ther. 1981 May;217(2):285-91.

PMID:7229972
Abstract

A study has been made of the transport of seven morphine analogs across short-circuited preparations of rat gastric mucosa, small intestine and colon in vitro. Net secretory transport of all of the compounds tested was observed in the experiments with stomach. In the intestine the weaker bases were not transported but the more ionized compounds were secreted; in the colon, the stronger bases were transported in the absorptive direction. These transport processes were not dependent on transmural gradients of pH and in some cases the pattern of transport was maintained in the presence of adverse pH gradients. Studies on the effects of concentration and of interactions between concurrently transported compounds provided no evidence for carrier-mediated mechanisms. It was suggested that these observations are explicable in terms of a double membrane system.

摘要

一项关于七种吗啡类似物在体外经大鼠胃黏膜、小肠和结肠短路制备物转运的研究。在胃部实验中观察到所有受试化合物的净分泌转运。在小肠中,碱性较弱的化合物不被转运,但离子化程度较高的化合物会分泌;在结肠中,碱性较强的化合物沿吸收方向转运。这些转运过程不依赖于跨膜pH梯度,在某些情况下,即使存在不利的pH梯度,转运模式仍能维持。关于浓度和同时转运的化合物之间相互作用的影响的研究没有提供载体介导机制的证据。有人提出这些观察结果可以用双膜系统来解释。

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