Chistiakov V V, Gegenava G P
Biokhimiia. 1976;41(7):1272-8.
Effect of morphine, codeine, dionine and nalorphine on the oxidative phosphorylation in rat liver mitochondria was studied. Morphine is found to inhibit both ATP-synthetase and ATP-ase activities in mitochondria, but not in submitochondrial particles. Morphine-suppressed oxidative phosphorylation was competitively reversed with high concentrations of ADP, but not of inorganic phosphate. The effect of other opiates (i.e. codeine, dionine, nalorphine) was similar. It is suggested, that opiates inhibit the transport of adenine nucleotides through inner mitochondrial membrane, as it does atractyloside. A significance of the hydrophobic interaction between the inhibitor and adenine nucleotide translocase is outlined, since the degree of the inhibition of oxidative phosphorylation is increased with the increase in the number of non-ionized opiate molecules (at alkaline pH values) and in the length of the carbon chain of narcotic molecule as follows: morphine--codeine--dionine--nalorphine.
研究了吗啡、可待因、地奥宁和烯丙吗啡对大鼠肝线粒体氧化磷酸化的影响。发现吗啡可抑制线粒体中的ATP合成酶和ATP酶活性,但对亚线粒体颗粒无此作用。吗啡抑制的氧化磷酸化可被高浓度的ADP竞争性逆转,但不能被无机磷酸盐逆转。其他阿片类药物(即可待因、地奥宁、烯丙吗啡)的作用相似。有人提出,阿片类药物抑制腺嘌呤核苷酸通过线粒体内膜的转运,就像苍术苷那样。概述了抑制剂与腺嘌呤核苷酸转位酶之间疏水相互作用的重要性,因为氧化磷酸化的抑制程度随着非离子化阿片类分子数量的增加(在碱性pH值下)以及麻醉分子碳链长度的增加而增加,顺序如下:吗啡 - 可待因 - 地奥宁 - 烯丙吗啡。