Saitoh H, Noujoh A, Chiba Y, Iseki K, Miyazaki K, Arita T
Department of Pharmacy, Hokkaido University Hospital, School of Medicine, Sapporo, Japan.
J Pharm Pharmacol. 1990 May;42(5):308-13. doi: 10.1111/j.2042-7158.1990.tb05417.x.
We have investigated the correlation between the molecular structures of various organic cations and their binding to rat small intestinal brush border membrane. The binding of small quaternary ammonium compounds such as tetramethylammonium and choline to brush border membrane was not sufficient to inhibit methylchlorpromazine binding. However, lauryltrimethylammonium and cetyltrimethylammonium, both quaternary amines with a long carbon chain, inhibited binding significantly. The inhibition was competitive. When the unbranched hydrocarbon chain of the quaternary amines was extended in steps from C1 (methyl) to C16 (cetyl), the inhibitory effect increased sharply with length from C7 (heptyl) to C16. These results suggest that the size of the hydrophobic part of the molecule is an important factor in binding of quaternary ammonium compounds to the brush border membrane. The structure of the hydrophilic part was another factor. In imipramine-related compounds, the order of binding was N-didesmethylimipramine (primary amine) greater than desipramine (secondary) greater than imipramine (tertiary) greater than methylimipramine (quaternary). However, with the small molecular ethylamine-related compounds, binding properties did not reflect differences in the hydrophilic component. Therefore, the effect of the hydrophilic part may be secondary and may depend on the size of the hydrophobic part. We suggest that organic cations which are amphiphilic can bind to a common binding site on brush border membrane through hydrophobic and/or hydrophilic interactions.
我们研究了各种有机阳离子的分子结构与其与大鼠小肠刷状缘膜结合之间的相关性。四甲基铵和胆碱等小分子季铵化合物与刷状缘膜的结合不足以抑制甲氯丙嗪的结合。然而,月桂基三甲基铵和十六烷基三甲基铵这两种具有长碳链的季胺,能显著抑制结合。这种抑制是竞争性的。当季胺的直链烃链从C1(甲基)逐步延伸到C16(十六烷基)时,抑制作用从C7(庚基)到C16随着链长急剧增加。这些结果表明,分子疏水部分的大小是季铵化合物与刷状缘膜结合的一个重要因素。亲水部分的结构是另一个因素。在与丙咪嗪相关的化合物中,结合顺序为N-去二甲基丙咪嗪(伯胺)大于去甲丙咪嗪(仲胺)大于丙咪嗪(叔胺)大于甲基丙咪嗪(季胺)。然而,对于小分子乙胺相关化合物,结合特性并未反映亲水成分的差异。因此,亲水部分的作用可能是次要的,且可能取决于疏水部分的大小。我们认为两亲性有机阳离子可通过疏水和/或亲水相互作用与刷状缘膜上的共同结合位点结合。