Housley G M, Born G V
Proc R Soc Lond B Biol Sci. 1983 Aug 22;219(1214):83-90. doi: 10.1098/rspb.1983.0060.
We have reported that the antihaemolytic effect of low concentrations of chlorpromazine is decreased after enzymic removal of sialopeptides from red cell membranes, suggesting that an interaction between negatively charged sialic acids and positively charged chlorpromazine is involved in its membrane stabilizing effect. We have now investigated the antihaemolytic action of simpler molecules with different charges Removal of membrane sialopeptides did not affect the membrane stabilizing actions of simple aliphatic mono- or diamines nor of similar aliphatic molecules carrying strong positive or negative charges, where those positively charged were more potent than those with negative charges. It appears, therefore, that membrane stabilizing activity is determined primarily by lipophilicity and secondarily by polarity and that it does not depend on interactions with enzymically accessible sialopeptides on the outer surface of biological membranes.
我们曾报道,从红细胞膜上酶解去除唾液酸肽后,低浓度氯丙嗪的抗溶血作用会降低,这表明带负电荷的唾液酸与带正电荷的氯丙嗪之间的相互作用涉及其膜稳定作用。我们现在研究了具有不同电荷的更简单分子的抗溶血作用。去除膜唾液酸肽并不影响简单脂肪族单胺或二胺以及带有强正电荷或负电荷的类似脂肪族分子的膜稳定作用,其中带正电荷的分子比带负电荷的分子更有效。因此,似乎膜稳定活性主要由亲脂性决定,其次由极性决定,并且它不依赖于与生物膜外表面上可被酶作用的唾液酸肽的相互作用。