Suzuki T, Ohishi K, Kida J, Uchida M
Eur J Pharmacol. 1984 Mar 2;98(3-4):347-55. doi: 10.1016/0014-2999(84)90283-8.
The study concerned the effects of lidocaine and mepivacaine on rat mast cell histamine release. At low concentrations these drugs inhibited the histamine release induced by concanavalin A and compound 48/80 although, at high concentrations, they caused cell lysis. The mechanism of their inhibition of histamine release was studied by examining the pH dependence of the inhibitory action. In the absence of drugs, the release of histamine was not affected by the pH of the medium, but the inhibitory effects of the drugs increased with increase in pH. The percent inhibition of histamine release by these drugs at each pH was plotted against the calculated concentration of the nonionized form of the drug, according to the Henderson-Hasselbalch equation. The inhibitory action was correlated with the concentration of nonionized molecules, which readily penetrate the cell membrane. From the interaction of lidocaine with the phospholipid bilayer, it was concluded that this drug penetrates the lipid bilayer and that this effect increases with increasing pH of the medium. Thus, it seems that it is the nonionized form of local anesthetics that inhibits histamine release and that it is nonionized molecules that penetrate the mast cell membrane.
该研究关注利多卡因和甲哌卡因对大鼠肥大细胞组胺释放的影响。在低浓度时,这些药物抑制伴刀豆球蛋白A和化合物48/80诱导的组胺释放,尽管在高浓度时它们会导致细胞裂解。通过研究抑制作用的pH依赖性来探讨它们抑制组胺释放的机制。在无药物情况下,组胺释放不受培养基pH的影响,但药物的抑制作用随pH升高而增强。根据亨德森-哈塞尔巴尔赫方程,将这些药物在每个pH下对组胺释放的抑制百分比与计算出的药物非离子化形式的浓度作图。抑制作用与易于穿透细胞膜的非离子化分子浓度相关。从利多卡因与磷脂双层的相互作用得出结论,该药物穿透脂质双层,且这种作用随培养基pH升高而增强。因此,似乎是局部麻醉药的非离子化形式抑制组胺释放,并且是非离子化分子穿透肥大细胞膜。