Gunn R B, Cooper J A
J Membr Biol. 1975;25(3-4):311-26. doi: 10.1007/BF01868581.
The self-exchange of chloride isotopes across the human erythrocyte membrane was inhibited by tetracaine, benzocaine, and lidocaine. The inhibition by tetracaine was increased at higher pH values, but was not exclusively due to the uncharged form of tetracaine. The inhibition was effective within 5 seconds, was reversible, was non competitive with chloride ions, and was not reversed by calcium ions. These findings indicate that local anesthetics react with the erythrocyte chloride carrier at a site separate from the chloride site and cause inhibition of anion transport by a specific mechanism not involving changes in the surface charge density on the erythrocyte membrane.
丁卡因、苯佐卡因和利多卡因可抑制氯离子同位素在人红细胞膜上的自我交换。在较高pH值下,丁卡因的抑制作用增强,但并非完全归因于丁卡因的不带电荷形式。这种抑制作用在5秒内即可生效,是可逆的,对氯离子无竞争性,且不受钙离子逆转。这些发现表明,局部麻醉药在与氯离子位点不同的部位与红细胞氯离子载体发生反应,并通过一种不涉及红细胞膜表面电荷密度变化的特定机制抑制阴离子转运。