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The mode of action of local anesthetics on nerve axons: A diffusion-reaction process.

机译:局麻药对神经轴突的作用方式:扩散反应过程。

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摘要

The mode of action of tertiary-amine local anesthetics on nerve axon activity was investigated. The axons were those from lobster (Homerus americanus) and squid (Loligo paelii). Anesthetics used were benzocaine, procaine, lidocaine, tetracaine and permanently-charged quaternary amine local anesthetic QX-314. The action potential and its time derivative were measured by the standard electrophysiological method, and a degree of anesthesia was determined as a reduction of the time derivative of the action potential to a certain degree. Using the model we developed for diffusion of local anesthetics into the axon and binding of the local anesthetics to the membrane receptor site, the permeability of uncharged form of local anesthetics and the binding constants of both positive charged and neutral forms were obtained. For squid axon at pHo, the permeability of the neutral form of procaine was 11 × 10−4 cm/sec and the binding constants of the positively charged and neutral forms of procaine were 293 M−1 and 166 M−1, respectively. For tetracaine, the respective values were 1.8 × 10−4 cm/sec, 3800 M−1 and 994 M−1. Comparable values were obtained for the case of lobster. The permanently charged local anesthetic, QX314, did not affect the axon activity extracellularly and supposedly did not permeate across the membrane. From these experimental results, the mode of action of local anesthetics is proposed as follows: when a tertiary amine local anesthetic is applied extracellularly, only the neutral form penetrates through the axon membrane and both positive charged and neutral forms act intracellularly. Therefore, the mode of action depends upon the pH values of intracellular and extracellular compartments, pKa of anesthetics, and the binding affinities of local anesthetics to the action sites of ionic channels. It was found that the charged form blocks up to 30 to 60 times more ion channels than the neutral form, although the neutral form also plays a definite role in contributing to the overall action but in a minor degree. The proposed mode of action has its originality in analyzing quantitatively the dual modes (both charged and neutral forms) of action of tertiary-amine anesthetics on nerve axon excitability.
机译:研究了叔胺局部麻醉药对神经轴突活性的作用方式。轴突是来自龙虾( Americanrususus )和鱿鱼( Loligo paelii )的轴突。所用的麻醉剂是苯佐卡因,普鲁卡因,利多卡因,丁卡因和永久充电的季胺局部麻醉剂QX-314。通过标准电生理学方法测量动作电位及其时间导数,并且将麻醉度确定为动作电位的时间导数在一定程度上的减小。使用我们开发的局部麻醉剂扩散到轴突中和局部麻醉剂与膜受体部位结合的模型,获得了不带电荷形式的局部麻醉剂的渗透性以及带正电荷和中性形式的结合常数。对于pH o 的鱿鱼轴突,普鲁卡因中性形式的渗透性为11×10 -4 cm / sec,带正电和中性形式的普鲁卡因的结合常数普鲁卡因分别为293 M -1 和166 M -1 。对于丁卡因,各自的值为1.8×10 -4 cm / sec,3800 M -1 和994 M -1 。对于龙虾,获得了可比的值。永久充电的局麻药QX314不会影响细胞外的轴突活性,并且据信不会渗透到整个膜上。从这些实验结果中,提出了局麻药的作用方式如下:当在细胞外施用叔胺局麻药时,只有中性形式穿透轴突膜,带正电和中性形式都在细胞内起作用。因此,作用方式取决于细胞内和细胞外区室的pH值,麻醉药的pK 以及局麻药对离子通道作用部位的结合亲和力。已经发现,带电形式比中性形式阻塞最多多达30至60倍的离子通道,尽管中性形式在总体作用中也起着一定作用,但程度较小。所提出的作用方式在定量分析叔胺麻醉药对神经轴突兴奋性的双重作用方式(带电和中性形式)方面具有独创性。

著录项

  • 作者单位

    State University of New York at Buffalo.;

  • 授予单位 State University of New York at Buffalo.;
  • 学科 Biophysics Medical.
  • 学位 Ph.D.
  • 年度 2001
  • 页码 149 p.
  • 总页数 149
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物物理学 ;
  • 关键词

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