Time course and effective spread of lidocaine and tetrodotoxin delivered via microdialysis: an electrophysiological study in cerebral cortex

被引:61
作者
Boehnke, SE
Rasmusson, DD
机构
[1] Dalhousie Univ, Dept Physiol & Biophys, Halifax, NS B3H 4H7, Canada
[2] Dalhousie Univ, Dept Psychol, Halifax, NS B3H 4H7, Canada
基金
英国医学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
cerebral cortex; evoked potentials; inactivation; lidocaine; microdialysis; raccoon; somatosensory; tetrodotoxin;
D O I
10.1016/S0165-0270(00)00348-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microdialysis is a useful tool for administering drugs into localized regions of brain tissue, but the diffusion of drugs from the probe has not been systematically examined. Lidocaine (10%) and tetrodotoxin (TTX, 10 muM), drugs typically used in neural inactivation studies, were infused through a microdialysis probe into raccoon somatosensory cortex while evoked responses were recorded at four electrodes equally spaced 0.5-2.0 mm from the probe. The decreases in evoked response amplitude as a function of time and distance from the probe were used as functional measures to describe the time course and spread of the drugs. TTX inactivated distant sites more quickly and to a greater extent than lidocaine. Responses recovered within approximately 40 min after termination of lidocaine, but did not recover for at least 2 h after TTX. Based on these measurements, we estimated that, at the concentrations used, lidocaine has a maximal spread of 2.1 mm, while TTX could spread as far as 4.8 mm from the microdialysis probe. However, in terms of significant inactivation of neuronal activity, lidocaine and TTX have an effective spread of 1 and 2 mm, respectively. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:133 / 141
页数:9
相关论文
共 20 条
  • [1] AN EXAMINATION OF THE FUNCTIONALLY EFFECTIVE SPREAD OF MU-L OF SLOWLY INFUSED LIDOCAINE
    ALBERT, DJ
    MADRYGA, FJ
    [J]. BEHAVIORAL AND NEURAL BIOLOGY, 1980, 29 (03): : 378 - 384
  • [2] BRAIN MICRODIALYSIS
    BENVENISTE, H
    [J]. JOURNAL OF NEUROCHEMISTRY, 1989, 52 (06) : 1667 - 1679
  • [3] BENVENISTE H, 1991, MICRODIALYSIS NEUROS, P81, DOI DOI 10.1016/B978-0-444-81194-3.50009-5
  • [4] CAULLER LJ, 1991, EXP BRAIN RES, V84, P607
  • [5] DELANGE ECM, 1995, BRIT J PHARMACOL, V116, P2538
  • [6] EFFECTS OF REVERSIBLE LESIONS AND STIMULATION OF OLIVOCEREBELLAR SYSTEM ON VESTIBULOOCULAR REFLEX PLASTICITY
    DEMER, JL
    ROBINSON, DA
    [J]. JOURNAL OF NEUROPHYSIOLOGY, 1982, 47 (06) : 1084 - 1107
  • [7] QUANTITATIVE EXAMINATION OF TISSUE CONCENTRATION PROFILES ASSOCIATED WITH MICRODIALYSIS
    DYKSTRA, KH
    HSIAO, JK
    MORRISON, PF
    BUNGAY, PM
    MEFFORD, IN
    SCULLY, MM
    DEDRICK, RL
    [J]. JOURNAL OF NEUROCHEMISTRY, 1992, 58 (03) : 931 - 940
  • [8] Hille B., 1992, IONIC CHANNELS EXCIT, P607
  • [9] A SURVEY ON QUANTITATIVE MICRODIALYSIS - THEORETICAL-MODELS AND PRACTICAL IMPLICATIONS
    KEHR, J
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 1993, 48 (03) : 251 - 261
  • [10] THE COMBINED EEG-INTRACEREBRAL MICRODIALYSIS TECHNIQUE - A NEW TOOL FOR NEUROPHARMACOLOGICAL STUDIES ON FREELY BEHAVING ANIMALS
    LUDVIG, N
    MISHRA, PK
    YAN, QS
    LASLEY, SM
    BURGER, RL
    JOBE, PC
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 1992, 43 (2-3) : 129 - 137