Characterization of Na+ currents in isolated dorsal unpaired median neurons of Locusta migratoria and effect of the alpha-like scorpion toxin BmK M1

被引:16
作者
Brône, B
Tytgat, J
Wang, DC
Van Kerkhove, E
机构
[1] Limburgs Univ Ctr, Physiol Lab, B-3590 Diepenbeek, Belgium
[2] Univ Leuven, Toxicol Lab, B-3000 Louvain, Belgium
[3] Chinese Acad Sci, Inst Biophys, Beijing 100101, Peoples R China
关键词
voltage gated Na+ current; isolated dorsal unpaired median neurons; Locusta migratoria; alpha-like toxin; Buthus martensi Karsch;
D O I
10.1016/S0022-1910(02)00263-9
中图分类号
Q96 [昆虫学];
学科分类号
摘要
A primary cell culture was developed for efferent dorsal unpaired median (DUM) neurons of the locust. The isolated somata were able to generate Tetrodotoxin (TTX)-sensitive action potentials in vitro. The a-like scorpion toxin BmK M1, from the Asian scorpion Buthus martensi Karsch, prolonged the duration of the action potential up to 50 times. To investigate the mechanism of action of BmK M1, the TTX-sensitive voltage gated Na+ currents were studied in detail using the whole cell patch clamp technique. BmK M1 slowed down and partially inhibited the inactivation of the TTX-sensitive Na+ current in a dose dependent manner (EC50 = 326.8 +/- 34.5 nM). Voltage and time dependence of the Na+ current were described in terms of the Hodgkin-Huxley model and compared in control conditions and in the presence of 500 nM BmK M1. The BmK M1 shifted steady state inactivation by 10.8 mV to less negative potentials. The steady state activation was shifted by 5.5 mV to more negative potentials, making the activation window larger. Moreover, BmK M1 increased the fast time constant of inactivation, leaving the activation time constant unchanged. In summary, BmK M1 primarily affected the inactivation parameters of the voltage gated Na+ current in isolated locust DUM neurons. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:171 / 182
页数:12
相关论文
共 62 条
[1]   Na+-dependent neuritic spikes initiate Ca2+-dependent somatic plateau action potentials in insect dorsal paired median neurons [J].
Amat, C ;
Lapied, B ;
French, AS ;
Hue, B .
JOURNAL OF NEUROPHYSIOLOGY, 1998, 80 (05) :2718-2726
[2]  
ASHBY GJ, 1972, UFAW HDB CARE MANAGE, P182
[3]   LIQUID JUNCTION POTENTIALS AND SMALL-CELL EFFECTS IN PATCH-CLAMP ANALYSIS [J].
BARRY, PH ;
LYNCH, JW .
JOURNAL OF MEMBRANE BIOLOGY, 1991, 121 (02) :101-117
[4]   The scorpion α-like toxin LQH III specifically alters sodium channel inactivation in frog myelinated axons [J].
Benoit, E ;
Gordon, D .
NEUROSCIENCE, 2001, 104 (02) :551-559
[5]   OMEGA-AGA-I - A PRESYNAPTIC CALCIUM-CHANNEL ANTAGONIST FROM VENOM OF THE FUNNEL WEB SPIDER, AGELENOPSIS-APERTA [J].
BINDOKAS, VP ;
ADAMS, ME .
JOURNAL OF NEUROBIOLOGY, 1989, 20 (04) :171-188
[6]   METABOLIC INTEGRATION IN LOCUST FLIGHT - THE EFFECT OF OCTOPAMINE ON FRUCTOSE 2,6-BISPHOSPHATE CONTENT OF FLIGHT-MUSCLE IN-VIVO [J].
BLAU, C ;
WEGENER, G .
JOURNAL OF COMPARATIVE PHYSIOLOGY B-BIOCHEMICAL SYSTEMIC AND ENVIRONMENTAL PHYSIOLOGY, 1994, 164 (01) :11-15
[7]  
Burrows M, 1996, NEUROBIOLOGY INSECT
[8]  
Cestèle S, 1998, J NEUROCHEM, V70, P1217
[9]   Scorpion α-like toxins, toxic to both mammals and insects, differentially interact with receptor site 3 on voltage-gated sodium channels in mammals and insects [J].
Cestèle, S ;
Stankiewicz, M ;
Mansuelle, P ;
De Waard, M ;
Dargent, B ;
Gilles, N ;
Pelhate, M ;
Rochat, H ;
Martin-Eauclaire, M ;
Gordon, D .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (03) :975-985
[10]   Molecular mechanisms of neurotoxin action on voltage-gated sodium channels [J].
Cestèle, S ;
Catterall, WA .
BIOCHIMIE, 2000, 82 (9-10) :883-892