Heterogeneous competition of Kv1 channel toxins with kaliotoxin for binding in rat brain: autoradiographic analysis

被引:5
作者
Bessone, R
Martin-Eauclaire, MF
Crest, M
Mourre, C
机构
[1] Univ Aix Marseille 1, Fac Sci St Jerome, UMR 6149, CNRS,Lab Neurobiol Integrat & Adapt, F-13397 Marseille 20, France
[2] Univ Mediterranee, Fac Med Marseille, IFR Jean Roche, CNRS,ITIS,UMR 6150, Marseille, France
[3] Univ Mediterranee, Fac Med Marseille, IFR Jean Roche, CNRS,UMR 6560,CNRS, F-13916 Marseille, France
关键词
potassium channel; kaliotoxin; dendrotoxin; mast cell degranulating peptide; neurotoxin; hippocampus; neocortex; basal ganglia; cerebellum; synaptic plasticity; binding; central nervous system; rat;
D O I
10.1016/j.neuint.2004.05.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The alpha-subunits of Kv1 channels display characteristic distributions and restricted co-assembly in mammalian brain. The heterogeneous composition of Kv1 channels has made it difficult to use specific toxins to label brain structures. We used autoradiography to analyse the competitive behaviour of three Kv1 channel toxins-alpha-dendrotoxin, kaliotoxin, and mast cell degranulating peptide-for binding to kaliotoxin binding sites in various brain structures. IC50 varied considerably between brain regions (by up to three orders of magnitude) for each ligand. alpha-dendrotoxin and kaliotoxin competed equally in some regions and to different extents in others, identifying two types of structure. Mast cell degranulating peptide competed with I-125-kaliotoxin less efficiently than alpha-dendrotoxin and kaliotoxin, in all regions. Thus, differences in the capacity of these three toxins to bind to kaliotoxin binding sites provide evidence of major differences in the composition of the Kv1 channels constituting the kaliotoxin binding sites. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1039 / 1047
页数:9
相关论文
共 36 条
[1]   2 POTENT CENTRAL CONVULSANT PEPTIDES, A BEE VENOM TOXIN, THE MCD PEPTIDE, AND A SNAKE-VENOM TOXIN, DENDROTOXIN-I, KNOWN TO BLOCK K+ CHANNELS, HAVE INTERACTING RECEPTOR-SITES [J].
BIDARD, JN ;
MOURRE, C ;
LAZDUNSKI, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 143 (01) :383-389
[2]   ANALOGIES AND DIFFERENCES IN THE MODE OF ACTION AND PROPERTIES OF BINDING-SITES (LOCALIZATION AND MUTUAL INTERACTIONS) OF 2 K+ CHANNEL TOXINS, MCD PEPTIDE AND DENDROTOXIN-I [J].
BIDARD, JN ;
MOURRE, C ;
GANDOLFO, G ;
SCHWEITZ, H ;
WIDMANN, C ;
GOTTESMANN, C ;
LAZDUNSKI, M .
BRAIN RESEARCH, 1989, 495 (01) :45-57
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   Immunohistochemical study on the distribution of six members of the Kv1 channel subunits in the rat basal ganglia [J].
Chung, YH ;
Shin, CM ;
Kim, MJ ;
Cha, CI .
BRAIN RESEARCH, 2000, 875 (1-2) :164-170
[5]   Immunohistochemical study on the distribution of six members of the Kv1 channel subunits in the rat cerebellum [J].
Chung, YH ;
Shin, CM ;
Kim, MJ ;
Lee, BK ;
Cha, CI .
BRAIN RESEARCH, 2001, 895 (1-2) :173-177
[6]   Immunohistochemical study on the distribution of voltage-gated K+ channels in rat brain following transient focal ischemia [J].
Chung, YH ;
Kim, HS ;
Shin, CM ;
Kim, MJ ;
Cha, CI .
NEUROSCIENCE LETTERS, 2001, 308 (03) :157-160
[7]   Age-related changes in the distribution of Kv1.1 and Kv1.2 channel subunits in the rat cerebellum [J].
Chung, YH ;
Shin, CM ;
Kim, MJ ;
Lee, BK ;
Cha, CI .
BRAIN RESEARCH, 2001, 897 (1-2) :193-198
[8]   Subunit composition of Kv1 channels in human CNS [J].
Coleman, SK ;
Newcombe, J ;
Pryke, J ;
Dolly, JO .
JOURNAL OF NEUROCHEMISTRY, 1999, 73 (02) :849-858
[9]  
CREST M, 1992, J BIOL CHEM, V267, P1640
[10]  
GRISSMER S, 1994, MOL PHARMACOL, V45, P1227