Voltage-gated ion channelopathies of the nervous system

被引:20
作者
Cannon, SC [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Dept Neurol, EDR 413, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
ion channel; periodic paralysis; myotonia; epilepsy; headache;
D O I
10.1016/S1566-2772(00)00011-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Mutations in genes coding for voltage-gated ion channels cause a diverse group of disorders affecting heart, skeletal muscle, and brain. Mutant channels alter the electrical excitability of cells. which increases the susceptibility, to paroxysmal symptoms including cardiac arrhythmia. periodic paralysis. myotonia, seizures. migraine headache. and episodic ataxia. This review provides an update on the genetics and physiology of diseases of skeletal muscle and brain caused h mutations in voltage-gated in ion channel genes. The discovery of specific ion channel defects provides a rational basis for designing pharmacological intervention, as ion channel,, are the molecular targets of many drugs in clinical use. Moreover, the advent of a molecular genetic-based diagnosis provides an important tool for clarifying the natural history and effectiveness of intervention in these disorders. (C) 2001 Association for Research in Nervous and Mental Disease. All rights reserved.
引用
收藏
页码:104 / 117
页数:14
相关论文
共 68 条
[1]   REPETITIVE DISCHARGE IN MYOTONIC MUSCLE-FIBERS [J].
ADRIAN, RH ;
BRYANT, SH .
JOURNAL OF PHYSIOLOGY-LONDON, 1974, 240 (02) :505-515
[2]  
[Anonymous], 1994, MYOLOGY
[3]  
Ashcroft F.M., 2000, Ion Channels and Disease
[4]   A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33 [J].
Baulac, S ;
Gourfinkel-An, I ;
Picard, F ;
Rosenberg-Bourgin, M ;
Prud'homme, JF ;
Baulac, M ;
Brice, A ;
LeGuern, E .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) :1078-1085
[5]   Molecular basis for decreased muscle chloride conductance in the myotonic goat [J].
Beck, CL ;
Fahlke, C ;
George, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :11248-11252
[6]   A potassium channel mutation in neonatal human epilepsy [J].
Biervert, C ;
Schroeder, BC ;
Kubisch, C ;
Berkovic, SF ;
Propping, P ;
Jentsch, TJ ;
Steinlein, OK .
SCIENCE, 1998, 279 (5349) :403-406
[7]   EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE, KCNA1 [J].
BROWNE, DL ;
GANCHER, ST ;
NUTT, JG ;
BRUNT, ERP ;
SMITH, EA ;
KRAMER, P ;
LITT, M .
NATURE GENETICS, 1994, 8 (02) :136-140
[8]   CABLE PROPERTIES OF EXTERNAL INTERCOSTAL MUSCLE FIBRES FROM MYOTONIC AND NONMYOTONIC GOATS [J].
BRYANT, SH .
JOURNAL OF PHYSIOLOGY-LONDON, 1969, 204 (03) :539-&
[9]   A novel sodium channel mutation in a family with hypokalemic periodic paralysis [J].
Bulman, DE ;
Scoggan, KA ;
van Oene, MD ;
Nicolle, MW ;
Hahn, AF ;
Tollar, LL ;
Ebers, GC .
NEUROLOGY, 1999, 53 (09) :1932-1936
[10]   A SODIUM-CHANNEL DEFECT IN HYPERKALEMIC PERIODIC PARALYSIS - POTASSIUM-INDUCED FAILURE OF INACTIVATION [J].
CANNON, SC ;
BROWN, RH ;
COREY, DP .
NEURON, 1991, 6 (04) :619-626