Mechanisms of epilepsy progression: current theories and perspectives from neuroplasticity in adulthood and development

被引:105
作者
Sutula, TP
机构
[1] Univ Wisconsin, Dept Neurol, Madison, WI 53792 USA
[2] Univ Wisconsin, Dept Anat, Madison, WI 53792 USA
关键词
seizures; kindling; hippocampus; chronic model; intractability; complex systems;
D O I
10.1016/j.eplepsyres.2004.07.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Clinical and epidemiological studies have repeatedly demonstrated that a subset of patients with epilepsy have progressive syndromes with increasing seizure frequency and cumulative adverse effects despite optimal anticonvulsant therapy. Recent longitudinal imaging studies and long-term neuropsychological studies have confirmed that a substantial subset of people with epilepsy undergo progressive brain atrophy accompanied by functional declines that worsen with duration of epilepsy. As further evidence of the progressive and adverse effects of inadequately controlled epilepsy, chronic experimental models of epilepsy and the phenomenon of kindling have provided abundant evidence that neural circuits undergo long-term progressive structural and functional alterations in response to seizures. This long-term seizure-induced plasticity in neural circuits appears to be "bidirectional", inducing progressive damage while also inducing resistance to additional damage, as a function of timing or inter-seizure interval. Seizure-induced plasticity has pronounced age-dependence, and influences long-term cognitive consequences of seizures dufing early life and acquired susceptibility to epilepsy in adulthood. While it is clear from clinical and epidemiological studies that human epilepsy is a heterogeneous disorder and that not all epileptic syndromes are progressive, emerging results from studies of activity-dependent and seizure-induced plasticity and perspectives from "complex systems" analysis are providing new insights into systematic neurobiological processes that are likely to influence the progressive features of epileptic syndromes and patterns of progression in individual patients. The emerging perspective is that phenomena of plasticity and genetic background exert powerful effects in development and adulthood through regulation of activity-dependent structural and functional remodeling of neural circuitry, and that these effects not only influence progression and consequences of seizures, but also offer new opportunities for therapeutic intervention. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:161 / 171
页数:11
相关论文
共 75 条
[1]  
Anderson V E, 1999, Adv Neurol, V79, P59
[2]   The lesional and epileptogenic consequences of lithium-pilocarpine-induced status epilepticus are affected by previous exposure to isolated seizures:: Effects of amygdala kindling and maximal electroshocks [J].
André, V ;
Ferrandon, A ;
Marescaux, C ;
Nehlig, A .
NEUROSCIENCE, 2000, 99 (03) :469-481
[3]   A population-based study of seizures after traumatic brain injuries [J].
Annegers, JF ;
Hauser, WA ;
Coan, SP ;
Rocca, WA .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (01) :20-24
[4]   Apoptosis and proliferation of dentate gyrus neurons after single and intermittent limbic seizures [J].
Bengzon, J ;
Kokaia, Z ;
Elmer, E ;
Nanobashvili, A ;
Kokaia, M ;
Lindvall, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10432-10437
[5]  
Bengzon J, 2002, PROG BRAIN RES, V135, P111
[6]   Seizure-associated hippocampal volume loss: A longitudinal magnetic resonance study of temporal lobe epilepsy [J].
Briellmann, RS ;
Berkovic, SF ;
Syngeniotis, A ;
King, MA ;
Jackson, GD .
ANNALS OF NEUROLOGY, 2002, 51 (05) :641-644
[7]   PROGRESSIVE NEURONAL LOSS INDUCED BY KINDLING - A POSSIBLE MECHANISM FOR MOSSY FIBER SYNAPTIC REORGANIZATION AND HIPPOCAMPAL SCLEROSIS [J].
CAVAZOS, JE ;
SUTULA, TP .
BRAIN RESEARCH, 1990, 527 (01) :1-6
[8]  
CAVAZOS JE, 1994, J NEUROSCI, V14, P3106
[9]   Febrile seizures impair memory and cAMP response-element binding protein activation [J].
Chang, YC ;
Huang, AM ;
Kuo, YM ;
Wang, ST ;
Chang, YY ;
Huang, CC .
ANNALS OF NEUROLOGY, 2003, 54 (06) :706-718
[10]   A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family [J].
Charlier, C ;
Singh, NA ;
Ryan, SG ;
Lewis, TB ;
Reus, BE ;
Leach, RJ ;
Leppert, M .
NATURE GENETICS, 1998, 18 (01) :53-55