A new hypothesis of drug refractory epilepsy: Neural network hypothesis

被引:139
作者
Fang, Min [1 ]
Xi, Zhi-Qin [1 ]
Wu, Yuan [1 ,2 ]
Wang, Xue-Feng [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Neurol, Chongqing Key Lab Neurol, Chongqing 400016, Peoples R China
[2] Guangxi Med Univ, Affiliated Hosp 1, Dept Neurol, Nanning 530022, Peoples R China
基金
中国国家自然科学基金;
关键词
TEMPORAL-LOBE EPILEPSY; HILAR BASAL DENDRITES; GENE-EXPRESSION; DENTATE GYRUS; GRANULE CELLS; PROTEIN-SYNTHESIS; AXON GUIDANCE; FUNCTIONAL IMPLICATIONS; NEUROLOGICAL DISORDERS; ANTIEPILEPTIC DRUGS;
D O I
10.1016/j.mehy.2011.02.039
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Drug refractory is an important clinical problem in epilepsy, affecting a substantial number of patients globally. Mechanisms underlying drug refractory need to be understood to develop rational therapies. Current two prevailing theories on drug refractory epilepsy (DRE) include the target hypothesis and the transporter hypothesis. However, those hypotheses could not be adequate to explain the mechanisms of all the DRE. Thus, we propose another possible mechanism of DRE, which is neural network hypothesis. It is hypothesized that seizure-induced alterations of brain plasticity including axonal sprouting, synaptic reorganization, neurogenesis and gliosis could contribute to the formation of abnormal neural network, which has not only avoided the inhibitory effect of endogenous antiepileptic system but also prevented the traditional antiepileptic drugs from entering their targets, eventually leading to DRE. We will illustrate this hypothesis at molecular and structural level based on our recent studies and other related researches. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:871 / 876
页数:6
相关论文
共 87 条
[1]
Recurrent excitation of granule cells with basal dendrites and low interneuron density and inhibitory postsynaptic current frequency in the dentate gyrus of macaque monkeys [J].
Austin, JE ;
Buckmaster, PS .
JOURNAL OF COMPARATIVE NEUROLOGY, 2004, 476 (03) :205-218
[2]
Refractory Epilepsy: A Clinically Oriented Review [J].
Beleza, Pedro .
EUROPEAN NEUROLOGY, 2009, 62 (02) :65-71
[3]
Astrocyte-neuron interactions Implications for epilepsy [J].
Benarroch, Eduardo E. .
NEUROLOGY, 2009, 73 (16) :1323-1327
[4]
Functional changes in astroglial cells in epilepsy [J].
Binder, Devin K. ;
Steinhaeuser, Christian .
GLIA, 2006, 54 (05) :358-368
[5]
Look who is weaving the neural web: glial control of synapse formation [J].
Bolton, M. McLean ;
Eroglu, Cagla .
CURRENT OPINION IN NEUROBIOLOGY, 2009, 19 (05) :491-497
[6]
Degeneration and proliferation of astrocytes in the mouse dentate gyrus after pilocarpine-induced status epilepticus [J].
Borges, Karin ;
McDermott, Dayna ;
Irier, Hasan ;
Smith, Yoland ;
Dingledine, Raymond .
EXPERIMENTAL NEUROLOGY, 2006, 201 (02) :416-427
[7]
The multidrug transporter hypothesis of drug resistance in epilepsy:: Proof-of-principle in a rat model of temporal lobe epilepsy [J].
Brandt, Claudia ;
Bethmann, Kerstin ;
Gastens, Alexandra M. ;
Loescher, Wolfgang .
NEUROBIOLOGY OF DISEASE, 2006, 24 (01) :202-211
[8]
Mechanisms of disease - Epilepsy [J].
Chang, BS ;
Lowenstein, DH .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (13) :1257-1266
[9]
Molecular mechanisms of axon guidance [J].
Chilton, JK .
DEVELOPMENTAL BIOLOGY, 2006, 292 (01) :13-24
[10]
Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis [J].
Christopherson, KS ;
Ullian, EM ;
Stokes, CCA ;
Mullowney, CE ;
Hell, JW ;
Agah, A ;
Lawler, J ;
Mosher, DF ;
Bornstein, P ;
Barres, BA .
CELL, 2005, 120 (03) :421-433