Basic mechanisms of MCD in animal models

被引:14
作者
Battaglia, Giorgio [2 ]
Becker, Albert J. [3 ]
LoTurco, Joseph [4 ]
Represa, Alfonso [5 ]
Baraban, Scott C. [6 ]
Roper, Steven N. [7 ]
Vezzani, Annamaria [1 ]
机构
[1] Mario Negri Inst Pharmacol Res, Lab Expt Neurol, Dept Neurosci, I-20156 Milan, Italy
[2] IRCCS Fdn Neurol Inst Carlo Besta, Mol Neuroanat & Pathogenesis Unit, Milan, Italy
[3] Univ Bonn, Med Ctr, Dept Neuropathol, D-5300 Bonn, Germany
[4] Univ Connecticut, Dept Physiol & Neurobiol, Storrs, CT 06269 USA
[5] Univ Mediterranee, INSERM, INMED, U901, Marseille, France
[6] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[7] Univ Florida, McKnight Brain Inst, Dept Neurol Surg, Gainesville, FL USA
关键词
epileptogenesis; glutamate receptors; methylazoxymethanol; pilocarpine; in utero irradiation; MAEUK proteins; MCD; animal model; SHORT-TERM PLASTICITY; DEVELOPMENTAL SWITCH; MIGRATION; NEURONS; HIPPOCAMPUS; RATS; EPILEPTOGENICITY; ABNORMALITIES; DOUBLECORTIN; HETEROTOPIA;
D O I
10.1684/epd.2009.0273
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Epilepsy-associated glioneuronal malformations (malformations of cortical development [MCD]) include focal cortical dysplasias (FCD) and highly differentiated glioneuronal tumors, most frequently gangliogliomas. The neuropathological findings are variable but suggest aberrant proliferation, migration, and differentiation of neural precursor cells as essential pathogenetic elements. Recent advances in animal models for MCDs allow new insights in the molecular pathogenesis of these epilepsy-associated lesions. Novel approaches, presented here, comprise RNA interference strategies to generate and study experimental models of subcortical band heterotopia and study functional aspects of aberrantly shaped and positioned neurons. Exciting analyses address impaired NMDA receptor expression in FCD animal models compared to human FCDs and excitatory imbalances in MCD animal models such as lissencephaly gene ablated mice as well as in utero irradiated rats. An improved understanding of relevant pathomechanisms will advance the development of targeted treatment strategies for epilepsy-associated malformations.
引用
收藏
页码:206 / 214
页数:9
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