Avanzini G, de Curtis M, Franceschetti S, Sancini G, Spreafico R
Department of Neurophysiology, Instituto Nazionale Neurologico C. Besta, Milan, Italy.
Epilepsy Res. 1996 Dec;26(1):37-44. doi: 10.1016/s0920-1211(96)00037-x.
Genetic absence epilepsy rats from Strasbourg (GAERS) have non-convulsive generalized seizures associated with spike-wave (SW) discharges, which are due to a hyperexcitable state of the thalamo-cortico circuits involving the reticular thalamic nucleus (nRt). Investigation of the primary genetically-determined defect responsible for GAERS epilepsy revealed the following abnormalities: (1) increased effectiveness of AMPA receptors dependent glutamate-mediated transmission; (2) impairment of GABA-mediated transmission in the neocortex; (3) increased amplitude of the voltage-dependent low-threshold Ca2(+)-current (I(T)) in the nRt. The maturational profile of these abnormalities supports the conclusion that the abnormality in the I(T) current in the nRt is the primary genetically-determined defect, which may secondarily induce the other changes found in the neocortex and thalamus of GAERS.
来自斯特拉斯堡的遗传性失神癫痫大鼠(GAERS)具有与棘波(SW)放电相关的非惊厥性全身性癫痫发作,这是由于涉及丘脑网状核(nRt)的丘脑 - 皮质回路的过度兴奋状态所致。对导致GAERS癫痫的原发性遗传决定缺陷的研究揭示了以下异常情况:(1)AMPA受体依赖性谷氨酸介导的传递效率增加;(2)新皮质中GABA介导的传递受损;(3)nRt中电压依赖性低阈值Ca2 +电流(I(T))的幅度增加。这些异常情况的成熟特征支持以下结论:nRt中I(T)电流的异常是原发性遗传决定缺陷,这可能继而诱发在GAERS的新皮质和丘脑中发现的其他变化。