Dailey J W, Jobe P C
Epilepsia. 1986 Nov-Dec;27(6):665-70. doi: 10.1111/j.1528-1157.1986.tb03593.x.
Norepinephrine concentrations and tyrosine hydroxylase activity were determined in the brains of moderate-seizure and severe-seizure genetically epilepsy-prone rats (GEPRs) and in nonepileptic control rats. Both moderate-seizure (GEPR-3) and severe-seizure (GEPR-9) animals had widespread abnormalities in brain norepinephrine concentrations. Abnormalities in tyrosine hydroxylase activity were restricted to the midbrain. The state of abnormal seizure susceptibility, but not severity, in the GEPR may be determined by noradrenergic deficits in the hypothalamus/thalamus. Both seizure severity and susceptibility may be determined by noradrenergic deficits in the telencephalon, midbrain, and pons-medulla. Seizure severity but not susceptibility may be determined by noradrenergic abnormalities in the cerebellum.
测定了中度癫痫发作和重度癫痫发作的遗传性癫痫易感大鼠(GEPRs)以及非癫痫对照大鼠大脑中的去甲肾上腺素浓度和酪氨酸羟化酶活性。中度癫痫发作(GEPR - 3)和重度癫痫发作(GEPR - 9)的动物大脑去甲肾上腺素浓度均存在广泛异常。酪氨酸羟化酶活性异常局限于中脑。GEPR中异常癫痫易感性而非严重程度的状态可能由下丘脑/丘脑的去甲肾上腺素能缺陷决定。癫痫严重程度和易感性可能由端脑、中脑和脑桥 - 延髓的去甲肾上腺素能缺陷决定。癫痫严重程度而非易感性可能由小脑的去甲肾上腺素能异常决定。