Bittigau Petra, Sifringer Marco, Ikonomidou Chrysanthy
Department of Pediatric Neurology, Children's Hospital, Charite-Virchow Clinics, Humboldt University, Berlin, Germany.
Ann N Y Acad Sci. 2003 May;993:103-14; discussion 123-4. doi: 10.1111/j.1749-6632.2003.tb07517.x.
Epilepsy is the most common neurologic disorder in young humans. Antiepileptic drugs (AEDs), used to treat seizures in children, infants, and pregnant women, cause cognitive impairment, microcephaly, and birth defects by unknown mechanisms. We tested whether common AEDs cause neurodegeneration in the developing rat brain. Rats aged 3-30 days received phenytoin, phenobarbital, diazepam, clonazepam, vigabatrin, or valproic acid. Histologic examination of the brains revealed that these drugs cause widespread and dose-dependent apoptotic neurodegeneration in the developing rat brain during the brain growth spurt period. Apoptotic neurodegeneration was triggered at plasma drug levels relevant for seizure control in humans. Antiepileptic drugs lead to reduced expression of neurotrophins and decreased concentrations of the active forms of ERK1/2, RAF, and AKT. beta-Estradiol, which stimulates pathways that are activated by neurotrophins, ameliorated AEDs-induced apoptotic neurodegeneration. Our findings present one possible mechanism to explain cognitive impairment and reduced brain mass associated with pre- or postnatal exposure of humans to antiepileptic therapy.
癫痫是年轻人中最常见的神经系统疾病。用于治疗儿童、婴儿和孕妇癫痫发作的抗癫痫药物(AEDs)通过未知机制导致认知障碍、小头畸形和出生缺陷。我们测试了常见的抗癫痫药物是否会导致发育中的大鼠大脑发生神经退行性变。3至30日龄的大鼠接受苯妥英钠、苯巴比妥、地西泮、氯硝西泮、氨己烯酸或丙戊酸治疗。对大脑的组织学检查显示,这些药物在大脑快速生长期间导致发育中的大鼠大脑广泛且剂量依赖性的凋亡性神经退行性变。在与人类癫痫控制相关的血浆药物水平时引发了凋亡性神经退行性变。抗癫痫药物导致神经营养因子表达减少,以及ERK1/2、RAF和AKT活性形式的浓度降低。刺激由神经营养因子激活的信号通路的β-雌二醇可改善抗癫痫药物诱导的凋亡性神经退行性变。我们的研究结果提出了一种可能的机制,以解释人类在产前或产后接受抗癫痫治疗相关的认知障碍和脑容量减少。