Ludvig N, Moshé S L
Department of Neurology, Albert Einstein College of Medicine, Rose F. Kennedy Center, Bronx, NY 10461.
Epilepsy Res. 1989 May-Jun;3(3):185-90. doi: 10.1016/0920-1211(89)90022-3.
The behavioral and electrographic effects of acoustic stimulation (100 dB) and injection of dibutyryl cyclic AMP (cAMP, 10 nmol) into the inferior colliculus were studied in normal and genetically epilepsy-prone (GEPR-9) rats. Acoustic stimulations induced behavioral seizures only in GEPR-9 rats; the seizures were associated with electrographic epileptiform discharges recorded from the inferior colliculus. Injections of dibutyryl cAMP into the inferior colliculus caused wild running episodes resembling the initial phase of audiogenic seizures in both groups. However, in GEPR-9 rats these episodes progressed to significantly more severe seizures than in normal rats and the convulsions culminated into status epilepticus. During drug-induced seizures, epileptiform activity was present in the inferior colliculus in both groups. The seizure generalization latency was markedly shorter in GEPR-9 rats than in normals. Furthermore, in GEPR-9 rats, the seizure generalization latency was in the same range with either acoustic stimulation-induced or dibutyryl cAMP-induced seizures. The data suggest that the increased susceptibility of genetically epilepsy-prone rats to acoustic stimuli may be related to a malfunction of the cyclic AMP system within the inferior colliculus.
在正常大鼠和遗传性癫痫易感(GEPR - 9)大鼠中,研究了听觉刺激(100分贝)以及向下丘注射二丁酰环磷酸腺苷(cAMP,10纳摩尔)的行为和脑电图效应。听觉刺激仅在GEPR - 9大鼠中诱发行为性癫痫发作;这些发作与下丘记录到的脑电图癫痫样放电有关。向下丘注射二丁酰环磷酸腺苷在两组中均引起类似听源性癫痫发作初始阶段的狂奔发作。然而,在GEPR - 9大鼠中,这些发作比正常大鼠发展为明显更严重的癫痫发作,惊厥最终演变为癫痫持续状态。在药物诱发的癫痫发作期间,两组下丘均出现癫痫样活动。GEPR - 9大鼠的癫痫发作扩散潜伏期明显短于正常大鼠。此外,在GEPR - 9大鼠中,癫痫发作扩散潜伏期在听觉刺激诱发或二丁酰环磷酸腺苷诱发的癫痫发作中处于相同范围。数据表明,遗传性癫痫易感大鼠对听觉刺激的易感性增加可能与下丘内环磷酸腺苷系统功能异常有关。