Department of Neurology, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
CNS Neurosci Ther. 2011 Oct;17(5):271-80. doi: 10.1111/j.1755-5949.2010.00168.x. Epub 2010 Jul 7.
It is unknown whether hypothermia can disrupt the progress of epileptogenesis. The present study aimed to determine the effect of hypothermia on brain edema and epileptogenesis and to establish whether brain edema is associated with epileptogenesis after severe status epilepticus (SE).
Rats were injected with a single dose of Kainic acid (KA) to produce either chronic epileptic rats (rats with spontaneous recurrent seizure, SRS) or rats without spontaneous recurrent seizure (no-SRS rats). A second KA injection was used to induce SE in SRS rats and in no-SRS rats. The number of SRS was counted and the brain edema induced by SE was assessed by brain water content measurement. The cognitive function was assessed by the radial-arm maze (RAM) test.
A second KA injection resulted in brain edema that was more severe in SRS rats than in no-SRS rats. After second injection of KA, hypothermia treatment attenuated the KA induced brain edema and reduced the SRS attack in SRS rats. Additionally cognitive function was better in hypothermia-treated SRS rats than in nomothermia treated SRS rats 1 month after the second KA injection.
Hypothermia treatment immediately after SE not only exhibited protective effects against the chronic spontaneous recurrent convulsant seizures but also improved cognitive function. These antiepileptogenic properties of hypothermia may be related to its attenuating effect on brain edema induced by SE. They therefore suggest that brain edema may be involved in the progress of epileptogenesis.
目前尚不清楚低温是否会干扰癫痫发生的进程。本研究旨在确定低温对脑水肿和癫痫发生的影响,并确定严重癫痫持续状态(SE)后脑水肿是否与癫痫发生有关。
向大鼠单次注射海人酸(KA),以产生慢性癫痫大鼠(具有自发性复发性癫痫发作的大鼠,SRS)或无自发性复发性癫痫发作的大鼠(无 SRS 大鼠)。对 SRS 大鼠和无 SRS 大鼠进行第二次 KA 注射以诱导 SE。通过脑水含量测量评估 SE 引起的脑水肿,并计数 SRS 的次数。通过放射臂迷宫(RAM)测试评估认知功能。
第二次 KA 注射导致 SRS 大鼠的脑水肿比无 SRS 大鼠更严重。第二次 KA 注射后,低温治疗减轻了 KA 诱导的脑水肿,并减少了 SRS 大鼠的 SRS 发作。此外,与未进行低温治疗的 SRS 大鼠相比,第二次 KA 注射 1 个月后,低温治疗的 SRS 大鼠的认知功能更好。
SE 后立即进行低温治疗不仅对慢性自发性复发性惊厥发作具有保护作用,而且改善了认知功能。低温的这种抗癫痫作用可能与其对 SE 引起的脑水肿的减轻作用有关。因此,它们表明脑水肿可能参与了癫痫发生的进程。