Su S W, Cilio M R, Sogawa Y, Silveira D C, Holmes G L, Stafstrom C E
Department of Neurology, Children's Hospital and Medical Center, Harvard Medical School, Boston, MA, USA.
Brain Res Dev Brain Res. 2000 Dec 29;125(1-2):131-8. doi: 10.1016/s0165-3806(00)00130-9.
Following kainic acid (KA)-induced status epilepticus (SE), the ketogenic diet (KD) retards the development of epileptogenesis, with fewer spontaneous recurrent seizures (SRS) and less mossy fiber sprouting than rats on a normal diet. In this study, we investigated whether there is a critical period for initiation of the KD, in terms of the diet's effectiveness in reducing SRS. In addition, we investigated whether early treatment with the KD prevents the deficits in spatial learning and memory that ordinarily follow KA-induced SE. Young rats (P30) underwent KA-induced SE, followed by assignment to one of three treatment groups: control diet ('KA'), KD begun 2 days after SE ('KD2'), and KD begun fourteen days after SE ('KD14'). For 12 weeks following SE, rats were monitored by closed circuit video recording (12 h/wk) to detect SRS. KD2 rats had significantly fewer SRS than rats in the control or KD14 groups. On water maze testing to assess spatial learning and memory, KD2 rats had significantly poorer acquisition of place learning than control (KA alone) or KD14 rats. KD2 rats also failed to gain weight well. There was no difference between groups on routine histologic examination of the hippocampus. In summary, P30 rats placed on the KD 2 days after SE were relatively protected from recurrent seizures, but showed behavioral and physical impairment. Rats placed on the KD 14 days after KA-induced SE did not differ from controls with regard to spontaneous seizure rate.
在给予 kainic 酸(KA)诱导的癫痫持续状态(SE)后,生酮饮食(KD)可延缓癫痫发生的发展,与正常饮食的大鼠相比,其自发性复发性癫痫发作(SRS)更少,苔藓纤维发芽也更少。在本研究中,我们从 KD 对减少 SRS 的有效性方面,研究了启动 KD 是否存在关键时期。此外,我们还研究了早期给予 KD 是否能预防通常在 KA 诱导的 SE 后出现的空间学习和记忆缺陷。幼鼠(P30)接受 KA 诱导的 SE,然后被分配到三个治疗组之一:对照饮食(“KA”)、SE 后 2 天开始的 KD(“KD2”)和 SE 后 14 天开始的 KD(“KD14”)。在 SE 后的 12 周内,通过闭路视频记录(每周 12 小时)对大鼠进行监测以检测 SRS。KD2 组大鼠的 SRS 明显少于对照组或 KD14 组大鼠。在用于评估空间学习和记忆的水迷宫测试中,KD2 组大鼠在位置学习的获取方面明显比对照组(仅 KA 组)或 KD14 组大鼠差。KD2 组大鼠体重增加也不佳。在海马的常规组织学检查中,各组之间没有差异。总之,SE 后 2 天开始给予 KD 的 P30 大鼠相对免受复发性癫痫发作的影响,但表现出行为和身体损伤。KA 诱导的 SE 后 14 天开始给予 KD 的大鼠在自发性癫痫发作率方面与对照组没有差异。