Fueta Y, Avoli M
Montréal Neurological Institute, Qué., Canada.
Can J Physiol Pharmacol. 1991 Sep;69(9):1301-4. doi: 10.1139/y91-191.
The effects induced by the antiepileptic drug valproic acid were studied in the CA3 subfield of in vitro hippocampal slices obtained from young (16- to 27-day-old) and adult (over 60-day-old) rats. Spontaneous epileptiform discharges were induced by the addition of the convulsant 4-aminopyridine to the medium. Valproic acid (0.5 mM) selectively blocked the ictal epileptiform discharges in slices obtained from young rats. Interictal epileptiform discharges disappeared during perfusion with higher doses of valproic acid (2 mM). This blockade of interictal epileptiform activity was not observed when valproic acid (0.5-5 mM) was tested in hippocampal slices from adult rats. Thus, in the hippocampus of young rats, 4-aminopyridine-induced ictal activity is more sensitive to valproic acid than are interictal discharges. Moreover, valproic acid is effective in controlling interictal discharges in the young, but not in the adult rat hippocampus.
在从幼龄(16至27日龄)和成年(60日龄以上)大鼠获取的体外海马切片的CA3亚区中,研究了抗癫痫药物丙戊酸所诱导的效应。通过向培养基中添加惊厥剂4-氨基吡啶来诱导自发性癫痫样放电。丙戊酸(0.5 mM)选择性地阻断了从幼龄大鼠获取的切片中的发作期癫痫样放电。在用更高剂量的丙戊酸(2 mM)灌注期间,发作间期癫痫样放电消失。当在成年大鼠的海马切片中测试丙戊酸(0.5 - 5 mM)时,未观察到对发作间期癫痫样活动的这种阻断作用。因此,在幼龄大鼠的海马中,4-氨基吡啶诱导的发作期活动比发作间期放电对丙戊酸更敏感。此外,丙戊酸在控制幼龄大鼠而非成年大鼠海马中的发作间期放电方面是有效的。