Le Gal La Salle G
Can J Physiol Pharmacol. 1980 Jan;58(1):7-11. doi: 10.1139/y80-002.
The anticonvulsant effect of aminooxyacetic acid (AOAA) was examined on a model of experimental epilepsy (kindling) induced by daily appropriate amygdaloid stimulation in the rat. Doses from 5 to 30 mg/kg were intraperitoneally administered in fully kindled animals 3--4 h before triggering a seizure. At low doses (less than 15 mg/kg) AOAA had no effect whereas at higher doses (greater than 15 mg/kg) it reduced the severity of the generalized kindled seizures in over half the cases, and even sometimes completely blocked them. The inhibition of epileptic activity by AOAA is in accordance with the hypothesis that an increase in GABA level is associated with a reduction of epileptic sensitivity. An unexpected lengthening of the afterdischarge duration was also observed in about 20% of the cases, independently of the amount administered. This fact is discussed in regard to the complex action of AOAA on gamma-aminobutyric acid related enzymes. Finally, since the afterdischarge threshold was shown to be unaffected by the drug, it is suggested that it may act on the afterdischarge propagation rather than at the focal amygdaloid level.
在大鼠实验性癫痫(点燃)模型中,研究了氨氧基乙酸(AOAA)的抗惊厥作用。该模型通过每日适当刺激大鼠杏仁核诱导产生。在引发癫痫发作前3 - 4小时,对完全点燃的动物腹腔注射5至30毫克/千克的AOAA。低剂量(低于15毫克/千克)时,AOAA无作用;而高剂量(高于15毫克/千克)时,在超过半数的情况下可减轻全身性点燃癫痫发作 的严重程度,甚至有时能完全阻断发作。AOAA对癫痫活动的抑制作用符合以下假说:γ-氨基丁酸(GABA)水平升高与癫痫敏感性降低相关。在约20%的案例中,还意外观察到后放电持续时间延长,且与给药量无关。针对AOAA对γ-氨基丁酸相关酶的复杂作用,对这一事实进行了讨论。最后,由于后放电阈值不受该药物影响,提示其可能作用于后放电的传播,而非作用于杏仁核局部水平。