Siporin S, Fuller J L
Pharmacol Biochem Behav. 1976 Mar;4(3):269-72. doi: 10.1016/0091-3057(76)90240-9.
An attempt was made to determine the effects of genetic and temporal factors on the inhibitory action of aminooxyacetic acid on priming for audiogenic seizures. SJL/J and C57BL/6J mice were administered 20 mug/g of AOAA subcutaneously, employing either a 2 hr or 5 hr injection-prime interval, and either a 2 day or a 9 day prime-test interval. It was found that an inhibitory effect on priming occurred only in C57BL/6J mice; this effect was significant only for the 9 day groups, and was observed when wild running was used as the criterion for seizures, but not when clonic convulsion was the criterion. Effects of AOAA are discussed in relation to theories of seizure development through disuse supersensitivity, or by chemical actions on the GABA system.
本研究试图确定遗传和时间因素对氨氧乙酸抑制听源性惊厥引发作用的影响。分别以2小时或5小时的注射-引发间隔,以及2天或9天的引发-测试间隔,给SJL/J和C57BL/6J小鼠皮下注射20微克/克的氨氧乙酸。结果发现,仅在C57BL/6J小鼠中对引发产生了抑制作用;这种作用仅在9天组中显著,并且当以狂奔作为惊厥标准时可观察到,但以阵挛性惊厥为标准时则未观察到。根据废用超敏反应或对γ-氨基丁酸(GABA)系统的化学作用导致惊厥发展的理论,对氨氧乙酸的作用进行了讨论。