Maxson S C, Cowen J S
Pharmacol Biochem Behav. 1977 Mar;6(3):349-50. doi: 10.1016/0091-3057(77)90035-1.
At 19 days of age, C57BL/6Bg mice received KCl-induced cortical spreading depression during which they were acoustically primed by exposure to an initial auditory stimulus. At 28 days of age, the mice were tested for susceptibility to audiogenic seizures. Cortical spreading depression had no effect on acoustic priming of C57BL/6Bg mice and it had been previously reported to have no effect on acoustic priming of SJL/J mice. These findings are discussed in the context of pharmacogenetic differences for the effects of aminooxyacetic acid on acoustic priming of C57BL/6 and SJL/J mice.
19日龄时,C57BL/6Bg小鼠接受了氯化钾诱导的皮质扩散性抑制,在此期间通过暴露于初始听觉刺激对它们进行声音启动。28日龄时,测试小鼠对听源性癫痫发作的易感性。皮质扩散性抑制对C57BL/6Bg小鼠的声音启动没有影响,并且先前已有报道称其对SJL/J小鼠的声音启动也没有影响。这些发现是在氨基氧基乙酸对C57BL/6和SJL/J小鼠声音启动影响的药物遗传学差异背景下进行讨论的。