Schreiber R A, Santos N N
Pharmacol Biochem Behav. 1977 May;6(5):603-5. doi: 10.1016/0091-3057(77)90126-5.
Donor C57BL/6J mice were given audiogenic priming (AP) by exposure to noise at 16 days of age (To) and sacrificed at intervals from 1 hr to 18 days therafter. Brains from AP and littermate non-AP mice were extracted in 1 M acetic acid, and passed through a filter with a nominal mol. wt. cutoff of 10,000 daltons. The filtrates were lyophilized and resuspended in H2O (0.1 ml/brain). Recipient C57BL/6J mice were also exposed to 30 sec of 127 +/- 2 dBA at 16 days of age, and injected IP with one brain-equivalent of extracts from either AP or non-AP donors immediately therafter. All recipients were tested for convulsability at 18 days of age. There were no differences in audiogenic convulsion rates between groups given AP or non-AP extracts from donors sacrificed 1 to 4 hr after To. Recipient convulsion rates were higher in AP relative to non-AP extract-injected mice whenAP donors were sacrificed 1 to 18 days after To. The extract taken from donors 1 day after To appears more potent than extract taken either before or later.
供体C57BL/6J小鼠在16日龄(T0)时通过暴露于噪声进行听源性启动(AP),并在之后1小时至18天的不同时间点处死。将AP小鼠和同窝非AP小鼠的大脑在1M乙酸中提取,然后通过标称分子量截留值为10,000道尔顿的滤器。滤液冻干后重悬于水中(0.1ml/脑)。受体C57BL/6J小鼠在16日龄时也暴露于127±2分贝的噪声30秒,随后立即腹腔注射相当于一个脑量的来自AP或非AP供体的提取物。所有受体在18日龄时进行惊厥易感性测试。在T0后1至4小时处死的供体给予的AP或非AP提取物组之间,听源性惊厥率没有差异。当T0后1至18天处死AP供体时,与注射非AP提取物的小鼠相比,注射AP提取物的受体惊厥率更高。T0后1天从供体提取的提取物似乎比之前或之后提取的提取物更有效。