Hall M E, Schlesinger K, Stamm E
Pharmacol Biochem Behav. 1976 Mar;4(3):353-5. doi: 10.1016/0091-3057(76)90256-2.
Female C57BL/6J mice were trained on a one trial passive avoidance response. Twenty-four hours later, they were treated with puromycin in combination with either 2.0 or 10.0 mg/kg of amphetamine, 0.3 mg/kg of strychnine, or 20.0 or 50.0 mg/kg of pentylenetetrazol. Tests one week after training revealed that treatment with these stimulant drugs prevented the memory loss characteristic of puromycin; an exception being those animals injected with the low dose of amphetamine. Biochemical determination of amino acid incorporation into protein revealed that none of the stimulant drugs used significantly altered the extent or the duration of protein synthesis inhibition induced by puromycin. These results are interpreted as showing that the amnesic effects of puromycin can be counteracted by a state of heightened nervous system excitation.
雌性C57BL/6J小鼠接受单次被动回避反应训练。24小时后,它们被给予嘌呤霉素,并分别联合2.0或10.0毫克/千克的苯丙胺、0.3毫克/千克的士的宁,或20.0或50.0毫克/千克的戊四氮。训练一周后的测试表明,这些兴奋性药物的治疗可防止嘌呤霉素所致的记忆丧失;注射低剂量苯丙胺的动物除外。对蛋白质中氨基酸掺入的生化测定表明所用的兴奋性药物均未显著改变嘌呤霉素诱导的蛋白质合成抑制的程度或持续时间。这些结果被解释为表明嘌呤霉素的失忆作用可被神经系统兴奋增强的状态所抵消。