Fagioli S, Rossi-Arnaud C, Castellano C
Department of Genetics and Molecular Biology, University La Sapienza, I-Rome, Italy.
Psychopharmacology (Berl). 1992;109(4):457-60. doi: 10.1007/BF02247723.
Groups of C57BL/6 mice were injected intraperitoneally with GM1 monosialoganglioside at different ages during development and subsequently tested for the retention of an inhibitory avoidance task 24 h after training. Results show improvements in inhibitory avoidance retention according to the age of the animals, the doses of GM1 used and the length of treatment. The effective doses ranged from 20 mg/kg for all age groups after 7 days treatment to 280 mg/kg for 6- and 7-week old animals after pre-trial treatment. Six- and 7-week-old mice are more sensitive to GM1 treatment than 5-week-old animals and, with decreasing lengths of treatment, increasing doses of GM1 are needed to improve the performance of the animals. These findings show that short treatment durations can be effective in improving inhibitory avoidance retention as long as the doses of GM1 administered are increased and that animals are more sensitive to the treatment when they are 6 or 7 weeks of age than when they are 5 weeks old.
在发育过程中的不同年龄,给C57BL/6小鼠腹腔注射单唾液酸神经节苷脂(GM1),随后在训练24小时后测试其对抑制性回避任务的记忆保持情况。结果显示,根据动物年龄、GM1使用剂量和治疗时长,抑制性回避记忆保持有所改善。有效剂量范围从7天治疗后所有年龄组的20毫克/千克到试验前治疗后6周和7周龄动物的280毫克/千克。6周和7周龄的小鼠比5周龄的动物对GM1治疗更敏感,并且随着治疗时长缩短,需要增加GM1剂量才能改善动物的表现。这些发现表明,只要增加GM1给药剂量,短疗程治疗就能有效改善抑制性回避记忆保持,而且动物在6或7周龄时比5周龄时对治疗更敏感。