Nagy Z M, Forster M J
Pharmacol Biochem Behav. 1982 Feb;16(2):203-6. doi: 10.1016/0091-3057(82)90148-4.
Experimental hyperthyroidism was induced in neonatal mice by thyroxine injections at 1-3 days of age. Control and thyroxine-treated mice were subsequently tested daily for locomotor activity following injections of methysergide, a serotonin antagonist, or saline from 10 through 15 days of age. Although thyroxine-treated mice were more active than controls, the ontogeny of methysergide-induced disinhibition of locomotor activity was similar for both thyroxine-treated and control mice. The results suggest that the early maturation of serotonin-mediated inhibition of behavioral arousal is not affected by thyroxine-accelerated development. Results are discussed in terms of the specificity of the pharmacological agent, methysergide.
在新生小鼠1至3日龄时注射甲状腺素诱导实验性甲状腺功能亢进。随后,在10至15日龄期间,对对照小鼠和经甲状腺素处理的小鼠每天注射5-羟色胺拮抗剂美西麦角或生理盐水后进行运动活性测试。尽管经甲状腺素处理的小鼠比对照小鼠更活跃,但美西麦角诱导的运动活性去抑制的个体发生在经甲状腺素处理的小鼠和对照小鼠中相似。结果表明,5-羟色胺介导的行为唤醒抑制的早期成熟不受甲状腺素加速发育的影响。根据药理剂美西麦角的特异性对结果进行了讨论。