Ago Yukio, Arikawa Shinsuke, Yata Miyuki, Yano Koji, Abe Michikazu, Takuma Kazuhiro, Matsuda Toshio
Laboratory of Medicinal Pharmacology, Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamada-oka, Suita, Osaka 565-0871, Japan.
Neuropharmacology. 2008 Dec;55(8):1355-63. doi: 10.1016/j.neuropharm.2008.08.026. Epub 2008 Aug 30.
Chronic corticosterone and isolation rearing paradigms may provide reliable mouse models of depression. Using these models, the present study examined if the specific glucocorticoid receptor antagonist, RU-43044, has an antidepressant-like effect, and studied the possible role of prefrontal neurotransmission on the behavioral effects. Chronic administration of corticosterone and isolation rearing increased the immobility time in the forced swim and tail suspension tests. Subchronic treatment with RU-43044 decreased the immobility time in the forced swim test in chronic corticosterone-treated and isolation-reared mice, but not the control mice. Chronic corticosterone decreased the levels of cortical glucocorticoid receptors and stress-induced increases in plasma corticosterone levels, and blocked the response of plasma corticosterone to dexamethasone, while isolation rearing did not cause any changes in the glucocorticoid receptor system. Both chronic corticosterone and isolation rearing markedly increased high K+ -induced dopamine release, but not serotonin release, in the prefrontal cortex. Subchronic RU-43044 reversed the enhanced release of dopamine in the prefrontal cortex of chronic corticosterone-treated and isolation-reared mice. These results suggest that chronic corticosterone and isolation rearing increase the depressive-like behavior in glucocorticoid receptor-dependent and independent manners, respectively, and that RU-43044 shows an antidepressant-like effect, probably via an inhibition of enhanced prefrontal dopaminergic neurotransmission in these mouse models.
慢性皮质酮和隔离饲养范式可能提供可靠的抑郁症小鼠模型。利用这些模型,本研究检验了特异性糖皮质激素受体拮抗剂RU - 43044是否具有抗抑郁样作用,并研究了前额叶神经传递在行为效应中的可能作用。慢性给予皮质酮和隔离饲养增加了强迫游泳和悬尾试验中的不动时间。在慢性皮质酮处理和隔离饲养的小鼠中,用RU - 43044进行亚慢性治疗可减少强迫游泳试验中的不动时间,但对对照小鼠无效。慢性皮质酮降低了皮质糖皮质激素受体水平以及应激诱导的血浆皮质酮水平升高,并阻断了血浆皮质酮对地塞米松的反应,而隔离饲养未引起糖皮质激素受体系统的任何变化。慢性皮质酮和隔离饲养均显著增加了前额叶皮质中高钾诱导的多巴胺释放,但未增加5 -羟色胺释放。亚慢性给予RU - 43044可逆转慢性皮质酮处理和隔离饲养小鼠前额叶皮质中多巴胺释放的增强。这些结果表明,慢性皮质酮和隔离饲养分别以糖皮质激素受体依赖性和非依赖性方式增加了抑郁样行为,并且RU - 43044在这些小鼠模型中可能通过抑制前额叶多巴胺能神经传递增强而显示出抗抑郁样作用。