Yau J L, Kelly P A, Sharkey J, Seckl J R
University of Edinburgh, Department of Medicine, Western General Hospital, U.K.
Neuroscience. 1994 Jul;61(1):31-40. doi: 10.1016/0306-4522(94)90057-4.
Both glucocorticoids and serotonin have been implicated in the regulation of mood and neuroendocrine control. In this study we have examined the effects of the psychomotor stimulant, 3,4-methylenedioxymethamphetamine on corticosteroid and 5-hydroxytryptamine receptor subtype gene expression within the hippocampal formation using in situ hybridization histochemistry. Animals were injected subcutaneously with 3,4-methylenedioxymethamphetamine (20 mg/kg) twice daily for four days. Two weeks following this dosage regimen, shown to markedly reduce 5-hydroxytryptamine terminals, both glucocorticoid receptor and mineralocorticoid receptor messenger RNA expression were significantly decreased (30-47% fall) in the granule cells of the dentate gyrus and pyramidal cells of CA1-CA4 fields of Ammon's horn, but not in parietal cortex neurons. In the same rats, 5-hydroxytryptamine1C receptor messenger RNA expression was significantly increased in CA3 pyramidal neurons (133% rise), but neither 5-hydroxytryptamine1A or 5-hydroxytryptamine2 receptor messenger RNA levels were altered in any dorsal hippocampal subfield. 3,4-Methylenedioxymethamphetamine treatment was associated with modest hypersecretion of coricosterone during the diurnal nadir, without other peripheral evidence of chronic glucocorticoid excess (unchanged thymic and adrenal weights and corticosterone-binding globulin levels). These results emphasize the importance of the serotonergic innervation in maintaining hippocampal corticosteroid receptor gene expression. It is suggested that 5-hydroxytryptamine1C receptors may be involved in mediating the effects of serotonin on hippocampal glucocorticoid receptor and mineralocorticoid receptor expression and perhaps mood.
糖皮质激素和血清素都与情绪调节和神经内分泌控制有关。在本研究中,我们使用原位杂交组织化学技术,研究了精神运动兴奋剂3,4-亚甲基二氧甲基苯丙胺对海马结构内皮质类固醇和5-羟色胺受体亚型基因表达的影响。动物每天皮下注射两次3,4-亚甲基二氧甲基苯丙胺(20mg/kg),持续四天。在这种给药方案两周后,结果显示5-羟色胺终末显著减少,齿状回颗粒细胞和海马CA1-CA4区锥体细胞中的糖皮质激素受体和盐皮质激素受体信使核糖核酸表达均显著降低(下降30-47%),但顶叶皮质神经元中未出现这种情况。在同一批大鼠中,CA3区锥体细胞中的5-羟色胺1C受体信使核糖核酸表达显著增加(升高133%),但任何背侧海马亚区的5-羟色胺1A或5-羟色胺2受体信使核糖核酸水平均未改变。3,4-亚甲基二氧甲基苯丙胺治疗与日间最低点时皮质酮的适度分泌过多有关,没有其他慢性糖皮质激素过量的外周证据(胸腺和肾上腺重量以及皮质酮结合球蛋白水平未改变)。这些结果强调了血清素能神经支配在维持海马皮质类固醇受体基因表达中的重要性。有人提出,5-羟色胺1C受体可能参与介导血清素对海马糖皮质激素受体和盐皮质激素受体表达的影响,也许还参与情绪调节。