Guidotti A, Dong E, Matsumoto K, Pinna G, Rasmusson A M, Costa E
Department of Psychiatry, Psychiatric Institute, College of Medicine, University of Illinois at Chicago, 1601 W. Taylor St., MC 912, Chicago, IL 60612, USA.
Brain Res Brain Res Rev. 2001 Nov;37(1-3):110-5. doi: 10.1016/s0165-0173(01)00129-1.
Allopregnanolone (3alpha,5alpha-TH PROG) and 5alpha-dihydroprogesterone (5alpha-DH PROG), the two most important neuroactive steroids synthesized in the brain, potently modulate neuronal activity by allosterically regulating GABA action at GABA(A) receptors or by changing specific GABA(A) receptor subunit gene expression, respectively. We recently reported [Proc. Natl. Acad. Sci. USA 95 (1998) 3239] that in patients with severe depression there is a decrease in the CSF levels of 3alpha,5alpha-TH PROG, which is normalized by treatment with drugs (i.e. fluoxetine) that improve psychopathology. The mechanism by which fluoxetine and other selective serotonin reuptake inhibitors normalize 3alpha,5alpha-TH PROG CSF levels appears to involve a direct stimulation of 3alpha-hydroxysteroidoxidoreductase (3alpha-HSD), an enzyme that catalyses the reduction of 5alpha-DH PROG into 3alpha,5alpha-TH PROG. Here, we propose the use of socially-isolated mice that have a downregulation of 3alpha,5alpha-TH PROG and of 5alpha-DH PROG expression to establish a model to study the behavioral consequences of this deficiency. After 4-6 weeks of isolation, these mice exhibit increased anxiety and aggressive behavior and also a decreased response to the administration of GABA-mimetic drugs. In these mice, the decrease in 3alpha,5alpha-TH PROG is selectively normalized by the use of fluoxetine in doses that reduce behavioral abnormalities. In addition, the expression of 5alpha-reductase Type I mRNA and protein was lower in socially-isolated mice than that in group-housed mice whereas 3alpha-HSD mRNA expression remained unchanged. The results of these studies may enable us to design drugs that specifically affect neurosteroidogenic enzymatic activities and may provide an efficacious treatment for the psychopathologies associated with psychiatric disorders.
别孕烯醇酮(3α,5α - 四氢孕酮)和5α - 双氢孕酮是大脑中合成的两种最重要的神经活性甾体,它们分别通过变构调节GABA在GABAA受体上的作用或改变特定GABAA受体亚基基因表达来有效调节神经元活动。我们最近报道[《美国国家科学院院刊》95 (1998) 3239],在重度抑郁症患者中,脑脊液中3α,5α - 四氢孕酮水平降低,而用改善精神病理学症状的药物(即氟西汀)治疗后该水平恢复正常。氟西汀和其他选择性5 - 羟色胺再摄取抑制剂使脑脊液中3α,5α - 四氢孕酮水平恢复正常的机制似乎涉及对3α - 羟基甾体氧化还原酶(3α - HSD)的直接刺激,该酶催化5α - 双氢孕酮还原为3α,5α - 四氢孕酮。在此,我们提议使用3α,5α - 四氢孕酮和5α - 双氢孕酮表达下调的社会隔离小鼠来建立一个模型,以研究这种缺乏的行为后果。隔离4 - 6周后,这些小鼠表现出焦虑和攻击行为增加,并且对给予GABA模拟药物的反应也降低。在这些小鼠中,使用能减少行为异常的剂量的氟西汀可选择性地使3α,5α - 四氢孕酮的降低恢复正常。此外,社会隔离小鼠中I型5α - 还原酶的mRNA和蛋白表达低于群居小鼠,而3α - HSD的mRNA表达保持不变。这些研究结果可能使我们能够设计出特异性影响神经甾体生成酶活性的药物,并可能为与精神疾病相关的精神病理学提供有效的治疗方法。