Kitagishi Yasuko, Kobayashi Mayumi, Kikuta Kanae, Matsuda Satoru
Department of Environmental Health Science, Nara Women's University, Kita-Uoya Nishimachi, Nara 630-8506, Japan.
Depress Res Treat. 2012;2012:752563. doi: 10.1155/2012/752563. Epub 2012 Dec 18.
Several pharmacological agents acting on monoamine neurotransmission are used for the management of mental illnesses. Regulation of PI3K/AKT and GSK3 pathways may constitute an important signaling center in the subcellular integration of the synaptic neurotransmission. The pathways also modulate neuronal cell proliferation, migration, and plasticity. There are evidences to suggest that inflammation of neuron contributes to the pathology of depression. Inflammatory activation of neuron contributes to the loss of glial elements, which are consistent with pathological findings characterizing the depression. A mechanism of anti-inflammatory reactions from antidepressant medications has been found to be associated with an enhancement of heme oxygenase-1 expression. This induction in brain is also important in neuroprotection and neuroplasticity. As enzymes involved in cell survival and neuroplasticity are relevant to neurotrophic factor dysregulation, the PI3K/AKT/GSK3 may provide an important signaling for the neuroprotection in depression. In this paper, we summarize advances on the involvement of the PI3K/AKT/GSK3 pathways in cell signaling of neuronal cells in mental illnesses.
几种作用于单胺神经传递的药物制剂被用于精神疾病的治疗。PI3K/AKT和GSK3信号通路的调节可能在突触神经传递的亚细胞整合中构成一个重要的信号中心。这些信号通路还调节神经元细胞的增殖、迁移和可塑性。有证据表明神经元炎症与抑郁症的病理过程有关。神经元的炎症激活会导致神经胶质成分的丧失,这与抑郁症的病理特征相符。已发现抗抑郁药物的抗炎反应机制与血红素加氧酶-1表达的增强有关。大脑中的这种诱导在神经保护和神经可塑性方面也很重要。由于参与细胞存活和神经可塑性的酶与神经营养因子失调有关,PI3K/AKT/GSK3可能为抑郁症的神经保护提供重要信号。在本文中,我们总结了PI3K/AKT/GSK3信号通路在精神疾病中神经元细胞信号传导中的研究进展。