Department of Pharmacology & Therapeutics, Clinical Science Institute, National University of Ireland, Galway, Ireland.
Translational Neuropsychiatry Unit, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Acta Neuropsychiatr. 2020 Feb;32(1):1-9. doi: 10.1017/neu.2019.17. Epub 2019 Jun 12.
Chronic low-grade inflammation has been observed in major depression and other major psychiatric disorders and has been implicated in metabolic changes that are commonly associated with these disorders. This raises the possibility that the effects of dysfunctional metabolism may facilitate changes in neuronal structure and function which contribute to neuroprogression. Such changes may have implications for the progress from major depression to dementia in the elderly patient. The purpose of this review is to examine the contribution of inflammation and hypercortisolaemia, which are frequently associated with major depression, to neurodegeneration and how they detrimentally impact on brain energy metabolism. A key factor in these adverse events is insulin insensitivity caused by pro-inflammatory cytokines in association with desensitised glucocorticoid receptors. Identifying the possible metabolic changes initiated by inflammation opens new targets to ameliorate the adverse metabolic changes. This has resulted in the identification of dietary and drug targets which are of interest in the development of a new generation of psychotropic drugs.
慢性低度炎症在重度抑郁症和其他重大精神疾病中被观察到,并与这些疾病常见的代谢变化有关。这就提出了这样一种可能性,即代谢功能障碍的影响可能促进神经元结构和功能的变化,从而导致神经进展。这些变化可能与老年患者从重度抑郁症到痴呆症的进展有关。本综述的目的是研究炎症和皮质醇过多症(这两种情况常与重度抑郁症相关)对神经退行性变的影响,以及它们如何对大脑能量代谢产生不利影响。这些不良事件的一个关键因素是促炎细胞因子引起的胰岛素不敏感,以及糖皮质激素受体脱敏。炎症引起的代谢变化的确定为改善不良代谢变化开辟了新的靶点。这导致了对炎症引发的可能代谢变化的识别,从而为新一代精神药物的开发确定了饮食和药物靶点。
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