Shelton R C
Department of Psychiatry, Vanderbilt University Medical Center, Nashville, TN, USA.
Harv Rev Psychiatry. 2000 Oct;8(4):161-74.
The action of antidepressant drugs on monoamines such as norepinephrine and serotonin has been described for three decades. However, more-recent research has looked beyond cell surface receptors to transductional cascades and gene expression. Antidepressant drug therapies seem to share several mechanisms involved in either activating the adenylyl cyclase-protein kinase A cascade or inhibiting the phospholipase C-protein kinase C mechanisms. These effects, ultimately, combine to regulate the expression of target genes. Several specific genes are known to be activated or inhibited by antidepressant therapies. Steady-state levels of mRNA for glucocorticoid and mineralocorticoid receptors, brain-derived neurotrophic factor and its receptor trkB, and preproenkephalin are enhanced, whereas those for corticotropin-releasing hormone, c-fos,N-methyl-D-aspartate receptor subunits, and nerve-growth factor 1A are reduced. New molecular genetic methods for identifying differentially expressed genes will aid in the development of targets for wholly new generations of antidepressant drug therapies.
抗抑郁药物对去甲肾上腺素和血清素等单胺类物质的作用已被描述了三十年。然而,最近的研究已超越细胞表面受体,深入到转导级联反应和基因表达层面。抗抑郁药物疗法似乎具有几种共同机制,这些机制要么涉及激活腺苷酸环化酶 - 蛋白激酶A级联反应,要么涉及抑制磷脂酶C - 蛋白激酶C机制。最终,这些效应共同调节靶基因的表达。已知几种特定基因会被抗抑郁疗法激活或抑制。糖皮质激素和盐皮质激素受体、脑源性神经营养因子及其受体trkB以及前脑啡肽原的mRNA稳态水平会升高,而促肾上腺皮质激素释放激素、c - fos、N - 甲基 - D - 天冬氨酸受体亚基和神经生长因子1A的mRNA稳态水平则会降低。用于识别差异表达基因的新分子遗传学方法将有助于开发全新一代抗抑郁药物疗法的靶点。