Jernigan Peter L, Hoehn Richard S, Grassmé Heike, Edwards Michael J, Müller Christian P, Kornhuber Johannes, Gulbins Erich
Department of Molecular Biology, University of Duisburg-Essen, Essen, Germany.
Neurosignals. 2015;23(1):49-58. doi: 10.1159/000442603. Epub 2015 Dec 19.
Major depression is one of the most common and severe diseases affecting the world's population. However, the pathogenesis of the disease remains inadequately defined. Previously, a lack of monoaminergic neurotransmitters was the focus of pathophysiological concepts; however, recent concepts focus on a alteration of neurogenesis in the hippocampus. This concept suggests that neurogenesis is decreased in major depression with a rarefication of neuronal networks and a lack of new, immature neurons in the hippocampus, events that may result in the clinical symptoms of major depression. However, molecular targets involved in the pathogenesis of major depression and, in particular, a reduction of neurogenesis, are largely unknown. We have recently discovered that an inhibition of the acid sphingomyelinase/ceramide system mediates the effects of tri- and tetracyclic antidepressants. Moreover, an accumulation of ceramide in the hippocampus results in depression-like symptoms. This suggests the acid sphingomyelinase/ceramide system is very important in the pathogenesis of major depression.
重度抑郁症是影响全球人口的最常见、最严重的疾病之一。然而,该疾病的发病机制仍未得到充分阐明。以前,单胺能神经递质的缺乏是病理生理学概念的重点;然而,最近的概念聚焦于海马体中神经发生的改变。这一概念表明,在重度抑郁症中神经发生减少,伴有神经网络稀疏以及海马体中缺乏新的未成熟神经元,这些情况可能导致重度抑郁症的临床症状。然而,参与重度抑郁症发病机制,尤其是神经发生减少的分子靶点在很大程度上尚不清楚。我们最近发现,酸性鞘磷脂酶/神经酰胺系统的抑制介导了三环和四环抗抑郁药的作用。此外,海马体中神经酰胺的积累会导致类似抑郁的症状。这表明酸性鞘磷脂酶/神经酰胺系统在重度抑郁症的发病机制中非常重要。