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New Molecular Targets for Antidepressant Drugs

期刊

PHARMACEUTICALS
卷 14, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/ph14090894

关键词

acid sphingomyelinase; ceramide; sphingomyelin; FIASMA; antidepressant drug; lysosome; neurogenesis; hippocampus; autophagy; brain-derived neurotrophic factor (BDNF)

资金

  1. DEUTSCHE FORSCHUNGSGEMEINSCHAFT [KO 947/13-3, Gu-335/29-3]

向作者/读者索取更多资源

Major depressive disorder (MDD) is a common and severe mental disorder that is usually recurrent and has a high risk of suicide. This disorder affects not only on psychological symptoms but also multiple changes throughout the body, including increased risks of obesity, diabetes, and cardiovascular disease. Studies have found elevated levels of peripheral markers of oxidative stress and inflammation in MDD patients. Pharmacological treatment with antidepressants takes several weeks before desired effects manifest, and recent research has focused on new mechanisms of action for long-standing antidepressants.
Major depressive disorder (MDD) is a common and severe mental disorder that is usually recurrent and has a high risk of suicide. This disorder manifests not only with psychological symptoms but also multiple changes throughout the body, including increased risks of obesity, diabetes, and cardiovascular disease. Peripheral markers of oxidative stress and inflammation are elevated. MDD is therefore best described as a multisystem whole-body disease. Pharmacological treatment with antidepressants usually requires several weeks before the desired effects manifest. Previous theories of depression, such as the monoamine or neurogenesis hypotheses, do not explain these characteristics well. In recent years, new mechanisms of action have been discovered for long-standing antidepressants that also shed new light on depression, including the sphingolipid system and the receptor for brain-derived neurotrophic factor (BDNF).

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