4.7 Article

Transcriptomic Studies of Antidepressant Action in Rodent Models of Depression: A First Meta-Analysis

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出版社

MDPI
DOI: 10.3390/ijms232113543

关键词

major depression; antidepressant; fluoxetine; hippocampus; transcriptomics

资金

  1. ERA-NET NEURON ANTaRES [ANR-19-NEUR-0005]
  2. Gebra (Imaging GEne and BRAin networks in stress susceptibility: novel pathways and biomarkers in mice and men) [ANR-19-CE37-0017]

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Antidepressants are currently the best treatment for moderate to severe major depressive episodes, but the trial-and-error prescription strategy and side effects are concerning. There is a lack of biomarkers to aid in treatment decisions, highlighting the need for further research.
Antidepressants (ADs) are, for now, the best everyday treatment we have for moderate to severe major depressive episodes (MDEs). ADs are among the most prescribed drugs in the Western Hemisphere; however, the trial-and-error prescription strategy and side-effects leave a lot to be desired. More than 60% of patients suffering from major depression fail to respond to the first AD they are prescribed. For those who respond, full response is only observed after several weeks of treatment. In addition, there are no biomarkers that could help with therapeutic decisions; meanwhile, this is already true in cancer and other fields of medicine. For years, many investigators have been working to decipher the underlying mechanisms of AD response. Here, we provide the first systematic review of animal models. We thoroughly searched all the studies involving rodents, profiling transcriptomic alterations consecutive to AD treatment in naive animals or in animals subjected to stress-induced models of depression. We have been confronted by an important heterogeneity regarding the drugs and the experimental settings. Thus, we perform a meta-analysis of the AD signature of fluoxetine (FLX) in the hippocampus, the most studied target. Among genes and pathways consistently modulated across species, we identify both old players of AD action and novel transcriptional biomarker candidates that warrant further investigation. We discuss the most prominent transcripts (immediate early genes and activity-dependent synaptic plasticity pathways). We also stress the need for systematic studies of AD action in animal models that span across sex, peripheral and central tissues, and pharmacological classes.

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