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Review
. 2023 Apr 25;13(5):719.
doi: 10.3390/brainsci13050719.

Study on the Mechanism for SIRT1 during the Process of Exercise Improving Depression

Affiliations
Review

Study on the Mechanism for SIRT1 during the Process of Exercise Improving Depression

Xiao Qiu et al. Brain Sci. .

Abstract

The mechanism behind the onset of depression has been the focus of current research in the neuroscience field. Silent information regulator 1 (SIRT1) is a key player in regulating energy metabolism, and it can regulate depression by mediating the inflammatory response (e.g., nuclear factor-kappa B (NF-κB), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β)), gene expression in the nucleus accumben (NAc) and CA1 region of the hippocampus (e.g., nescient helix-loop-helix2 (NHLH2), monoamine oxidase (MAO-A), and 5-Hydroxyindole-3-acetic acid (5-HIAA)), and neuronal regeneration in the CA3 region of the hippocampus. Exercise is an important means to improve energy metabolism and depression, but it remains to be established how SIRT1 acts during exercise and improves depression. By induction and analysis, SIRT1 can be activated by exercise and then improve the function of the hypothalamic-pituitary-adrenal (HPA) axis by upregulating brain-derived neurotrophic factors (BDNF), inhibit the inflammatory response (suppression of the NF-κB and TNF-α/indoleamine 2,3-dioxygenase (IDO)/5-Hydroxytryptamine (5-HT) pathways), and promote neurogenesis (activation of the insulin-like growth factor1 (IGF-1) and growth-associated protein-43 (GAP-43) pathways, etc.), thereby improving depression. The present review gives a summary and an outlook based on this finding and makes an analysis, which will provide a new rationale and insight for the mechanism by which exercise improves depression.

Keywords: SIRT1; depression; exercise; gene expression; inflammatory factor; neurogenesis.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Mechanism of SIRT1 in exercise improving depression.

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References

    1. Ménard C., Hodes G.E., Russo S.J. Pathogenesis of depression: Insights from human and rodent studies. Neuroscience. 2016;321:138–162. doi: 10.1016/j.neuroscience.2015.05.053. - DOI - PMC - PubMed
    1. Zhang Y., Anoopkumar-Dukie S., Davey A.K. SIRT1 and SIRT2 Modulators: Potential Anti-Inflammatory Treatment for Depression? Biomolecules. 2021;11:353. doi: 10.3390/biom11030353. - DOI - PMC - PubMed
    1. Khan H., Tiwari P., Kaur A., Singh T.G. Sirtuin Acetylation and Deacetylation: A Complex Paradigm in Neurodegenerative Disease. Mol. Neurobiol. 2021;58:3903–3917. doi: 10.1007/s12035-021-02387-w. - DOI - PubMed
    1. Liu T., Ma Y., Zhang R., Zhong H., Wang L., Zhao J., Yang L., Fan X. Resveratrol ameliorates estrogen deficiency-induced depression- and anxiety-like behaviors and hippocampal inflammation in mice. Psychopharmacology. 2019;236:1385–1399. doi: 10.1007/s00213-018-5148-5. - DOI - PubMed
    1. Hou L., Miao J., Meng H., Liu X., Wang D., Tang Y., Li C. Sirtuin Type 1 Mediates the Antidepressant Effect of S-Ketamine in a Chronic Unpredictable Stress Model. Front. Psychiatry. 2022;13:855810. doi: 10.3389/fpsyt.2022.855810. - DOI - PMC - PubMed