SIRT1 mediates depression-like behaviors in the nucleus accumbens

Hee Dae Kim, Jennifer Hesterman, Tanessa Call, Samantha Magazu, Elizabeth Keeley, Kristyna Armenta, Hope Kronman, Rachael L. Neve, Eric J. Nestler, Deveroux Ferguson

Research output: Contribution to journalArticle

45 Citations (Scopus)

Abstract

Depression is a recurring and life-threatening illness that affects up to 120 million people worldwide. In the present study, we show that chronic social defeat stress, an ethologically validated model of depression in mice, increases SIRT1 levels in the nucleus accumbens (NAc), a key brain reward region. Increases in SIRT1, a well characterized class III histone deacetylase, after chronic social defeat suggest a role for this enzyme in mediating depression-like behaviors. When resveratrol, a pharmacological activator of SIRT1, was directly infused bilaterally into the NAc, we observed an increase in depression- and anxiety-like behaviors. Conversely, intra-NAc infusions of EX-527, a SIRT1 antagonist, reduced these behaviors; EX-527 also reduced acute stress responses in stress-naive mice. Next, we increased SIRT1 levels directly in NAc by use of viral-mediated gene transfer and observed an increase in depressive- and anxiety-like behaviors when mice were assessed in the open-field, elevated-plus-maze, and forced swim tests. Using a Cre-inducible viral vector system to overexpress SIRT1 selectively in dopamine D1 or D2 subpopulations of medium spiny neurons (MSNs) in the NAc, we found that SIRT1 promotes depressive-like behaviors only when overexpressed in D1 MSNs, with no effect seen in D2 MSNs. Conversely, selective ablation of SIRT1 in the NAc using viral-Cre in floxed Sirt1 mice resulted in decreased depression- and anxiety-like behaviors. Together, these results demonstrate that SIRT1 plays an essential role in the NAc in regulating mood-related behavioral abnormalities and identifies a novel signaling pathway for the development of innovative antidepressants to treat major depressive disorders.

Original languageEnglish (US)
Pages (from-to)8441-8452
Number of pages12
JournalJournal of Neuroscience
Volume36
Issue number32
DOIs
StatePublished - Aug 10 2016

Fingerprint

Nucleus Accumbens
Depression
Anxiety
Neurons
Histone Deacetylases
Viral Genes
Major Depressive Disorder
Reward
Antidepressive Agents
Dopamine
Pharmacology
Brain
Enzymes

Keywords

  • Anxiety
  • Cell-type specific
  • Depression
  • Epigenetic
  • Stress
  • Striatum

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Kim, H. D., Hesterman, J., Call, T., Magazu, S., Keeley, E., Armenta, K., ... Ferguson, D. (2016). SIRT1 mediates depression-like behaviors in the nucleus accumbens. Journal of Neuroscience, 36(32), 8441-8452. https://doi.org/10.1523/JNEUROSCI.0212-16.2016

SIRT1 mediates depression-like behaviors in the nucleus accumbens. / Kim, Hee Dae; Hesterman, Jennifer; Call, Tanessa; Magazu, Samantha; Keeley, Elizabeth; Armenta, Kristyna; Kronman, Hope; Neve, Rachael L.; Nestler, Eric J.; Ferguson, Deveroux.

In: Journal of Neuroscience, Vol. 36, No. 32, 10.08.2016, p. 8441-8452.

Research output: Contribution to journalArticle

Kim, HD, Hesterman, J, Call, T, Magazu, S, Keeley, E, Armenta, K, Kronman, H, Neve, RL, Nestler, EJ & Ferguson, D 2016, 'SIRT1 mediates depression-like behaviors in the nucleus accumbens', Journal of Neuroscience, vol. 36, no. 32, pp. 8441-8452. https://doi.org/10.1523/JNEUROSCI.0212-16.2016
Kim HD, Hesterman J, Call T, Magazu S, Keeley E, Armenta K et al. SIRT1 mediates depression-like behaviors in the nucleus accumbens. Journal of Neuroscience. 2016 Aug 10;36(32):8441-8452. https://doi.org/10.1523/JNEUROSCI.0212-16.2016
Kim, Hee Dae ; Hesterman, Jennifer ; Call, Tanessa ; Magazu, Samantha ; Keeley, Elizabeth ; Armenta, Kristyna ; Kronman, Hope ; Neve, Rachael L. ; Nestler, Eric J. ; Ferguson, Deveroux. / SIRT1 mediates depression-like behaviors in the nucleus accumbens. In: Journal of Neuroscience. 2016 ; Vol. 36, No. 32. pp. 8441-8452.
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