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Role of Sirtuins in Linking Metabolic Syndrome with Depression

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Specialty Cell Biology
Date 2016 Apr 12
PMID 27065808
Citations 5
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Abstract

Depression is now widely regarded as a common disabling disorder that affects negatively the social functioning all over the world. Depression is associated with diverse phenomenon in brain such as neuroinflammation, synaptic dysfunction, and cognitive deficit. Recent studies reported that depression occurs by various metabolic changes, leading to metabolic syndrome. Sirtuins (SIRTs) are NAD(+)-dependent class III histone deacetylases, known to regulate diverse biological mechanism such as longevity, genomic stability, and inflammation. The modulation of sirtuin activity has been highlighted as a promising approach to reduce neurodegenerative processes. In this review, we summarize the recent discoveries regarding the potential relationship between SIRTs and depression caused by metabolic disorders (Mets). Ultimately, we suggest the possibility that SIRTs will be novel targets to alleviate neuropathogenesis induced by depression.

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References
1.
Maciag D, Hughes J, ODwyer G, Pride Y, Stockmeier C, Sanacora G . Reduced density of calbindin immunoreactive GABAergic neurons in the occipital cortex in major depression: relevance to neuroimaging studies. Biol Psychiatry. 2009; 67(5):465-70. PMC: 2823848. DOI: 10.1016/j.biopsych.2009.10.027. View

2.
Levitan R, Davis C, Kaplan A, Arenovich T, Phillips D, Ravindran A . Obesity comorbidity in unipolar major depressive disorder: refining the core phenotype. J Clin Psychiatry. 2012; 73(8):1119-24. DOI: 10.4088/JCP.11m07394. View

3.
Michan S, Sinclair D . Sirtuins in mammals: insights into their biological function. Biochem J. 2007; 404(1):1-13. PMC: 2753453. DOI: 10.1042/BJ20070140. View

4.
McGaugh J . Memory--a century of consolidation. Science. 2000; 287(5451):248-51. DOI: 10.1126/science.287.5451.248. View

5.
Patel N, Gordon M, Connor K, Good R, Engelman R, Mason J . Caloric restriction attenuates Abeta-deposition in Alzheimer transgenic models. Neurobiol Aging. 2005; 26(7):995-1000. DOI: 10.1016/j.neurobiolaging.2004.09.014. View