期刊
MOLECULAR NEUROBIOLOGY
卷 54, 期 7, 页码 5385-5399出版社
SPRINGER
DOI: 10.1007/s12035-016-0048-3
关键词
Huntington's disease; Lysine (de)acetylation; Mitochondria; Nicotinamide; Resveratrol; Sirtuins
资金
- Fundo Europeu de Desenvolvimento Regional (FEDER) funds through the Programa Operacional Factores de Competitividade (COMPETE) [PEst-C/SAU/LA0001/2013-2014, UID/NEU/04539/2013]
- national funds through Fundacao para a Ciencia e a Tecnologia (FCT) [PTDC/SAU-FCF/108056/2008, EXPL/BIM-MEC/2220/2013]
- Santa Casa da Misericordia de Lisboa (SCML), Portugal
- FCT PhD fellowship [SFRH/BD/86655/2012]
- FCT postdoctoral fellowships [SFRH/BPD/44246/2008, SFRH/BPD/91811/2012]
- FCT technician fellowship [EXPL/BIM-MEC/2220/2013]
- Programa Operacional Potencial Humano (POPH), QREN
- European Union
- Mantero Belard Neuroscience prize
- Fundação para a Ciência e a Tecnologia [SFRH/BD/86655/2012, EXPL/BIM-MEC/2220/2013] Funding Source: FCT
Sirtuin 1 (SIRT1) is a nicotinamide adenine dinucleotide (NAD(+))-dependent lysine deacetylase that regulates longevity and enhances mitochondrial metabolism. Both activation and inhibition of SIRT1 were previously shown to ameliorate neuropathological mechanisms in Huntington's disease (HD), a neurodegenerative disease that selectively affects the striatum and cortex and is commonly linked to mitochondrial dysfunction. Thus, in this study, we tested the influence of resveratrol (RESV, a SIRT1 activator) versus nicotinamide (NAM, a SIRT1 inhibitor) in counteracting mitochondrial dysfunction in HD models, namely striatal and cortical neurons isolated from YAC128 transgenic mice embryos, HD human lymphoblasts, and an in vivo HD model. HD cell models displayed a deregulation in mitochondrial membrane potential and respiration, implicating a decline in mitochondrial function. Further studies revealed decreased PGC-1 alpha and TFAM protein levels, linked to mitochondrial DNA loss in HD lymphoblasts. Remarkably, RESV completely restored these parameters, while NAM increased NAD(+) levels, providing a positive add on mitochondrial function in in vitro HD models. In general, RESV decreased while NAM increased H3 acetylation at lysine 9. In agreement with in vitro data, continuous RESV treatment for 28 days significantly improved motor coordination and learning and enhanced expression of mitochondrial-encoded electron transport chain genes in YAC128 mice. In contrast, high concentrations of NAM blocked mitochondrial-related transcription, worsening motor phenotype. Overall, data indicate that activation of deacetylase activity by RESV improved gene transcription associated to mitochondrial function in HD, which may partially control HD-related motor disturbances.
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