期刊
JOURNAL OF NEUROCHEMISTRY
卷 125, 期 3, 页码 410-419出版社
WILEY
DOI: 10.1111/jnc.12190
关键词
BDNF; glucose metabolism; huntingtin; PGC-1; PPAR-; Sirt6
资金
- NIH [NS072344]
Huntington's disease (HD) is a devastating genetic neurodegenerative disease caused by CAG trinucleotide expansion in the exon-1 region of the huntingtin gene. Currently, no cure is available. It is becoming increasingly apparent that mutant Huntingtin (HTT) impairs metabolic homeostasis and causes transcriptional dysregulation. The peroxisome proliferator-activated receptor gamma (PPAR-) is a transcriptional factor that plays a key role in regulating genes involved in energy metabolism; recent studies demonstrated that PPAR- activation prevented mitochondrial depolarization in cells expressing mutant HTT and attenuated neurodegeneration in various models of neurodegenerative diseases. PPAR--coactivator 1 (PGC-1 ) transcription activity is also impaired by mutant HTT. We now report that the PPAR- agonist, rosiglitazone (RSG), significantly attenuated mutant HTT-induced toxicity in striatal cells and that the protective effect of RSG is mediated by activation of PPAR-. Moreover, chronic administration of RSG (10mg/kg/day, i.p) significantly improved motor function and attenuated hyperglycemia in N171-82Q HD mice. RSG administration rescued brain derived neurotrophic factor(BDNF) deficiency in the cerebral cortex, and prevented loss of orexin-A-immunopositive neurons in the hypothalamus of N171-82Q HD mice. RSG also prevented PGC-1 reduction and increased Sirt6 protein levels in HD mouse brain. Our results suggest that modifying the PPAR- pathway plays a beneficial role in rescuing motor function as well as glucose metabolic abnormalities in HD.
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