Electroacupuncture Upregulates SIRT1-Dependent PGC-1α Expression in SAMP8 Mice

Med Sci Monit. 2015 Nov 4:21:3356-62. doi: 10.12659/msm.894864.

Abstract

Background: Abnormalities of brain energy metabolism are involved in Alzheimer disease (AD). Sirtuin 1 (SIRT1) is a class III histone deacetylase and activates peroxisome proliferator-activated receptor-γ co-activator-1α (PGC-1α), which enhances mitochondrial biogenesis and energy homeostasis. Electroacupuncture (EA) has been reported to improve brain energy metabolism in AD. However, the effect of EA on SIRT1 and PGC-1α in AD remains unclear.

Material and methods: ATP levels were measured using assay kits in the hippocampus and frontal cortex of senescence-accelerated mouse prone 8 (SAMP8) mice. Western blotting analysis and quantitative real-time RT-PCR were performed to measure the expression of SIRT1 and PGC-1a in the hippocampus of SAMP8 mice. PGC-1α acetylation was analyzed using immunoprecipitation.

Results: Compared with senescence-accelerated resistant mice 1 (SAMR1) mice, SAMP8 mice had a decline in ATP levels and the expression of SIRT1 and PGC-1α. EA treatment improved ATP levels, upregulated the expression of SIRT1 and PGC-1α, and decreased PGC-1α acetylation.

Conclusions: These data suggest that EA improved brain energy metabolism, potentially associated with the upregulation of SIRT1-dependent PGC-1α expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Adenosine Triphosphate / chemistry
  • Alzheimer Disease / metabolism
  • Animals
  • Disease Models, Animal
  • Electroacupuncture*
  • Frontal Lobe / metabolism
  • Gene Expression Regulation*
  • Hippocampus / metabolism
  • Homeostasis
  • Immunoprecipitation
  • Male
  • Mice
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Sirtuin 1 / metabolism*
  • Transcription Factors / metabolism*
  • Up-Regulation*

Substances

  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, mouse
  • Transcription Factors
  • Adenosine Triphosphate
  • Sirt1 protein, mouse
  • Sirtuin 1