Dietary supplementation with decaffeinated green coffee improves diet-induced insulin resistance and brain energy metabolism in mice

Nutr Neurosci. 2012 Jan;15(1):37-45. doi: 10.1179/1476830511Y.0000000027.

Abstract

Objectives: There is accumulating evidence that coffee consumption may reduce risk for type 2 diabetes, a known risk factor for Alzheimer's and other neurological diseases. Coffee consumption is also associated with reduced risk for Alzheimer's disease and non-Alzheimer's dementias. However, preventive and therapeutic development of coffee is complicated by the cardiovascular side effects of caffeine intake. As coffee is also a rich source of chlorogenic acids and many bioactive compounds other than caffeine, we hypothesized that decaffeinated coffee drinks may exert beneficial effects on the brain.

Methods: We have investigated whether dietary supplementation with a standardized decaffeinated green coffee preparation, Svetol®, might modulate diet-induced insulin resistance and brain energy metabolism dysfunction in a high-fat diet mouse model.

Results: As expected, dietary supplementation with Svetol® significantly attenuated the development of high-fat diet-induced deficits in glucose-tolerance response. We have also found that Svetol®) treatment improved brain mitochondrial energy metabolism as determined by oxygen consumption rate. Consistent with this evidence, follow-up gene expression profiling with Agilent whole-genome microarray revealed that the decaffeinated coffee treatment modulated a number of genes in the brain that are implicated in cellular energy metabolism.

Discussion: Our evidence is the first demonstration that dietary supplementation with a decaffeinated green coffee preparation may beneficially influence the brain, in particular promoting brain energy metabolic processes.

MeSH terms

  • Animals
  • Beverages
  • Blood Glucose
  • Brain / drug effects
  • Brain / metabolism
  • Caffeine*
  • Chlorogenic Acid / analysis
  • Chlorogenic Acid / pharmacology
  • Coffee / chemistry*
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diet, High-Fat*
  • Dietary Supplements*
  • Energy Metabolism / drug effects*
  • Female
  • Follow-Up Studies
  • Gene Expression Profiling / methods
  • Insulin Resistance*
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism
  • Risk Factors

Substances

  • Blood Glucose
  • Coffee
  • Chlorogenic Acid
  • Caffeine