Improved glucose metabolism by Eragrostis tef potentially through beige adipocyte formation and attenuating adipose tissue inflammation

PLoS One. 2018 Aug 2;13(8):e0201661. doi: 10.1371/journal.pone.0201661. eCollection 2018.

Abstract

Background: Teff is a staple food in Ethiopia that is rich in dietary fiber. Although gaining popularity in Western countries because it is gluten-free, the effects of teff on glucose metabolism remain unknown.

Aim: To evaluate the effects of teff on body weight and glucose metabolism compared with an isocaloric diet containing wheat.

Results: Mice fed teff weighed approximately 13% less than mice fed wheat (p < 0.05). The teff-based diet improved glucose tolerance compared with the wheat group with normal chow but not with a high-fat diet. Reduced adipose inflammation characterized by lower expression of TNFα, Mcp1, and CD11c, together with higher levels of cecal short chain fatty acids such as acetate, compared with the control diet containing wheat after 14 weeks of dietary treatment. In addition, beige adipocyte formation, characterized by increased expression of Ucp-1 (~7-fold) and Cidea (~3-fold), was observed in the teff groups compared with the wheat group. Moreover, a body-weight matched experiment revealed that teff improved glucose tolerance in a manner independent of body weight reduction after 6 weeks of dietary treatment. Enhanced beige adipocyte formation without improved adipose inflammation in a body-weight matched experiment suggests that the improved glucose metabolism was a consequence of beige adipocyte formation, but not solely through adipose inflammation. However, these differences between teff- and wheat-containing diets were not observed in the high-fat diet group.

Conclusions: Teff improved glucose tolerance likely by promoting beige adipocyte formation and improved adipose inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue, Beige / metabolism*
  • Adipose Tissue, Beige / pathology
  • Animals
  • Apoptosis Regulatory Proteins / genetics
  • Apoptosis Regulatory Proteins / metabolism
  • Blood Glucose / analysis
  • Body Temperature
  • CD11c Antigen / genetics
  • CD11c Antigen / metabolism
  • Carbohydrate Metabolism / drug effects*
  • Dietary Fiber / pharmacology*
  • Eragrostis / metabolism*
  • Fatty Acids, Volatile / analysis
  • Fatty Acids, Volatile / chemistry
  • Feces / chemistry
  • Glucose Tolerance Test
  • Inflammation / metabolism
  • Inflammation / prevention & control
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Uncoupling Protein 1 / genetics
  • Uncoupling Protein 1 / metabolism

Substances

  • Apoptosis Regulatory Proteins
  • Blood Glucose
  • CD11c Antigen
  • Cidea protein, mouse
  • Dietary Fiber
  • Fatty Acids, Volatile
  • Tumor Necrosis Factor-alpha
  • Uncoupling Protein 1

Grants and funding

The Department of Medicine at SUMS received research promotion grants [SHOGAKUKIFU] from Boehringer Ingelheim, and Astellas to HM. ML received support from the MEXT fellowship program from the Japanese government. Teff flour was provided by The Teff Company (USA). These funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. CMIC Pharma Science provided support in the form of equipment and salaries for authors (FN and AN), but did not have any additional role in the study design, data collection, analysis, decision to publish or preparation of the manuscript. The specific roles of these authors are articulated in the 'author contributions' section.