The effect of dietary supplementation with blueberry, cyanidin-3-O-β-glucoside, yoghurt and its peptides on gene expression associated with glucose metabolism in skeletal muscle obtained from a high-fat-high-carbohydrate diet induced obesity model

PLoS One. 2022 Sep 16;17(9):e0270306. doi: 10.1371/journal.pone.0270306. eCollection 2022.

Abstract

Obesity is a leading global health problem contributing to various chronic diseases, including type II diabetes mellitus (T2DM). The aim of this study was to investigate whether blueberries, yoghurt, and their respective bioactive components, Cyanidin-3-O-β-glucoside (C3G) and peptides alone or in combinations, alter the expression of genes related to glucose metabolism in skeletal muscles from diet-induced obese mice. In extensor digitorum longus (EDL), yoghurt up-regulated the expression of activation of 5'adenosine monophosphate-activated protein kinase (AMPK), insulin receptor substrate-1 (IRS-1), phosphatidylinositol-3 kinase (PI3K) and glucose transporter 4 (GLUT4), and down-regulated the expression of angiotensin II receptor type 1 (AGTR-1). The combination of blueberries and yoghurt down-regulated the mRNA expression of AGTR-1 and Forkhead box protein O1 (FoxO1) in the EDL. Whereas the combination of C3G and peptides down-regulated AGTR-1 and up-regulated GLUT4 mRNA expression in the EDL. In the soleus, blueberries and yoghurt alone, and their combination down-regulated AGTR-1 and up-regulated GLUT4 mRNA expression. In summary blueberries and yoghurt, regulated multiple genes associated with glucose metabolism in skeletal muscles, and therefore may play a role in the management and prevention of T2DM.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Adenosine Monophosphate / metabolism
  • Animals
  • Anthocyanins* / metabolism
  • Anthocyanins* / pharmacology
  • Blueberry Plants* / chemistry
  • Diabetes Mellitus, Type 2* / metabolism
  • Diet, High-Fat / adverse effects
  • Dietary Supplements
  • Forkhead Box Protein O1 / metabolism
  • Gene Expression
  • Glucose Transport Proteins, Facilitative / metabolism
  • Glucose* / metabolism
  • Insulin Receptor Substrate Proteins / metabolism
  • Mice
  • Mice, Obese
  • Muscle, Skeletal / metabolism
  • Obesity* / genetics
  • Obesity* / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphatidylinositols / metabolism
  • RNA, Messenger / metabolism
  • Receptors, Angiotensin / metabolism
  • Yogurt*

Substances

  • Anthocyanins
  • Forkhead Box Protein O1
  • Glucose Transport Proteins, Facilitative
  • Insulin Receptor Substrate Proteins
  • Phosphatidylinositols
  • RNA, Messenger
  • Receptors, Angiotensin
  • cyanidin-3-O-beta-glucopyranoside
  • Adenosine Monophosphate
  • AMP-Activated Protein Kinases
  • Glucose

Associated data

  • Dryad/10.5061/dryad.41ns1rnhd

Grants and funding

This research is supported by a PhD scholarship to Min Shi by Victoria University, Australia.