Dendrobium officinale polysaccharide prevents neuronal apoptosis via TET2-dependent DNA demethylation in high-fat diet-induced diabetic mice

Int J Biol Macromol. 2023 Apr 1:233:123288. doi: 10.1016/j.ijbiomac.2023.123288. Epub 2023 Jan 16.

Abstract

Dendrobium officinale polysaccharide (DP) has the potential function to prevent diabetes-induced neuronal apoptosis, whereas the mechanism is not completely clear. Ten eleven translocation dioxygenase 2 (TET2) is one of the most important therapeutic target for repairing neuronal damage in diabetic mice. The aim of the present study was to investigate whether DP could prevent neuronal apoptosis by regulating TET2 in the brain of HFD-induced diabetic mice. C57BL/6J mice were randomly divided into four groups (n = 12), control group (CON), high-fat diet group (HFD, negative control), metformin group (MET, positive control), and DP group (DP). Compared with HFD group, the neuronal apoptosis of brain was significantly lower in the DP group. The levels of TET2 protein, 5-hydroxymethylcytosine (5hmC) and 5-formylcytosine (5fC) were significantly lower in the HFD group than in both the DP and CON groups in the cerebral cortex of mice. The ratio of p-AMPK/AMPK and α-KG/(fumaric acid + succinic acid) were significantly lower in the HFD group than in the other groups. The present study suggests that DP has a preventive effect on diabetes-induced neuronal apoptosis by regulating TET2 function through improving phosphorylate AMPK and mitochondrial function, thus remodeling DNA epigenetics profile of mice brain.

Keywords: DNA demethylation; Dendrobium officinale polysaccharide; Neuronal apoptosis.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Apoptosis
  • DNA Demethylation
  • DNA-Binding Proteins / metabolism
  • Dendrobium*
  • Diabetes Mellitus, Experimental* / drug therapy
  • Diet, High-Fat / adverse effects
  • Dioxygenases* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Polysaccharides / pharmacology
  • Polysaccharides / therapeutic use

Substances

  • AMP-Activated Protein Kinases
  • Polysaccharides
  • Tet2 protein, mouse
  • DNA-Binding Proteins
  • Dioxygenases