Galectin-12 is Involved in Corn Silk-Induced Anti-Adipogenesis and Anti-Obesity Effects

Am J Chin Med. 2018;46(5):1045-1063. doi: 10.1142/S0192415X18500544. Epub 2018 Jul 5.

Abstract

Obesity is a significant risk factor for various diseases. It is a clinical condition caused by the excessive accumulation of fat, which has a negative impact on human health. Galactin-12 is an adipocyte-expressed protein and possesses adipocyte-inducing activity. We investigated the expression level of candidate proteins involved in galactin-12-mediated adipocyte differentiation pathway. We performed a high-throughput screening assay to monitor galectin-12 promoter activity using 105 traditional Chinese herbs. Corn silk extract and [Formula: see text]-sitosterol reduced the expression of galactin-12 promoter in 3T3-L1 cells. In addition, corn silk extract and [Formula: see text]-sitosterol decreased the level of lipid droplets and downregulated the gene and protein expression level of C/EBP[Formula: see text], C/EBP[Formula: see text], PPAR[Formula: see text], Ap2, and adipsin in 3T3-L1 pre-adipocytes via AKT and ERK1/2 inhibition. In vivo study with the oral administration of corn silk extract and [Formula: see text]-sitosterol in a mouse model showed a significant weight reduction and decrease in adipocytes in several organs such as the liver and adipose tissue. Taken together, corn silk extract and [Formula: see text]-sitosterol may effectively reduce pre-adipocyte differentiation by inhibiting galectin-12 activity and exerting anti-obesity effects. These findings highlight the potential use of corn silk extract and [Formula: see text]-sitosterol as potential candidates for the prevention and treatment of obesity.

Keywords: -Sitosterol; Adipogenesis; Corn Silk; Galectin-12; Obesity.

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Adipogenesis / drug effects*
  • Animals
  • Anti-Obesity Agents / pharmacology*
  • CCAAT-Enhancer-Binding Proteins / genetics
  • CCAAT-Enhancer-Binding Proteins / metabolism
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Cell Survival / drug effects
  • Galectins / genetics
  • Galectins / metabolism*
  • Humans
  • Mice
  • NIH 3T3 Cells
  • Obesity / drug therapy
  • Obesity / genetics
  • Obesity / metabolism*
  • Obesity / physiopathology
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Plant Extracts / pharmacology*
  • Zea mays / chemistry*

Substances

  • Anti-Obesity Agents
  • CCAAT-Enhancer-Binding Proteins
  • Cell Cycle Proteins
  • Galectins
  • Lgals12 protein, mouse
  • PPAR gamma
  • Plant Extracts