Anti-Obesity Effects of Grateloupia elliptica, a Red Seaweed, in Mice with High-Fat Diet-Induced Obesity via Suppression of Adipogenic Factors in White Adipose Tissue and Increased Thermogenic Factors in Brown Adipose Tissue

Nutrients. 2020 Jan 24;12(2):308. doi: 10.3390/nu12020308.

Abstract

Obesity is a serious metabolic syndrome characterized by high levels of cholesterol, lipids in the blood, and intracellular fat accumulation in adipose tissues. It is known that the suppression of adipogenic protein expression is an effective approach for the treatment of obesity, and regulates fatty acid storage and transportation in adipose tissues. The 60% ethanol extract of Grateloupia elliptica (GEE), a red seaweed from Jeju Island in Korea, was shown to exert anti-adipogenic activity in 3T3-L1 cells and in mice with high-fat diet (HFD)-induced obesity. GEE inhibited intracellular lipid accumulation in 3T3-L1 cells, and significantly reduced expression of adipogenic proteins. In vivo experiments indicated a significant reduction in body weight, as well as white adipose tissue (WAT) weight, including fatty liver, serum triglycerides, total cholesterol, and leptin contents. The expression of the adipogenic proteins, SREBP-1 and PPAR-γ, was significantly decreased by GEE, and the expression of the metabolic regulator protein was increased in WAT. The potential of GEE was shown in WAT, with the downregulation of PPAR-γ and C/EBP-α mRNA; in contrast, in brown adipose tissue (BAT), the thermogenic proteins were increased. Collectively, these research findings suggest the potential of GEE as an effective candidate for the treatment of obesity-related issues via functional foods or pharmaceutical agents.

Keywords: Grateloupia elliptica; adipocyte; adipogenesis; anti-obesity; red seaweed; thermogenesis.

MeSH terms

  • 3T3-L1 Cells
  • Adipogenesis / drug effects*
  • Adipose Tissue, Brown / drug effects*
  • Adipose Tissue, Brown / metabolism
  • Adipose Tissue, Brown / physiopathology
  • Adipose Tissue, White / drug effects*
  • Adipose Tissue, White / metabolism
  • Adipose Tissue, White / physiopathology
  • Adiposity / drug effects
  • Animals
  • Anti-Obesity Agents / isolation & purification
  • Anti-Obesity Agents / pharmacology*
  • CCAAT-Enhancer-Binding Proteins / metabolism
  • Diet, High-Fat
  • Disease Models, Animal
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity / drug therapy*
  • Obesity / metabolism
  • Obesity / physiopathology
  • PPAR gamma / metabolism
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology*
  • Rhodophyta* / chemistry
  • Seaweed* / chemistry
  • Signal Transduction
  • Sterol Regulatory Element Binding Protein 1 / metabolism
  • Thermogenesis / drug effects*

Substances

  • Anti-Obesity Agents
  • CCAAT-Enhancer-Binding Proteins
  • CEBPA protein, mouse
  • PPAR gamma
  • Plant Extracts
  • Pparg protein, mouse
  • Srebf1 protein, mouse
  • Sterol Regulatory Element Binding Protein 1