Potential of Nutraceutical Supplementation in the Modulation of White and Brown Fat Tissues in Obesity-Associated Disorders: Role of Inflammatory Signalling

Int J Mol Sci. 2021 Mar 25;22(7):3351. doi: 10.3390/ijms22073351.

Abstract

The high incidence of obesity is associated with an increasing risk of several chronic diseases such as cardiovascular disease, type 2 diabetes and non-alcoholic fatty liver disease (NAFLD). Sustained obesity is characterized by a chronic and unsolved inflammation of adipose tissue, which leads to a greater expression of proinflammatory adipokines, excessive lipid storage and adipogenesis. The purpose of this review is to clarify how inflammatory mediators act during adipose tissue dysfunction in the development of insulin resistance and all obesity-associated diseases. In particular, we focused our attention on the role of inflammatory signaling in brown adipose tissue (BAT) thermogenic activity and the browning of white adipose tissue (WAT), which represent a relevant component of adipose alterations during obesity. Furthermore, we reported the most recent evidence in the literature on nutraceutical supplementation in the management of the adipose inflammatory state, and in particular on their potential effect on common inflammatory mediators and pathways, responsible for WAT and BAT dysfunction. Although further research is needed to demonstrate that targeting pro-inflammatory mediators improves adipose tissue dysfunction and activates thermogenesis in BAT and WAT browning during obesity, polyphenols supplementation could represent an innovative therapeutic strategy to prevent progression of obesity and obesity-related metabolic diseases.

Keywords: BAT; WAT; browning; inflammation; metabolic diseases; nutraceutical supplementation; obesity; polyphenols.

Publication types

  • Review

MeSH terms

  • Adipogenesis
  • Adipose Tissue / metabolism
  • Adipose Tissue, Brown / metabolism*
  • Adipose Tissue, White / metabolism*
  • Animals
  • Curcumin / chemistry
  • Diet
  • Dietary Supplements*
  • Endoplasmic Reticulum / metabolism
  • Fatty Acids, Unsaturated / metabolism
  • Humans
  • Inflammation / metabolism*
  • Insulin Resistance
  • Intestines / chemistry
  • Lipids / chemistry
  • Macrophages / metabolism
  • Obesity / metabolism*
  • Polyphenols / chemistry
  • Resveratrol / pharmacology
  • Signal Transduction
  • Thermogenesis*

Substances

  • Fatty Acids, Unsaturated
  • Lipids
  • Polyphenols
  • Curcumin
  • Resveratrol