| Literature DB >> 33805912 |
Federica Scarano1,2, Micaela Gliozzi1,2, Maria Caterina Zito1,2, Lorenza Guarnieri1,2, Cristina Carresi1,2, Roberta Macrì1,2, Saverio Nucera1,2, Miriam Scicchitano1,2, Francesca Bosco1,2, Stefano Ruga1,2, Anna Rita Coppoletta1,2, Rocco Mollace1,2, Jessica Maiuolo1,2, Irene Bava1,2, Antonio Cardamone1,2, Monica Ragusa3, Ernesto Palma1,2, Vincenzo Musolino1,2, Vincenzo Mollace1,2.
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.Entities:
Keywords: BAT; WAT; browning; inflammation; metabolic diseases; nutraceutical supplementation; obesity; polyphenols
Year: 2021 PMID: 33805912 PMCID: PMC8037903 DOI: 10.3390/ijms22073351
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923