Influence of Polyphenols on Adipose Tissue: Sirtuins as Pivotal Players in the Browning Process.
Lorenzo FloriEugenia PiragineJacopo SpezziniValentina CitiVincenzo CalderoneAlma MartelliPublished in: International journal of molecular sciences (2023)
Adipose tissue (AT) can be classified into two different types: (i) white adipose tissue (WAT), which represents the largest amount of total AT, and has the main function of storing fatty acids for energy needs and (ii) brown adipose tissue (BAT), rich in mitochondria and specialized in thermogenesis. Many exogenous stimuli, e.g., cold, exercise or pharmacological/nutraceutical tools, promote the phenotypic change of WAT to a beige phenotype (BeAT), with intermediate characteristics between BAT and WAT; this process is called "browning". The modulation of AT differentiation towards WAT or BAT, and the phenotypic switch to BeAT, seem to be crucial steps to limit weight gain. Polyphenols are emerging as compounds able to induce browning and thermogenesis processes, potentially via activation of sirtuins. SIRT1 (the most investigated sirtuin) activates a factor involved in mitochondrial biogenesis, peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α), which, through peroxisome proliferator-activated receptor γ (PPAR-γ) modulation, induces typical genes of BAT and inhibits genes of WAT during the transdifferentiation process in white adipocytes. This review article aims to summarize the current evidence, from pre-clinical studies to clinical trials, on the ability of polyphenols to promote the browning process, with a specific focus on the potential role of sirtuins in the pharmacological/nutraceutical effects of natural compounds.
Keyphrases
- adipose tissue
- insulin resistance
- weight gain
- high fat diet induced
- high fat diet
- clinical trial
- fatty acid
- body mass index
- oxidative stress
- genome wide
- palliative care
- physical activity
- cell death
- type diabetes
- high resolution
- randomized controlled trial
- blood pressure
- open label
- reactive oxygen species
- dna methylation
- transcription factor
- single molecule
- endoplasmic reticulum