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Updated: Oct 2, 2025

Isolation and Differentiation of Stromal Vascular Cells to Beige/Brite Cells
Published on: March 28, 2013
Palmitoylethanolamide Promotes White-to-Beige Conversion and Metabolic Reprogramming of Adipocytes: Contribution of
Chiara Annunziata1, Claudio Pirozzi1, Adriano Lama1
1Department of Pharmacy, School of Medicine, University of Naples Federico II, 80131 Naples, Italy.
Palmitoylethanolamide (PEA) helps convert white fat to brown-like fat, improving metabolism and combating obesity. PEA activates peroxisome proliferator-activated receptor alpha (PPAR-α) to restore white adipose tissue homeostasis.
Area of Science:
- Adipose tissue biology
- Metabolic regulation
- Obesity research
Background:
- Brown and beige adipose tissues play a role in combating obesity.
- Browning of white adipose tissue (WAT) improves adipocyte function.
- High-fat diets (HFD) impair adipose tissue plasticity.
Purpose of the Study:
- To investigate the effect of palmitoylethanolamide (PEA) on adipose tissue plasticity in mice on HFD.
- To elucidate the mechanisms underlying PEA's effects on adipocytes.
Main Methods:
- Mice were fed a control or HFD, with PEA administration.
- Analysis of adipose tissue morphology, gene expression (UCP1, thermogenic genes), and signaling pathways (PPAR-α, AMPK).
- In vitro studies using 3T3-L1 adipocytes and human adipose-derived stromal cells (ASCs).
Main Results:
- PEA restored brown fat morphology and function, increasing UCP1 and noradrenergic innervation.
- PEA promoted beige-conversion of subcutaneous WAT, enhancing thermogenic markers and leptin signaling.
- PEA improved mitochondrial bioenergetics and activated AMPK via PPAR-α.
Conclusions:
- PEA rewires white adipocytes into energy-consuming brown-like adipocytes.
- PEA-mediated effects involve PPAR-α activation and AMPK phosphorylation.
- PEA restores WAT homeostasis and metabolic flexibility, offering a potential strategy against obesity.
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