Cyclopia intermedia (Honeybush) Induces Uncoupling Protein 1 and Peroxisome Proliferator-Activated Receptor Alpha Expression in Obese Diabetic Female db/db Mice

Previously, we reported that a crude polyphenol-enriched fraction of Cyclopia intermedia (CPEF), a plant consumed as the herbal tea, commonly known as honeybush, reduced lipid content in 3T3-L1 adipocytes and inhibited body weight gain in obese, diabetic female leptin receptor-deficient (db/db) mice. In the current study, the mechanisms underlying decreased body weight gain in db/db mice were further elucidated using western blot analysis and in silico approaches. CPEF induced uncoupling protein 1 (UCP1, 3.4-fold, p < 0.05) and peroxisome proliferator-activated receptor alpha (PPAR alpha, 2.6-fold, p < 0.05) expression in brown adipose tissue. In the liver, CPEF induced PPAR alpha expression (2.2-fold, p < 0.05), which was accompanied by a 31.9% decrease in fat droplets in Hematoxylin and Eosin (H&E)-stained liver sections (p < 0.001). Molecular docking analysis revealed that the CPEF compounds, hesperidin and neoponcirin, had the highest binding affinities for UCP1 and PPAR alpha, respectively. This was validated with stabilising intermolecular interactions within the active sites of UCP1 and PPAR alpha when complexed with these compounds. This study suggests that CPEF may exert its anti-obesity effects by promoting thermogenesis and fatty acid oxidation via inducing UCP1 and PPAR alpha expression, and that hesperidin and neoponcirin may be responsible for these effects. Findings from this study could pave the way for designing target-specific anti-obesity therapeutics from C. intermedia.

Automated summary

Previous studies have shown that crude polyphenol-enriched fraction of Cyclopia intermedia (CPEF), commonly known as honeybush, can reduce lipid content in adipocytes and inhibit body weight gain in obese mice. This study further explored the mechanisms behind these effects and found that CPEF induces the expression of UCP1 and PPAR alpha in brown adipose tissue, promoting thermogenesis and fatty acid oxidation. The compounds hesperidin and neoponcirin in CPEF were found to have specific interactions with UCP1 and PPAR alpha, respectively, suggesting their potential role in the anti-obesity effects.