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May 6, 2026Foods1 citationsOpen Access

Chemical Composition, Antioxidant Activity, Anti-Fatigue Function and Mechanism of Pomegranate Peel Polyphenols on Exercise-Induced Fatigue in Mice

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XMXing-Yu MaYWYu-Mei WangYHYu-Dong Hu

Key Points

  • The study aims to evaluate the effects of pomegranate peel polyphenols on exercise-induced fatigue and determine the underlying mechanisms.
  • Identified twenty main compounds from pomegranate peel using LC-MS/MS.
  • Assessed antioxidant activity in H2O2-induced HepG2 cells and evaluated anti-fatigue function in endurance swimming-induced fatigue mice.
  • Analyzed oxidative stress effects through the Keap1/Nrf2 pathway and mitochondrial biogenesis through the AMPK/PGC-1α/PPAR-α pathway.
  • Pomegranate peel polyphenols prolonged exhaustion times in mice during endurance swimming.
  • Reduced levels of fatigue-related metabolites such as malondialdehyde, BUN, LA, LDH, and CK.
  • Enhanced the expression of antioxidant enzymes and promoted mitochondrial biogenesis.

Abstract

Pomegranate peel is a food industry waste rich in polyphenols. To date, its effect in alleviating fatigue remains unclear. This study aimed to characterize the chemical composition of pomegranate peel polyphenols (PPPs), evaluate its antioxidant and anti-fatigue capacities, and investigate the underlying mechanism. In the current study, twenty main compounds, primarily flavonoids, phenolic acids, and anthocyanins, were identified from PPPs using LC-MS/MS. In H2O2-induced HepG2 cells, PPPs promoted cellular repair and reduced the production of intracellular malondialdehyde (MDA) and reactive oxygen species (ROS) via enhancing the activity of antioxidant enzymes (SOD, CAT, and GSH-Px). In the endurance swimming-induced fatigue mice model, PPPs prolonged mice exhaustion times, reduced accumulation of fatigue-related metabolites (BUN, LA, BA, LDH and CK), and alleviated liver and muscle tissue damage. Mechanistically, PPPs mitigated oxidative stress via activation of the Keap1/Nrf2 pathway, leading to increased expression of hemeoxygenase-1 (HO-1) and NAD(P)H quinone oxidoreductase 1 (NQO1). Furthermore, PPPs stimulated energy metabolism by activating the AMPK/PGC-1α/PPAR-α pathway, promoting mitochondrial biogenesis, enhancing glycogen storage, increasing ATPase activity (Na+-K+-ATPase, Ca2+-Mg2+-ATPase, and T-ATPase) and accelerating lipid β-oxidation. These findings suggest that PPPs is a promising anti-fatigue supplement and could be further utilized in the nutritional industry.

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Cite This Study

Ma et al. (2026) studied this question.

synapsesocial.com/papers/69fa979b04f884e66b531909https://doi.org/10.3390/foods15091576
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