Is there good evidence for the anti-inflammatory properties of Urolithin A (UA)?

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Last updated: June 10, 2025View editorial policy

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From the Guidelines

There is evidence suggesting the anti-inflammatory properties of Urolithin A, although it is not directly stated in the provided study. The study 1 discusses various compounds that modulate autophagy, including urolithin A, which is a metabolite produced by gut microbiota from compounds found in many fruits and vegetables. While the study does not explicitly mention the anti-inflammatory properties of urolithin A, it does mention that urolithin A has been shown to induce mitophagy in cell cultures, increase longevity in nematodes, and prevent age-related muscle impairment in mouse models 1.

Key Points

  • Urolithin A is a metabolite produced by gut microbiota from compounds found in many fruits and vegetables 1.
  • It has been shown to induce mitophagy in cell cultures, increase longevity in nematodes, and prevent age-related muscle impairment in mouse models 1.
  • The study suggests that compounds that modulate autophagy, such as urolithin A, may have potential anti-aging properties 1.
  • However, the study does not provide direct evidence for the anti-inflammatory properties of urolithin A.

Clinical Implications

Given the potential benefits of urolithin A, further research is needed to fully understand its effects on human health, including its potential anti-inflammatory properties. While the current evidence is promising, it is essential to consult with a healthcare provider before starting any supplement regimen, including urolithin A. A combination of dietary sources rich in ellagitannins and possibly supplements may be beneficial, particularly for inflammatory conditions, but more research is needed to establish optimal dosing protocols and to fully understand the effects of urolithin A on human health 1.

From the Research

Anti-Inflammatory Properties of Urolithin A

  • Urolithin A (UA) has been shown to possess anti-inflammatory properties in various studies 2, 3, 4, 5, 6.
  • The anti-inflammatory effects of UA have been demonstrated in both in vitro and in vivo studies, including models of colitis, carrageenan-induced paw edema, and rheumatoid arthritis 2, 3.
  • UA has been found to attenuate the production of pro-inflammatory factors, such as IL-6, IL-1β, and NOS2, and to inhibit the activation of inflammatory signaling pathways, including the NF-κB pathway 2, 3.
  • The anti-inflammatory effects of UA are thought to be mediated by its ability to modulate the activity of various molecular targets, including aryl hydrocarbon receptors, protein kinase B, and p53 2.
  • UA has also been shown to induce mitophagy, a process that helps to remove damaged mitochondria and reduce oxidative stress, which can contribute to inflammation 5, 6.

Mechanisms of Action

  • The exact mechanisms by which UA exerts its anti-inflammatory effects are not fully understood, but are thought to involve the modulation of multiple signaling pathways, including the AMPK/NF-κB pathway 3.
  • UA has been found to inhibit the phosphorylation of NF-κB, a key transcription factor involved in the regulation of inflammatory gene expression, and to activate the phosphorylation of AMPK, a key regulator of cellular energy metabolism 3.
  • UA has also been shown to inhibit the production of pro-inflammatory cytokines, such as TNF-α, and to increase the production of anti-inflammatory cytokines, such as IL-10 4.

Potential Therapeutic Applications

  • The anti-inflammatory properties of UA make it a potential therapeutic agent for the treatment of various inflammatory diseases, including rheumatoid arthritis, cancer, and age-related diseases 2, 3, 5, 6.
  • UA has been shown to be safe and well-tolerated in animal models and human clinical trials, and its potential therapeutic applications are currently being explored in various research studies 2, 5, 6.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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