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Naringenin reduces inflammatory pain in mice
Felipe A Pinho-Ribeiro1, Ana C Zarpelon1, Victor Fattori1
1Departamento de Ciências Patológicas-Centro de Ciências Biológicas, Universidade Estadual de Londrina, 86057970 Londrina, Brazil.
Neuropharmacology
|February 25, 2016
Summary
Naringenin, a natural flavonoid, effectively reduces inflammatory and acute pain by modulating nociceptors and inhibiting inflammatory pathways. This study demonstrates its analgesic potential with no observed toxicity in mice.
Area of Science:
- Pharmacology
- Pain Research
- Natural Products Chemistry
Background:
- Naringenin is a flavonoid with known anti-inflammatory properties and low toxicity.
- Previous research indicated naringenin's analgesic effects in neuropathic pain models.
- The current study investigates naringenin's efficacy in various inflammatory pain models.
Purpose of the Study:
- To evaluate the analgesic effects of naringenin in multiple models of inflammatory pain.
- To explore the underlying mechanisms of naringenin's pain-relieving actions.
Main Methods:
- Mice were treated orally with naringenin (16.7-150 mg/kg) or control drugs.
- Pain behaviors were assessed using acetic acid-induced visceral pain, formalin, capsaicin, and CFA-induced paw tests.
- Mechanical hyperalgesia was measured using electronic von Frey filaments after various inflammatory stimuli.
Main Results:
- Naringenin (50 mg/kg) significantly reduced pain behaviors across all tested stimuli, including both phases of the formalin test.
- Naringenin inhibited mechanical hyperalgesia induced by carrageenan, capsaicin, and PGE2.
- Mechanisms involved inhibition of oxidative stress, pro-inflammatory cytokines (IL-33, TNF-α, IL-1β), NF-κB activation, and activation of the NO-cGMP-PKG pathway.
Conclusions:
- Naringenin exhibits potent analgesic effects in inflammatory pain models, suggesting direct nociceptor modulation.
- The compound demonstrates anti-inflammatory and analgesic properties through multiple molecular pathways.
- Naringenin presents a promising therapeutic agent for inflammatory and neurogenic pain with no observed gastric or hepatic toxicity.

