Peripheral Anti-nociceptive and Anti-inflammatory Effect of OleanoliAcid in a Rat Model of Osteoarthritis
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Bentham Science Publishers
Abstract
Background: Oleanolic acid (OA) is a naturally occurring pentacyclic triterpenoid with multifarious actions. The anti-inflammatory effect it exerts when taken orally is the most important; however, the underpinning mechanisms of such effects have not yet been fully explored. Methods: In the present study, we evaluated the anti-inflammatory and anti-nociceptive effect of OA by injecting it directly into the knee joint using an animal model of osteoarthritis. Behavioral and electrophysiological studies were conducted to determine whether OA exerts a direct modulatory effect on primary sensory afferents that can lead to a decrease in pain-related behaviors and inflammatory responses. Rats were divided into two main groups: a pre-and a post-treatment group. Knee joint inflammation was induced by injecting a mixture of 3% kaolin and carrageenan (K/C). In the pre-treatment group, two different doses of OA [5 mg/ml (n=5) and 30 mg/ml (n=4); 0.1 ml per injection] were administered into the synovial cavity of the knee joint before induction of inflammation. In the post-treatment group, rats received only one dose [5 mg/ml (n=5)] of OA after induction of inflammation. Results: Results indicate that intra-articular injection of OA improves motor coordination and attenuates nociceptive behavior and inflammatory reactions. More importantly, we observed a direct depolarizing action of OA on articular sensory fibers, a crucial mechanism that activates descending inhibitory pathways and controls incoming nociceptive signals to the spinal cord. Conclusion: Overall, our findings suggest that OA can be used as a preventive and therapeutic approach for the management of osteoarthritis. © 2021 Bentham Science Publishers.
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Inflammation, Kaolin/carrageenan, Motor coordination, Nociception, Oleanolic acid, Osteoarthritis, Pain, Animals, Anti-inflammatory agents, Disease models, animal, Injections, intra-articular, Knee joint, Rats, Carrageenan, Isoflurane, Kaolin, Ketamine, Xylazine, Antiinflammatory agent, Action potential, Adult, Allodynia, Analgesic activity, Animal experiment, Animal model, Antiinflammatory activity, Article, Controlled study, Down regulation, Electrophysiology, Epineurium, Experimental behavioral test, Heat hyperalgesia, Hot plate test, Hyperalgesia, Knee, Male, Mechanoreceptor, Nerve cell plasticity, Nerve regeneration, Nonhuman, Orbital cortex, Pain threshold, Pilot study, Rat, Sciatic nerve injury, Spinal ganglion, Tibial nerve, Animal, Disease model, Intraarticular drug administration, Metabolism