Peripheral Anti-nociceptive and Anti-inflammatory Effect of OleanoliAcid in a Rat Model of Osteoarthritis

dc.contributor.authorSalman, Israa
dc.contributor.authorFakhoury, Marc
dc.contributor.authorFouani, Malak
dc.contributor.authorLawand, Nada Bashir
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.departmentNeurology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:37:10Z
dc.date.available2025-01-24T11:37:10Z
dc.date.issued2021
dc.description.abstractBackground: 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.
dc.identifier.doihttps://doi.org/10.2174/1871523019999201111191754
dc.identifier.eid2-s2.0-85122165922
dc.identifier.pmid33183210
dc.identifier.urihttp://hdl.handle.net/10938/28808
dc.language.isoen
dc.publisherBentham Science Publishers
dc.relation.ispartofAnti-Inflammatory and Anti-Allergy Agents in Medicinal Chemistry
dc.sourceScopus
dc.subjectInflammation
dc.subjectKaolin/carrageenan
dc.subjectMotor coordination
dc.subjectNociception
dc.subjectOleanolic acid
dc.subjectOsteoarthritis
dc.subjectPain
dc.subjectAnimals
dc.subjectAnti-inflammatory agents
dc.subjectDisease models, animal
dc.subjectInjections, intra-articular
dc.subjectKnee joint
dc.subjectRats
dc.subjectCarrageenan
dc.subjectIsoflurane
dc.subjectKaolin
dc.subjectKetamine
dc.subjectXylazine
dc.subjectAntiinflammatory agent
dc.subjectAction potential
dc.subjectAdult
dc.subjectAllodynia
dc.subjectAnalgesic activity
dc.subjectAnimal experiment
dc.subjectAnimal model
dc.subjectAntiinflammatory activity
dc.subjectArticle
dc.subjectControlled study
dc.subjectDown regulation
dc.subjectElectrophysiology
dc.subjectEpineurium
dc.subjectExperimental behavioral test
dc.subjectHeat hyperalgesia
dc.subjectHot plate test
dc.subjectHyperalgesia
dc.subjectKnee
dc.subjectMale
dc.subjectMechanoreceptor
dc.subjectNerve cell plasticity
dc.subjectNerve regeneration
dc.subjectNonhuman
dc.subjectOrbital cortex
dc.subjectPain threshold
dc.subjectPilot study
dc.subjectRat
dc.subjectSciatic nerve injury
dc.subjectSpinal ganglion
dc.subjectTibial nerve
dc.subjectAnimal
dc.subjectDisease model
dc.subjectIntraarticular drug administration
dc.subjectMetabolism
dc.titlePeripheral Anti-nociceptive and Anti-inflammatory Effect of OleanoliAcid in a Rat Model of Osteoarthritis
dc.typeArticle

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