Wilkerson, Jenny L.Ghosh, SudeshnaMason, Brittany L.Crowe, Molly S.Hsu, KulungWise, Laura E.Kinsey, Steven G.Damaj, Mohamad ImadCravatt, Benjamin F.Lichtman, Aron H.2022-10-122022-10-122016-02-16Wilkerson, J. L. vd. (2016). "Diacylglycerol lipase beta inhibition reverses nociceptive behaviour in mouse models of inflammatory and neuropathic pain". British Journal of Pharmacology, 173(10), Special Issue, 1678-1692.0007-11881476-5381https://doi.org/10.1111/bph.13469https://bpspubs.onlinelibrary.wiley.com/doi/10.1111/bph.13469http://hdl.handle.net/11452/29061Background and PurposeInhibition of diacylglycerol lipase (DGL) prevents LPS-induced pro-inflammatory responses in mouse peritoneal macrophages. Thus, the present study tested whether DGL inhibition reverses allodynic responses of mice in the LPS model of inflammatory pain, as well as in neuropathic pain models. Experimental ApproachInitial experiments examined the cellular expression of DGL and inflammatory mediators within the LPS-injected paw pad. DAGL- (-/-) mice or wild-type mice treated with the DGL inhibitor KT109 were assessed in the LPS model of inflammatory pain. Additional studies examined the locus of action for KT109-induced antinociception, its efficacy in chronic constrictive injury (CCI) of sciatic nerve and chemotherapy-induced neuropathic pain (CINP) models. Key ResultsIntraplantar LPS evoked mechanical allodynia that was associated with increased expression of DGL, which was co-localized with increased TNF- and prostaglandins in paws. DAGL- (-/-) mice or KT109-treated wild-type mice displayed reductions in LPS-induced allodynia. Repeated KT109 administration prevented the expression of LPS-induced allodynia, without evidence of tolerance. Intraplantar injection of KT109 into the LPS-treated paw, but not the contralateral paw, reversed the allodynic responses. However, i.c.v. or i.t. administration of KT109 did not alter LPS-induced allodynia. Finally, KT109 also reversed allodynia in the CCI and CINP models and lacked discernible side effects (e.g. gross motor deficits, anxiogenic behaviour or gastric ulcers). Conclusions and ImplicationsThese findings suggest that local inhibition of DGL at the site of inflammation represents a novel avenue to treat pathological pain, with no apparent untoward side effects.eninfo:eu-repo/semantics/openAccessPharmacology & pharmacyMonoacylglycerol lipaseEndogenous cannabinoidsCell-differentiationConcise guideAlphaPharmacologyResponsesBlockadeAgonistSystemAnimalsDisease models, animalDose-response relationship, drugEnzyme inhibitorsInflammationLipopolysaccharidesLipoprotein lipaseMaleMiceMice, inbred C57BLMice, knockoutNeuralgiaNociceptionStructure-activity relationshipArticle0003749760000102-s2.0-849626349461678169217310, Special Issue26915789Pharmacology & pharmacyAcylglycerol Lipase; Fatty-Acid Amide Hydrolase; AnimalsDiacylglycerol lipase betaDiclofenacEsteraseEsterase inhibitorKt 195LipopolysaccharideProstaglandin E2Tumor necrosis factor alphaUnclassified drug[4 [(1,1' biphenyl) 4 yl] 1h 1,2,3 triazol 1 yl](2 benzylpiperidin 1 yl)methanoneDiacylglycerol lipase betaMouseEnzyme inhibitorLipopolysaccharideLipoprotein lipaseAdultAllodyniaAnalgesic activityAnimal experimentAnimal modelAnimal tissueAntinociceptionAnxietyArticleControlled studyDrug efficacyEnzyme inhibitionHyperalgesiaInflammatory painMaleMotor dysfunctionMouseNeuropathic painNonhumanPriority journalProtein expressionSciatic nerve injuryStomach hemorrhageStomach ulcerAnimalAntagonists and inhibitorsC57BL mouseChemistryDeficiencyDisease modelDose responseDrug effectsInflammationKnockout mouseMetabolismNeuralgiaNociceptionStructure activity relation