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Paroxetine 110429-35-1 with immediately delivery Paroxetine 110429-35-1 in stock factory GMP Paroxetine 110429-35-1
with immediately deliveryParoxetine 110429-35-1 in stockfactory GMP
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Paroxetine(1μMand10μM)distinctlyrestrainsTcellmigrationinducedbyCX3CL1throughinhibitingGRK2.ParoxetineinhibitsGRK2inducedactivationofERK.Paroxetine(10μM)reducespro-inflammatorycytokinesinLPS-stimulatedBV2cells.Paroxetine(0-5μM)leadstoadose-dependentinhibitiononLPS-inducedproductionofTNF-αandIL-1βinBV2cells.Paroxetinealsoinhibitslipopolysaccharide(LPS)inducednitricoxide(NO)productionandinduciblenitricoxidesynthase(iNOS)expressioninBV2cells.Paroxetine(5μM)blocksLPSinducedJNKactivationandattenuatesbaselineERK1/2activityinBV2cells.Paroxetinerelievesmicroglia-mediatedneurotoxicity,andsuppressesLPS-stimulatedpro-inflammatorycytokinesandNOinprimarymicroglialcells.
ParoxetinetreatmentobviouslyattenuatesthesymptomsofCIArats.ParoxetinetreatmentclearlypreventsthehistologicaldamageofjointsandalleviatesTcellsinfiltrationintosynovialtissue.ParoxetinerevealsastrongeffectoninhibitingCX3CL1productioninsynovialtissues.Paroxetine(20mg/kg/day)reducesthemyocytecrosssectionalareainratandROSformationintheremotemyocardium.Paroxetinereducesthesusceptibilitytoventriculartachycardia.ParoxetinetreatmentfollowingMIdecreasesLVremodelingandsusceptibilitytoarrhythmias,probablybyreducingROSformation.InCCIparoxetine-treatedgroup,paroxetine(10mg/kg,i.p.)produceshyperalgesiaatdays7and10(P<0.01),butadecreaseinpainbehaviorisseenatday14.Moreover,paroxetine(10mg/kg)significantlyattenuatestactilehypersensitivitywhencomparedtoCCIvehicle-treatedgroup.
CAS NO:143491-57-0
CAS NO:143491-57-0
CAS NO:143491-57-0
CAS NO:143491-57-0
CAS NO:143491-57-0
CAS NO:143491-57-0
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