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微量注射cnqx对大鼠臂旁核感官反应的影响
在roped,中央nuk膝(cea)是马蹄莲的一个发射包的发射包的一个发射包的一个发射包的信息,从pe面向sultan,从u体制中的一个分配信息,从u体制中的一个分配信息到另一个分配信息。这也是为什么分配的。从遗传因素到非正统阶段,有一个或两个生命体征,三个特征的痕迹,一个或两个生命体征的特征,三个特征的痕迹,一个或两个生命体征的特征,以及三个微带中的一个或两个微带的特征。这也表明,这是一个评估精度的过程,而不是努力或行为的过程。此外,这一过程中的一些迹象也表明,这是一个过程。体制改革或预算活动中的非物质丝没有形成,这是可以接受的。Inthecentralnervoussystem,glutaminergictransmissionplaysanimportantroleintheneuralmechanismoftasteformation.Ithasbeenshownthatglutamateisanexcitatoryneurotransmittermediatingchordatympani(CT)gustatoryafferentinputtothetaste-responsiveNSTareas,andthatthisneurotransmitterprimarilyactsonAMPAreceptors.Intheinsulargustatorycortex(IGC),thenormalexcitatorytransmissionoftasteafferentsisalsomediatedbyAMPAreceptors.Immunohistochemicalstudieshaveshownthattherearemanyglutamateimmunoreactiveneuronsintheamygdaloidcomplex,includingtheCeA.Thereisevidencethattheseneuronsareinvolvedintheformationofconditionedtasteaversion(CTA),andthatAMPAreceptorsareindispensablefortheacquisitionandexpressionoftheCTA.ThesefindingssuggestthatglutamatereceptorsareinvolvedintheexcitatorytransmissionoftasteintheCeA.However,noreportshavesofarbeenmadetoinvestigatetheroleofglutamatereceptorswithintheCeAinmodulatingthegustatoryresponsesofthePBN.Theaimofthepresentstudywastoassesstheeffectsofmicroinjectionof6-cyano-7-nitro-quinoxaline-2,3-dione(CNQX),aselectiveantagonistofAMPAreceptor,intotheCeAonthetasteresponsesofthePBNneurons.WerecordedresponsesofsinglePBNneurontogustatorystimulibeforeandaftertheipsilateraladministrationofCNQXtotheCeAandfoundthattheresponsesofthePBNneuronstoHClandQHClweresignificantlyinhibitedafterdrugapplication.1杏仁杏仁1.1ualiinstiagesin网络MaleSprague-Dawleyratsweighing220~290gwerehousedindividuallyinstainlesssteelcageswithlaboratorychowandtapwatercontinuouslyavailableexceptontheexperimentday.Roomlightswereon12hperdayandtemperaturewasmaintainedat(25±1)℃.1.2应用因子trepbn体的细胞系统见表3Theratswereanesthetizedwithethylcarbamate(urethane)(1.4~1.5g/kg,i.p.),andadditionalanestheticwasgivenasneededduringthecourseofeachexperiment.Theanimalwassecuredinastereotaxicinstrumentbyusingnonpunctureearbarsandabitebar.ForaccesstotheCeA,a2-mmtrephineholewascentered3.8~4.4mmlateraltothemidline,2.1~2.8mmposteriortobregma,asdescribedinPaxinosandWatson.AguidecannulawasimplantedintotheCeA.ForipsilateralPBNpenetration,thetrephinewascenteredat9.0~9.7mmposteriortobregmaand1.5~2.1mmlateraltothemidline.ThetransversesinusoverlyingthePBNwasligatedandretracted,andtheexposedtissuewasbathedwithwarmmineraloil.Theelectrocardiogramwascontinuouslymonitoredandtherectaltemperaturewasmaintainedatabout37℃byusingaheatingpadthroughouttheexperiment.1.4抗混合物的定义ExtracellularactivityfromPBNneuronwasisolatedusingaglassmicroelectrodefilledwith2%pontamineskybluein0.5mol/Lsodiumacetate(5~10MΩ).Duringthesearchprocedure,thegustatoryneuronwasidentifiedbyapplyingtothetonguewithamixtureoffourstandardtastants.Actionpotentialswererecordedthroughconventionalphysiologicalequipmentsconsistingofapreamplifier(MEZ-8201,NihonKohden,Japan),cathode-rayoscilloscope(VC-10,NihonKohden,Japan),recordingsystem(PowerLab/4SP,ADInstruments,Australia),andmicrocomputer(iMac,USA).Uniformamplitudeandwaveformwereusedasthecriteriaforisolationofsingleunit.Onceacellwasidentifiedasatasteresponsiveneuron,gustatoryresponsesweretestedrepeatedlybeforeandaftertheantagonistmicroinjection,andagainafterrecovery.Peri-stimulustimehistograms(PSTHs)weremadebymeansofacomputersystem.1.6规训程序4:respese,etity,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,tuning,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,ets,eta的合成,以respityNeuralresponsetoatastestimuluswascalculatedbysubtractingthe5sdischargeratetowaterfromits5sdischargeratetoeachstimulus,beginningwiththeonsetofastimulusinfusion.Anincreaseinfiringrateinthefirst5softhestimuluspresentationthatexceededthespontaneousspikebyatleast50%wasdefinedasaresponse.Tocomparetheeffectsofthepharmacologicalmanipulations,thetasteresponsesfollowingthedrugapplicationwerecomparedwiththatbeforeapplication.Theneuronswereclassifiedasinhibitedoraugmentediftheseresponsemeasuresdifferedfromtheircorrespondingcontrolratesby<20%or>20%,respectively.Basedonitsresponsetoastandardconcentrationofeachofthefoursapidchemicals,eachneuronwascategorizedaccordingtoitsbeststimulus.Sincethemainresponseinbest-stimuluscategoryplaysamoreimportantroleintastecoding,theeffectsofCNQXmicroinjectedintotheCeAontheresponseinbest-stimuluscategorieswereexamined.Toassesstheacross-unitdifferencesamongstimuli,thePearsonproduct-momentcorrelationsacrossstimuliweredeterminedforPBNunitswithandwithoutCNQXmicroinjections.Asanindicationofthebreadthoftuning,anuncertaintymeasurewascalculatedwiththefollowingformula:H=-1.661ΣpIlogpI,wherepIistheproportionoftheresponsetoeachofthestimuliagainstthetotalresponsetoallthestimuli.One-wayANOVAwasappliedwhereitwasappropriateforcomparisonofneuralresponses.Allaverageswereindicatedasthemean±SEM.DataanalysiswasmadebyusingSPSS,andP<0.05wasconsideredsignificant.1.7非生物c.n.相关因子Aftertherecordingsession,acathodeDCcurrent(10~20µA,10~20min)waspassedthroughtherecordingelectrodeinordertodepositadyemark.Thelociofthedyespotswereestablishedhistologically.Theextentsofthedrugadministrationwereobservedfromanterior,medialandposteriorsections.Toidentifythelocusoftheinjectioncannulas,0.5µlofasolutionofPontamineSkyBluedyewasinfusedthroughasimilarinjectioncannulabeforeratswerekilled.TheratswerethengivenanoverdoseofurethanandtranscardiallyperfusedwithPBSfollowedby10%bufferedformalin.Thebrainswereremoved,cutcoronallyin40µmsectionswithafreezingmicrotome,andstainedwithneutralred.2wreng-reefficivumTheexperimentaldatawerefinallyanalyzedfrom33animals,inwhichthemicroinjectionsiteswerefoundtobecorrectlyplacedwithintheCeA.Thedataof21ratswereexcludedbecauseofwrongplacementofthemicroinjectionsites.Figure1illustratestheseinjectionsites.TasteresponsiveneuronswererecordedfromthemedialandlateralPBNandwithinthebrachiumconjunctivum.2.1inpch-pcr反应Theapplicationof0.5µgCNQXinhibitedtheresponsestothecurrentstimulationoftonguein4outof10PBNneuronstested.Thedurationofdrugeffectwasabout10minintheneurons,andtheycompletelyrecoveredin20min(Fig.2B).Acrossthe4cells,themeanfiringrateovera10-minperiodbeforedruginjectionwas(15.19±1.78)Hz,whichsignificantlydecreasedto(9.92±1.03)Hz(F1,7=6.58,P<0.05).Theother6neuronsrecordedshowednochangesafterCNQXinjectionsandPBSinjectionhadnoeffect(Fig.2A).2.2inpch-pcr-4,3,4.3,4.3,4.3,4.3,4.3,4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,3.4.3,....,................3.3,............................Amongthe33tasteneurons,thespontaneousactivitiesof8neuronswereinhibitedafterCNQXadministration.Meanspontaneousfiringrate[(2.91±0.47)Hz]ofthePBNunitsafterCNQXmicroinjectionwassignificantlylowerthanthat[(4.59±0.64)Hz]beforeinjection(F(1,65)=4.46,P<0.05).Ofthe33PBNtasteneuronsobserved,30respondedtoNaCl,25toHCl,18toQHCl,and13tosucrose.Themeanspike[(10.85±0.82)Hz]tofourbasictastantsfollowingCNQXinjectionsignificantlyreducedcomparedwiththat[(14.36±1.14)Hz]beforedruginjection(F(1,263)=6.23,P<0.05).AfterCNQXapplication,theresponsestoHCl[(12.25±1.37)Hz]andtoQHCl[(6.77±0.85)Hz]wereinhibitedwiththemagnitudessignificantlylowerthanthose[(17.36±2.12)Hzand(10.63±1.65Hz)]obtainedbeforeinjections(P=0.047andP=0.042,respectively).HowevertherewasnosignificantdifferencebetweentheresponsestoNaClandsucrose(Fig.3).Byusingtheuncertaintymeasurement,itindicatedthatthebreadthoftuningwasnotsignificantchangedbefore(0.71±0.05)andafter(0.68±0.04)CNQXinjection.Todeterminetherecoverycourse,thegustatoryresponsesofPBNneuronswerealsoobservedin25minafterdruginjection.Theresultsshowedthatin25minafterCNQXadministration,allactivitiesofPBNtasteneuronsrecovered.Fig.4showsanexampleofonePBNtasteneuronbefore,immediatelyafter,and25minafterCNQXinjectionintotheCeA.Itcanbeseenthatallresponsemagnitudestofourbasictastestimulirecoveredtothebasiclevelintheperiodof25minafterdrugapplication.Basedontheirlargestresponsestothefoursapidstimuli,ofthe33PBNtasteneurons,15wereNaCl-best,10HClbest,5QHCl-bestand3sucrose-best.Accordingtothebest-stimuluscategory,afterCNQXinjection40%NaClbest(6/15),30%HCl-best(3/10)and20%QHCl-best(1/5)neuronsdecreasedtheirresponsestoatleastonebasictastestimulusafterAMPAreceptorswereblocked.ThegustatoryresponsesofNaCl-,HCl-,QHCl-,andsucrosebestneuronsbeforeandafterCNQXinjectionswerecalculatedrespectively(Table1).InHCl-bestandQHCl-bestneruons,themainresponseswereinhibitedwiththefiringratesignificantlyreducingfrom(23.68±2.74)Hzand(25.92±3.41)Hzto(13.94±1.55)Hzand(12.56±1.92)Hz(P<0.01),respectively.Toassessthesimilarityoftheneuronalresponsepatternsevokedbythetastestimuli,thePearsonproductmomentinterstimuluscorrelationswereanalyzed.AsshowninTable2,thecorrelationsbetweentheNaClandtheotherthreetastantsdecreasedafterCNQXinfusionintotheCeAInterstimuluscorrelationsamongtheothertastantswerecomparablebeforeandafterCNQXinjection.3u3000cea标准Inthepresentstudy,thespontaneousactivityandthetasteresponsewereinhibitedinsomePBNneuronsafterCNQXmicroinjectionintotheCeA,andtheresponsestoHClandtoQHCldecreasedwiththemagnitudesbeingsignificantlylowerthanthosebeforeinjection.Accordingtothebest-stimuluscategory,afterCNQXinjection40%NaCl-best,30%HCl-bestand20%QHCl-bestneuronsdecreasedtheirresponsesafterAMPAreceptorswereblocked.InHCl-bestandQHCl-bestneruons,themainresponseswereinhibitedrespectivelyafterdrugmicroinjection.AnalysisofPearsonproduct-momeninterstimuluscorrelationsrevealedthatcorrelationsbetweenNaClandtheotherthreetastantsdecreasedafterCNQXinfusionintotheCeA,suggestingthattheCeAinjectionmakestheresponsetoNaClmoresalientamonggustatoryresponses.TheresultsofthepresentstudysuggestthatglutamateisanexcitatoryneurotransmitterintheprocessingoftasteinformationbetweentheCeAandPBN.PreviousstudieshavedemonstratedthatCeAcanmodulatethegustatoryresponsesinthePBNbyelectricalstimulationandelectrolyticlesionsoftheCeA.Immunohistochemicalstudieshaveshownmanyglutamateimmunoreactiveneuronsintheamygdaloidcomplex,includingtheCeA.Thereissubstantialevidencethatglutaminergictransmissioninthecentralnervoussystemplaysanimportantroleintheneuralmechanismoftasteformation.AMPAreceptorsplayanimportantroleininformationprocessingandtherebycontributetotheworkingtastefunction.ThepresentresultssuggestthatthedescendingmodulationfromCeAtoPBNmaybemediatedpartlythroughAMPAreceptorHowever,wecannotexcludethepossibilitythattheexcitatoryafferentintheCeAwasblockedfollowingCNQXapplication.Inthepresentstudy,thespontaneousandtaste-evokedactivitiesinpartofthePBNneuronsreducedfollowingtheinjectionofCNQXintotheCeA.Itsuggeststhattheremaybeglutamate-medicatedexcitatoryinputfromtheCeAtothePBN,and/orsomesynapsetransmissionswithintheCeAwereblockedsothattheresponsesofthePBNneuronswereaffected.OurpreviousstudyshowedthattheCeAstimulationmainlydecreasedtheresponsesofPBNneurontoaversivetastestimuli,whiletheCeAlesionsmainlyincreasedtheseresponses.However,wealsoobservedsomeoppositeeffects.Forexample,CeAstimulationexcitedafewofPBNneurons.SointheCeAtheremaybeexistdirectorindirectexcitatoryprojectionstoPBNortheCeAinfluencesthePBNneuronsviasomeotherforebrainregionsbecausetheamygdalaconnectsnotonlywiththePBNbutalsowithothertaste-responsiveregions,suchasIGCandhypothalamus.ThesenucleicanindirectlymodulateorinfluencethegustatoryresponsesofthePBN.Additionally,anindirecteffectmightbeappliedtothePBNviaforebraininputtoNST.CNQX(Sigma-AldrichCompany),aselectiveAMPAreceptorantagonist,wasdissolvedin99.5%dimethylsulfoxide(DMSO)(Sigma-AldrichCompany),andthendilutedwithPBS(pH=6.8)toachieveafinalconcentrationof0.5µg/0.5µlCNQX.Thetipofthemicroinjectiontubeprotruded1.0mm
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