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圍產(chǎn)期低劑量雙酚AF暴露對(duì)成年子代小鼠認(rèn)知功能的影響及其性別效應(yīng)研究摘要:
目的:探討圍產(chǎn)期低劑量雙酚AF(BPA)暴露對(duì)成年子代小鼠認(rèn)知功能的影響及其性別效應(yīng)。
方法:雌性和雄性C57BL/6J小鼠在懷孕期和哺乳期分別暴露于0、10或100μg/kgBPA。子代小鼠在青春期和成年期分別完成行為學(xué)測(cè)試,分析其識(shí)別記憶能力、空間記憶能力、情緒行為等方面的表現(xiàn)。同時(shí),采集大腦組織,檢測(cè)甲基化水平和相關(guān)基因表達(dá)。
結(jié)果:BPA暴露組小鼠在識(shí)別記憶測(cè)試中表現(xiàn)出遲鈍,空間記憶測(cè)試和情緒行為測(cè)試結(jié)果變化不明顯。同時(shí),BPA暴露組小鼠的海馬區(qū)和前額葉皮質(zhì)DNA甲基化水平明顯升高,與控制組相比,基因表達(dá)也發(fā)生了變化。性別效應(yīng)驗(yàn)證表明,雌性小鼠對(duì)BPA的敏感性較高,表現(xiàn)出更為明顯的識(shí)別記憶下降和神經(jīng)發(fā)育異常。
結(jié)論:圍產(chǎn)期低劑量BPA暴露能夠影響子代小鼠認(rèn)知功能和神經(jīng)發(fā)育,這種影響表現(xiàn)出性別效應(yīng)。這些發(fā)現(xiàn)為環(huán)境因素與神經(jīng)發(fā)育疾病的關(guān)聯(lián)提供了新的證據(jù)。
關(guān)鍵詞:低劑量雙酚AF,子代小鼠,認(rèn)知功能,性別效應(yīng),環(huán)境因素
Abstract:
Objective:Toinvestigatetheeffectsofperinatallow-dosebisphenolA(BPA)exposureoncognitivefunctioninadultoffspringmiceanditsgendereffects.
Method:PregnantandlactatingfemaleandmaleC57BL/6Jmicewereexposedto0,10or100μg/kgBPA,respectively.Theoffspringmicecompletedbehavioraltestsinthejuvenileandadultstagestoanalyzetheirperformanceinrecognitionmemory,spatialmemory,andemotionalbehavior.BraintissuewasalsocollectedtodetectDNAmethylationlevelsandrelatedgeneexpression.
Result:TheBPAexposuregroupshowedcognitiveimpairmentinrecognitionmemorytests,butnosignificantchangeswereobservedinspatialmemorytestsandemotionalbehavior.Meanwhile,thehippocampalandfrontalcortexDNAmethylationlevelsintheBPAexposuregroupweresignificantlyincreased,andgeneexpressionchangeswereobservedcomparedtothecontrolgroup.ThegendereffectsverificationshowedthatfemalemiceweremoresensitivetoBPA,exhibitingmoresignificantcognitiveimpairmentsandabnormalneurodevelopment.
Conclusion:Perinatallow-doseBPAexposurecanaffectcognitivefunctionandneurodevelopmentinoffspringmice,showinggendereffects.Thesefindingsprovidenewevidencefortheassociationbetweenenvironmentalfactorsandneurodevelopmentaldisorders.
Keywords:BisphenolA,Offspringmice,Cognitivefunction,Gendereffects,EnvironmentalfactorsTheuseofBisphenolA(BPA)inthemanufacturingofplasticproductshasbecomeaseriouspublichealthconcern.WhileseveralstudieshavedemonstratedtheadverseeffectsofBPAexposureonvariousbodysystems,particularlythenervoussystem,thegender-specificneurotoxiceffectsofperinatallow-doseexposuretoBPAarestillunclear.
Inarecentstudy,researchersinvestigatedthegender-specificeffectsofperinatallow-doseBPAexposureoncognitivefunctionandneurodevelopmentinoffspringmice.TheresultsshowedthatfemalemiceweremoresusceptibletoBPAexposure,exhibitingmoresignificantcognitiveimpairmentsandabnormaldevelopmentoftheirnervoussystemcomparedtomalemice.
Thestudyfindingsprovidenewevidenceforthepotentialassociationbetweenenvironmentalfactors,particularlyBPAexposure,andneurodevelopmentaldisorders.Theresultsdemonstratetheneedforfurtherresearchtoinvestigatethepossiblegender-specificmechanismsunderlyingtheneurotoxiceffectsofBPAandotherenvironmentalfactors.Furthermore,thefindingssupporttheimportanceofreducinghumanexposuretoBPAandotherhazardouschemicalstoprotectthedevelopingnervoussystemofoffspringInadditiontoBPA,thereareotherenvironmentalfactorsthathavebeenlinkedtoneurodevelopmentaldisorders,suchaslead,mercury,andpesticides.Thesechemicalshavebeenshowntoalterbraindevelopmentandfunction,leadingtocognitiveandbehavioraldeficits.Furthermore,exposuretothesechemicalsduringcriticalperiodsofbraindevelopment,suchasgestationandearlychildhood,mayhavelastingeffectsonbrainhealthandfunction.
LeadexposurehasbeenassociatedwithdecreasedIQandattentiondeficitsinchildren.Childrenexposedtohighlevelsofleadcanalsoexhibithyperactivityandaggressivebehavior.Mercuryexposurecanleadtocognitivedeficits,particularlyinlanguage,memory,andattention.Prenatalexposuretopesticideshasbeenlinkedtodevelopmentaldelaysandautismspectrumdisorders.
Inadditiontochemicals,otherenvironmentalfactors,suchasmaternalstressandmalnutrition,canalsoimpactneurodevelopment.Maternalstressduringpregnancyhasbeenassociatedwithbehavioralandcognitiveproblemsinchildren.Poormaternalnutritioncanleadtomalformationofthedevelopingbrainandimpairedcognitivefunction.
Overall,thesefindingshighlighttheimportanceofidentifyingandreducingexposuretoenvironmentalfactorsthatcanimpactneurodevelopment.Thisincludesreducingexposuretochemicals,improvingnutritionduringpregnancy,andminimizingmaternalstress.Futureresearchshouldcontinuetoinvestigatethemechanismsunderlyingtheneurotoxiceffectsofenvironmentalfactors,particularlywithregardstogender-specificeffects.Byreducingexposuretohazardouschemicalsandotherenvironmentalfactors,wecanprotectthedevelopingnervoussystemandimproveneurodevelopmentaloutcomesforchildrenInadditiontotheenvironmentalfactorsdiscussedabove,thereareseveralotherfactorsthatcanimpactneurodevelopment.Theseincludegenetics,culturalandsocioeconomicfactors,andearlylifeexperiences.
Geneticsplayacriticalroleinneurodevelopment,notonlyindeterminingachild’sbasictraitsbutalsoinshapingthewaythebraindevelopsandfunctions.Recentadvancesingeneticresearchhaveledtonewinsightsintothegeneticsofneurodevelopmentaldisorderssuchasautism,schizophrenia,andintellectualdisability.Understandingthecomplexinterplaybetweengeneticsandenvironmentalfactorsiscrucialforadvancingourunderstandingofhowthebraindevelopsandhowwecanbestsupporthealthyneurodevelopmentinchildren.
Culturalandsocioeconomicfactorscanalsoplayasignificantroleinshapingneurodevelopment.Poverty,forexample,isassociatedwitharangeofnegativeoutcomesforchildren,includingreducedcognitiveandsocial-emotionaldevelopment.Childrenfromlow-incomefamiliesarealsomorelikelytoexperienceenvironmentalstressorssuchasexposuretoviolence,whichcanfurtherimpactneurodevelopment.
Earlylifeexperiences,includingthosethatoccurduringpregnancyandinfancy,canalsohaveaprofoundimpactonneurodevelopment.Stressfulortraumaticexperiencesduringtheseearlystagesoflifehavebeenlinkedtoarangeofnegativeoutcomes,includingincreasedriskofneurodevelopmentaldisordersandmentalhealthproblemslaterinlife.Conversely,positiveearlyexperiencessuchasresponsivecaregivingandenrichedenvironmentscansupporthealthyneurodevelopmentandpromoteresilienceinchildren.
Inconclusion,neurodevelopmentisacomplexandmultifacetedprocessthatisshapedbyarangeofenvironmental,genetic,andexperientialfactors.Whileth
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