Bartzokis_Age-related-myelin-breakdown-a-developmental-model-of-cognitive-decline-and-Alzheimer’s-disease_2004

Bartzokis_Age-related-myelin-breakdown-a-developmental-model-of-cognitive-decline-and-Alzheimer’s-disease_2004

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时间:2019-07-31

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1、NeurobiologyofAging25(2004)518OpenpeercommentaryAge-relatedmyelinbreakdown:adevelopmentalmodelofcognitivedeclineandAlzheimersdiseaseGeorgeBartzokisa,b,c,∗aDepartmentofNeurology,UCLAAlzheimer’sDiseaseCenter,710WestwoodPlaza,Room2-238,LosAngeles,CA90095,

2、USAbLaboratoryofNeuroimaging,DepartmentofNeurology,DivisionofBrainMapping,UCLA,LosAngeles,CA90095,USAcGreaterLosAngelesVAHealthcareSystem,WestLosAngeles,CA90073,USAReceived24January2003;accepted21March2003AbstractAhypotheticalmodelofAlzheimersdisease(A

3、D)asauniquelyhumanbraindisorderrootedinitsexceptionalprocessofmyelinationispresented.CorticalregionswiththemostprotracteddevelopmentaremostvulnerabletoADpathology,andthisprotracteddevelopmentisdrivenbyoligodendrocytes,whichcontinuetodifferentiateintomy

4、elinproducingcellslateintothefifthdecadeoflife.Theuniquemetabolicdemandsofproducingandmaintainingtheirvastmyelinsheathsandsynthesizingthebrainscholesterolsupplymakeoligodendrocytesespeciallysusceptibletoavarietyofinsults.Theirvulnerabilityincreaseswithi

5、ncreasingageatdifferentiationaslater-differentiatingcellsmyelinateincreasingnumbersofaxonalsegments.Thesevulnerablelate-differentiatingcellsdrivetheprotractedprocessofintracorticalmyelinationandbyincreasinglocalcholesterolandironlevels,progressivelyinc

6、reasethetoxicityoftheintracorticalenvironmentformingthebasisfortheageriskfactorforAD.Atolderages,theroughlybilaterallysymmetricalcontinuumofoligodendrocytevulnerabilitymanifestsasaprogressivepatternofmyelinbreakdownthatrecapitulatesthedevelopmentalproc

7、essofmyelinationinreverse.Theensuinghomeostaticresponsestomyelinbreakdownfurtherincreaseintracorticaltoxicityandresultsintherelentlessprogressionandnon-randomanatomicaldistributionofADlesionsthateventuallycauseneuronaldysfunctionanddegeneration.Thispro

8、cesscausesaslowlyprogressivedisruptionofneuralimpulsetransmissionthatdegradesthetemporalsynchronyofwidelydistributedneuralnetworksunderlyingnormalbrainfunction.Theresultingnetworkdisconnectionsfirstimpactfunctionsthataremostdependentonla

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