Identification and Repair of Novel Axonal Pathology in Demyelinating Disease
Identification and Repair of Novel Axonal Pathology in Demyelinating Disease
批准号:
8998612
负责人:
Jeffrey L. Dupree
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-04-01 至 2019-03-31
关键词:
Action PotentialsAffectAxonBlurred visionCellsCentral Nervous System DiseasesCognitive deficitsDataDemyelinating DiseasesDemyelinationsDiseaseDisease ProgressionEventExperimental Autoimmune EncephalomyelitisFunctional disorderHealthImpaired cognitionInflammationInflammatoryLimb structureLocationMediatingMicrogliaModelingMolecularMotorMultiple SclerosisMyelinNeocortexNeuronsNumbnessOnset of illnessPathologicPathologyPlayProteinsRanvier&aposs NodesReportingResolutionRoleSensoryStagingStructureTeenagersTestingThinkingTimeVeteransWorkabstractingaxonal degenerationbasecell injurycell typechronic demyelinationdesignfunctional lossloss of functionmotor deficitneuron lossnovelrepairedwhite matter
中文摘要
描述(由申请人提供):
英文摘要
DESCRIPTION (provided by applicant):
Project Summary/Abstract Multiple sclerosis is a devastating disease of the central nervous system that affects thousands of US veterans. MS frequently initially presents as temporary tingling or numbness in extremities or blurred vision. However, with time these "events" result in an accumulation of deficits leading to irreversible motor, sensory and cognitive dysfunction. Presently, there are no cures for MS. Treatment are available but their efficacy is highly variable
and loss of motor function appears irreversible. Although classically described as a demyelinating disease, more recent studies have shown that axonal pathology is prevalent in MS and that this axonal pathology may be responsible for the irreversible loss of function associated with the disease. Here, we present strong preliminary data that challenge this view of MS. We show that a specific domain along the axon, known as the axon initial segment is structurally disrupted independent of demyelination indicating that axonal pathology in MS is a primary event and not merely consequential to demyelination. Structural disruption of the axon initial segment is functional devastating to the CNS since it is within the initial segment where i is decided whether an action potential will be generated. If our hypothesis is current, then disease onset does not parallel demyelinating episodes but occurs significantly earlier. Although our findings could revolutionize the view of MS onset, more importantly, we present strong preliminary data that disruption of the axon initial segment is reversible. Presently, we provide morphologic data suggesting reversibility. In this proposal we will test functional reversibility. Together, the studies outlined in this proposal are designed to challenge the current thinking of MS onset and the pathologic mechanisms that mediate the earliest stages of the disease. Moreover, we will further investigate the possibility that dysfunction that results form MS is reversible.
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会议论文
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依托单位:
海外基金