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Gene Transfer for Prevention of Diabetic Neuropathy

Gene Transfer for Prevention of Diabetic Neuropathy
预防糖尿病神经病变的基因转移
批准号:
7618659
负责人:
DAVID J. FINK
金额:
$33.25万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-07-23 至 2013-04-30
关键词:
Adverse effectsAfferent NeuronsAgeAnalgesicsAnimal ModelAnimalsAutonomic DysfunctionBehavioralBinding SitesBiological AssayC FiberCell DeathCisplatinCodeComplicationComplications of Diabetes MellitusDNADNA Binding DomainDataDetectionDevelopmentDiabetes MellitusDiabetic NeuropathiesDiabetic PolyneuropathiesDiabetic mouseDiseaseDoseElementsEngineeringEnzyme-Linked Immunosorbent AssayErythropoietinEventFiberFunctional disorderFundingGene ExpressionGene TransferGenesGenetic ModelsGenetic TranscriptionGenomicsGreen Fluorescent ProteinsHSV vectorHeterodimerizationHistologicHomebound PersonsHomologous GeneHumanHyperglycemiaImmunophilinsImmunosuppressive AgentsIn VitroInjection of therapeutic agentInsulin-Dependent Diabetes MellitusKineticsLifeLigationLipidsMeasuresMediatingMediator of activation proteinModelingMonitorMotorMusNTF3 geneNerveNerve FibersNerve Growth FactorsNervous system structureNeural ConductionNeurogliaNeurologic DeficitNeuronsNeuropathyNeurotrophin 3Non-Insulin-Dependent Diabetes MellitusOutcome MeasurePan GenusPathogenesisPeptidesPeripheralPeripheral NervesPeripheral Nervous SystemPharmacologic SubstancePhase I Clinical TrialsPhosphotransferasesPolyneuropathyPreventionProteinsRNARattusRecombinantsResearch DesignReverse Transcriptase Polymerase Chain ReactionReverse TranscriptionRodentSensorySimplexvirusSkinSolutionsSpinal CordSpinal GangliaSpinal nerve structureStaining methodStainsStimulusStreptozocinStreptozocin DiabetesSurfaceSystemTacrolimus Binding ProteinsTestingTimeTissuesToxic effectTransgenesTranslationsTropismVascular Endothelial Growth FactorsWithdrawalWorkafferent nerveautonomic neuropathybasebehavior measurementdb/db mousediabeticdiabetic patienteffective therapyexpression vectorfootgene transfer vectorhuman diseasein vivomouse modelnerve supplyneurotrophic factornovelpainful neuropathypre-clinicalpreclinical studypreventpromoterprotective effectpublic health relevancepyridoxinereceptorresearch studyresponsesecondary outcomesmall moleculesubcutaneoustransgene expressiontype I and type II diabetesvector

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中文摘要
翻译
描述(由申请人提供):我们已经开发出基于单纯疱疹病毒(HSV)的重组、复制能力不强的基因组载体,用于将基因转移到神经系统。在之前的资助期间,我们已经证明了HSV介导的神经营养素-3(NT-3)、血管内皮生长因子(VEGF)或促红细胞生成素(EPO)在体内背根节(DRG)的表达可以预防链脲佐菌素(STZ)诱导的糖尿病小鼠神经病变的进展。在这次相互竞争的更新中,我们将继续利用HSV载体对周围感觉神经元(DRG)的自然取向,以进一步测试假设,即通过基于HSV的载体将神经保护因子的基因转移到DRG可以用于防止糖尿病神经病变的进展,最终目的是开发一种治疗人类神经病变的有效方法。描述了四个具体目标。(1)确定单纯疱疹病毒(HSV)介导的神经保护因子的表达是否能防止1型糖尿病链佐菌素模型中DRG神经元的丢失;(2)检测HSV介导的神经保护因子表达在2型糖尿病db/db小鼠模型中的治疗作用;(3)构建具有可调控开关的载体,以安全地控制转基因表达;以及(4)检测间歇调节保护因子表达对STZ糖尿病和db/db小鼠糖尿病神经病变进展的影响。公共卫生相关性:神经病变是1型和2型糖尿病的一种重要且经常致残的并发症,目前还没有有效的治疗方法来有效地防止并发症的发展。这些研究旨在开发可用于有效治疗这种疾病的新型药物。
英文摘要
DESCRIPTION (provided by applicant): We have developed recombinant, replication-incompetent, genomic herpes simplex virus (HSV)-based vectors for gene transfer to the nervous system. In the previous period of funding we have demonstrated that HSV- mediated expression of neurotrophin-3 (NT-3), vascular endothelial growth factor (VEGF), or erythropoietin (EPO) in dorsal root ganglion (DRG) in vivo prevents the progression of neuropathy in mice with streptozotocin (STZ)-induced diabetes. In this competing renewal, we will continue to exploit the natural tropism of HSV vectors for peripheral sensory neurons of the (DRG) to further test the hypothesis that gene transfer of neuroprotective factors to the DRG by means of an HSV-based vector can be used to prevent the progression of diabetic neuropathy, with the ultimate aim of developing a therapy that will be effective for the treatment of human neuropathy. Four specific aims are described. (1) to determine whether HSV-mediated neuroprotective factor expression prevents the loss of DRG neurons in the streptozocin model of type 1 diabetes; (2) to examine the effect of HSV-mediated delivery of neuroprotective factors in the treatment of diabetic neuropathy in the db/db mouse model of type 2 diabetes; (3) to construct a vector with a regulatable switch to control transgene expression safely; and, (4) to test the effect of intermittent regulated protective factor expression on the progression of diabetic neuropathy in the STZ-diabetic and db/db mouse. PUBLIC HEALTH RELEVANCE: Neuropathy is an important and often disabling complication of both type 1 and type 2 diabetes mellitus, and there are no currently available treatments that are effective in preventing the progression of the complication. These studies are designed to develop novel agents that could be used to treat the disease effectively.
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Regulatable Gene Expression for Prevention of Neuropathy
  • 批准号:
    8540668
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2013
  • 负责人:
    DAVID J. FINK
  • 依托单位:
Regulatable Gene Expression for Prevention of Neuropathy
  • 批准号:
    8966656
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2013
  • 负责人:
    DAVID J. FINK
  • 依托单位:
Preclinical Development of an NT3-expressing HSV Vector
Preclinical Development of an NT3-expressing HSV Vector
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