Mapping and Serotonergic Regulation of Multiple BDNF Transcript Isoforms in Mice
Mapping and Serotonergic Regulation of Multiple BDNF Transcript Isoforms in Mice
批准号:
7258654
负责人:
ANNE MILASINCIC ANDREWS
金额:
$6.66万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-05-09 至 2009-04-30
关键词:
AccountingAddressAdultAlzheimer&aposs DiseaseAntidepressive AgentsAnxietyAnxiety DisordersAtrophicBehaviorBehavioralBrainBrain DiseasesBrain StemBrain regionBrain-Derived Neurotrophic FactorChronicChronic stressCodeComplexDegenerative DisorderDevelopmentDisruptionDrug abuseEnvironmental Risk FactorEpigenetic ProcessExonsFutureGenbankGene ExpressionGenesGenetic TranscriptionGenetically Engineered MouseHippocampus (Brain)HumanIndividualInvestigationLearningMapsMediatingMemoryMental DepressionMessenger RNAMolecularMusNeuronsNumbersPatternPersonality TraitsPhenotypePlayPopulationPredispositionProtein IsoformsProteinsQuantitative Reverse Transcriptase PCRRNA SplicingRangeRattusRegulationRoleSchizophreniaSeizuresSelective Serotonin Reuptake InhibitorSerotoninSignal PathwaySignal TransductionStressStructureTimeTranscriptTranscriptional RegulationTricyclic Antidepressive AgentsVariantcell typeclinically relevantconditioned feardesignfrontal lobemood regulationmouse modelneurogenesisnovel therapeuticspromoterresponsereuptakeserotonergic regulationserotonin receptorserotonin transportertranscription factor
中文摘要
描述(由申请人提供):了解两种临床相关形式的5-羟色胺再摄取减少对单个BDNF mRNA剪接变体的调节将有助于我们了解BDNF在情绪和焦虑相关行为调节中的作用。这也将有助于我们解决长期的问题,如为什么BDNF受到复杂的转录调控,以及这是如何反映在不同的BDNF蛋白水平在特定的亚区或神经元亚型在精神和退行性脑疾病?最终,我们预计,在不同细胞类型和大脑区域的转录水平上选择性调节BDNF的能力将成为未来开发治疗抑郁症,焦虑症和阿尔茨海默病的新型疗法的有力途径。
英文摘要
DESCRIPTION (provided by applicant): Understanding the modulation of individual BDNF mRNA splice variants by two clinically relevant forms of reduced serotonin reuptake will facilitate our understanding of the role of BDNF in the regulation of mood and anxiety-related behavior. It will also assist us in addressing long-range questions such as why BDNF is subject to complex transcriptional regulation and how this is reflected in different BDNF protein levels in specific subregions or neuronal subtypes in psychiatric and degenerative brain disorders? Ultimately, we anticipate that having the capability to selectively modulate BDNF at the level of transcription in different cell types and brain regions will be a powerful avenue for the future development of novel therapeutics for the treatment of depression, anxiety disorders and Alzheimer's disease.
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会议论文
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Sert Expression and Survival of Serotonin Neurons
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海外基金