The role of TRPM8 and Nav1.8 channels in cold tolerance of hibernators
The role of TRPM8 and Nav1.8 channels in cold tolerance of hibernators
批准号:
9312901
负责人:
Elena Gracheva
金额:
$45.97万
依托单位:
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:
2015-09-15 至 2020-06-30
关键词:
Action PotentialsAcuteAffectAnalgesicsAnimal ModelAnimalsAreaBehavioral ParadigmBioinformaticsBiologicalBiophysicsBloodBody TemperatureCalciumCationsCellular biologyDataDetectionDevelopmentDropsDrug or chemical Tissue DistributionElectrodesElectrophysiology (science)EnvironmentEsthesiaEventGangliaGenomicsGleanGoalsHealthHeart ArrestHibernationHumanImageIn Situ HybridizationIon ChannelKnowledgeLaboratoriesMedicalMentholModelingModificationMolecularMusNeuraxisNeuronsOutcomePainPathologicPathway interactionsPerceptionPeriodicityPharmacologyPhenotypePhysiologic ThermoregulationPhysiologicalPhysiologyPlayProcessPropertyProtein IsoformsRNARNA SplicingRegulationResistanceRodentRoleSensorySignal TransductionSodium ChannelSpermophilusSquirrelStimulusStrokeSystemTRP channelTemperatureTetrodotoxinTherapeuticTraumaVariantallodyniabasebiophysical propertieschemotherapycold temperaturein vivoinsightinterdisciplinary approachnatural hypothermianerve injurynovelnovel strategiespainful neuropathypatch clamppost strokepublic health relevanceratiometricresponsesomatosensorytranscriptomicstransmission processvirtualvoltagevoltage clamp
中文摘要
描述(由申请人提供):热敏性和耐热性是影响人体生理学几乎所有方面的基本过程。人类对寒冷的感觉--从清爽到令人不快和寒冷--依赖于初级感觉传入神经将这些刺激转化为电信号的能力,从而触发适应性的
生物反应。温度感觉失调是冷异常性疼痛的基础,冷异常性疼痛是化疗、神经损伤和中风后引起的神经性疼痛的共同标志,其中即使是轻微的冷却也可以被认为是极度痛苦的。尽管具有重要的医学意义,但在正常、适应性和病理条件下冷感觉的分子方面,以及该过程背后的事件序列仍然是谜和有争议的。将温度敏感性调节到极限的动物提供了理想的模型来描述一般的耐热性和温度感知的细胞和分子方面。我们正在使用哺乳动物冬眠作为自然可逆模型来理解这些过程。与标准的实验室啮齿动物不同,冬眠动物在-2 ° C之前不会感到寒冷的温度不舒服。这种非凡的能力有助于它们在冬眠期间对寒冷的抵抗力,当动物的核心体温下降到2-4°C时。在本研究中,我们的目标是利用多学科方法,包括生理学、成像学、行为学、细胞生物学、差异转录组学、基因组学和生物信息学,在体感系统水平上研究TRPM 8和Nav1.8离子通道对冬眠松鼠冷适应的贡献。
英文摘要
DESCRIPTION (provided by applicant): Thermosensitivity and thermotolerance are fundamental processes that affect virtually all aspects of human physiology. Human sensation of cold - ranging from refreshingly cool to unpleasant and frigid - relies on the ability of primar sensory afferents to transduce these stimuli into electrical signaling, thereby triggering adaptive
biological response. Dysregulation of thermosensation underlie cold allodynia - a common hallmark of chemotherapy-, nerve injury- and post-stroke-induced neuropathic pain, in which even mild cooling can be perceived as excruciatingly painful. Despite significant medical relevance, the molecular aspects of cold sensation under normal, adaptive and pathological conditions, and the sequence of events that underlies this process still remain enigmatic and controversial. Animals that tune temperature sensitivity to the extreme provide ideal model to delineate cellular and molecular aspects of thermotolerance and temperature perception in general. We are using mammalian hibernation as a naturally-reversible model to understand these processes. Unlike the standard laboratory rodents, hibernating animals do not perceive cold temperature as uncomfortable until -2°C. This remarkable ability contributes to their unusual resistance to cold during hibernation, when the animals drop their core body temperature to 2-4°C. In this proposal, we are aiming to examine contribution of TRPM8 and Nav1.8 ion channels into cold adaptations in hibernating squirrels at the level of somatosensory system using multi-disciplinary approach, including physiology, imaging, behavioral paradigms, cell biology, differential transcriptomics, genomics and bioinformatics.
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会议论文
Molecular and cellular basis of reversible hypothermia
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批准号:10583822
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项目类别:
-
资助金额:$51.53万
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财政年份:2022
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负责人:Elena Gracheva
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依托单位:
The role of TRPM8 and Nav1.8 channels in cold tolerance of hibernators
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批准号:9026719
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项目类别:
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资助金额:$35.55万
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财政年份:2015
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负责人:Elena Gracheva
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依托单位:
海外基金