TRH and Energy Homeostasis
TRH and Energy Homeostasis
批准号:
7066642
负责人:
RONALD Michael LECHAN
金额:
$22.46万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-06-01 至 2008-05-31
关键词:
bioenergeticsbrain mappingcell population studygenetically modified animalsgreen fluorescent proteinshormone regulation /control mechanismlaboratory mouseleptinneural information processingneuroendocrine systemparaventricular nucleussuid alphaherpesvirus 1thyrotropin releasing hormonetransfection /expression vector
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Thyrotropin-releasing hormone (TRH) has an important role in the regulation of energy homeostasis not only through effects on thyroid function, but also on feeding behavior, thermogenesis, and autonomic regulation. We hypothesize that two distinct populations of TRH-producing neurons located in the medial/periventricular vs anterior parvocellular subdivision of the hypothalamic paraventricular nucleus (PVN) have critical roles in a coordinated effort to mediate the effects of TRH on energy homeostasis. To determine how these two TRH neuronal populations are integrated into energy control systems in the brain and elucidate their specific functions, we will develop transgenic mice in which Cre recombinase is selectively targeted to TRH-producing cells. This approach, together with the use of genetically modified pseudorabies virus (PRV) that exploits the Cre-loxP system for conditional replication and expression of the fluorescent marker protein, GFP, will be used to elucidate the complex, multisynaptic circuitries regulating of each of these neuronal groups and their regulation by leptin. In addition, using Cre-lox-site-specific recombination, we propose to construct a PRV derivative that is dependent on a Cre-mediated recombination event for replication, yet unable to infect other adjacent or transsynaptic neuronal populations due to a mutation in gB, a major membrane protein required for membrane fusion and transneuronal passage of virions. Thus, only neurons that express Cre will be targeted for cell death, allowing selective loss of the TRH neuronal population in each defined anatomical region of the PVN without any effects on adjacent populations. The use of these novel "suicide" viruses to selectively ablate TRH neurons in each subdivision of the PVN, will ultimately allow the elucidation of the full gambit of physiologic effects exerted by TRH neurons in the anterior vs medial/periventricular subdivision in the regulation of energy homeostasis, and may become of general value as a new neuroanatomical tool for neuroscience research.
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会议论文
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财政年份:2009
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资助金额:$3.56万
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CART AND THE HYPOTHALAMIC-PITUITARY-THYROID AXIS
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批准号:6629368
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资助金额:$3.66万
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D2 TANTYCYTES IN THE REGULATION OF HPT AXIS
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D2 TANTYCYTES IN THE REGULATION OF HPT AXIS
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批准号:6089907
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CRH STIMULATION W/WO DEXAMETHASONE IN DIAGNOSIS OF CUSHINGS SYNDROME
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依托单位:
PROTRH DERIVED PEPTIDES DURING OPIATE WITHDRAWAL
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资助金额:$36.13万
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依托单位:
PROTRH DERIVED PEPTIDES DURING OPIATE WITHDRAWAL
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批准号:2668169
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资助金额:$33.83万
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财政年份:1997
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依托单位:
PROTRH DERIVED PEPTIDES DURING OPIATE WITHDRAWAL
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财政年份:1994
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负责人:RONALD Michael LECHAN
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依托单位:
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财政年份:1994
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依托单位:
海外基金