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Taste Transduction and its Regulation

Taste Transduction and its Regulation
味觉传导及其调节
批准号:
7172339
负责人:
TIMOTHY A. GILBERTSON
金额:
$23.62万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-08-01 至 2009-02-28

项目摘要

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中文摘要
翻译
描述(由申请人提供):味觉系统的主要作用之一是识别生物体生存所需的营养物质。历史上,味觉系统一直被认为是不灵活的,仅仅报告味觉刺激的存在。然而,最近的证据表明,味觉系统可能受到许多激素的调节,这些激素可能会改变参与营养味觉转导的元素的表达和/或功能。提出的研究的主要目标是探索味觉系统对调节线索(如激素)的反应能力,这些信号可能通过作用于特定的转导元件来调节周围味觉系统。该项目的一个目标是进一步确定参与大鼠味觉细胞中盐和水转导的通道。该项目的第一个目标是验证这样一个假设,即在其他盐和水运输上皮中表达的许多相同的离子通道和水通道也在外周味觉系统中表达。分子生物学、免疫细胞化学和电生理技术将用于确定可能在盐和水转导途径中发挥作用的通道的表达和功能。这些包括鉴定和表征参与钠盐味觉的上皮钠通道(ENaC), CIC家族的氯通道和囊性纤维化跨膜传导调节剂(CFTR),水通道蛋白(AQP)水通道,向内校正钾通道,ROMK1,所有这些都通过初步数据显示存在于哺乳动物味觉细胞中。本研究的第二个目标是研究几种利钠激素(醛固酮、血管加压素和心房利钠肽)调节这些已确定元素的表达和功能的能力。上述通道的一个共同特征是它们受一种或多种这些激素的调节,这些激素在运输上皮时维持帮助盐和水的平衡。我们将验证味觉细胞中促进盐和水运输的转导元件对其他上皮中调节盐和水运动的一种或多种钠性激素作出反应的假设。我们将利用实时荧光定量PCR和电生理记录在大鼠味觉细胞中检测这三种激素对ENaC、CIC、CFTR、AQP和ROMK1相对表达和功能的影响。综上所述,这些研究将有助于进一步阐明哺乳动物味觉细胞中盐和水的转导途径。此外,它应该提供一些第一手的直接证据,证明味觉转导通路中特定元素受激素信号调节的能力,并确定这种调节的机制。这些研究将试图提供直接的证据,证明味觉系统是灵活的,它在帮助维持和恢复营养平衡方面起着积极的作用。
英文摘要
DESCRIPTION (provided by applicant): One of the main roles of the taste system is to identify nutrients an organism needs to survive. Historically, the taste system has been thought of as inflexible, merely reporting the presence of taste stimuli. However, recent evidence suggests that the taste system may be modulated by a number of hormones that may alter the expression and/or function of elements involved in nutrient taste transduction. The primary goal of the proposed studies is to explore the ability of the taste system to respond to regulatory cues, like hormones, that may modulate the peripheral gustatory system by acting on specific transduction elements. One goal of the project is to further identify channels that participate in salt and water transduction in rat taste cells. The first aim of the project will test the hyposthesis that many of the same ion channels and water channels that are expressed in other salt and water transporting epithelia are also expressed in the peripheral gustatory system. Molecular biological, immunocytochemical and electrophysiological techniques will be used to determine the expression and function of channels that may play roles in both salt and water transduction pathways. These include identification and characterization of the epithelial sodium channel (ENaC) involved in sodium salt taste, the chloride channels of the CIC family and the cystic fibrosis transmembrane conductance regulator (CFTR), aquaporin (AQP) water channels, the inward rectifying potassium channel, ROMK1, all that shown to be present in mammalian taste cells by preliminary data. The second goal of the proposed research will investigate the ability of several natriferic hormones (aldosterone, vasopressin and atrial natriuretic peptide) to modulate expression and function of these identified elements. A common feature of the aforementioned channels is that they are regulated by one or more of these hormones that maintain help salt and water balance in transporting epithelia. We will test the hypothesis that the transduction elements that contribute to salt and water transport in taste cells respond to one or more of the natriferic hormones that regulate salt and water movement in other epithelia. Using quantitative real-time PCR and electrophysiological recording in rat taste cells we will examine the ability of these three hormones to alter the relative expression and function of ENaC, CIC, CFTR, AQP and ROMK1. Taken together, these studies should help to further elucidate the transduction pathways for salts and water in mammalian taste cells. In addition, it should provide some of the first direct evidence as to the ability of specific elements in taste transduction pathways to be modulated by hormonal signals and to identify the mechanism underlying such modulation. These studies will attempt to provide direct evidence that the gustatory system is flexible and that it plays an active role in helping maintain and restore nutrient balance.
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Chemosensory pathways in food intake
  • 批准号:
    8636331
  • 项目类别:
  • 资助金额:
    $21.15万
  • 财政年份:
    2013
  • 负责人:
    TIMOTHY A. GILBERTSON
  • 依托单位:
MECHANISMS OF PERIPHERAL FAT DETECTION
  • 批准号:
    7924065
  • 项目类别:
  • 资助金额:
    $34.68万
  • 财政年份:
    2009
  • 负责人:
    TIMOTHY A. GILBERTSON
  • 依托单位:
MECHANISMS OF PERIPHERAL FAT DETECTION
  • 批准号:
    7730887
  • 项目类别:
  • 资助金额:
    $34.75万
  • 财政年份:
    2009
  • 负责人:
    TIMOTHY A. GILBERTSON
  • 依托单位:
MECHANISMS OF PERIPHERAL FAT DETECTION
  • 批准号:
    6616209
  • 项目类别:
  • 资助金额:
    $25.3万
  • 财政年份:
    2000
  • 负责人:
    TIMOTHY A. GILBERTSON
  • 依托单位:
海外基金