课题基金 / 基金详情

ABLATION OF HYPOTHALAMIC POMC/CART NEURONS

ABLATION OF HYPOTHALAMIC POMC/CART NEURONS
下丘脑 POMC/CART 神经元的消融
批准号:
6397745
负责人:
Suzanne M Appleyard
金额:
$4.02万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
未结题
起止时间:
2001-04-01 至

项目摘要

项目成果

Suzanne M Appleyard的其他基金

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中文摘要
翻译
肥胖症是美国的一个主要健康问题,影响着大部分人口。 它可能导致严重的疾病,如心力衰竭,中风和糖尿病。 需要更详细地了解体重的稳态调节,以找到预防和治疗这种严重疾病的最佳方法。 下丘脑中的POMC神经元已被证明在体重稳态中起关键作用。黑皮质素抑制进食,并且对于适当的体重稳态是必不可少的,因为黑皮质素信号传导缺陷的小鼠是肥胖的。 β-内啡肽对体重平衡的影响尚不清楚。 令人惊讶的是,我们的初步结果表明,缺乏β-内啡肽的小鼠也会肥胖。 这项资助的第一个目标是建立β-内啡肽缺陷小鼠肥胖的机制,并确定这种肥胖是否与MC 4受体缺陷小鼠相加。 NPY调节从这些神经元释放α-MSH和β-内啡肽,并且已经显示阿片样物质拮抗剂阻断NPY刺激的食物摄入。 因此,我们计划检验β-内啡肽是NPY作用所必需的假设,并预测缺乏β-内啡肽的小鼠将缺乏NPY刺激的进食。腹侧基底下丘脑对体重稳态和高水平的瘦素受体表达具有抑制作用。POMC和NPY神经元在该区域都有胞体,并表达瘦素受体。 除了黑皮质素,POMC神经元还表达CART,这是一种有效抑制进食的递质,预计在体重稳态中起重要作用,以及潜在的未识别递质。我们推测,除了黑皮质素,POMC神经元中的其他递质对体重稳态和瘦素作用也很重要。 为了测试这一点,我们建议通过特异性消融成年小鼠的POMC神经元来去除通过这些POMC神经元的所有信号。 然后将这些小鼠中的体重稳态和瘦素功能与仅缺乏POMC信号传导的小鼠进行比较。
英文摘要
Obesity is a major health problem in the United States affecting a large portion of the population. It can lead to serious diseases such as heart failure, stroke and diabetes. A more detailed understanding of the homeostatic regulation of weight is required to find the best method of both preventing and treating this serious disease. POMC neurons in the hypothalamus have been demonstrated to play a critical role m weight homeostasis. Melanocortins inhibit feeding and are essential for appropriate weight homeostasis as mice deficient in melanocortin signaling are obese. The effects of beta-endorphin on weight homeostasis are less clear. Surprisingly, our preliminary results indicate that mice lacking beta-endorphin are also obese. The first goal of this grant is to establish the mechanism of the obesity in beta-endorphin deficient mice and to determine whether this obesity is additive with MC4 receptor deficient mice. NPY modulates the release of alpha-MSH and beta-endorphin from these neurons, and opioid antagonists have been shown to block NPY stimulated food intake. We therefore plan to test the hypothesis that beta-endorphin is required for the action of NPY and predict that mice lacking beta-endorphin will be deficient in NPY- stimulated feeding. The ventrobasal hypothalamus has an inhibitory tone on weight homeostasis and high levels of expression of leptin receptors. Both POMC and NPY neurons have cell bodies in this region and express leptin receptors. In addition to the melanocortins, POMC neurons also express CART, a transmitter shown to potently inhibit feeding and predicted to play an important role in weight homeostasis, as well as potentially unidentified transmitters. We hypothesize that other transmitters in the POMC neurons, aside from the melanocortins, are important for weight homeostasis and leptin action. To test this, we propose to remove all signaling through these POMC neurons by specifically ablating the POMC neurons in adult mice. Weight homeostasis and leptin function in these mice will then be compared to mice deficient solely in POMC signaling.
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Integration of Peripheral and Central Appetite Signals by Brainstem Neurons
  • 批准号:
    9210080
  • 项目类别:
  • 资助金额:
    $33.98万
  • 财政年份:
    2009
  • 负责人:
    Suzanne M Appleyard
  • 依托单位:
Integration of Peripheral and Central Appetite Signals by Brainstem Neurons
  • 批准号:
    8052786
  • 项目类别:
  • 资助金额:
    $25.64万
  • 财政年份:
    2009
  • 负责人:
    Suzanne M Appleyard
  • 依托单位:
Integration of Peripheral and Central Appetite Signals by Brainstem Neurons
  • 批准号:
    8888987
  • 项目类别:
  • 资助金额:
    $33.98万
  • 财政年份:
    2009
  • 负责人:
    Suzanne M Appleyard
  • 依托单位:
Integration of Peripheral and Central Appetite Signals by Brainstem Neurons
  • 批准号:
    8583361
  • 项目类别:
  • 资助金额:
    $0.15万
  • 财政年份:
    2009
  • 负责人:
    Suzanne M Appleyard
  • 依托单位: