Energy sensing mechanism of the brain regulating feeding and reproduction

大脑调节摄食和繁殖的能量传感机制

基本信息

  • 批准号:
    14360177
  • 负责人:
  • 金额:
    $ 8.96万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    2002
  • 资助国家:
    日本
  • 起止时间:
    2002 至 2005
  • 项目状态:
    已结题

项目摘要

The present study aimed to understant the energy sensing mechanism in the brain to regulate feeding and reproduction.Glucokinase (GK), an enzyme playing a key role in sensing blood glucose levels, is expressed in the various brain areas. The present study revealed that the transcription start sites of GK gene in the brain areas, such as the wall of the fourth ventricle (4V), hypothalamic ventromedial nucleus, lateral hypothalamus, and raphe obsculus nuclei, were located near the pancreatic-type promoter. Of the above brain areas, the wall of the 4V sowed decreased transcription of the major B1 isoform of GK after the peripheral injection of 2-deoxyglucose, a glucose inhibitor, suggesting that the brain area may sense the decreased availability of glucose at the transcriptional level.Diabetic rats show increased food intake and severe ketosis. The present study revealed that injection of 3-hydroxybutylate (3HB), a ketone body, into the 4V hunger responses, such as increased food intake … More and decreased gonadotropin release in normal rats. Next, we hypothesized that the ependymocytes lining, the 4V sense ketone bodies, as well as glucose, to regulate reproductive functions and feeding behavior. To determine if the increased food intake is mediated by monocarboxylate transporter in the 4V in diabetic rats and if the ependymocytes lining 4V respond to 3HB in vitro, p-Chloromercuri benzese sulphonic acid (pCMBS), a monocarboxylate transporter 1 (MCT1) inhibitor, was injected into the 4V of normal or streptozotocin (STZ)-induced diabetic rats. In addition, in vitro responses of the intracellular calcium concentration ([Ca^<2+>]i) to ketone bodies was determined in dispersed ependymocytes taken from the 4V of normal rats. The results showed that increased food intake was reduced by the administration pCMBS into the 4V in a dose-dependent manner in the diabetic rats. In vitro [Ca^<2+>]i was increased by 3HB in the ependymocytes. Immunohistochemistry showed that MCT1 was located in the 4V ependymocytes. These results suggest that increased food intake is induced by the increased ketone bodies in the circulation. The ependymocytes in the hindbrain may be a ketone body sensor mediating pathological or physiological changes in the food intake. Less
葡萄糖激酶(Glucokinase,GK)是一种在感知血糖水平中起关键作用的酶,它在脑的不同区域均有表达。本研究发现GK基因在第四脑室壁(4V)、下丘脑腹内侧核、下丘脑外侧核和中缝隐核等脑区的转录起始位点位于胰腺型启动子附近。在上述脑区中,在外周注射2-脱氧葡萄糖(一种葡萄糖抑制剂)后,4V区壁的GK主要B1亚型的转录减少,表明该脑区可能在转录水平上感受到葡萄糖可用性的减少。目前的研究表明,注射3-羟基丁酸酯(3 HB),一种酮体,到4V饥饿反应,如增加食物摄入, ...更多信息 正常大鼠促性腺激素释放减少。接下来,我们假设室管膜细胞衬里,4V感觉酮体,以及葡萄糖,调节生殖功能和摄食行为。为探讨糖尿病大鼠4V内单羧酸转运体介导的摄食量增加以及4V内室管膜细胞对3 HB的反应,将单羧酸转运体1(MCT 1)抑制剂对氯汞苯磺酸(pCMBS)注射到正常或链脲佐菌素(STZ)诱导的糖尿病大鼠4V内。此外,在离体条件下测定了正常大鼠4V室管膜细胞内游离钙浓度([Ca^<2+>]i)对酮体的反应。结果表明,在糖尿病大鼠中,通过将pCMBS以剂量依赖性方式施用到4V中来减少增加的食物摄入。在体外实验中,3 HB可增加室管膜细胞[Ca^<2+>]i。免疫组化显示MCT 1定位于4V室管膜细胞。这些结果表明,食物摄入量增加是由循环中酮体增加引起的。后脑的室管膜细胞可能是介导食物摄入的病理或生理变化的酮体感受器。少

项目成果

期刊论文数量(34)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Fourth ventricular alloxan injection suppresses pulsatile luteinizing hormone release in female rats.
第四心室四氧嘧啶注射抑制雌性大鼠脉动黄体生成激素释放。
Moriyama, R.: "Glucoprivation-induced Fos expression in the hypothalamus and medulla oblongata in female rats"Journal of Reproduction and Development. (in press). (2003)
Moriyama, R.:“雌性大鼠下丘脑和延髓中葡萄糖缺乏诱导的 Fos 表达”生殖与发育杂志。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
脳の性分化
大脑的性别分化
  • DOI:
  • 发表时间:
    2006
  • 期刊:
  • 影响因子:
    0
  • 作者:
    山内 兄人;新井 康允(共編著)
  • 通讯作者:
    新井 康允(共編著)
前多敬一郎: "ブルーバックス「生命を操るホルモン」"講談社. 238 (2003)
前田敬一郎:“Bluebacks‘控制生命的激素’”讲谈社 238 (2003)。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Lactation-associated infertility in Japanese monkeys (Macaca fuscata) during the breeding season
日本猴(Macaca fuscata)在繁殖季节与哺乳相关的不孕症
  • DOI:
    10.1002/zoo.10073
  • 发表时间:
    2003
  • 期刊:
  • 影响因子:
    1.3
  • 作者:
    M. Kondo;H. Kishi;C. Kojima;W. Jin;J. Suzuki;K. Shimizu;M. Itoh;S. Ohkura;H. Tsukamura;K. Maeda;G. Watanabe;K. Taya
  • 通讯作者:
    K. Taya
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MAEDA Kei-ichiro其他文献

MAEDA Kei-ichiro的其他文献

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{{ truncateString('MAEDA Kei-ichiro', 18)}}的其他基金

Establishment of transgenic musk shrews (Suncus murinus)
转基因麝鼩(Suncus murinus)的建立
  • 批准号:
    23650233
  • 财政年份:
    2011
  • 资助金额:
    $ 8.96万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Brain energy-sensing mechanism controlling reproduction and food intake.
控制生殖和食物摄入的大脑能量传感机制。
  • 批准号:
    18208025
  • 财政年份:
    2006
  • 资助金额:
    $ 8.96万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Metabolic Control of Reproductive system by the brain
大脑对生殖系统的代谢控制
  • 批准号:
    09044215
  • 财政年份:
    1997
  • 资助金额:
    $ 8.96万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B).
Neuroendocrine mechanism mediating the nutritional infertility
介导营养性不孕的神经内分泌机制
  • 批准号:
    08456151
  • 财政年份:
    1996
  • 资助金额:
    $ 8.96万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Central regulation of luteinizing hormone-releasing hormone release by nitric oxide in female rsts.
女性中一氧化氮对黄体生成素释放激素释放的中枢调节。
  • 批准号:
    06454125
  • 财政年份:
    1994
  • 资助金额:
    $ 8.96万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Analysis of the brain mechanism regulating the reproductive system using small laboratory animals.
利用小型实验动物分析调节生殖系统的大脑机制。
  • 批准号:
    06044101
  • 财政年份:
    1994
  • 资助金额:
    $ 8.96万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Brain mechanism regulating pulsatile secretion of luteinizing hormone-releasing hormone
调节黄体生成素释放激素脉动分泌的脑机制
  • 批准号:
    04660289
  • 财政年份:
    1992
  • 资助金额:
    $ 8.96万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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G6PC 酶学、结构、功能及其在空腹血糖调节中的作用
  • 批准号:
    10584866
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    10588351
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    10827641
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    2023
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    $ 8.96万
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Behavioral and neural measures of oral carbohydrate and sweetener reward signals
口服碳水化合物和甜味剂奖励信号的行为和神经测量
  • 批准号:
    10532978
  • 财政年份:
    2022
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The cellular molecular regulation of differing mechanisms of insulin resistance.
胰岛素抵抗不同机制的细胞分子调节。
  • 批准号:
    10531044
  • 财政年份:
    2022
  • 资助金额:
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The cellular molecular regulation of differing mechanisms of insulin resistance.
胰岛素抵抗不同机制的细胞分子调节。
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  • 批准号:
    10364251
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    2022
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    $ 8.96万
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Biochemical Mechanism of Beta-Cell Destruction
β细胞破坏的生化机制
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Behavioral and neural measures of oral carbohydrate and sweetener reward signals
口服碳水化合物和甜味剂奖励信号的行为和神经测量
  • 批准号:
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Mitochondrial ADP privation: A unifying model for glucose-induced insulin secretion.
线粒体 ADP 缺乏:葡萄糖诱导的胰岛素分泌的统一模型。
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    10597083
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    $ 8.96万
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