Clock gene response against skelton type entrainment stimulation in mice

小鼠中针对骨架型夹带刺激的时钟基因反应

基本信息

  • 批准号:
    18390071
  • 负责人:
  • 金额:
    $ 10.21万
  • 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:
    2006
  • 资助国家:
    日本
  • 起止时间:
    2006 至 2007
  • 项目状态:
    已结题

项目摘要

The aim of this experiment is to elucidate the mechanism of skeleton-type photic and non-photic entrainment like food entrainment in mice. First we examined the circadian pattern of clock gene expression in the liver under one-hr light stimulation in the morning and one-hr light stimulation in the evening. This lighting schedule could entrain the locomotor activity rhythm and also liver dock gene expression rhythm. Thus, skeleton lighting schedule can entrain the circadian dock just like usual 12-hr light-dark schedule. Next, we examined the circadian pattern of clock gene expression in the liver under 2-hr feeding in the morning and 2-hr feeding in the evening. This feeding schedule could entrain the liver clock gene expression rhythm, and its pattern was very similar to adlib feeding group. Thus, two feeding times per day with morning and evening could entrain the peripheral circadian rhythm. In the third experiment, we changed the ratio of feeding volume in the morning and evening. If the more feeding volume was applied in the morning, there was little effect on the phase of dock gene expression. However, if the more feeding volume was applied in the evening, phase of dock gene expression rhythm was strongly delayed. Taken together these results suggest that food intake in the morning is important to keep the phase of dock gene expression the peripheral organs.
本实验的目的是阐明小鼠骨骼型光和非光夹带(如食物夹带)的机制。首先,我们检查了早晨一小时光刺激和晚上一小时光刺激下肝脏中时钟基因表达的昼夜节律模式。这种照明时间表可以控制运动活动节律以及肝脏码头基因表达节律。因此,骨架照明时间表可以像通常的 12 小时明暗时间表一样引导昼夜节律码头。接下来,我们检查了早晨 2 小时喂养和晚上 2 小时喂养下肝脏中时钟基因表达的昼夜节律模式。这种喂养方案可以带动肝脏时钟基因的表达节律,其模式与adlib喂养组非常相似。因此,每天早上和晚上两次喂食可以控制周围的昼夜节律。在第三个实验中,我们改变了早上和晚上的饲喂量比例。如果早上施加更多的饲喂量,则对码头基因表达的阶段影响很小。然而,如果在晚上施加更多的饲喂量,则码头基因表达节律的阶段被强烈延迟。综上所述,这些结果表明早上的食物摄入对于保持外周器官的码头基因表达阶段很重要。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
PPARalpha is a potential therapeutic target of drugs to treat circadian rhythm sleep disorders
PPARα 是治疗昼夜节律睡眠障碍药物的潜在治疗靶点
  • DOI:
  • 发表时间:
    2007
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Shirai H;Oishi K;Kudo T;Shibata S;Ishida N.
  • 通讯作者:
    Ishida N.
Multifactorial rugulation of daily rhythms in expression of the metabolically responsive gene spot14 in the mouse liver
小鼠肝脏中代谢反应基因spot14表达的日常节律的多因素调控
  • DOI:
  • 发表时间:
    2007
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Ishihara A;Matsumoto E;Horikawa K;Kudo T;Shibata S;Takiguchi M.
  • 通讯作者:
    Takiguchi M.
Clock mutation facilitates accumulation of cholesterol in the liver of mice fed a cholesterol and/or cholic acid diet
Attenuating effect of Clock mutation on triglyceride contents in the ICR mouse liver under a high-fat diet
  • DOI:
    10.1177/0748730407302625
  • 发表时间:
    2007-08-01
  • 期刊:
  • 影响因子:
    3.5
  • 作者:
    Kudo, Takashi;Tarnagawa, Toru;Shibata, Shigenobu
  • 通讯作者:
    Shibata, Shigenobu
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SHIBATA Shigenobu其他文献

SHIBATA Shigenobu的其他文献

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{{ truncateString('SHIBATA Shigenobu', 18)}}的其他基金

Role of breakfast in food-induced entrainment of mouse circadian clock
早餐在食物诱导的小鼠生物钟中的作用
  • 批准号:
    20390065
  • 财政年份:
    2008
  • 资助金额:
    $ 10.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Studies of association of metabolic syndrome and circadian rhythms
代谢综合征与昼夜节律关联的研究
  • 批准号:
    15390074
  • 财政年份:
    2003
  • 资助金额:
    $ 10.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Research on molecular mechanism of sleep-wakefulness rhythm and development of new hypnotics
睡眠-觉醒节律分子机制研究及新型安眠药开发
  • 批准号:
    13470016
  • 财政年份:
    2001
  • 资助金额:
    $ 10.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Circadian clock function as a neuron-glia complex
昼夜节律时钟作为神经元-胶质细胞复合体发挥作用
  • 批准号:
    09470018
  • 财政年份:
    1997
  • 资助金额:
    $ 10.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Development of animal models for Parkinson's desease and new drugs for this desease by the study of synaptic plasticity
通过突触可塑性研究开发帕金森病动物模型及新药
  • 批准号:
    07672366
  • 财政年份:
    1995
  • 资助金额:
    $ 10.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Attenuating effect of drugs on an impairment of anticipatory activity in various animal models.
药物对各种动物模型预期活动损害的减弱作用。
  • 批准号:
    05671900
  • 财政年份:
    1993
  • 资助金额:
    $ 10.21万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
Development of effective drugs on impairments of Circardian rhythms and anticipatory behaivior in old rats.
开发针对老年大鼠昼夜节律和预期行为损伤的有效药物。
  • 批准号:
    03671098
  • 财政年份:
    1991
  • 资助金额:
    $ 10.21万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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