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Development Alcohol and Circadian Clock Function

Development Alcohol and Circadian Clock Function
开发酒精和生物钟功能
批准号:
6509437
负责人:
DAVID J EARNEST
金额:
$21.6万
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:
已结题
起止时间:
2001-07-01 至 2006-03-31

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中文摘要
翻译
描述(申请人提供):估计有2000 - 12000名婴儿
英文摘要
DESCRIPTION (Provided by applicant): It is estimated that 2,000-12,000 babies are born each year with fetal alcohol syndrome (FAS) (Stratton et al., 1996). By far the most debilitating feature of FAS in CNS dysfunction that results from structure are known to persist into adulthood. However, information on the long-term neurobehavioral correlates of this alcohol-related brain damage is limited. The circadian regulation of most body processes by the clock in the suprachiasmatic nucleus (SCN) represents an area in which limited information is available on the consequences of developmental alcohol exposure in humans or animal models. Offspring exposed to heavy maternal alcohol consumption during pregnancy have been reported to show disturbances in their sleep-wake patterns (Rosett et al., 1979). Consistent with this finding, our PRELIMINARY STUDIES demonstrate that alcohol exposure during the third trimester equivalent in rats produces permanent changes in the circadian rhythm of activity. Therefore, experiments in this proposal will utilize multidisciplinary approaches to examine the long-term effects of three different alcohol doses on the circadian rhythm of activity on the anatomical, cellular and molecular organization of the SCN clock. The patterns of wheel- running behavior in adult rats will be assessed for alcohol-related changes in fundamental properties such as circadian period and rhythm amplitude. Subsequent to this behavioral analysis, the SCN will be evaluated for evidence of general cell loss and perturbations in its rhythmic expression of the putative clock genes, Perl, Per2 and Cry2, and the output signals, vasopressin (AVP), vasoactive intestinal polypeptide (VIP) and brain-derived neurotrophic factor (BDNF). Unlike CNS involvement in the neural regulation of most other behaviors, the discrete localization of circadian clock function to the SCN provides a unique opportunity to identify cellular and molecular correlates of alcohol-related neurobehavioral disturbances. By determining how the SCN and its circadian function are affected by developmental alcohol exposure, these studies are expected to yield important information on the basic mechanisms underlying alcohol-induced brain injury during development. Such information could lead to new strategies in the treatment of known behavioral correlates of FAS related to sleep problems and to mental and physical disorders associated with sleep-wake abnormalities.
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会议论文
Circadian Clock Disruption and Ischemic Stroke Outcomes: Age and Sex Differences
Intercellular Integration of SCN Output Signals
  • 批准号:
    7168075
  • 项目类别:
  • 资助金额:
    $21.15万
  • 财政年份:
    2006
  • 负责人:
    DAVID J EARNEST
  • 依托单位:
Development Alcohol and Circadian Clock Function
Development Alcohol and Circadian Clock Function
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