MATERNAL DEHYDRATION--FETAL & AMNIOTIC FLUID HOMEOSTASIS

母体脱水--胎儿

基本信息

项目摘要

Pregnant women may be exposed to exercise, thermal, or gastrointestinal (hyperemesis) water loss, all of which commonly induce a >10 mOsm increase in plasma osmolality (osm). Although fetal plasma is dependent on maternal osm the impact of maternal dehydration and subsequent rehydration on the fetus has not been explored. Increases in maternal plasma osm well within the physiologic range result in significant fetal endocrine responses (stimulation of arginine vasopressin and renin secretion and perhaps a suppression of atrial natriuretic factor) and subsequent alterations in fetal water dynamics and blood volume. Despite maternal rehydration, fetal endocrine and fluid responses persist beyond a return to basal maternal and fetal plasma osm. As a result, episodic maternal dehydration may contribute to the development of oligohydramnios, premature labor, and/or fetal growth retardation. This project will utilize the chronically catheterized ovine model to investigate the ontogeny of fetal and amniotic fluid water and electrolyte responses to maternal dehydration and subsequent rehydration. A compartmental model will be utilized to quantify alterations in fetal water acquisition (fetal swallowing and transplacental flow) and excretion (urine and lung fluid). Specifically, we have developed and confirmed a method for the measurement of fetal swallowing activity and volume. Fetal urine and lung fluid production will be measured directly, and transplacental flow calculated. The resultant effects on fetal blood volume and the impact on amniotic and allantoic water compartments will be evaluated. The response of selected fetal endocrine systems central to water homeostasis will be examined and the mechanisms of endocrine regulation of fetal fluid and electrolytes and swallowing responses will be studied using selective agonists and antagonists. As maternal and fetal responses to rehydration differ depending upon the mode of hydration, this project also will examine the fetal endocrine and fluid responses to several means of maternal rehydration. Studies of dehydration and rehydration of the ovine model represent a promising approach to understanding maternal-fetal water dynamics, while addressing a potentially critical problem in perinatal medicine.
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项目成果

期刊论文数量(0)
专著数量(0)
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会议论文数量(0)
专利数量(0)

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Michael Glenn Ross其他文献

Michael Glenn Ross的其他文献

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{{ truncateString('Michael Glenn Ross', 18)}}的其他基金

Mechanisms of Programmed Gestational Hyperphagia
程序性妊娠期食欲过盛的机制
  • 批准号:
    7614207
  • 财政年份:
    2008
  • 资助金额:
    $ 12.41万
  • 项目类别:
Mechanisms of Programmed Gestational Hyperphagia
程序性妊娠期食欲过盛的机制
  • 批准号:
    7467418
  • 财政年份:
    2008
  • 资助金额:
    $ 12.41万
  • 项目类别:
Mechanisms of Programmed Gestational Hyperphagia
程序性妊娠期食欲过盛的机制
  • 批准号:
    7799747
  • 财政年份:
    2008
  • 资助金额:
    $ 12.41万
  • 项目类别:
Mechanisms of Programmed Gestational Hyperphagia
程序性妊娠期食欲过盛的机制
  • 批准号:
    8250374
  • 财政年份:
    2008
  • 资助金额:
    $ 12.41万
  • 项目类别:
Mechanisms of Programmed Gestational Hyperphagia
程序性妊娠期食欲过盛的机制
  • 批准号:
    8052762
  • 财政年份:
    2008
  • 资助金额:
    $ 12.41万
  • 项目类别:
DO IONIZED MAGNESIUM LEVELS PREDICT CLINICAL EFFECTS BETTER THAN TOTAL MAGNESIS
离子镁水平比总镁水平更能预测临床效果吗
  • 批准号:
    7606211
  • 财政年份:
    2007
  • 资助金额:
    $ 12.41万
  • 项目类别:
AQUAPORIN GENE EXPRESSION IN HUMAN FETAL MEMBRANE
人胎膜中水通道蛋白基因的表达
  • 批准号:
    7606210
  • 财政年份:
    2007
  • 资助金额:
    $ 12.41万
  • 项目类别:
AQUAPORIN GENE EXPRESSION IN HUMAN FETAL MEMBRANE
人胎膜中水通道蛋白基因的表达
  • 批准号:
    7376108
  • 财政年份:
    2005
  • 资助金额:
    $ 12.41万
  • 项目类别:
THE COMPARISON OF PLACENTAL AND UMBILICAL NUCLEATED RED BLOOD CELL COUNT
胎盘和脐带有核红细胞计数的比较
  • 批准号:
    7376109
  • 财政年份:
    2005
  • 资助金额:
    $ 12.41万
  • 项目类别:
THE COMPARISON OF PLACENTAL AND UMBILICAL NUCLEATED RED BLOOD CELL COUNT
胎盘和脐带有核红细胞计数的比较
  • 批准号:
    7206410
  • 财政年份:
    2004
  • 资助金额:
    $ 12.41万
  • 项目类别:

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精氨酸加压素的 PET 配体发现
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    10283131
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RGC 释放的精氨酸加压素对昼夜节律和精神功能的生理作用
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精氨酸加压素受体 1A 在周围神经病理性疼痛中的作用机制的鉴定
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    16K09448
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精氨酸加压素 1a 受体 (AVPR1a) 基因的变异、社会环境、总体健康和福祉
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  • 财政年份:
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