MATERNAL DEHYDRATION--FETAL/AMNIOTIC FLUID HOMEOSTASIS
母体脱水--胎儿/羊水稳态
基本信息
- 批准号:6322273
- 负责人:
- 金额:$ 13.29万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1989
- 资助国家:美国
- 起止时间:1989-04-01 至 2003-03-31
- 项目状态:已结题
- 来源:
- 关键词:RNase protection assay amniotic fluid arginine vasopressin blood volume body water dehydration drug screening /evaluation electrolyte balance embryo /fetus homeostasis hormone receptor hormone regulation /control mechanism hyponatremia in situ hybridization laboratory rat nonhuman therapy evaluation northern blottings placental transfer pregnancy pregnancy disorder chemotherapy prenatal stress radioimmunoassay scintillation counter sheep swallowing ultrasound blood flow measurement urinalysis
项目摘要
Amniotic fluid (AF) is an essential accompaniment of normal pregnancy,
necessary for fetal movement, growth and development. Oligohydramnios,
or reduced AF volume, occurs in 8 to 38 percent of all pregnancies. The
majority of oligohydramnios patients have no identifiable medical or
antepartum complication and only 7 percent of cases have associated
fetal malformations. However, oligohydramnios is often associated with
conditions of chronic fetal stress, such as intrauterine growth
retardation, preeclampsia and postterm pregnancy. These conditions,
together with the direct effect of reduced AF volume, results in
significant perinatal morbidity and mortality. Increasing AF volume in
laboring patients with oligohydramnios improves fetal outcome, though
this generally requires rupture of fetal membranes. However, our
studies demonstrate that modulation of AF production (fetal urine flow)
and AF resorption (fetal swallowing and intramembranous flow) may be
utilized to increase AF volume in patients with intact membranes. We
have developed a novel model to increase AF volume utilizing maternal
administration of the arginine vasopressin (AVP) antidiuretic agonist
[desamino, D-Arg8]-AVP (DDAVP). Our studies in the ovine model indicate
that maternal hydration and DDAVP induces maternal and fetal plasma
hyponatremia, marked increases in fetal urine flow, reduced fetal
swallowing and expansion of AF volume. Our human studies have supported
the clinical utility of these interventions. Despite these promising
results, critical issues of efficacy and safety of DDAVP therapy for
both the mother and fetus must be resolved prior to clinical use.
Firstly, in studies of efficacy, we will determine the minimum level of
maternal hyponatremia which induces and maintains fetal fluid responses,
and examine the effects of alterations in placental osmolality
gradients. Long term studies will examine the effects of hyponatremia
on ovine AF volume, maternal plasma volume and umbilical and uterine
blood flows in both normal and oligohydramnios ovine pregnancies.
Secondly, in studies of fetal safety, we will determine if fetal brain
edema and/or loss of brain electrolytes are induced by hyponatremia.
As AVP has important fetal fluid and cardiovascular regulatory roles,
we will determine the effect of hyponatremia on fetal osmotic and non-
osmotic stimulated AVP secretion. Finally, as permanent imprinting of
AVP synthesis and secretion regulatory systems may occur in response
chronic tonicity alterations in newborn rats, we will examine the
effects of chronic tonicity alterations on fetal AVP transcription and
translation. Physiologic assessments will focus on measurements of
fetal fluid exchange and fetal plasma and AF volume and composition.
Endocrine and molecular assessments will include determination of fluid
regulatory hormones and hypothalamic AVP mRNA and pituitary AVP
contents, utilizing our newly developed ovine 130 bp cDNA probe and
solution and in situ hybridization techniques. The goal of this project
is to determine critical efficacy and fetal safety issues central to
maternal DDAVP treatment, prior to widespread clinical use in human
pregnancies with oligohydramnios.
羊水(AF)是正常妊娠必不可少的伴随物,
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)
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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:
$ 13.29万 - 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:
$ 13.29万 - 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:
$ 13.29万 - 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:
$ 13.29万 - 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:
$ 13.29万 - 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:
$ 13.29万 - 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:
$ 13.29万 - 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:
$ 13.29万 - 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:
$ 13.29万 - 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:
$ 13.29万 - 项目类别:
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