NEW PRENATAL THERAPY FOR CONGENITAL DIAPHRAGMATIC HERNIA
NEW PRENATAL THERAPY FOR CONGENITAL DIAPHRAGMATIC HERNIA
批准号:
2211177
负责人:
JAY J SCHNITZER
金额:
$8.34万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-09-01 至 1999-06-30
关键词:
apoptosis congenital disorders developmental genetics diaphragm disease /disorder model embryo /fetus pharmacology embryo /fetus tissue /cell culture embryology endothelin gene expression gene targeting genetic enhancer element gestational age glucocorticoids hernia hormone therapy immunocytochemistry laboratory rat messenger RNA nitric oxide synthase organ culture polymerase chain reaction pulmonary surfactants sheep subtraction hybridization
中文摘要
CDH的情况发生在膈肌分离的时候
英文摘要
The condition of CDH occurs when the diaphragmatic muscle, which separates
the chest from the abdomen, falls to form completely in the developing
fetus. The intestines, no longer confined to the abdomen, herniate into
the thorax. The defect is often associated with immaturity of the lungs;
it is not a rare condition, affecting nearly one in 2,000 pregnancies.
Despite many major advances in the surgery and intensive care of infants
with CDH, the mortality from the malformation remains as high as 60%. The
infants die from inadequate lung function, which is a combination of 1)
pulmonary hypoplasia and 2) persistent pulmonary hypertension of the
newborn. Lungs of full term infants with CDH are similar to lungs of
premature infants. We have used the nitrofen-induced model of CDH in the
fetal rat to demonstrate that the lungs are immature by biochemical,
morphometric, physiologic, and molecular biologic criteria. We have shown
further that the lethally immature lungs of the full term CDH rats can be
improved by treating the mothers with parenteral glucocorticoids at doses
extrapolated from the current therapy used to accelerate lung development
of premature human babies. Addition of thyroid hormone augments this
effect. We will search for more potent pulmonary growth enhancers at the
gene level, evaluate expression of developmentally regulated genes in CDH,
and investigate the role of apoptosis in CDH. We have developed an in
vitro organ culture system of nitrofen-induced pulmonary hypoplasia using
quantitative mathematical and fractal techniques to screen new agents; we
will test their efficacy and optimize dosing in the rat model, then extend
these experiments to fetal sheep in whom CDH has been surgically, rather
than pharmacologically, created. Combination of these systems will allow
us to pretest and develop appropriate therapies for CDH that can be used
in future clinical trials for prenatal treatment of humans in whom CDH has
been detected in utero by ultrasound.
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MECHANISMS OF CDH-ASSOCIATED PULMONARY HYPOPLASIA
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批准号:6184724
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项目类别:
-
资助金额:$31.73万
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财政年份:1999
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负责人:JAY J SCHNITZER
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依托单位:
MECHANISMS OF CDH-ASSOCIATED PULMONARY HYPOPLASIA
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批准号:6390367
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项目类别:
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资助金额:$32.35万
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财政年份:1999
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负责人:JAY J SCHNITZER
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依托单位:
MECHANISMS OF CDH-ASSOCIATED PULMONARY HYPOPLASIA
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批准号:6527433
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项目类别:
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资助金额:$32.99万
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财政年份:1999
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负责人:JAY J SCHNITZER
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依托单位:
MECHANISMS OF CDH-ASSOCIATED PULMONARY HYPOPLASIA
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批准号:6654862
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项目类别:
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资助金额:$33.66万
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财政年份:1999
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负责人:JAY J SCHNITZER
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依托单位:
MECHANISMS OF CDH-ASSOCIATED PULMONARY HYPOPLASIA
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批准号:6042827
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项目类别:
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资助金额:$31.12万
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财政年份:1999
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负责人:JAY J SCHNITZER
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依托单位:
NEW PRENATAL THERAPY FOR CONGENITAL DIAPHRAGMATIC HERNIA
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批准号:2211178
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项目类别:
-
资助金额:$8.45万
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财政年份:1995
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负责人:JAY J SCHNITZER
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依托单位:
NEW PRENATAL THERAPY FOR CONGENITAL DIAPHRAGMATIC HERNIA
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批准号:2445002
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项目类别:
-
资助金额:$8.45万
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财政年份:1995
-
负责人:JAY J SCHNITZER
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依托单位:
NEW PRENATAL THERAPY FOR CONGENITAL DIAPHRAGMATIC HERNIA
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批准号:2734925
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项目类别:
-
资助金额:$8.45万
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财政年份:1995
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负责人:JAY J SCHNITZER
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依托单位:
海外基金