DETERMINANTS OF MUSCLE MAXIMAL 02 UPTAKE AND PERFORMANCE
DETERMINANTS OF MUSCLE MAXIMAL 02 UPTAKE AND PERFORMANCE
批准号:
3457329
负责人:
MICHAEL C HOGAN
金额:
$9.31万
依托单位国家:
美国
项目类别:
财政年份:
1991
资助国家:
美国
项目状态:
已结题
起止时间:
1991-09-30 至 1996-08-31
关键词:
adenosine triphosphate dogs gastrocnemius muscle glycolysis human in situ hybridization mathematical model membrane activity microcirculation muscle function muscle metabolism nicotinamide adenine dinucleotide oxidation reduction reaction oxygen consumption oxygen transport pulmonary diffusion striated muscles
中文摘要
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英文摘要
DESCRIPTION: (Adapted from applicant's abstract): The objective of this
study is to elucidate the factors that limit maximal 02 consumption
(V02max) and performance in working skeletal muscle. 1) The hypothesis
that V02 max can be limited by the capacity for 02 diffusion in the
peripheral tissue will be tested using an isolated, in situ canine
gastrocnemius model, and the isolated knee extensor muscle model in humans.
A mathematical model incorporating diffusion limitation has been developed
from a combination of Fick's law of diffusion and the Fick principle. A.
This model will be used to predict the outcome of various experiments in
which 02 delivery is altered through lowered arterial P02, anemia, and
ischemia. Special experiments in which the )2 delivery (muscle blood flow
X arterial 02 content) will be kept equal between varied conditions of
hypoxemia, anemia, and muscle blood flow will be used in both the animal
and human studies in an attempt to separate perfusion limitation from
diffusion limitation. B. Because muscle blood flow to V02 heterogeneity
can mimic 02 diffusion limitation, the problem of tissue heterogeneity will
also be investigated in the canine gastrocnemius model using step changes
in inert gas and 02 levels of arterial blood and following the muscle
venous responses, using methodology developed investigating for pulmonary
heterogeneity. 2) Several factors that determine muscle function and
performance during high-intensity work will also be investigated. A. The
NAD redox state during progressive work will be measured to determine
tissue oxygenation and its control of metabolism. B. The role of
glycolysis during intense work and the impact of increased
activation-relaxation cycles on contractile function and fatigue will be
investigated. These experiments will also provide information concerning
the amount of ATP produced by glycolysis that is used for membrane
functions. C. In all of the experiments in which 02 delivery is
manipulated, the development of fatigue will be studied along with changes
in blood and muscle acid-base balance. D) Finally, the potential role of
granulocyte plugging of muscle microcirculatin after surgery in reducing in
situ maximal blood flow will also be investigated.
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会议论文
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资助金额:$41.02万
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财政年份:2008
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资助金额:$41.02万
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财政年份:2008
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O2 dependence of isolated single skeletal muscle fibers
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资助金额:$24.62万
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O2 dependence of isolated single skeletal muscle fibers
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资助金额:$24.62万
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财政年份:1991
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O2 Dependence of Isolated Single Skeletal Muscle Cells
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负责人:MICHAEL C HOGAN
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依托单位:
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项目类别:
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资助金额:$23.89万
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依托单位:
O2 Dependence of Isolated Single Skeletal Muscle Cells
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项目类别:
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资助金额:$31.7万
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财政年份:1991
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项目类别:
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资助金额:$32.3万
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财政年份:1991
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负责人:MICHAEL C HOGAN
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依托单位:
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资助金额:$28.73万
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依托单位:
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依托单位:
海外基金