T
Tuan Khanh Tran
Researcher at University of California, Davis
Publications - 7
Citations - 468
Tuan Khanh Tran is an academic researcher from University of California, Davis. The author has contributed to research in topics: Myoglobin & Gastrocnemius muscle. The author has an hindex of 7, co-authored 7 publications receiving 453 citations.
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Journal ArticleDOI
Comparative analysis of NMR and NIRS measurements of intracellular PO2 in human skeletal muscle
Tuan Khanh Tran,Napapon Sailasuta,Ulrike Kreutzer,Ralph E. Hurd,Youngran Chung,Paul A. Molé,Shinya Kuno,Thomas Jue +7 more
TL;DR: The experimental results establish the feasibility and methodology to observe the deoxyMb and Hb signals in skeletal muscle, help clarify the origin of the NIRS signal, and set a stage for continuing study of O2regulation in skeletal Muscle.
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Myoglobin desaturation with exercise intensity in human gastrocnemius muscle
TL;DR: The O2 gradient from hemoglobin to the mitochondria can modulate the O2flux to meet the increased V˙o 2 in exercising muscle, but declining cellular levels during enhanced mitochondrial respiration suggests that O2 availability is not limiting during exercise.
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Control of respiration and bioenergetics during muscle contraction.
TL;DR: In this article, the authors determined intracellular O2 consumption (Vo2) with oxymyoglobin (MbO2) desaturation kinetics in human calf muscle during plantar flexion exercise at 0.75, 0.92, and 1.17 Hz.
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Spatial distribution of deoxy myoglobin in human muscle: an index of local tissue oxygenation
TL;DR: One and two‐dimensional chemical shift imaging experiments reveal clearly the localized deoxy Mb signal in muscle and consequently the spatial distribution of the cellular oxygenation, indicating the feasibility to assess the pO2 in tissue regions and to directly study the regulation of oxidative metabolism in human tissue.
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Role of oxygen in limiting respiration in the in situ myocardium.
TL;DR: Oxygen availability does not appear to limit oxygen consumption nor oxidative phosphorylation under dopamine enhanced work state in myocardium.