M
Michael S. DeBuysere
Researcher at University of Texas Health Science Center at San Antonio
Publications - 18
Citations - 564
Michael S. DeBuysere is an academic researcher from University of Texas Health Science Center at San Antonio. The author has contributed to research in topics: Pyruvate dehydrogenase complex & Pyruvate decarboxylation. The author has an hindex of 13, co-authored 18 publications receiving 559 citations.
Papers
More filters
Journal ArticleDOI
The Regulation of Pyruvate Dehydrogenase in the Isolated Perfused Rat Heart
TL;DR: A combination of measurements of metabolic flux rates, the active/total pyruvate dehydrogenase activities, and the tissue levels of various effector molecules of this regulatory system represents an effective approach to a precise determi- nation of the responses of a very complex regulatory system for this multienzyme complex during physiolog- ically meaningful metabolic state changes in cardiac tissue.
Journal ArticleDOI
Studies on the regulation of the branched chain alpha-keto acid dehydrogenase in the perfused rat liver.
TL;DR: The evidence presented indicates that (alpha) the metabolic flux through the branched chain alpha-keto acid dehydrogenase complex can be monitored effectively in a continuous fashion in the perfused liver by following the release of 14CO2 from infused 1-14C-labeled substrates.
Journal ArticleDOI
Identification of receptors for platelet-activating factor in rat Kupffer cells.
TL;DR: It is suggested that rat Kupffer cells have specific and functionally active AGEPC receptors which are involved in signaling mechanisms which govern the production of several other autacoid-type mediators in the liver.
Journal ArticleDOI
Studies on the relationship between ketogenesis and pyruvate oxidation in isolated rat liver mitochondria.
Journal ArticleDOI
The effect of acetylglyceryl ether phosphorylcholine on glycogenolysis and phosphatidylinositol 4,5-bisphosphate metabolism in rat hepatocytes.
TL;DR: AGEPC is a chemical mediator which induces the degradation of phosphatidylinositol 4,5-bisphosphate without activating glycogenolysis in hepatocytes.