Your browser doesn't support javascript.
loading
Effects of different oxidative insults on intermediary metabolism in isolated perfused rat hearts.
Jones, J G; Le, T H; Storey, C J; Sherry, A D; Malloy, C R; Burton, K P.
Afiliação
  • Jones JG; Department of Radiology, University of Texas Southwestern Medical Center, Dallas, USA.
Free Radic Biol Med ; 20(4): 515-23, 1996.
Article em En | MEDLINE | ID: mdl-8904292
ABSTRACT
13C and 31P NMR were used to evaluate exogenous substrate utilization and endogenous phosphate metabolites in perfused rat hearts exposed to tert-butylhydroperoxide (tert-BOOH) and hydrogen peroxide (H2O2). Both reagents caused a reduction in developed pressure compared to controls and, in agreement with previous 31P NMR data, had different effects on intracellular high-energy phosphates and glycolysis. 13C Isotopomer analysis of tissue extracts showed that H2O2 and tert-BOOH also had significantly different effects on substrate utilization by the citric acid cycle. The contribution of exogenous lactate and glucose to acetyl-CoA was 43% in controls and increased to over 80% in the presence of either oxidant. With tert-BOOH, exogenous glucose and lactate were both significant contributors to acetyl-CoA (44 +/- 2 and 41 +/- 3%). However, with H2O2, exogenous lactate supplied a much higher fraction of acetyl-CoA (72 +/- 2%) than glucose (9 +/- 1%). Also, when [2-(13)C] glucose was supplied, accumulation of [2-(13)C] and [5-(13)C] fructose 1,6-bisphosphate was observed in the presence of H2O2, indicating inhibition of glyceraldehyde-3-phosphate dehydrogenase. These results indicate that despite this glycolytic inhibition, H2O2 increased the utilization of pyruvate precursors when lactate was present as an alternative carbohydrate substrate.
Assuntos
Buscar no Google
Base de dados: MEDLINE Assunto principal: Miocárdio Limite: Animals Idioma: En Ano de publicação: 1996 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Miocárdio Limite: Animals Idioma: En Ano de publicação: 1996 Tipo de documento: Article