Properties of thiamine transport in isolated perfused hearts of chronically alcoholic guinea pigs

Can J Physiol Pharmacol. 2008 Apr;86(4):160-5. doi: 10.1139/Y08-013.

Abstract

The aim of this study was to determine the mechanism of transport of (14)C-thiamine in the hearts of healthy (nonalcoholic) and chronically alcoholic guinea pigs. We used the single-pass, paired-tracer dilution method on isolated and retrogradely perfused guinea pig hearts. The maximal cellular uptake (U(max)) and total cellular uptake (U(tot)) of (14)C-thiamine were determined under control conditions and under influence of possible modifiers. We tested how the presence of unlabeled thiamine, metabolic inhibitors, or absence of sodium ions influence the transport of (14)C-thiamine. The results of our experiments show that the transport of (14)C-thiamine is specific and energy-dependent and that its properties are significantly changed under the influence of chronic alcoholism. The latter effect occurs by increase in both U(max) and U(tot), as a manifestation of a compensatory mechanism in thiamine deficiency.

MeSH terms

  • Alcoholism / metabolism*
  • Animals
  • Biological Transport, Active
  • Carbon Radioisotopes
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone / pharmacology
  • Disease Models, Animal
  • Enzyme Inhibitors / pharmacology
  • Female
  • Guinea Pigs
  • Kinetics
  • Male
  • Myocardium / enzymology
  • Myocardium / metabolism*
  • Ouabain / pharmacology
  • Oxidative Phosphorylation / drug effects
  • Perfusion
  • Radioisotope Dilution Technique
  • Sodium / metabolism
  • Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Thiamine / metabolism*
  • Uncoupling Agents / pharmacology
  • Vitamin B Complex / metabolism*

Substances

  • Carbon Radioisotopes
  • Enzyme Inhibitors
  • Uncoupling Agents
  • Vitamin B Complex
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone
  • Ouabain
  • Sodium
  • Sodium-Potassium-Exchanging ATPase
  • Thiamine