• Corpus ID: 99035509

Hepatic uptake, intracellular accumulation and biliary secretion of 5-methyltetrahydrofolate.

@article{Wb1980HepaticUI,
  title={Hepatic uptake, intracellular accumulation and biliary secretion of 5-methyltetrahydrofolate.},
  author={Strum Wb and Li Hh},
  journal={Research communications in chemical pathology and pharmacology},
  year={1980},
  volume={30},
  pages={493-507},
  url={https://api.semanticscholar.org/CorpusID:99035509}
}
  • Strum WbLi Hh
  • Published 1 December 1980
  • Medicine, Chemistry
  • Research communications in chemical pathology and pharmacology
These studies indicate that hepatic uptake and biliary secretion of 5-methyltetrahydrofolate occurs by an energy-dependent, carrier-mediated process in which the coenzyme accumulates in the liver, is secreted into bile against a high concentration gradient and undergoes enterohepatic circulation.

Kinetic profile of overall elimination of 5-methyltetrahydropteroylglutamate in rats.

It is concluded that the hepatobiliary excretion is a relatively low-affinity process with a constant clearance, whereas the renal tubular reabsorption is saturated at higher plasma 5-CH3-H4PteGlu concentration (∼0.5 μM).

Transport of Folates and Antifolates in Liver

    D. W. Horne
    Medicine, Biology
  • 1993
The hepatocyte has separate systems for uptake of the naturally occurring, reduced folates and for the 4-amino-substituted antifolates, which are taken up by the perfused liver and secreted into bile by apparently active processes.

Reduced folate derivatives are endogenous substrates for cMOAT in rats.

Results indicate that 5-CH3-H4PteGlu and other derivatives are transported via cMOAT, which are the first endogenous substrates for c MOAT that do not contain glutathione, glucuronide, or sulfate moieties.

Effects of folic acid and pyrimethamine, a dihydrofolate reductase inhibitor, on intestinal absorption of folates in rats.

The findings indicate that PteGlu competes with the bile reduced folates for the intestinal transport system and potentiates the decrease of plasma 5-methyltetrahydrofolic acid concentration induced by pyrimethamine in rats.

Non-fasting reference intervals for the Abbott IMxTM homocysteine and AxSYMTM plasma folate assays: influence of the methylenetetrahydrofolate reductase 677 C→T mutation on homocysteine

Plasma homocysteine comes under both genetic and nutritional control. B vitamins and particularly folate are important factors in homocysteine metabolism. We have obtained reference intervals for