Folic Acid
- 1 January 2001
- journal article
- review article
- Published by Taylor & Francis in Critical Reviews in Clinical Laboratory Sciences
- Vol. 38 (3) , 183-223
- https://doi.org/10.1080/20014091084209
Abstract
Folic acid is an essential nutrient from the B complex group of vitamins. Folate, as a cofactor, is involved in numerous intracellular reactions, and this is reflected in the various derivatives that have been isolated from biological sources. Folic acid is involved in single carbon transfer reactions and serves as a source of single carbon units in different oxidative states. The processes involved in the absorption, transport, and intracellular metabolism of this cofactor are complex. Much of folate is bound tightly to enzymes, indicating that there is not excess of this cofactor and that its cellular availability is protected as well as being strictly regulated. In animals, the liver controls the supply of folate through first pass metabolism, biliary secretion, enterohepatic recirculation, as well as through senescent erythrocyte recycling. Deficiencies of folate can occur for many reasons, including reduced intake, increased metabolism, and/or increased requirements as well as through genetic defects. The effects of folate deficiency include hyperhomocysteinemia, megaloblastic anemia, and mood disorders. Folate deficiency has also been implicated in disorders associated with neural tube defects. Supplementation of grain products such as cereals has been undertaken in several countries as a cost-effective means of reducing the prevelance of neural tube defects. Recently, common polymorphisms have been discovered in several genes associated with folate pathways that may play a role in diseases associated with folate deficiency, particularly mild folate deficiency.Keywords
This publication has 177 references indexed in Scilit:
- The Effect of Folic Acid Fortification on Plasma Folate and Total Homocysteine ConcentrationsNew England Journal of Medicine, 1999
- Long-term treatment of congenital folate malabsorptionThe Journal of Pediatrics, 1996
- A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductaseNature Genetics, 1995
- Molecular Cloning of the Human Placental Folate TransporterBiochemical and Biophysical Research Communications, 1995
- Expression of the Human Placental Folate Receptor Transcript is Regulated in Human TissuesJournal of Molecular Biology, 1993
- Gastrointestinal function in patients with progressive systemic sclerosisClinical Rheumatology, 1985
- Noninvolvement of a rat intestinal folate binding protein in physiological folate absorptionCellular and Molecular Life Sciences, 1984
- Cell cycle patterns of thymidylate synthetase and 5,10-methylenetetrahydrofolate polyglutamates in cultured mouse hepatoma cellsCellular and Molecular Life Sciences, 1982
- Therapy of congenital folate malabsorptionThe Journal of Pediatrics, 1981
- Isolation of methyl-B12 from Escherichia coli B N5-methyl-H4-folate-homocysteine vitamin-B12 transmethylaseBiochemical and Biophysical Research Communications, 1967