RIBOFLAVIN (B2)
Structure:
- Flavin - yellow colored, seen in urine
- Ribitol
Coenzymes:
DIGESTION, ABSORPTION, METABOLISM, and EXCRETION
FUNCTION/MOA
2 coenzyme forms of Riboflavin - FAD FMN
- Flavoproteins exhibit a wide range of redox potentials so can play a variety of roles in intermediary metabolism
- FAD and FMN have ability to accept a pair of hydrogen atoms
- Reduction of FAD and FMN results in FADH2 and FMNH2
Role in Nutrition and Energy Production
- Electron transport chain
- B6 metabolism
- Pyridoxine phosphate oxidase (converts PMP and PNP to PLP, dependant on FMN)
- L-amino oxidase uses FMN in the dehydrogenase of L-amino acids to imino acids
- Oxidative decarboxylation of pyruvate and a-ketoglutarate
- Succinate dehydrogenase removes electrons from succinic acid to form fumarate
- Fatty acid beta-oxidation, acyl-coA dehydrogenase requires FAD
- Sphingonine oxidase, requires FADA
- Coenzyme for an oxidase such as Xanthine Oxidase involved in purine metabolism
- Aldehyde oxidate
- Synthesis of folate
- Synthesis of niacin from tryptophan
- Choline metabolism
- Monoamine oxidate (dopamine)
- Glutathione reductase
- Eral and sulfhydryl oxidases, impair folding with B2 deficiency
- THioredoxin reductase
- Ribonucleotide reductase
- Hydrogen peroxide production from O2
USES
- Migraine headaches 400 mg
- Glutaric acid type 1
- Beta-oxidation of fatty acids in mitochondria
RDA
1.3 mg/d and 1.1 mg/dDeficiency
Ariboflavinosis
- 3-4 months of inadequate intake
- cheliosis, angular stomatitis, glossitis
- skin becomes reddened scaly greasy painful
- conjuctivitis
- neuropathy
- RXb5-30mg daily
At risk: etoh, hypothyroidism, adrenal insufficiency, DM, trauma, stress, TCAs
Toxicity
no TUL
Assessment
Measurement of activity of FAD-dependent enzyme erythrocyte glutathione reductase
- Activity Coefficients
- AC 1.2 to 1.4 normal
- AC>1.4 riboflavin deficiency
FAD-dependent enzyme pyridoxamine phosphate oxidase
Urinary riboflavin excretion with <25 ug/g creatinine = deficiency
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