Vitamin E Flashcards
evans and bishop
identify a factor in
vegetable oil that is required for production
in rats, also in wheat germ. Proposes
“Vitamin E”. Tokos-childbirth, pherin- to bear
or carry—tocopherol.
Kerrer
vitamin E
synthesized.
Human Requirement
α-tocopherol is the
only form to meet RDA. Forms are not
convertible
food
vegetable oils,
margarine, mayonnaise, wheat germ, nuts
α- Tocopherol Transfer protein
transfer of α-
tocopherol from liver to lipoproteins. Plasma
concentrations dependent on the affinity. Other
forms are absorbed and delivered to liver in
chylomicrons but poorly packaged in lipoproteins for
transport. Relates back to structure.
Binding to α-TTP
Requires it to be in the form
of RRR- α-tocopherol
Transport
Does not have a specific transport
protein. Liver exports α-tocopherol into plasma
as VLDL. Genetic defect in synthesis of α-TTP
leads to deficiency.
Cellular uptake
Lipoprotein lipase-mediated catabolism. Lipoprotein
receptors. Membrane lipid transporters.
Storage & Excretion
Storage is in adipose (>90%). Excretion is fecal.
Forms
8 different forms. 4
tocopherols & 4
tocotrienols. Trienols have 3
double bonds in chain
RDA
1 mg/ 1.49 IU
UL
> 1000 mg (bleeding in
brain/ can’t form clots b/c antagonized Vit. K)
Applies to all synthetic forms.
Antioxidant function-
lipid soluble chain-breaking antioxidant.
Neutralizes lipid peroxyl radicals, involved in the oxidation of lipids
(lipid peroxidation). Protects PUFA within phospholipids of biological
membranes and in plasma lipoproteins.
Lipid peroxidation
In initiation, propagation and termination.
Donates a hydrogen to the lipid peroxyl radical to form lipid
peroxide and a vitamin E radical. Chain reaction is terminated
because the Vitamin E radical is relatively stable and will not react
with an adjacent unsaturated fatty acid.
Symptoms-
oxidative damage of tissues, membrane damage of
cells/ sub-cellular organelles, damage of structural and functional
compounds, neurological abnormalities, muscular function,
membrane instability hemolytic anemia. VERY RARE. Babies with
VLBW. Fat malabsorption disorders. Ataxia with Vitamin E disorder.