Vitamin A: Functions, Forms, Food sources, Deficiency and Toxicity
What
are the functions of vitamin A?
Stanfield and Hui (2011), define vitamins as a group
of essential organic compounds required daily in very small amounts (mostly milligrams) for the
normal functioning of the body. According to Ball (2008), Vitamins have unique
varying functions in the body including the regulation of gene expression (Vitamins A
and D, thiamin, vitamin B12), structural roles in visual pigments (vitamin A as retinal), function as anti-oxidants (vitamins A, E,
and C) and, as enzyme cofactors (the B group vitamins and Vitamin K (Dryden,
2008).
Vitamin A along with other fat soluble vitamins is found in foodstuffs in association with lipids and is absorbed along with dietary fats by mechanisms similar to fat absorption (McDowell, 2008).
Vitamin A along with other fat soluble vitamins is found in foodstuffs in association with lipids and is absorbed along with dietary fats by mechanisms similar to fat absorption (McDowell, 2008).
According to Seth (2011), the various functional
forms of vitamin A have correspondingly
different functions in the body. Retinol aids in transport and reproduction
(Dente and Hopkins, 2010), retinyl esters are important in storage, retinal plays a key role in vision whereas the function of retinoic acid
is demonstrated in epithelial differentiation, growth and transformation. The most
widely recognized role played by vitamin A is its function in vision (Combs,
2012). Retinol is utilized in the aldehyde form (trans-form to 11-cis-retinal)
in the retina of the eye as the prosthetic group in rhodopsin for adaptation to
darkness i.e. rods (Berdainer, 2010) and as the prosthetic group in iodopsin
for bright light and color vision i.e. cones (McDowell, 2008). In maintenance
of integrity of the cornea, retinoic acid is needed to sustain appropriate cell
differentiation (Herrmann and Obeid, 2011).
Vitamin A has gained a reputation as an
anti-infective vitamin (Whitney et al., 2011) essential for normal immune
system maturation and function. There is evidence to suggest that vitamin A
deficiency is a risk factor for low antibody production (Hulea, 2008) and, that vitamin A plays a role in maintenance of
integrity of epithelial surfaces and
development of the lymphoid system
(Shetty, 2010). Vitamin A stimulates antitumor activity in cancer cell lines.
All-trans-retinoic acid exhibited an inhibitory effect on cell growth, cell
cycle and alkaline phosphatase activity in human pancreatic cancer cells in
vitro (Guo et al., 2006).
Vitamin A especially as retinoic acid is required
for differentiation of epithelial cells. Cell differentiation is a process by
which immature cells are transformed into specific type of mature cells, which
form protective linings on many of the body’s organs (Gropper et al., 2009). The integrity of the respiratory,
gastrointestinal, and urogenital tracts, as well as the eye, are protected from
environmental influences by mucous membranes (Elias and Ketcham 2007). Retinoids
perform the latter function in a way that steroid hormones do; this is by
binding to the nuclear chromatin to signal transcriptional processes. Further
retinoic acid has been found to stimulate, synergistically with thyroid
hormone, the production of growth hormone in cultured pituitary cells (Combs,
2012).
Vitamin A functions as an antioxidant to reduce
markers of oxidative damage and inflammation, and therefore may be helpful in
preventing initiation and progression of diseases due to oxidative stress
(Prasad, 2008). Beta carotene is one of the many dietary anti-oxidants present
in foods- others include, vitamin E, Vitamin C, the mineral selenium and
various phytochemicals (Whitney et al., 2011). A study from 1989 to 1995 showed
that higher serum levels of beta- carotene, total carotene, provitamin A and
total carotenoid reduced the harzadous ratios for mortality rates of patients
with cardiovascular diseases and cancer at all sites. (Ito et al., 2006).Vitamin A itself is physiologically significant in
this regard, as retinol and retinal cannot quench singlet oxygen and have only
weak capacities to scavenge free radicals. It however can affect tissue levels
of other antioxidants. Several carotenoids, on the other hand, have been shown
to have direct antioxidant activities. These include beta-carotene, lycopene
and some oxycarotenoids (like lutein and zeaxanthin), which can quench singlet
oxygen or free radicals in the lipid membranes into which they partition (Combs,
2012).
Forms and Sources of Vitamin A
Vitamin A is generally classified into two main groups
possessing biological activity: (i) C-20 unsaturated hydrocarbons including
retinol and its derivatives from animal origin (b) C-40 unsaturated
hydrocarbons including carotene and a number of other provitamin A carotenoids
of plant origin (Heldman and Lund, 2006).
Preformed vitamin A is found in foods of animal
origin the richest sources being liver and fish oil. Milk and milk products and
vitamin A fortified foods such as enriched cereals can also be good sources.
Even butter and eggs provide some vitamin A (Sizer and Whitney, 2013). Eating liver once a week or so is
enough to provides the recommended daily intake. Butter and eggs also provide
some vitamin A to the diet. Because vitamin A is fat soluble, it is lost when
milk is skimmed. To compensate, reduced-fat, low-fat and fat-free milk are
often fortified with vitamin A. Margerine is also usually fortified so as to
provide the same amount of vitamin A as butter (Whitney et al., 2011).
Retinoids refer to any natural or synthetic form of
vitamin A ( Messonnier, 2010). Retinol is the alcohol form of vitamin A. Replacement of the alcohol group by an aldehyde group gives retinal, and
replacement by an acid group gives retinoic acid. Esters of retinol are called
retinyl esters. Vitamin A in animal products exists in several forms, but the
principally exists as long chain fatty acid esters (McDowell, 2008). In several
varieties of seawater and freshwater fish, vitamin A2 is present as a major
form of vitamin A. Vitamin A2 differs from vitamin A in chemical structure as
it has an addition double bond in the cyclohexene ring at the 3,4 position (
Herrmann and obeid, 2011). The most active form of vitamin A is the all-trans
vitamin A. the cis-forms may arise from the all trans-form, and there is a loss
of vitamin A potency due to the conversion. These changes are promoted by
moisture, heat, light and catalysts (McDowell, 2008).
Carotenoids are usually found in plants and plant
products as in inactive forms. They are referred to as provitamin A or vitamin
precursors because the body can convert them into active vitamin A (Insel et
al., 2012). The carotenoids are a diverse group of more than 600 naturally
occurring pigments. All of the carotenoids are antioxidants, and approximately
50 are considered vitamins because they have pro-vitamin A activity (Morley and
Thomas, 2007). Four of these including α-carotene, β-carotene, γ-carotene, and
cryptoxanthine have vitamin A activity of which β-carotene has the greatest
activity. Theoretically, I mol of β-carotene could be converted to 2 mol of
retinal whereas 1 mole of other provitamin A carotenoids yield only one mol of
retinal (McDowell, 2008). Carotenoids can further be classified into provitamin
A and non-provitamin A carotenoids. Provitamin A carotenoids include beta
–carotene, alpha-carotene, gamma-carotene, beta-cryptoxanthin and
alpha-cryptoxanthin (Victor, 2012). Provitamin A carotenoid absorption is
usually low, at around 10-20% and not all absorbed provitamin A carotenoids are
cleaved into vitamin A activitive compounds (Bohn, 2008). Non-provitamin A
carotenoids include lutein, lycopene, zeaxanthin and astaxanthin and according
to Sayo et al., (2013) the molecular
basis of their biological activities is not fully known.
Many plant foods contain beta-carotene, the orange
pigment responsible for the bold colors of many fruits and vegetables. Carrots,
sweet potatoes, pumpkins, cantaloupe, and apricots are all rich sources and
their bright orange color enhances the eye appeal of the plate. Dark green
vegetables, such as spinach, other greens, and broccoli, owe their color to
both chlorophyll and beta-carotene. However colorful vegetables like iceberg,
lettuce, beets and sweet corn don’t contain beet carotene as it my perceived
(Whitney et al., 2011). The vitamin A activity of fruits is generally lower
than that of leafy vegetable. However fruits have more acceptance than
vegetables especially in children.
Mango, papaya and watermelon have the highest concentration of provitamin
A carotenoids (Sommerburg et al.,
2013). The carotenoid content of foods is highly variable and is affected by a
number of factors including genotype (variety and cultivar), season, geography,
cultivation variation, stage of maturity at harvest, handling and postharvest
storage conditions (Tanumihardjo, 2012).
Vitamin A and Night Vision
Vitamin A allows for night and color vision as is a
functioning part of the retina. The retina contains both rod and cone cells.
The former are of interest in low light vision and are rich in a purple pigment
rhodopsin also known as visual purple (Insel et al., 2012). Retinol is utilized in the aldehyde form in the
retina of the eye as the prosthetic group in rhodopsin for dim light vision
(rods) (McDowell, 2008). Each rhodopsin molecule is composed of a protein
called opsin bonded to a molecule of the retinal form of vitamin A (Whitney et al., 2011).
When light strikes rhodopsin, cis-retinal changes in configuration to trans-retinal, subsequently separating from opsin. This metabolic
conversion, in turn, causes a series of reactions leading to a decrease in
sodium entry to sodium channels and a change in membrane potential that is
transmitted to the brain. This neural signal is seen as light and is
transformed into an image that you recognize (Desai, 2000). A visual cycle is
completed when trans-retinal is converted back to cis- retinal which in turn combines with opsin in the outer segment
to form rhodopsin. (Gibney et al., 2012). However, trans-retinal is not recycled to cis-retinal with 100% efficiency.
Instead, some trans-retinal is converted to retinoic acid, which cannot be used
to form rhodopsin. Extra retinal must therefore always be available for vision
to remain optimal. Without enough retinal to reform, night vision becomes
especially difficult, resulting in a condition called night blindness (Mcguire
and Beerman, 2011).The role played by vitamin A in night vision (dark
adaptation) is illustrated in figure 1.
Vitamin A Deficiency
McDowell (2008), states that vitamin A is one of the
few vitamins whose deficiency or excessive amounts constitute a health hazard. Vitamin
A deficiency affects over 250 million preschool children of which close to
500,000 become blind every year and half of them die within 12 months of losing
their sight (WHO, 2013). The deficiency is more prevalent in the developing
world due to inadequate intake whereas toxicity is commonly found in the
developed world as a result of supplementation. Up to a year’s supply of
vitamin A can be stored in the body, 90 percent of it in the liver (Whitney et al., 2013). The extent of vitamin A deficiency can be
assessed by biochemical measures such as plasma or serum retinol or
retinol-binding concetrations (Semba and Bloem, 2008).
According
to McDowell (2008), a diet deficient in Vitamin A causes lesions in the eye, the
process of keratinization leads to drying and hardening of the cornea, which
may progress to permanent blindness. Vitamin A deficiency is the major cause of
preventable blindness in children (Whitney eta al, 2013), loss of vision due to a failure of rhodopsin
formation in the retina; defects in bone growth; defects in reproduction (e.g.,
failure of spermatogenesis in the male and resorption of the fetus in the
female); and defects in growth and differentiation of epithelial tissues
frequently resulting in keratinization of tissues including; the alimentary
,the genital, reproductive, respiratory and urinary tracts (McDowell, 2008).To prevent
the severe deficiencies of vitamin A, the RDI is recommending 5,000
international units for men and women, and 8,000 international units for
pregnant and lactating women (Bruning and Lieberman, 2007).
Vitamin A Toxicity
For optimum general health, the basic optimum daily
intakes for Vitamin A are 5,000-25,000 IU for men and women respectively and
for beta-carotene are 11,000-25,000IU for men and women respectively (Lieberman
et al., 2007). Unlike the water soluble vitamins B and C that are easily eliminated
from the body, vitamin A is fat soluble and therefore hard for the body to
eliminate it (Asprey and Asprey, 2012). The hepatic storage of vitamin A tends
to mitigate against the development of intoxication due to intakes in excess of
physiological needs (combs, 2012). Both forms of active vitamin A i.e. both fat
and water soluble are stored in the liver and can hence be toxic in excess
amounts. However, toxicity is commonly due to persistent large overdoses of
preformed vitamin A in foods derived from animals, fortified foods, or
supplements (Whitney et al.,
2011). More than 1,000 times the
nutritionally required amount can exceed the capacity of the liver to store and
catabolize and will thus produce intoxication (Combs, 2012).
The condition attached to vitamin A toxicity is
called hypervitaminosis A (Nix, 2012).
It may be either acute or chronic. Acute toxicity usually follows a large
single dose of vitamin A and is recognizes by symptoms suggesting an acute rise
in intracranial pressure (McLaren and Kraemer, 2012). Acute symptoms may
include; nausea, headache, fatigue, dizziness and loss of appetite. Chronic
symptoms may include; dry skin, desquamation, cerebral edema, bone and joint
pain, liver damage including cirrhosis, hemorrhages into the skin, and coma
(Higdon and Drake, 2012). Natural beta-carotene, on the other hand, can be
given for long periods of time virtually without risk of toxicity because the
conversion of beta-carotene to active vitamin A is slow (Whitney et al., 2011). The only adverse effect
of taking too much beta-carotene is the possibility of carotenemia, a harmless
condition in which the skin turns a slight orange color (Lieberman et al.,
2007). People take large doses of vitamin A with the aim of having improved
vision, improved skin and resistance to disease. A pregnant woman who takes excess
vitamin A is at a risk of miscarriages, or giving birth to a baby with
malformations (Frankenburg, 2009). Too much vitamin A for a pregnant woman may
disrupt a child’s brain cell activity. Vitamin A competes with vitamin D inside
the body and therefore deprives the body of vitamin D creating a risk of
osteoporosis (Asprey and Asprey, 2012).
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