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Vitamin A
Vitamin A has multiple functions, it is important for
growth and development, for the maintenance of
the immune system and good vision.
Vitamin A is needed by the retina of the eye in the
form of retinal, which combines with protein opsin
to form rhodopsin the light-absorbing molecule
color vision.[4]
Vitamin A also functions in a very different role as
an irreversibly oxidized form of retinol known as
retinoic acid, which is an important hormone-like
growth factor for epithelial and other cells.[5]
Vision
Gene transcription
Immune function
Embryonic development and reproduction
Bone metabolism
Haematopoiesis
Skin and cellular health
Antioxidant activity
Defisiensi vitamin A
Rabun senja : Nictalopia
Bitot's spots
Xerophthalmi
Sumber vitamin A
Liver
Deficiency
Vitamin A deficiency
Prevalence of vitamin A deficiency. Source: WHO
Vitamin A deficiency is common in developing
countries but rarely seen in developed
countries. Approximately 250,000 to 500,000
malnourished children in the developing world
go blind each year from a deficiency of vitamin
A.
Night blindness is one of the first signs of
vitamin A deficiency. Vitamin A deficiency
contributes to blindness by making the cornea
very dry and damaging the retina and cornea.
Retinol is one of the animal forms of vitamin A. It is a diterpenoid and an alcohol. It is convertible
to other forms of vitamin A, and the retinyl ester derivative of the alcohol serves as the storage
form of the vitamin in animals.
When converted to the retinal (retinaldehyde) form, vitamin A is essential for vision, and when
converted to retinoic acid is essential for skin health, teeth remineralization and bone growth.
These chemical compounds are collectively known as retinoids, and possess the structural motif of
all-trans retinol as a common feature in their structure. Structurally, all retinoids also possess a
-ionone ring and a polyunsaturated side chain, with either an alcohol, aldehyde, a carboxylic acid
group or an ester group. The side chain is composed of four isoprenoid units, with a series of
conjugated double bonds which may exist in trans- or cis-configuration.[1]
Retinol is produced in the body from the hydrolysis of retinyl esters, and from the reduction of
retinal. Retinol in turn is ingested in a precursor form; animal sources (liver and eggs) contain
retinyl esters, whereas plants (carrots, spinach) contain pro-vitamin A carotenoids (these may also
be considered simply vitamin A). Hydrolysis of retinyl esters results in retinol, while pro-vitamin A
carotenoids can be cleaved to produce retinal by carotene dioxygenase in the intestinal mucosa.
Retinal, also known as retinaldehyde, can be reversibly reduced to produce retinol or it can be
irreversibly oxidized to produce retinoic acid, which then cannot function as the vitamin in the eye.
Commercial production of retinol typically requires retinal synthesis through reduction of a
pentadiene derivative and subsequent acidification/hydrolysis of the resulting isomer to produce
retinol. Pure retinol is extremely sensitive to oxidization and is prepared and transported at low
temperatures and oxygen free atmospheres. When prepared as a dietary supplement, retinol is
stabilized as the ester derivatives retinyl acetate or retinyl palmitate.[2]
Biosynthesis of retinol
Retinol is synthesized from the breakdown of -carotene.
First the -carotene 15-15-monooxygenase cleaves carotene at the central double bond, creating an epoxide.
This epoxide is then attacked by water creating two
hydroxyl groups in the center of the structure.
The cleavage occurs when these alcohols are reduced to
the aldehydes using NADH.
This compound is called retinal. Retinal is then reduced
to retinol by the enzyme retinol dehydrogenase. Retinol
dehydrogenase is an enzyme that is dependent on NADH.
[6]
Ujian blok
Peranan vitamin A pada penglihatan
Sumber vitmin A yang murah
-