Vitamin B12 (Cyanocobalamin or Cobamide)
(Anti pernicious anaemia factor, Extrinsic factor of
Castle)
Introduction
In 1948 Smith and Parker isolated Cyanocobalamin
from the liver, In 1955 its complex structure was determined,
Chemistry
The central portion of the molecule consists of four
reduced and extensively substituted pyrrol rings surrounding single cobalt
atom. The central structure is referred to as a corrin ring. Below the ring
system it contains the base dimethyl benziminazole linked with ribose and
phosphoric acid.
Properties
·
Red crystalline substance
·
soluble in water
·
contains cobalt (45%)
·
Molecular weight is 1,500
Distribution
Animal
sources
·
Liver (1 unit of liver extract contains
approximately 1 micro-gram of B12)
·
kidney
·
eggs
·
meat
·
milk
Plant
sources
·
Absent
Absorption
and excretion
Absorption takes place from the ileum. Intrinsic It
is stored in the liver. Vitamin B12 is excreted in the faeces and
urine.
Functions
(1) Essential for the formation and
maturation of red blood cells.
(2) It plays an essential role in
the synthesis of nucleic acid.
(3) Increases the white cell count
and the platelets through its action in the bone-marrow.
(4) Concerned with the maintenance
of normal health and activity of certain parts of the nervous system.
(5) Biosynthesis of methyl group is increased
by vitamin B12, and this vitamin plays a part in increasing enzymatic rate in
one carbon metabolism and synthesis.
(6)This vitamin has also helps in
transmethylation process,
(7) Formation of lipid from
carbohydrate is influenced by vitamin B12
(9) A coenzyme of vitamin B12 helps
in isomerization of glutamic acid to methyl aspartate.
Deficiency
signs
(1) Pernicious or macrocytic or
megaloblastic anaemia is produced. It brings about hyperglycemia.
(2) Other important features in
vitamin B12 deficiency are mucosal atrophy and inflammation of tongue, mouth,
etc.
(3) Degenerative lesions of the
posterior and lateral columns of the spinal cord.
Daily
requirement
A daily intake of 1.0 gm is sufficient to prevent
deficiency.
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