PHG 413 - Vitamin C b1 b2 b3
PHG 413 - Vitamin C b1 b2 b3
PHG 413 - Vitamin C b1 b2 b3
Vitamin B1 (Thiamine)
Vitamin B1 (Thiamine)
The 1st water-soluble B-vitamin family to be discovered.
Since body reserve of thiamine is small (~30mg), a steady
dietary supply of it is important to avoid deficiency.
Because of its central role in energy production, most of
thiamine is located in the muscles.
Once thiamine absorbed, it is rapidly transformed into the
active form, thiamin pyrophosphate (TPP) which acts
as a coenzyme.
Methyl
Bridge Thiazole Ring
Pyrimidine
Ring
Thiamin or Aneurine
(Coenzyme form)
Daily Required amount and Sources
RDA (Recommended Dietary Allowance )is based on
the number of calories in diet:
Thiochrome
Functions of Vitamin B1
1. It act as co-enzyme (TPP) in carbohydrate metabolism
(for glycolysis and Kreb’s cycle enzymes: pyruvate
dehydrogenase and α-ketoglutarate dehydrogenase), which
enable conversion of glucose into biological energy
through oxidative decarboxylation reactions. This role is
important:
To provide energy to the brain.
To improve transmission of nerve impulses by
providing nerves with energy.
To increase the efficiency of the heart muscles.
For the formation of RBC’s.
2. It act as co-enzyme for transketolase which functions in:
The pentose phosphate pathway to synthesize
NADPH.
The pentose sugars: deoxyribose and ribose are
involved in nucleic acids biosynthesis.
Thiamine Antagonists
Oxythiamine is a competitive inhibitor (Amino group
in pyrimidine ring is replaced by hydroxyl group).
Neopyrithiamine (It prevents the phosphorilation of
hydroxy ethyl group that is essential for activity
of the vitamin B1).
Thiaminase (found in raw fish destroys vitamin B1).
Riboflavin phosphate
Ribose moiety
Riboflavin = Vitamin B2
Malnutrition.
Lumiflavin method:
Riboflavin solution or biological
sample is irradiated in alkaline
medium to yielded a chloroform-
soluble lumiflavin, measured by
fluoremetry.
VITAMIN B3
(NIACIN & NIACINAMIDE)
Vitamin B3 (Niacin & Niacinamide)
Two main forms of Vitamin B3 are found in foods:
nicotinic acid (niacin) and nicotinamide
(niacinamide).
Niacin can be partially satisfied by intake of
tryptophan, which is converted by the liver
into niacin.
60 mg of tryptophan can be converted into
about 1mg of niacin.
Dietary requirements for niacin are described in
terms of niacin equivalents (NEs):
1NE = 60mg of tryptophan = 1mg of niacin
RDA: 13- 20 mg/day
Sources of Vitamin B3
Nicotinic acid or Niacin Nicotinamide or Niacinamide
Yeast Bran
Pharmacokinetics of Vitamin B3
Absorption:
At low concentration by active transportation.
At high concentration by passive diffusion.
Transportation:
Both Nicotinic acid and Nicotinamide bind to
plasma proteins for transportation.
Biosynthesis:
The liver can synthesize Niacin from the essential
amino acid Tryptophan, but the synthesis is
extremely slow and requires vitamin B1, B2, and
B6 (60 mg of Tryptophan 1mg of niacin).
Bacteria in the gut may also perform the conversion
but are inefficient.
Functions of Vitamin B3
Treatment of Pellagra.
Toxicity and side effects of vitamin B3
Large doses (500 mg) of niacin (but not niacinamide)
can cause dilation of capillaries tingling and
flushing of the skin.
Flushing of the skin is usually worse if nicotinic acid
is taken on an empty stomach, therefore it should
be taken just after meals.
Niacin in the form of niacinamide does not produce
these side effects.
At doses of > 2.5 g / day, it can produce hypotension,
dizziness, increased blood sugar and uric acid,
liver dysfunction, and increased risk of peptic
ulcer. These effects are gradually adopted and
decreased and are reversible on withdrawal of
nicotinic acid.
Vitamin B3 – Drug Interactions