Water soluble vitamins
Lecture by
Dr.Ilakkia
Thiamine (Vitamin B1)
• 1st
B-complex vitamin to be identified
• Coenzyme of vit B1, (TPP) thiamine
pyrophosphate is involved in
carbohydrate metabolism.
• Thiamine & biotin(sulphur containing
vitamins) contain sulphur in their
structure
Thiamine (Vitamin B1)
RDA : 1-1.5 mg/day
Dietary Sources : whole grain cereals,
yeast, legumes,oilseeds,nuts (groundnuts),
pork, beef & sheep liver
Biochemical functions :
 The multienzyme complex PDH requires
TPP as coenzymes.
Thiamine (Vitamin B1)
Oxidative decarboxylation of α-ketoglutarate to
succinyl CoA &CO2 by α-ketoglutarate
dehydrogenase in TCA cycle requires TPP as
coenzyme.
Oxidative decarboxylation of branched chain
aminoacids (valine, leucine, isoleucine)
requires TPP.
Transketolase of HMP shunt utilises TPP as
coenzyme.
Thiamine (Vitamin B1)
Thiamine triphosphate & thiamine
pyrophosphate are required for acetyl choline
synthesis.
Biochemical changes in Thiamine deficiency
• In thiamine deficiency, glucose metabolism is
impaired & CNS is affected.
• Accumulation of pyruvate & lactate cause
vasodilation and increased cardiac output.
• Transketolase activity in RBCs is decreased
Thiamine (Vitamin B1)
Clinical manifestations
• Prolonged thiamine deficiency causes a
condition known as beri-beri
• Two types
1. Wet beriberi
2. Dry beriberi
Wet Beri-beri
• Characterised by cardiovascular signs & symptoms
such as edema of legs,face & trunk.
• Other CVS manifestations include palpitation,
breathelessness, rapid pulse &tachycardia.
• The underlying mechanisms involve an impaired
energy metabolism in the myocardium leading to
peripheral vasodilation, biventricular heartfailure
with pulmonary congestion and retention of sodium
& water, leading to edema.
• Death may occur due to heart failure.
Dry beriberi
• Nervous system is affected in this type
• It presents with progressive muscle
wasting & peripheral neuropathy.
• Lower limbs are worst affected & walking
becomes difficult.
Infantile Beriberi
• Seen in infants of thiamine
deficient mothers
• Infantile beri-beri occurs
suddenly and severely with
sleepnessness,restlessnes
s vomiting & convulsions.
• Death may occur due to
heart failure.
Wernicke - Korsakoff syndrome
• Inadequate intake & impaired intestinal absorption
of thiamine in chronic alcoholics results in certain
CNS manifestation like paralysis of extraocular
muscles & cerebellar ataxia known as wernicke’s
encephalopathy.
• When there is mental impairment with loss of
memory and apathy, it is called as korsakoff’s
psychosis.When both occur together, the condition
is referred to as Wernicke - Korsakoff‘s
Vitamin B2 (Riboflavin)
• Riboflavin is a yellow fluorescent
substance that is widely distributed in
plant and animal origin.
• Riboflavin in its coenzymic form takes
part in a wide variety of oxidation-
reduction reactions involved in ETC
linked to carbohydrates, lipids and
proteins metabolism.
Vitamin B2 (Riboflavin)
Coenzymes of Riboflavin
Riboflavin exists in 2 active coenzyme forms
1. Flavin mononucleotide (FMN)- formed by
phosphorylation of riboflavin
2. Flavin adenine dinucleotide (FAD)-
synthesised from FMN by addition of AMP
moiety.
Vitamin B2 (Riboflavin)
RDA : 1.5 mg/day
Dietary Sources : Milk & diary products,lean
meat, fish, eggs and legumes. Germination
enhances riboflavin content in cereals and
pulses.
Biochemical Functions
1. FMN & FAD acts as potential redox carriers.
Vitamin B2 (Riboflavin)
2. FMN is an integral component of complex I &
FAD is a part of complex II of ETC.
3. During the transport of reducing equivalents
(NADH) from cytosol to mitochondria FAD is
used.
4. Riboflavin plays a role in Niacin metabolism
5. FMN & FAD are required for the oxidised and
reduced form of NAD & NADP.
Vitamin B2 (Riboflavin)
Deficiency manifestations
• It usually affects the tongue and lips
characterised by glossitis (magenta tongue),
angular stomatitis, cheilosis (fissure like lesions
at the corners of the mouth) and genital
dermatitis.
• FAD- dependent glutathione reductase activity in
RBC is used to measure riboflavin deficiency.
GLOSSITIS
Vitamin B2 (Riboflavin)
• Riboflavin deficiency may occur in newborn
infants suffering from jaundice. Riboflavin is
light sensitive.
Niacin (Vitamin B3)
• Niacin can be synthesised in the body from
tryptophan (60 mg of tryptophan is used to
produce 1 mg of niacin) and it participates in
the metabolism of carbohydrates, fat and
protein. Coenzymes of Niacin
1. Nicotinamide adenine dinucleotide (NAD+)
2. Nicotinamide adenine dinucleotide
phosphate (NADP+)
Niacin (Vitamin B3)
RDA : 20 mg/day
Dietary sources : Liver, meat, beans,
legumes,egg, whole grains & dried yeast
Biochemical Functions
1. NAD+ & NADP+ acts as hydrogen
acceptors and donors in metabolic
pathways.
Niacin (Vitamin B3)
Deficiency Manifestations
Pellagra is a disease caused by the deficiency
of niacin. It is characterised by 3 D’s-
Dermatitis (erythema resembling sunburns),
Diarrhea (loose stools with blood & mucus)
and Dementia (mental changes including
depression and loss of memory)
Pantothenic acid (vitamin B5)
• In greek pantos- everywhere
• Pantothenic acid participates in carbohydrate,
protein & lipid metabolism as coenzyme A
(coenzyme form of pantothenic acid)
RDA : 10 mg/day
Sources : (Plant & animal sources – egg
yolk,liver, yeast,legumes,wholegrains &
vegetables)
Pantothenic acid (vitamin B5)
Biochemical functions
1. More than 70 enzymes in various metabolism
are dependent on CoA.
2. As a component of acetyl CoA, coenzyme A is
considered to be central to the integration of
metabolism.
3. Acyl CoA, Acetyl CoA, propionyl CoA, succinyl
CoA & HMG CoA are derivatives of coenzyme
A.
Pyridoxine (Vitamin B6)
• Vitamin B6 refers to a family of closely related
compounds- pyridoxine, pyridoxal, pyridoxamine.
• The active form of Vitamin B6 is Pyridoxal
phosphate (PLP).
• PLP acts as coenzyme for more than 100
enzymes in metabolic reactions.
Pyridoxine (Vitamin B6)
RDA : 2 mg/day
Sources : wheat bran, rice bran, dried yeast, legumes,
nuts, milk, fish, eggs & leafy vegetables
Biochemical functions
1. Transamination reactions require PLP as
coenzyme
2. PLP is required as a coenzyme by many
decarboxylase enzymes for decarboxylation.
(Histidine, catecholamines, GABA)
Pyridoxine (Vitamin B6)
3. Production of niacin coenzymes require
PLP.
4. The regulatory enzyme of heme
synthesis, ALA synthase is dependent
on PLP and hence B6 deficiency
causes anemia.
5. The phosphorylase enzyme of
glycogenolysis requires PLP
Pyridoxine (Vitamin B6)
6. PLP is involved in the synthesis of
sphingolipids and formation of myelin.
7. Transsulphuration (transfer of sulphur from
methionine to serine to form cysteine) is PLP
dependent.
8. Serine is synthesised from glycine by PLP-
dependent hydroxy methyl transferase.
Pyridoxine (Vitamin B6)
Deficiency Manifestations
• Vitamin B6 deficiency is rare as it is available in
most of the foods
• When deficiency occurs, the symptoms are
Neurological, Hematological and
Dermatological
• Carpel Tunnel syndrome characterised by
synovial swelling and tenderness may occur
due to Vit B6 deficiency
Biotin (Vitamin B7)
• Biotin is a sulphur containing enzyme participates
in carboxylation reactions.
• It plays an important role in gluconeogenesis &
fatty acid synthesis.
• Biotin is popularly known as anti-egg-white injury
factor.
RDA : 200-300 mg/day
Sources : It is widely distributed in foods of plant &
animal origin.
Biotin (Vitamin B7)
• Biotin in food sources occurs in a protein bound form,
an enzyme biotinidase dissociates the vitamin from
the protein and helps in absorption and transport.
Deficiency Manifestations
• Biotin deficiency is uncommon since it is synthesised
by intestinal microflora
• Prolonged use of antibiotics kills the gut bacteria and
consumption of raw eggs result in biotin deficiency.
(symptoms- dermatitis, depression, glossitis &
nausea)
Biotin (Vitamin B7)
Biochemical Functions
1. Conversion of pyruvate to oxaloacetate an
important reaction in gluconeogenesis is
catalysed by biotin dependent pyruvate
carboxylase.
2. Biotin is required for the initial reaction of fatty
acid biosynthesis
3. Propionyl CoA & branched chain aminoacids
requires biotin for its further metabolism.
Folic acid (Vitamin B9)
• The word folate comes from the latin word
folia (meaning leaf)
Coenzyme of Folic Acid
Tetrahydrofolate is the coenzyme form of folic
acid .
Folic acid is reduced to THF by the enzyme
folate reductase.
Folic acid (Vitamin B9)
RDA : 200 µg/day, 400 µg/day during pregnancy &
300 µg/day during lactation
Sources : Green leafy vegetables, cereals,fruits,
eggs & diary products.
Bananas,oranges,cauliflower and broccoli
contain high levels of folate.
Biochemical functions
THF serves as a donor or acceptor of one
carbon units (formyl,methyl).
Folic acid (Vitamin B9)
• THF is involved in the conversion of serine to
glycine, the catabolism of Histidine and the
synthesis of methionine.
• THF is required for the formation of N-
formylmethionine, which initiates protein
biosynthesis
• The one carbon groups are utilised for the
synthesis of C2 & C3 of purine ring.
Folic acid (Vitamin B9)
Deficiency Manifestations
 Pregnant women are more susceptible to folate
deficiency due to their increased requirements.
Macrocytic anemia with megaloblastic changes
in the bone marrow is the characteristic feature
of folate deficiency
Folate deficiency during the first trimester of
pregnancy may lead to neural tube defects in
the fetus.(spina bifida, anencephaly)
Folic acid (Vitamin B9)
Folate deficiency may block the conversion of
homocysteine to methionine, causing the
accumulation of homocysteine.
Hyperhomocysteinemia is known to increase the
risk of coronary heart disease.
Folate deficiency may be associated with different
types of malignancy, especially cervical cancer &
colon cancer.(FIGLU – formimino glutamate is
accumulated & excreted in folate deficiency)
Vitamin B12
• Vitamin B12 is also known as cobalamin,
is required for the maturation of RBC.
• Vitamin B12 is a complex organometallic
compound with a centrally placed cobalt
atom.
• Methylcobalamin & deoxyadenosyl
cobalamine acts as the coenzymes of Vit
B12.
Vitamin B12
RDA : 1µg/day, during pregnancy and
lactation 3µg/day
Sources : It occurs in foods of animal origin. It is not
found in foods of plant origin. Liver, meat,
fish,eggs,milk, curd & cheese.
Vitamin B12
Biochemical Functions
Vitamin B12 is a component of enzymes found in
bacteria.
There are only two reactions identified in humans
1. Synthesis of methionine
2. Conversion of methylmalonyl CoA to succinyl
CoA.
Vitamin B12
Deficiency Manifestations
1. Megaloblastic anemia
2. Subacute combined degeneration
3. Pernicious anemia
4. Coronary artery disease.
Vitamin C
• Also known as ascorbic acid
• Vitamin c is involved in the formation of
collagen.
• Plants & most animals synthesise Vit C
through uronic acid pathway.
• Humans, monkeys, guinea pigs and bats
cannot synthesise ascorbic acid because they
lack an enzyme L- gulanolactone oxidase
Vitamin C
RDA : 60-75 mg/day, 100 mg/day during pregnancy
and lactation.
Sources : Fresh fruits & green leafy vegetables ,
citrus fruits & germinating pulses contain large
amount of vit C
Biochemical functions
1. Collagen formation
Vitamin C
2. Wound healing – post operative cases vit c is
prescribed for surgical wound healing
3. Antioxidant
4. Role in Aminoacid metabolism
5. Role in lipid metabolism
6. Role in iron metabolism
7.Role in hemoglobin metabolism
Vitamin C
8. Phagocytosis
9. Synthesis of hormones
10. Drug metabolism
11. Cell respiration
Deficiency Manifestations
• Vitamin C deficiency causes scurvy
• Poor wound healing & anemia
Vitamin C
• Swollen and painful gums
• Scurvy in infants is known as Barlows disease

Water soluble biochem vitamins- MBBS.pptx

  • 1.
  • 3.
    Thiamine (Vitamin B1) •1st B-complex vitamin to be identified • Coenzyme of vit B1, (TPP) thiamine pyrophosphate is involved in carbohydrate metabolism. • Thiamine & biotin(sulphur containing vitamins) contain sulphur in their structure
  • 4.
    Thiamine (Vitamin B1) RDA: 1-1.5 mg/day Dietary Sources : whole grain cereals, yeast, legumes,oilseeds,nuts (groundnuts), pork, beef & sheep liver Biochemical functions :  The multienzyme complex PDH requires TPP as coenzymes.
  • 5.
    Thiamine (Vitamin B1) Oxidativedecarboxylation of α-ketoglutarate to succinyl CoA &CO2 by α-ketoglutarate dehydrogenase in TCA cycle requires TPP as coenzyme. Oxidative decarboxylation of branched chain aminoacids (valine, leucine, isoleucine) requires TPP. Transketolase of HMP shunt utilises TPP as coenzyme.
  • 6.
    Thiamine (Vitamin B1) Thiaminetriphosphate & thiamine pyrophosphate are required for acetyl choline synthesis. Biochemical changes in Thiamine deficiency • In thiamine deficiency, glucose metabolism is impaired & CNS is affected. • Accumulation of pyruvate & lactate cause vasodilation and increased cardiac output. • Transketolase activity in RBCs is decreased
  • 7.
    Thiamine (Vitamin B1) Clinicalmanifestations • Prolonged thiamine deficiency causes a condition known as beri-beri • Two types 1. Wet beriberi 2. Dry beriberi
  • 8.
    Wet Beri-beri • Characterisedby cardiovascular signs & symptoms such as edema of legs,face & trunk. • Other CVS manifestations include palpitation, breathelessness, rapid pulse &tachycardia. • The underlying mechanisms involve an impaired energy metabolism in the myocardium leading to peripheral vasodilation, biventricular heartfailure with pulmonary congestion and retention of sodium & water, leading to edema. • Death may occur due to heart failure.
  • 10.
    Dry beriberi • Nervoussystem is affected in this type • It presents with progressive muscle wasting & peripheral neuropathy. • Lower limbs are worst affected & walking becomes difficult.
  • 12.
    Infantile Beriberi • Seenin infants of thiamine deficient mothers • Infantile beri-beri occurs suddenly and severely with sleepnessness,restlessnes s vomiting & convulsions. • Death may occur due to heart failure.
  • 13.
    Wernicke - Korsakoffsyndrome • Inadequate intake & impaired intestinal absorption of thiamine in chronic alcoholics results in certain CNS manifestation like paralysis of extraocular muscles & cerebellar ataxia known as wernicke’s encephalopathy. • When there is mental impairment with loss of memory and apathy, it is called as korsakoff’s psychosis.When both occur together, the condition is referred to as Wernicke - Korsakoff‘s
  • 14.
    Vitamin B2 (Riboflavin) •Riboflavin is a yellow fluorescent substance that is widely distributed in plant and animal origin. • Riboflavin in its coenzymic form takes part in a wide variety of oxidation- reduction reactions involved in ETC linked to carbohydrates, lipids and proteins metabolism.
  • 15.
    Vitamin B2 (Riboflavin) Coenzymesof Riboflavin Riboflavin exists in 2 active coenzyme forms 1. Flavin mononucleotide (FMN)- formed by phosphorylation of riboflavin 2. Flavin adenine dinucleotide (FAD)- synthesised from FMN by addition of AMP moiety.
  • 16.
    Vitamin B2 (Riboflavin) RDA: 1.5 mg/day Dietary Sources : Milk & diary products,lean meat, fish, eggs and legumes. Germination enhances riboflavin content in cereals and pulses. Biochemical Functions 1. FMN & FAD acts as potential redox carriers.
  • 17.
    Vitamin B2 (Riboflavin) 2.FMN is an integral component of complex I & FAD is a part of complex II of ETC. 3. During the transport of reducing equivalents (NADH) from cytosol to mitochondria FAD is used. 4. Riboflavin plays a role in Niacin metabolism 5. FMN & FAD are required for the oxidised and reduced form of NAD & NADP.
  • 18.
    Vitamin B2 (Riboflavin) Deficiencymanifestations • It usually affects the tongue and lips characterised by glossitis (magenta tongue), angular stomatitis, cheilosis (fissure like lesions at the corners of the mouth) and genital dermatitis. • FAD- dependent glutathione reductase activity in RBC is used to measure riboflavin deficiency.
  • 19.
  • 22.
    Vitamin B2 (Riboflavin) •Riboflavin deficiency may occur in newborn infants suffering from jaundice. Riboflavin is light sensitive.
  • 23.
    Niacin (Vitamin B3) •Niacin can be synthesised in the body from tryptophan (60 mg of tryptophan is used to produce 1 mg of niacin) and it participates in the metabolism of carbohydrates, fat and protein. Coenzymes of Niacin 1. Nicotinamide adenine dinucleotide (NAD+) 2. Nicotinamide adenine dinucleotide phosphate (NADP+)
  • 24.
    Niacin (Vitamin B3) RDA: 20 mg/day Dietary sources : Liver, meat, beans, legumes,egg, whole grains & dried yeast Biochemical Functions 1. NAD+ & NADP+ acts as hydrogen acceptors and donors in metabolic pathways.
  • 25.
    Niacin (Vitamin B3) DeficiencyManifestations Pellagra is a disease caused by the deficiency of niacin. It is characterised by 3 D’s- Dermatitis (erythema resembling sunburns), Diarrhea (loose stools with blood & mucus) and Dementia (mental changes including depression and loss of memory)
  • 26.
    Pantothenic acid (vitaminB5) • In greek pantos- everywhere • Pantothenic acid participates in carbohydrate, protein & lipid metabolism as coenzyme A (coenzyme form of pantothenic acid) RDA : 10 mg/day Sources : (Plant & animal sources – egg yolk,liver, yeast,legumes,wholegrains & vegetables)
  • 27.
    Pantothenic acid (vitaminB5) Biochemical functions 1. More than 70 enzymes in various metabolism are dependent on CoA. 2. As a component of acetyl CoA, coenzyme A is considered to be central to the integration of metabolism. 3. Acyl CoA, Acetyl CoA, propionyl CoA, succinyl CoA & HMG CoA are derivatives of coenzyme A.
  • 28.
    Pyridoxine (Vitamin B6) •Vitamin B6 refers to a family of closely related compounds- pyridoxine, pyridoxal, pyridoxamine. • The active form of Vitamin B6 is Pyridoxal phosphate (PLP). • PLP acts as coenzyme for more than 100 enzymes in metabolic reactions.
  • 29.
    Pyridoxine (Vitamin B6) RDA: 2 mg/day Sources : wheat bran, rice bran, dried yeast, legumes, nuts, milk, fish, eggs & leafy vegetables Biochemical functions 1. Transamination reactions require PLP as coenzyme 2. PLP is required as a coenzyme by many decarboxylase enzymes for decarboxylation. (Histidine, catecholamines, GABA)
  • 30.
    Pyridoxine (Vitamin B6) 3.Production of niacin coenzymes require PLP. 4. The regulatory enzyme of heme synthesis, ALA synthase is dependent on PLP and hence B6 deficiency causes anemia. 5. The phosphorylase enzyme of glycogenolysis requires PLP
  • 31.
    Pyridoxine (Vitamin B6) 6.PLP is involved in the synthesis of sphingolipids and formation of myelin. 7. Transsulphuration (transfer of sulphur from methionine to serine to form cysteine) is PLP dependent. 8. Serine is synthesised from glycine by PLP- dependent hydroxy methyl transferase.
  • 32.
    Pyridoxine (Vitamin B6) DeficiencyManifestations • Vitamin B6 deficiency is rare as it is available in most of the foods • When deficiency occurs, the symptoms are Neurological, Hematological and Dermatological • Carpel Tunnel syndrome characterised by synovial swelling and tenderness may occur due to Vit B6 deficiency
  • 33.
    Biotin (Vitamin B7) •Biotin is a sulphur containing enzyme participates in carboxylation reactions. • It plays an important role in gluconeogenesis & fatty acid synthesis. • Biotin is popularly known as anti-egg-white injury factor. RDA : 200-300 mg/day Sources : It is widely distributed in foods of plant & animal origin.
  • 34.
    Biotin (Vitamin B7) •Biotin in food sources occurs in a protein bound form, an enzyme biotinidase dissociates the vitamin from the protein and helps in absorption and transport. Deficiency Manifestations • Biotin deficiency is uncommon since it is synthesised by intestinal microflora • Prolonged use of antibiotics kills the gut bacteria and consumption of raw eggs result in biotin deficiency. (symptoms- dermatitis, depression, glossitis & nausea)
  • 35.
    Biotin (Vitamin B7) BiochemicalFunctions 1. Conversion of pyruvate to oxaloacetate an important reaction in gluconeogenesis is catalysed by biotin dependent pyruvate carboxylase. 2. Biotin is required for the initial reaction of fatty acid biosynthesis 3. Propionyl CoA & branched chain aminoacids requires biotin for its further metabolism.
  • 36.
    Folic acid (VitaminB9) • The word folate comes from the latin word folia (meaning leaf) Coenzyme of Folic Acid Tetrahydrofolate is the coenzyme form of folic acid . Folic acid is reduced to THF by the enzyme folate reductase.
  • 37.
    Folic acid (VitaminB9) RDA : 200 µg/day, 400 µg/day during pregnancy & 300 µg/day during lactation Sources : Green leafy vegetables, cereals,fruits, eggs & diary products. Bananas,oranges,cauliflower and broccoli contain high levels of folate. Biochemical functions THF serves as a donor or acceptor of one carbon units (formyl,methyl).
  • 38.
    Folic acid (VitaminB9) • THF is involved in the conversion of serine to glycine, the catabolism of Histidine and the synthesis of methionine. • THF is required for the formation of N- formylmethionine, which initiates protein biosynthesis • The one carbon groups are utilised for the synthesis of C2 & C3 of purine ring.
  • 39.
    Folic acid (VitaminB9) Deficiency Manifestations  Pregnant women are more susceptible to folate deficiency due to their increased requirements. Macrocytic anemia with megaloblastic changes in the bone marrow is the characteristic feature of folate deficiency Folate deficiency during the first trimester of pregnancy may lead to neural tube defects in the fetus.(spina bifida, anencephaly)
  • 40.
    Folic acid (VitaminB9) Folate deficiency may block the conversion of homocysteine to methionine, causing the accumulation of homocysteine. Hyperhomocysteinemia is known to increase the risk of coronary heart disease. Folate deficiency may be associated with different types of malignancy, especially cervical cancer & colon cancer.(FIGLU – formimino glutamate is accumulated & excreted in folate deficiency)
  • 42.
    Vitamin B12 • VitaminB12 is also known as cobalamin, is required for the maturation of RBC. • Vitamin B12 is a complex organometallic compound with a centrally placed cobalt atom. • Methylcobalamin & deoxyadenosyl cobalamine acts as the coenzymes of Vit B12.
  • 44.
    Vitamin B12 RDA :1µg/day, during pregnancy and lactation 3µg/day Sources : It occurs in foods of animal origin. It is not found in foods of plant origin. Liver, meat, fish,eggs,milk, curd & cheese.
  • 45.
    Vitamin B12 Biochemical Functions VitaminB12 is a component of enzymes found in bacteria. There are only two reactions identified in humans 1. Synthesis of methionine 2. Conversion of methylmalonyl CoA to succinyl CoA.
  • 46.
    Vitamin B12 Deficiency Manifestations 1.Megaloblastic anemia 2. Subacute combined degeneration 3. Pernicious anemia 4. Coronary artery disease.
  • 47.
    Vitamin C • Alsoknown as ascorbic acid • Vitamin c is involved in the formation of collagen. • Plants & most animals synthesise Vit C through uronic acid pathway. • Humans, monkeys, guinea pigs and bats cannot synthesise ascorbic acid because they lack an enzyme L- gulanolactone oxidase
  • 48.
    Vitamin C RDA :60-75 mg/day, 100 mg/day during pregnancy and lactation. Sources : Fresh fruits & green leafy vegetables , citrus fruits & germinating pulses contain large amount of vit C Biochemical functions 1. Collagen formation
  • 49.
    Vitamin C 2. Woundhealing – post operative cases vit c is prescribed for surgical wound healing 3. Antioxidant 4. Role in Aminoacid metabolism 5. Role in lipid metabolism 6. Role in iron metabolism 7.Role in hemoglobin metabolism
  • 50.
    Vitamin C 8. Phagocytosis 9.Synthesis of hormones 10. Drug metabolism 11. Cell respiration Deficiency Manifestations • Vitamin C deficiency causes scurvy • Poor wound healing & anemia
  • 51.
    Vitamin C • Swollenand painful gums • Scurvy in infants is known as Barlows disease