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The discovery of the first vitamin was published in 1911 by a Polish biochemist, Casimir Funk. The term vitamine is derived from the words vita (meaning lifegiving) and amine (were originally thought to be amines). Although not all vitamins are amines, they are organic compounds req
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1. Vitamins 1
2. The discovery of the first vitamin was published in 1911 by a Polish biochemist, Casimir Funk.
The term vitamine is derived from the words vita (meaning lifegiving) and amine (were originally thought to be amines).
Although not all vitamins are amines, they are organic compounds required by humans in small amounts from the diet.
Usually only a few milligrams (mg) or micrograms (ľg) are needed per day, but these amounts are essential for health. 2
3. Most vitamins cannot be made by the body, so have to be provided by the diet.
An exception is vitamin D which can be obtained by the action of sunlight on the skin.
Small amounts of a B vitamin (niacin) can be made from the essential amino acid, tryptophan.
Vitamin K is formed by bacterial action in the large intestine. 3
4. Vitamins do not contain energy per se, but they help regulate energy process in the body.
Vitamins have a variety of functions in the body: some are co-factors in enzyme activity, some are antioxidants (prevent oxygen from doing damage in the body) and one (vitamin D) is a pro-hormone.
If insufficient amounts of vitamins are available to the body because of a poor diet or some medical condition (e.g. malabsorption of nutrients), specific symptoms will appear and can develop into a deficiency disease.
Vitamin deficiency diseases are rare in the westernized society, but still occur in some parts of the world.
Vitamins and minerals are measured in milligrams (mg), micrograms (ľg) and international units (IU). 4 deficiency di´finsideficiency di´finsi
5. How much of the vitamins do we need? The body requires different amounts of each vitamin because each of them has a different function.
People have different requirements too, according to their age, gender, level of activity and state of health.
5
6. Vitamin supplements
Although most people are able to meet their requirements for vitamins by eating a varied diet, there are certain groups of the population who have higher than normal requirements, e.g. the sick, those taking certain drugs and pregnant women.
Infants and young children are recommended to have supplements of vitamins A and D for at least 2 years.
Some women many require additional iron if menstrual losses are high.
The evidence for benefits from antioxidant supplementation for athletes is mixed.
6
7. Vitamins have been traditionally grouped into two categories:
the fat soluble vitamin (A, D, E, K),
and the water soluble vitamins (C, B complex).
Originally, vitamins were given letters (A, B, C, etc.) but now are usually referred to by their chemical names, e.g. folate. 7
8. The fat soluble vitamins are stored in the body and their deficiencies are relatively rare.
On the other hand, excessive intakes may be toxic.
The water soluble vitamins are not stored to any significant extent in the body.
Excess supplements of these vitamins are usually excreted in the urine. 8
9. The water soluble vitamins
10. Vitamin C (Ascorbic acid ) Vitamin C is the most famous vitamin.
sources: almost exclusively in foods from plant sources (citrus fruits, broccoli, peppers, kiwi, strawberries, potatoes, tomatoes), although fresh milk and liver contain small amounts.
RDA: 80 mg
one kiwi, small orange or 4 strawberries provides 100% of RDA
10
11. Vitamin C - Ascorbic Acid Structure
Metabolism
oxidation/reduction
dehydroascorbic acid
dehydroascorbate reductase
glutathione (GSH)
glutamate-cysteine-glycine 11
12. ASCORBIC ACID AND DEHYDROASCOBIC ACID
13. Major function in the body helps form collagen
helps in growth and repair of body tissue and blood vessels
prevents scurvy
a strong antioxidant
aids in absorption of iron
helps regulate the metabolism of cholesterol and amino acids
13
14. Functions of Vitamin C Enhances absorption of iron
reduces iron to more absorbable ferrous form
chelates with ferrous ion to make it more soluble 14
15. Functions of Vitamin C Hydroxylation of proline and lysine
post-translational reaction of procollagen
hydroxylated collagen can be cross-linked to triple helix collagen
Scurvy - weak collagen 15
16. Functions of Vitamin C Hydroxylation Reactions
Involves O2 and metal coenzyme
(ferrous, cuprous)
Carnitine synthesis
Tyrosine synthesis & catabolism
16
17. Functions of Vitamin C Hydroxylation Reactions
Synthesis of Neurotransmitters
Dopamine
Norepinephrine
Serotonin
Bile acid synthesis 17
18. Functions of Vitamin C Antioxidant Activity
Reacts and removes active oxygen species
Pro-oxidant Activity
Reduces metals to their pro-oxidant forms 18
19. Scurvy Bleeding gums
petechiae
easy bruising
impaired wound healing and bone repair
joint pain
anemia 19
20. RDA for Vitamin C 10 mg/day prevents scurvy
historic RDAs 45-70 mg (60mg in 1989), 75mg in 2000
prevention of scurvy vs antioxidant effect with supplements? 20
22. Ascorbic acid defiency: scurvy
hemorrhage from mucous membranes, mouth and GIT, skin and muscles
gingivitis: swelling, tenderness, redness and ulceration of gums
loosening or loss of teeth
swelling of joints
rarefaction of bones and dentine
23. deficiency: weakness, slows wound healing, bleeding gums, scurvy
The vitamin can be decreased by cigarette smoking, stressful injuries, stress and oral contraceptives.
hypervitaminosis: excessive doses can cause kidney stones and break down red blood cells 23
24. Toxicity of Vitamin C UL adults: 2000mg/d
Osmotic diarrhea
Oxalate kidney stones
Decreases uric acid reabsorption resulting in increased risk of gout
Affects diagnostic tests in feces and gout
fecal blood
urinary glucose 24
25. VITAMIN B COMPLEX Eight vitamins that make up the B Complex of vitamins:
B1 - Thiamine
B2 - Riboflavin
B3 - Niacin
B5 - Panthotenic acid
B6 - Pyridoxine
B7 Biotin
B9 - Folate (folic acid)
B12 (Cobalamin, cyanocobalamin)
25
26. Vitamins B group Vitamin B1 (Thiamine)
Vitamin B2 (Riboflavin)
Vitamin B3 or Vitamin P or Vitamin PP (Niacin)
Vitamin B5 (Pantothenic acid)
Vitamin B6 (Pyridoxine and Pyridoxamine)
Vitamin B7 or Vitamin H (Biotin)
Vitamin B9 or Vitamin M and Vitamin B-c (Folic acid)
Vitamin B12 (Cyanocobalamin)
27. Thiamin (Vitamin B1) sources: whole grains, nuts and meat.
White and brown flour and many breakfast cereals are usually fortified with thiamin.
RDA: 1,5 mg for men, 1,1 mg for women
function: Thiamin is needed to release energy from carbohydrate. It is involved in the normal function of the nervous system and the heart.
27
28. 28
29. Thiamin Structure
pyrimidine ring
thiazole ring
methyl bridge 29
30. 30
31. Conversion of thiamine to TPP
32. 32
33. 33
34. 34
35. 35
36. Chemical Characteristics Very labile nutrient
Heat
stable in crystalline form
less stable in solution
Alkali - very unstable with heat
baking soda 36
37. Chemical Characteristics Sulfites - decomposes B-1
High cooking/processing losses
heat
leaching 37
38. Absorption of B-1 in duodenum
active transport (low thiamin levels)
requires sodium and folic acid
passive transport (hi B-1 levels) 38
39. Absorption of B-1 phosphorylation to active form inside cells (TPP)
transported via portal blood
no significant storage, excess to urine 39
40. 40
41. Thiamin Deficiency Beri-Beri
anorexia, fatigue, depression
effects on
cardiovascular system
nervous system 41
42. Infantile Beri-Beri first 6 months
breast milk deficient in B-1
mother w/o symptoms
rapid onset
cyanosis, tachycardia, labored breathing
heart failure and death 42
43. Wet Beri Beri symptoms similar to congestive heart failure
Pitting edema - trunk, limbs, face
labored breathing, tachycardia
rapid deterioration
fatal cirulatory collapse
responds rapidly to B-1 supplements 43
44. Dry Beri-Beri no edema
progressive wasting
numbing and weakening of extremities
chronic infections 44
45. Thiamine assay biologic assay in animals time consuming and costly (curative or protective)
microbiologic using bacteria which require thiamine for growth
chemical/fluorescent assay conversion of thiamine to thiochrome by alkaline ferricyanide
46. Assessment of Thiamin Status Urinary thiamin excretion
Blood or serum thiamin concentration
[pyr + lac] in blood
erythrocyte transketolase activity
stimulation with B-1 46
47. Lipoic acid lipoic acid is a co-factor found in pyruvate dehydrogenase and a-ketoglutarate dehydrogenase, two multienzymes involved in a-keto acid oxidation
lipoic acid functions to couple acyl group transfer and electron transfer during oxidation and decarboxylation of a-ketoacids
no evidence exists of a dietary lipoic acid requirement in humans; therefore it is not considered a vitamin
49. Riboflavin (Vitamin B2) sources: milk, eggs, fortified breakfast cereals, liver and green vegetables.
RDA: 1,7 mg for men, 1,3 mg for women
function: Riboflavin is required to release energy from protein, carbohydrate and fat. It is also involved in the transport and metabolism of iron in the body and is needed for the normal structure and function of mucous membranes and skin.
deficiency: Although there is no specific deficiency disease, low intakes lead to dryness and cracking of the skin around the mouth and nose.
hypervitaminosis: general lack of toxicity, excess riboflavin is excreted in the urine.
51. Riboflavin vitamin B2, lactoflavin (ovo, hepato, verdo), vitamin G
a heterocyclic flavin linked to ribose analogous to the nucleosides in RNA
orange-yellow fluorescent compound
found in significant quantities in green leafy vegetables, milk and meats
heat stable, but easily destroyed by light
recommended intake is related to energy intake (kcal) RDA 1 2 mg/day
54. 54
55. 55
56. 56
57. 57
58. Riboflavin 2 cofactors are involved:
riboflavin phosphate (flavin mononucleotide, FMN)
flavin adenine dinucleotide (FAD)
involved in the metabolism of carbohydrates, fats and proteins (flavin dehydrogenases/flavoproteins)
hydrogen carriers in the respiratory chain
61. Riboflavin
63. Riboflavin
64. Riboflavin Enzymes utilizing riboflavin cofactors:
NADH dehydrogenase
succinate dehydrogenase
d and l-amino acid oxidases
pyridoxine-5-phosphate oxidase
glutathione reductase
xanthine oxidase
In some enzymes, the cofactor is covalently bonded to an amino acid (dehydrogenases)
65. Dehydrogenase reaction
66. Amino acid oxidases
67. Xanthine oxidase
68. Fatty acyl-CoA desaturase
69. Riboflavin deficiency seldom seen in industrialized societies
deficiency when seen:
cheilosis (vertical fissure in the lips)
angular stomatitis (craks in the corner of the mouth)
glossitis
photophobia
seborrheic dermatitis
normochromic normocytic anemia
usually encountered along with pellagra (niacin deficiency)
newborns treated for hyperbilirubinemia by phototherapy (riboflavin is unstable to light)
70. Niacin Structure
Nicotinic Acid = Niacin
Nicotinamide = Niacinamide 70
71. Niacin (nicotinic acid, B 3) sources: Niacin is found in most foods, although meat is the major source. It can also be made by the body from the amino acid tryptophan.
RDA: 19 mg for men, 15 mg for women
function: It is required for the release of energy from food, for the normal structure of the skin and mucous membranes and for normal functioning of the nervous system.
71
72. deficiency: a disease called pellagra (symptoms: high sensitivity to sunlight, aggression, dermatitis, red skin lesions, insomnia...)
Nicotinic acid is sometimes prescribed by doctors (as a drug) to treat high blood lipid levels, i.e. hyperlipidaemia (excess fat in the blood).
hypervitaminosis: rare, headache, nausea, burning and itching skin
72
74. 74
75. Cofactor Forms of Niacin Nicotinamide Adenine Dinucleotide
NAD
nicotinamide-ribose-PP-ribose-adenine
Nicotinamide Adenine Dinucleotide Phosphate
NADP
nicotinamide-ribose-PP-(ribose-P)-adenine 75
76. 76
77. 77
78. Chemical Characteristics of Niacin relatively stable to
light
heat
oxidation
alkali
major losses due to leaching 78
79. Digestion and Absorption of Dietary Niacin Coenzyme form in food
hydrolysis in small intestine to free vitamin
absorbed in duodenum
nicotinic acid protein bound in corn
requires alkali treatment (lime) to release niacin 79
80. Metabolism of B-3 conversion of free vitamin to coenzyme in all cells
no storage
excesses metabolized in liver to variety of chemicals
metabolites excreted in urine 80
81. Synthesis of B-3 from Tryptophan
pathway requires B-6 (also B2)
60 mg of TRY required to make 1 mg B-3
corn is low in both B-3 and TRY 81
82. Biochemical Functions of B-3 Oxidation-Reduction Reactions (NAD/NADH
Dehydrogenases
Electron Transport System
Involved in energy production 82
83. Biochemical Functions of B-3 Synthetic Pathways (NADPH)
FA synthesis
Cholesterol synthesis
Purine & Pyrimidine synthesis
83
84. Cofactor Forms of Niacin Nicotinamide Adenine Dinucleotide
NAD
nicotinamide-ribose-PP-ribose-adenine
Nicotinamide Adenine Dinucleotide Phosphate
NADP
nicotinamide-ribose-PP-(ribose-P)-adenine 84
85. 85
86. Deficiency of B-3 Pellegra (fig 4-18)
Dermatitis
scaly dermatitis, sun exposed
Dementia
confused, disoriented
Diarrhea
irritation/inflammation of mucous membranes 86
87. Assessment of B-3 Status Urinary excretion of niacin metabolites
N-methyl nicotinamide
2-pyridone 87
88. Niacin Toxicity 1-3g/day for treatment of hypercholesterolemia
increases histamine release
skin flushing
increase risk of peptic ulcers
liver injury
time release forms greater risk of liver injury 88
89. Pantothenic acid (Vitamin B 5) sources: beef liver, lean meats, milk, eggs, legumes, whole grain products, most vegetables
A recent study also suggests that gut bacteria in humans can generate pantothenic acid
RDA: 47 mg 89
90. 90
91. Vitamin B5(Pantothenic acid) It is a peptide substance composed of Pantoic acid and b-Alanine.
It can be present as the Calcium salt or the Alcohol Pantothenol.
92. Pantothenic acid (vitamin B5)
93. Pantothenic acid a yellow viscous oil (free acid)
stable to moist heat (not to dry heat) and to oxidizing and reducing agents
hydrolyzed in acid or alkaline medium
sources (numerous): liver, kidney, eggs, lean beef, milk, molasses, cabbage, cauliflower, broccoli, peanuts, sweet potatoes, kale (derive its name from everywhere)
94. Pantothenic acid serves in its activated form as the cofactor for coenzyme A (CoA) and the acyl carrier protein (ACP)
first phosphorylated by ATP to 4-phosphopantothenate
next is the formation of 4-phosphopantetheine by addition of cysteine and decarboxylation
adenylation by ATP forms dephospho-CoA
phosphorylation to the 3-OH of the ribose generates CoA (coenzyme A)
96. Coenzyme A performs a vital role by transporting acetyl groups from one substrate to another
the key to this action is the reactive thioester bond in the acetyl form of CoA
the thioester bond is stable enough that it can survive inside the cell, but unstable enough that acetyl-CoA can readily transfer the acetyl group to another molecule
97. Example of an acetylation reaction
98. Pantothenic acid Deficiency:
rats
graying of hair/fur in black rats
dermatitis
inflammation of nasal mucosa
hemorrhage of adrenal cortex
humans
has not been encountered or extremely rare
difficult to induce with either synthetic diets and/or with antagonists (omega-methylpantothenic acid
99. Pantothenic acid vague symptoms in human deficiency:
numbness and tingling in feet burning foot
fatigue
GIT disturbances
available pharmaceutically as calcium pantothenate (d-isomer) and as racemic mixture
5 - 7 mg/day appear to prevent signs of deficiency
appears to be non-toxic (up to 10-20 gm have been tolerated)
100. Pyridoxine (Vitamin B6) Vitamin B6 comprising 3 forms pyridoxine, pyridoxal and pyridoxamine.
sources: is found in a variety of foods: beef, fish and poultry are rich sources. It also occurs in eggs, whole-grains and some vegetables.
RDA: 2 mg for men, 1,6 mg for women
100
101. 101
102. 102
103. 103
104. 104
105. 105
106. Pyridoxine (vitamin B6)
107. Other forms of B-6
108. Pyridoxine
widespread occurrence
pyridoxine: mostly in vegetable products
pyridoxal and pyridoxamine: mostly in animal products
pyridoxine is stable in acid solution, but unstable in neutral or alkaline solutions (destroyed by light)
109. Pyridoxal phosphate pyridoxine is converted to pyridoxal phophate by phosphorylation and oxidation to the aldehyde
pyridoxal phosphate is then attached to the holoenzyme via a covalent bond to a lysine residue (a Schiffs base)
the Schiffs base bond is readily broken and reformed
this reversibility is very important in the biochemical action of this cofactor
110. Pyridoxal phosphate Biochemical functions:
Decarboxylation of amino acids
Transaminase reactions
Racemization reactions
Aldol cleavage reactions
Transulfuration reactions
Conversion of tryptophan to niacin
Conversion of linoleic acid into arachidonic acid (prostaglandin precursor)
Formation of sphingolipids
111. Important transaminases ALT ( alanine aminotransferase)
formerly known as SGPT (serum glutamate pyruvate transaminase)
alanine + alpha-ketoglutarate = pyruvate + glutamate
increased serum level in liver injury
112. Important transaminases AST (aspartate aminotransferase)
formerly known as SGOT (serum glutamate oxaloacetate transaminase)
aspartate + alpha-ketoglutarate = oxaloacetate + glutamate
elevated when heart and/or liver are damaged
113. Important decarboxylases
114. Mechanism for transamination reaction
115. Pyridoxine deficiency:
difficult to produce in humans
may be accomplished artificially with a pyridoxine antagonist (deoxypyridoxine)
symptoms include: nausea and vomiting, seborrheic dermatitis, depression and confusion, mucous membrane lesions, peripheral neuritis, anemia
116. Pyridoxine antagonists
117. Biotin (Vitamin B 7 or H) sources: meats, legumes, milk, egg yolk, whole grain products, most vegetables
RDA: 300 ľg
function: It is a coenzyme in the metabolism of carbohydrates, fats, and protein.
deficiency: rare, fatigue, nausea, skin rashes
hypervitaminosis: general lack of toxicity
Biotin supplements are often recommended as a natural product to counteract the problem of hair loss. 117
118. Biotin
119. 119
120. Biotin an imidazole sulfur containing compound
sometimes referred to as vitamin B7 or vitamin H
widely distributed in foods (liver, kidney, milk, molasses)
a large portion of the daily need of biotin is met by synthesis by intestinal bacteria
deficiency is usually the result of a defect in utilization rather than simple dietary deficiency
121. Reactions involving biotin enzymes
122. Biotin like lipoic acid, biotin is converted to its coenzyme form (called biotinyllysine or biocytin) by formation of a covalent amide bond to the nitrogen of a lysine residue
like lipoic acid it performs a highly specialized function : adds a carboxyl group to substrates
123. Biotin deficiency:
quite uncommon
can be induced by feeding raw egg white (avidin)
avidin is a protein which binds tighly with biotin (MW 70,000)
symptoms are: anorexia, nausea, muscle pain, fine scaly desquamation of the skin
requirements: 150 200 mcg/day
therapeutic use: in babies with infantile seborrhea (cradle cap) and Leiners disease
124. Folate (vitamin B 9) Folic acid is the synthetic form of the vitamin and the most stable. It is used in supplements and for food fortification. Various folates are found in both plant and animal foods.
sources: liver, yeast extract, orange juice and green leafy vegetables. Various foods, e.g. breakfast cereals and bread may be fortified with folic acid.
124
125. 125
126. 126
127. Folic Acid / Folacin Structure
pteridine ring - PABA - glutamate
Stability
very sensitive to heat
easily oxidized
leached 127
128. FOLIC ACID absorbed by both active and passive transport
on the average we absorb 50 -200ug per day (about 10 -25% of dietary intake)
storage is in the form of 5-methyl THF (5 -20 mg)
found in green vegetable, dietary yeasts, liver, kidney
bacteria synthesize their own folic acid (dihydropteroate synthetase)
129. Digestion & Absorption dietary form: polyglutamyl folate
glutamate gamma linked
folate absorbed as monoglutamate (free folate)
dietary supplement: free folate 129
130. 130
131. Folate Metabolism Intestinal Cells
folate reduced to tetrahydrofolate
folate reductase
inhibited by methotrexate (chemotheraputic drug)
methylated to N5-methyl-THF
primary blood form 131
132. Folate Functions Single carbon metabolism 132
133. 133
134. Folic acid Biochemical functions
one carbon fragment transfer (formyl, methyl, hydroxymethyl)
conversion of homocysteine to methionine
conversion of serine to glycine
synthesis of thymidylic acid
synthesis of purines (de novo)
histdine metabolism
synthesis of glycine
137. Deficiency of folic acid abnormal metabolism of folates
folic acid antagonists (dihydrofolate reductase inhibibitors - methotrexate, pyrimethamine, trimethoprim)
enzyme deficiency
vitamin B12 deficiency
oral contraceptives
increased requirement
pregnancy, infancy
138. Folate Functions Interconversion of serine and glycine
ser + THF <---> gly + 5,10-Me-THF
Degradation of histidine
his->->->formiminoglutamate(FIGLU)
FIGLU+THF -> glu + 5-forminino-THF
histidine load test
Functional test for folate status 138
139. Folate Functions Purine and Pyrimidine Synthesis
dUMP + 5,10-Me-THF -> dTMP + THF
Methionine Synthesis
homocysteine + 5-Me-THF -> MET + THF
MET as a methyl donor for choline synthesis 139
140. Folate Deficiency Megaloblastic Anemia
decreased DNA synthesis
failure of bone marrow cells to divide
normal protein synthesis
results in large immature RBCs
contrast with microcytic hypochromic anemia 140
141. Deficiency of folic acid Inadequate intake
defective absorption (most common)
sprue
gastric resection and intestinal disorders
acute and chronic alcoholism
drugs (anticonvulsants and oral contraceptives)
pregnancy
pellagra
142. Folate and Neural Tube Defects Defects in formation of neural tube (brain & spinal cord)
First two months gestation
Anencephaly
absence of cerebral hemispheres 142
143. Folate and Neural Tube Defects Spina bifida
defective closure of vertebral column
spinal cord protrusion from spinal column results in damage to spinal cord
lower limb and hip paralysis
rectal and bladder problems
143
144. NTD Prevalence US:
4000 live births with NTDs/yr
1/1000 pregnancies
World:
400,000 live births with NTDs/yr 144
145. Cyanocobalamin (Vitamin B12) sources: Dietary intake is exclusively from animal sources, e.g. milk, meat and eggs (and fortified foods). Although some bacteria can make vitamin B12, it is probably not in a form that can be used by the body. Fortified breakfast cereals can be a useful source of this vitamin.
145 virtually (ve:celi) prakticky, fakticky
neurological njuere´lodikl
paralysis pe´relesisvirtually (ve:celi) prakticky, fakticky
neurological njuere´lodikl
paralysis pe´relesis
146. 146
147. Vitamin B-12 Structure
cobalamine
methyl cobalamine
transport and coenzyme form
adenosyl cobalamine
storage and coenzyme form
147
150. Vitamin B12 the corrin ring is similar to the porphyrin ring system found in hemoglobin except that in corrin 2 of the pyrroles are linked directly (without methylene bridges)
the cobalt is coordinated to the 4 pyrrole nitrogens
one of the axial cobalt ligands is a nitrogen of the dimethylbenzimidazole group
the other axial ligand may be CN, OH, CH3 or the 5-carbon of a 5-deoxyadenosyl group
152. Vitamin B12 synthesized by bacteria only
red in color, levorotatory and stable to heat
commercially available either as cyano or hydroxocobalamin
stored in the liver as the coenzyme
absorbed only in the presence of the intrinsic factor (a glycoprotein released by parietal cells)
transported to tissues via transcobalamin II
present in foods such as liver, fish, eggs, milk
absent in vegetables and fruits
153. Vitamin B12 by far the most complex vitamin in structure
made up of a planar corrin ring (4 pyrroles)
the only vitamin that possesses a metal ion (cobalt) as part of its structure
the major cofactor form of B12 is adenosylcobalamin or 5-deoxyadenosylcobalamin
small amounts of methylcobalamin also occur (intermediate in methyl transfer reactions)
154. Vitamin B12 biochemical functions (mediated by coenzymes)
mutase reaction (rearrangement reaction
methylmalonyl CoA to succinyl CoA (lipid metabolism)
methylation reactions
uracil to thymine
homocysteine to methionine
aminoethanol to choline
activation of amino acids for protein synthesis
ribonucleotides to deoxyribonucleotides for DNA synthesis in certain bacteria
155. Causes of B12 deficiency Pernicious anemia (autoimmune gastritis against parietal cells - loss of intrinsic factor)
rarely due dietary deficiency
oral contaceptive drugs
intestinal parasite
gastrectomy
chronic gastritis
Schilling test
156. Manifestation of B12 deficiency macrocytic megaloblastic anemia
spinal cord degeneration (irreversible)
this cannot be treated with folic acid!!
157. Digestion & Absorption of B12 Intrinsic Factor
gastric glycoprotein
binds with B12 in small intestine
IF-B12 complex binds to B12receptor in ileum for absorption
B12 absorption requires functioning stomach, pancreas, and ileum 157
158. Shilling Test for Malabsorption Saturation of B12 by injection
Oral administration of radiolabeled B12
free B12
IF-B12
Measure urinary excretion of labeled B12 158
159. The fat soluble vitamins
160. Vitamin A (Retinol) Retinol and betacarotene preformed vitamin A.
Beta carotene can be converted to retinol in the body; 6mg of beta carotene is equivalent to 1mg of retinol.
sources:
Retinol is found in liver, whole milk, cheese and butter.
Carotenes are found in milk, carrots, dark green leafy vegetables and orange coloured fruits, e.g. mango and apricots.
The law states that margarine must be fortified with vitamin A (and vitamin D).
160
161. 161
162. Major function in the body vital to good vision
prevents night blindness
antioxidant
necessary for healthy skin, hair growth
keeps mucous membranes healthy
promotes bone development
162
163. Vitamin A is stored in the body in relatively large amounts, and thus deficiencies are rare.
deficiency: night blindness, intestinal infections, impaired growth
hypervitaminosis: nausea, headache, fatigue, liver and spleen damage, skin peeling, risk of birth defect
It is for this reason that women who are pregnant, or who might become pregnant, are advised not to take vitamin A supplements unless they are advised to do so by a health professional. Liver and liver products may contain a large amount of vitamin A, so these should also be avoided.
163
164. Vitamin A Exits in 3 forms:
all trans-retinol
long chain fatty acyl ester of retinol (main storage form)
retinal (the active form in the retina)
retinoic acid is also considered to be physiologically active
provitamin A or carotene can be converted to retinol in vivo
167. Vitamin A Diseases of deficiency:
Nigh blindness and xerophthalmia (dry eye)
Skin disorders
Lack of growth
Hypervitaminosis:
A serious potential problem (CNS disorders; birth defects)
168. Vision and the role of vitamin A photoreception is the function of 2 specialized cell types: rods and cones
both types of cells contain a photosensitive compound called opsin
in rod cells opsin is called scotopsin and the receptor is called rhodopsin or visual purple
rhodopsin is a receptor in the membrane of the rod cell; it is a complex between scotopsin and 11-cis retinal
169. Vision and the role of vitamin A intracellularly, rhodopsin is coupled to a G-protein called transducin
when rhodopsin is exposed to light, it is bleached releasing the 11-cis-retinal from opsin
absorption of photons by 11-cis-retinal triggers the conversion to all-trans-retinal (one important conformational intermediate is metarhodopsin II); also there is a change in conformation of the photoreceptor
170. Vision and the role of vitamin A these transformations activate a phosphodiesterase (which hydrolyzes c-GMP to GMP)
c-GMP is necessary to maintain the Na+ channels in the rods in the open conformation
with a decrease in c-GMP, there occurs a closure of the Na+ channels, which leads to hyperpolarization of the rod cells with concomittant propagation of nerve impulses to the brain
173. Additional role of retinol retinol also functions in the synthesis of certain glycoproteins and mucopolysaccharides necessary for mucous production and normal growth regulation
this is accomplished by phosphorylation of retinol to retinyl phosphate which then functions similarly to dolichol phosphate
175. Vitamin D (Cholecalciferol) Vitamin D is found in foods in two main forms, mostly as cholecalciferol and in small amounts as ergocalciferol.
The physiologically active form is calcitriol, which is the hormone of this vitamin.
The ultraviolet rays from sunshine convert a compound found in the skin into cholecalciferol which is released into the blood and is eventually converted by the liver and kidneys into active hormone calcitriol. In this form it works as a hormone in controlling the amount of calcium absorbed by the intestine.
It is also essential for the absorption of phosphorus and for normal bone mineralization and structure. 175
176. sources: fish liver oils, eggs, tuna, salmon, fortified foods like dairy products and margarine, and some breakfast cereals, action of sunlight on the skin = deficiencies are unusual
RDA (cholecalciferol): 10 micrograms or 400 IU
one glass of milk provides 25% of RDA
one tin of sardines provides 100% of RDA 176
177. Vitamin D There are 2 major precursor forms:
7-dehydrocholesterol
ergosterol
UV irradiation affords cholecalciferol (vitamin D3) and ergocalciferol (vitamin D2)
Discovery:
1890 sunlight prevents rickets
1924 Steanbock and Hess found that irradiating certain foods produced vitamin D2
1970 hormonally active form of vitamin D discovered
178. Vitamin D RDA 20 mg (required in minute amounts)
disease of deficiency: rickets
Malformation of bones due to improper bone mineralization
Hypervitaminosis
Toxic dose only 10X higher than the RDA
Causes hypercalcemia can lead to cardiac arrest
vitamin D is not a vitamin (or a cofactor) it is a steroid hormone
181. Major function in the body acts as a hormone to increase intestinal absorption of calcium
promote bone and tooth formation
prevents rickets in children and osteomalacia in adults
181
182. Biological functions Calcium homeostasis it is critical for the body to maintain the proper calcium level in the blood stream
Intestinal calcium absorption: acts as a signal to tell intestinal cells to take up more calcium from the gut
Bone calcium mobilization
Signals osteoclast (bone cells) to release calcium into the blood stream in response to low calcium levels
183. deficiency: rickets in children and osteomalatia in adults,
Deficiencies are rare. Some groups of people (e.g. older adults, and children) are at risk of vitamin D deficiency because of low vitamin D intake from food and/or inadequate exposure of skin to sunshine.
hypervitaminosis: loss of appetite, nausea, joint pains, loss of muscle tone, damage to soft tissues such as the kidney, heart, and blood vessels due to deposits of calcium.
In general, vitamin D supplement are not recommended.
183 rickets rikits
osteomalatia - ostieumaleiierickets rikits
osteomalatia - ostieumaleiie
185. Vitamin E (alpha-tocopherol) Vitamin E is a group of compounds called tocopherols and tocotrienols, of which alpha tocopherol is the most active.
sources: vegetable oils, margarine, green leafy vegetables, wheat germ, whole grain products, egg yolks
RDA (tocopherol): 10 mg for men, and 8 mg for women
one tablespoon of margarine provides 74% of RDA 185
186. Major function in the body helps breakdown polyunsaturated fats
antioxidant, protect cells against oxidative damage by free radicals, for example oxidation of the lipids in the cell membranes
plays a role in aging, sexual performance, or prevention of cancer and/or heart disease
186
187. deficiency: disruption of red blood cell membranes, anemia
Deficiencies are extremely rare.
hypervitaminosis: headache, fatigue, diarrhea, general lack of toxicity with doses up to 400 mg
Vitamin E is one of the most popular nutrient supplements. There are many health claims for supplementation slowing of the aging process or an improvement in sexual potency. 187
188. Vitamin K (phylloquinone) Vitamin K is found in foods from both plant and animal sources and is also made by bacteria in the gut.
sources: beef liver, eggs, spinach, cauliflower, broccoli, tomatoes
RDA: 80 ľg for men, 65 ľg for women 188
189. Major function in the body essential for clotting of blood (vitamin K is named antihemorrhagic vitamin)
normal bone structure
189
190. Vitamin K the coagulation vitamin
exists in 2 forms:
plant origin: phylloquinone or vit K1
bacterial origin: menaquinones or vit K2
also certain synthetic quinones have vitamin K activity
menadione (vitamin K3)
menadiol sodium phosphate (vitamin K4)
195. deficiency: increased bleeding and hemorrhage
Deficiency states are rare, they may occur in some individuals when antibiotic medications kill the intestinal bacteria that produce the vitamin.
hypervitaminosis: thrombosis, vomiting 195
196. Vitamin E alpha (E1), beta (E2) and gamma(E3) tocopherol
sources: plant oils (corn, peanut, wheat germ), green leafy vegetables, meat, eggs
value resides in the antioxidant properties of vitamin E (may prevent the formation of peroxides)
197. Vitamin E Estimated requirements: 5 mg/day + 0.6 mg/day of unstaurated fat
Biological function antioxidant for fatty acids
Acts like vitamin C; prevents lipid peroxidation and/or damage to cells by lipid hydroperoxides
198. Uses for vitamin E hemolytic anemia in premature infants, unresponsive to B12, Fe and folic acid
macrocytic megaloblastic anemia seen in children with severe protein-calorie malnutrition
199. ALPHA TOCOPHEROL