Vitamins
Feb 25, 2016
Vitamins
Vitamins
Fat-soluble
• Vitamin A: vision, epithelial tissue, growth in children
• Vitamin D: bone mineralization, blood Ca2+
regulation• Vitamin E: antioxidant• Vitamin K: clotting factor
Water-soluble
Energy metabolism
Amino acid metabolism
RBC/Neural development
Collagen synthesis
• Thiamine (B1)• Riboflavin (B2)• Niacin (B3)• Biotin• Pantothenic acid (B5)
• Pyridoxine pyridoxal, pyridoxamine (B6)
• Folic acid• Cobalamin (B12)
• Ascorbic acid
(Vitamin C)
Water-soluble Vitamins
A) B-Complex 1. Thiamine (B1) • Sources: whole-grain cereals, meats, legumes, nuts• Active form is thiamine pyrophosphate (TPP)Functions : 1. Oxidative decarboxylation of pyruvic acids,conversion of
pyruvic acid to acetyl coA.2. In transketolation reaction,transfer of ketol group.3. TPP is also essential for the process of nerve conduction and
structure of nerve membrane.Deficiency: most common in alcoholics and malnourished
individuals• Decreased ATP production
Manifestations Wet beri-beri:Affects cardiovascular
system 1. Extensive edema. 2. Congestive heart failure. Dry beri-beri: Affects nervous system. 1. Polyneuritis. 2. Hyperesthesia Muscle wasting and loss of weight. Wernicke’s disease 1. Occular distrubance 2.Ataxia
Cont. Korsakoff’s syndrome Defective memory. Impaired learning ability. Recommended dietary allowance:RDA 1-1.5mg/day.
2. Riboflavin (B2) (UV sensitive) • Sources: milk, eggs, meat, poultry, fish, green leafy
vegetables
• Active forms are FMN and FAD
• FAD: cofactor in succinate dehydrogenase reaction (TCA)
• FMN: component of ETC – accepts 2 electrons from NADH in NADH dehydrogenase reaction
Deficiency: not associated with major human disease but commonly seen in conjunction with other vitamin deficiencies
Deficiency symptoms include: dermatitischeilosisglossitis
Cont. Occular disturbance. 1. photophobia 2. vascularization of cornea. Angular stomatitis: inflammation of
angles of mouth. 3. Seborrheic dermatitis:inflammtion of
sebaceous glands of skin. Requirements: 1.3 -1.7 mg/day.
3. Niacin (nicotinic acid) (B3) • Sources: meat, whole-grain cereals, synthesis from
tryptophan-containing foods (milk, eggs)
• Active forms are NAD+ and NADP+
• Excess tryptophan is metabolized to niacin and supplies approx. 10% of RDA
Clinical correlations:
• deficiency causes pellagra(4D)
• RDA effective in treatment of type IIb hyperlipoproteinemia ( reduces lipolysis of fatty acids, activates lipoprotein lipase , less VLDL and LDL)
Requirements Niacin 13-19mg/day depending upon the
age and sex Tryptophan 13 x 60 mg/day to 19 x 60
mg/day. Hypervitaminonsis 1. Skin flushing. 2. Gastrointestinal disturbance. 3. Pruritis
4. Pantothenic acid (B5) • present in a wide variety of foods esp. eggs, liver, yeast
• Active form is Cofactor A (i.e. succinyl CoA, acetyl CoA, fatty acyl CoA)
• part of fatty acid synthase complex
Clinical correlations:
• deficiency is uncommon
• no RDA established
5. Pyridoxine, pyridoxal, pyridoxamine (B6 derivatives) • Sources: whole-grain cereals, eggs, meat, fish,
soybeans, nuts
• Active form is pyridoxal phosphate
• Important function in transamination, deamination, decarboxylation, and condensation reactions
5. Pyridoxine, pyridoxal, pyridoxamine (B6 derivatives)
Clinical correlations:
Isoniazid (isonicotinic acid hydrazide) used to treat TB may induce B6 deficiency -> need B6 supplement while taking isoniazid
Deficiencies seen in alcoholics, infants given deficient formula, and women on oral contraceptives
Toxicity: neurological symptoms if >2g/day
6. Cobalamin (B12) contains Co, corrin ring system • Sources: meats, shellfish, poultry, eggs, dairy products
(not present in plants)
• Active forms are 5’-deoxyadenosylcobalamin (fatty acid oxidation) and methyl cobalamin (met synthesis)
• Needed for synthesis of methionine from homocysteine, forming tetrahydrofolate
• isomerization of methyl malonyl CoA to succinyl CoA.• Vit B12 hepls in the formation of myelin sheath through
the metabolism of odd numbers fatty acids.
Vitamin B12 Metabolism
1. The absorption of vitamin B12 ,it combines with a glycoprotein secreted by the gastric parietal cells called intrinsic factors
2. This IF-B12 complex binds with specific ileal receptors.3. A pH above 6 and Ca ions required to promote vitamin
absorption.4. Vitamin B12 passes via portal circulation to the liver to
the general circulation.5. Vitamin B12 is carried in the plasma by number of
carrier globulins ,namely transcobalmin II ,transcobalmin I and R proteins.They transport B12 to the tissue .It bind to specific cell receptor cell surface to enter the cell.
Clinical correlations:
Deficiency causes accumulation of abnormal fatty acids -> neurological effects
Pernicious anemia – not usually a vitamin deficiency but inability to absorb B12 (no intrinsic factor) because of autoimmune destruction of parietal cells
Treatment: Lifetime intramuscular injections of cyanocobalamin
Anemia reversible, but not CNS effects
Clinical correlations: deficiency in either vitamin B12 or folic acid causes
increase in plasma homocysteine levels, which damages blood vessels and poses a risk for thrombosis
megaloblastic anemia must be treated with both folate and vitamin B12
other causes of B12 deficiency: pure vegan diet terminal ileal disease (i.e. Chron’s disease)
6. Biotin • Sources: bacterial synthesis in intestine,egg yolk,yeast,
animal tissues and tomatoes.
• Important function as cofactor in carboxylation reactions (I.e. pyruvate carboxylase, acetyl CoA carboxylase)
Clinical correlations:
• Deficiency (uncommon) caused by:
1. eating raw egg whites (contain avidin)2. broad-spectrum antibiotics (kill intestinal bacteria)
7. Folic acid • Sources: green leafy vegetables, liver, lima beans, whole-
grain cereals
• Active forms are tetrahydrofolate derivatives
• Important in 1-C transfer reactions especially in DNA synthesisMetabolism:
1. Folic acid ingested as polyglutamates -> converted to monoglutamates in jejunum by intestinal conjugase enzyme
2. Monoglutamate is reabsorned in jejunum.
3. Folic acid circulated and is measured in blood as methyltetrahydrofolate.
4. Only a 3-4 month supply is stored in the liver.
Clinical correlations:• Folic acid deficiency is most common vitamin deficiency
in U.S., most common in pregnant women and alcoholics
• Folic acid before pregnancy reduces risk of neural tube defects.
Deficiency caused by:1. Diet lacking in fruit and vegetable
2. Drugs: methotrexate, trimethoprim (chemotherapeutic drugs which inhibit dihydrofolate reductase thus preventing purine and pyrimidine biosynthesis -> kills blast cells and causes macrocytic anemia)
4. Oral contraceptives (block reabsorption of monoglutamate in jejunum)
5. Alcohol (block reabsorption of monoglutamate in jejunum)6. Rapidly-growing cancers (malignant cells use folic acid)7. Small bowel malabsorption (I.e. celiac disease)8. Sulfa drugs (sulfanilamide) inhibits folic acid synthesis
B. Non-B-ComplexAscorbic acid Source: citrus fruits, potatoes, tomatoes, green vegetables
• Action – coenzyme in hydroxylation reactions esp. proline and lysine in collagen synthesis
• antioxidant activity – helps prevent formation of free radicals• Clinical correlations:• deficiency and cigarette smoking causes scurvy
• megadoses claimed to be effective against common cold (very controversial)
• no toxic effects but oxidized form (dehydroascorbic acid) is toxic
• Excess intake may cause renal calculi (kidney stones)
Classification and Functions of Vitamins
Vitamins
Fat-soluble
• Vitamin A: vision, epithelial tissue, growth in children
• Vitamin D: bone mineralization, blood Ca2+
regulation• Vitamin E: antioxidant• Vitamin K: clotting factor
Water-soluble
Energy metabolism
Amino acid metabolism
RBC/Neural development
Collagen synthesis
• Thiamine (B1)• Riboflavin (B2)• Niacin (B3)• Biotin• Pantothenic acid (B5)
• Pyridoxine pyridoxal, pyridoxamine (B6)
• Folic acid• Cobalamin (B12)
• Ascorbic acid
(Vitamin C)
Vitamin A
• Vitamin A consists of three biologically active molecules, retinol, retinal (retinaldehyde) and retinoic acid
• Essential for vision, reproduction, growth and maintenance of epithelial tissues
• Associated with reduced heart disease, lung cancer, skin cancer, lower cataract risk
• Sources: liver, kidney, cream, butter, egg yolk
• RDA: 1000 retinol equivalents (RE) for males 800 retinol equivalents (RE) for females
1 RE = 1 mg retinol, 6 mg b-carotene, or 12 mg of other carotenoids
Each of these compounds are derived from the plant precursor molecule, b-carotene (a member of a family of molecules known as carotenoids).
Beta-carotene, which consists of two molecules of retinal linked at their aldehyde ends, is also referred to as the provitamin form of vitamin A.
Retinol -> dietary supplementsRetinoic acid -> dermatological applications
Metabolism of Vitamin A
1. Ingested b-carotene is cleaved in the lumen of the intestine by b-carotene dioxygenase to yield retinal.
2. Retinal is reduced to retinol by retinaldehyde reductase, an NADPH requiring enzyme within the intestines.
• vision is the function of 11-cis retinal coupled to opsin to form rhodopsin
• Rhodopsin is coupled to a G-protein called transducin. When exposed to light 11-cis is converted to all-trans-retinal. This conformational change activates transducin. Increased GTP binding.
• cGMP maintains Na+ channels in open state
• activation of cGMP phosphodiesterase
• drop in cGMP closes channels and leads to hyperpolarization of the rod cell
Vision and the Role of Vitamin A
Additional Roles of Retinol
1. Growth – retinoic acid required for appetite, bone growth
2. Spermatogenesis (males) and prevention of fetal resorption (females) – requires retinal or retinol (retinoic acid doesn’t work!)
3. Maintenance of epithelial cells + mucus secretion
Vitamin A - Clinical Correlations
2. Acne, psoriasis
• Retinoic acid used to treat mild acne (Darier’s disease)
• Tretinoin (all-trans retinoic acid) used to treat skin aging (topical)
• Isotretinoin (13-cis retinoic acid) used to treat severe acne (oral admin)
** teratogeniccontraindicated for women with childbearing
potentialprolonged treatment with isotretinoin causes
hyperlipidemia and increased LDL/HDL ratio
Vitamin A - Clinical Correlations
1. Dietary Deficiency
• treated with retinol or retinyl esters• night blindness early sign of Vitamin A deficiency• increased susceptibility to infection and cancer
• severe deficiency leads to progressive keratinization of the cornea
(xerophthalmia)
Vitamin A - Clinical Correlations
3. Toxicity
• Hypervitaminosis A = > 7.5 mg per day
• Early signs of Hypervitaminosis A : dry, pruritic skin, hepatomegaly, rise in intracranial pressure (can mimic brain tumor)
• teratogenic
Vitamin D(calciferol) Sources : generated from the provitamin
ergosterol(in plants)and 7-dehydrocholesterol(in human and animals) by ultra violet irradiation of sun.
Liver ,egg and yeast are rich diet Fish liver oils.cod liver oil,shark liver oil.
Metabolism of Vitamin D
D2 and D3 are activated in vivo by 2 sequential hydroxylation reactions
1. 25-hydroxylase in liver
2. 25-cholecalciferol-1-hydroxylase in kidney
product is 1,25-dihydroxycholecalciferol (1,25-diOH D3)
Function of Vitamin D – to increase plasma Ca2+
• stimulates calcium (and phosphate) uptake
by intestine by inducing synthesis of a calcium-binding protein
• increases calcium reabsorption by the kidney
• mobilizes bone calcium by resorption
Vitamin D - Clinical Correlations
Deficiency of vitamin D
1. Rickets – in children• collagen matrix formed but mineralization is incomplete• soft pliable bones – “bow-legged”• mutation in vitamin D receptor can cause vitamin D-
independent rickets
2. Osteomalacia – in adults• demineralization of bones = fractures• (less sunlight) problem more severe
3. Renal rickets (renal osteodystrophy) = chronic renal failure• results in low synthesis of 1,25 vitamin D3 (calcitrol)• calcitrol supplementation is effective treatment
Toxicity
• Very toxic
• vitamin D can be stored -> accumulates in liver and fat
• high doses = loss of appetite, nausea, thirst, hypercalcemia (leads to calcium deposits in arteries and kidneys
Vitamin D - Clinical Correlations
Vitamin k Three forms : K1,K2 and K3 Sources: 1. leafy vegetable(K1), intestinal flora
present in small intestine (K2),K3 is synthetic ,it is water soluble and more potent than vitamin K1 and K2.
Vitamin K • Role = posttranslational carboxylation of blood clotting factors
• Sources: cabbage, cauliflower, spinach, egg yolk, liver, synthesis from intestinal bacteria
• RDA: no RDA but recommendation is 70-140 mg/day
• Exists in several forms:phylloquinone = vitamin K1 (plants)menaquinone = vitamin K2 (intestinal bacteria)menadione = synthetic derivative of vitamin K1
Interaction of prothrombin with platelets
1. g -carboxylates chelate calcium and allow prothrombin to associate with membrane phospholipids in platelets 2. conversion to thrombin is stimulated
Vitamin K - Clinical Correlations
Deficiency of vitamin K
• deficiencies are unusual
• antibiotic treatment can lead to hypothrombinemia in undernourished/ very ill patients
• second generation cephalosporins have warfarin-like activity
• supplement treatment with vitamin K
• newborns are deficient and breast milk below RDA
• prophylactic i.m. injection can be used
Toxicity
• prolonged treatment causes hemolytic anemia, jaundice in infants (rbc membrane effects)
Vitamin K - Clinical Correlations
Vitamin E• 8 different types – a-tocopherol is most common
• absorbed in intestines
• Major storage site is adipose tissue
• function – antioxidant activity inhibits nonenzymatic oxidation by free radicals
• sources – vegetable oils, liver, eggs
• RDA = 10 mg/day for males 8 mg/day for females• RDA increases as intake of polyunsaturated fats increases
Vitamin E - Clinical Correlations
Deficiency
• restricted to premature infants
• in adults, deficiency associated with defective lipid transport/absorption
-> results – rbc membrane fragility, abnormal cell membranes
Toxicity
• none known
Vitamin E - Clinical Correlations
Benefits
• may protect against chronic disease
(heart disease, cancer, cataracts, aging) due to its antioxidant activity
Fat soluble Vitamins