Vitamins and Minerals II Flashcards

1
Q

describe vitamin E and its function

A
  • alpha tocopherol is the most active form
  • vitamin E functions as a lipid soluble antioxidant in cell membranes
    • prevents perioxidation of membrane lipids
    • prevents formation of oxidized LDL
    • scavenges free radicals
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2
Q

name the 3 antioxidant vitamins

A

vitamin C, vitamin E and beta-carotene

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3
Q
A
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4
Q

describe vitamin E deficiency

A
  • hemolytic anemia (abnormal cellular membranes)
  • reduces deep tendon reflexes and gait problems due to axonal degeneration
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5
Q

describe function and deficiency of vit. K

A
  • required as coenzyme for post-translational modification (gamma-carboxylation) of various clotting factors
    • II, VII, IX and X
    • proteins C and S
  • also synthesized by intestinal bacteria therefore broad spectrum antibiotics is a risk factor for deficiency
  • vit. K stored in the least amount among fat soluble vitamins therefore deficiency is the earliest to manifest
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6
Q

describe gamma carboxylation and role of vit K

A
  • gamma-carboxylation of the clotting factors II, VII, IX and X occurs in the liver to form mature clotting factors
  • vit. K is converted from the hydroquinone form to the epoxide form
  • warfarin prevents regeneration of hydroquinone form of vit. K
    • increased prothrombin/INR time
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7
Q

describe functions of vitamin C (ascorbic acid)

A
  • required for the maintenance of normal CT (collagen synthesis) and wound healing
    • vit. C acts as a coenzyme for hydroxylation of proline and lysine residues in collagen (prolyl and lysyl hydroxylase): facilitates formation of H-bonds
  • required for absorption of iron: reduces iron to the ferrous state in the stomach which facilitates absorption of iron
  • water soluble anti-oxidant
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8
Q

what are earliest signs of vit. C deficiency?

A

perifollicular hemorrhage

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9
Q

name the enzymes requiring vitamin B1 (thiamine) as a coenzyme

A
  • coenzyme form = TPP (thiamine pyrophosphate)
    • pyruvate dehydrogenase
    • alpha-KG dehydrogenase
    • branched chain alpha-keto acid dehydrogenase
    • transketolase in the PPP
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10
Q

describe thiamine deficiency

A
  • beriberi
    • common when rice is the major diet component
    • affects highly aerobic tissues (brain + cardiac)
    • polyneuropathy: disruption of motor, sensory and reflex arcs which could progress to paralysis (dry beriberi)
    • cardiovascular symptoms = cardiac failure (wet beriberi)
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11
Q

explain what a lab test for thiamine deficiency would show

A
  • low erythrocyte transketolase activity and increased activity on addition of TPP
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12
Q

describe Wernicke-Korsakoff syndrome

A
  • thiamine deficiency
  • associated with chronic alcoholism
  • ophthalmoplegia and nystagmus
  • ataxia, confusion, disorientation and loss of memory
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13
Q

describe use of vitamin B2 (riboflavin) in reactions

A
  • coenzyme forms:
    • flavin mononucleotide (FMN)
    • flavin dinucleotide (FAD)
  • found in oxidation-reduction reactions:
    • TCA cycle: succinate dehydrogenase, PDH
    • beta-oxidation: acyl CoA DH
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14
Q

describe riboflavin deficiency

A
  • nutritional
  • signs and symptoms:
    • cheilosis: areas of pallor, cracks and fissures at the angles of the mouth
    • glossitis: inflammation and atrophy of the tongue
    • facial dermatitis
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15
Q

describe function of vitamin B3 (niacin) and therapeutic use

A
  • coenzyme forms:
    • NAD+
    • NADP+
  • act as coenzymes in oxidation-reduction reactions
    • NAD: dehydrogenases
    • NADP: reactions in the HMP shunt and fatty acid and cholesterol synthesis (HMG CoA reductase)
  • therapeutic use: niacin inhibits lipolysis in the adipose tissue and greatly reduces production of free fatty acids; treatment of type IIb hyperlipoproteinemia
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16
Q

describe niacin deficiency

A
  • Pellagra (4 D’s)
    • dermatitis
    • diarrhea
    • dementia
      • loss of memory
    • death
17
Q

explain how tryptophan is related to niacin/pellagra

A
  • tryptophan can be used to synthesize NAD+ and NADP+
  • corn based diets can cause pellagra
  • patients with Hartnup disease can have pellagra
    • need supplementation of dietary niacin
  • patients with carcinoid syndrome since there is excessive conversion of tryptophan to serotonin
    • less availability of trpytophan for NAD formation
18
Q

describe function of biotin

A
  • biotin is the prosthetic group for most carboxylation reactions
    • pyruvate carboxylase
    • acetyl-CoA carboxylase
    • propionyl CoA carboxylase
  • avidin, present in raw egg whites, inhibits absorption of biotin
19
Q

describe functions of vitamin B6 (pyridoxine)

A
  • serves as precursors for PLP, which acts as a coenzyme for:
    • transamination
    • amino acid decarboxylation (neurotransmitter synthesis)
    • condensation (ALA synthase in heme synthesis)
    • glycogen phosphorylase
    • conversion of homocysteine to cysteine
      • many children with homocystinuria respond to B6 supplementation
20
Q

name the reactions that require PLP as a coenzyme

21
Q

describe how isoniazid therapy can affect pyridoxine

A
  • administration of isoniazid (anti-TB drug):
    • inactivates pyridoxine
    • pyridoxine supplements are given as a part of anti-TB regimens
    • peripheral neuropathy is observed as an adverse effect when pyridoxine supplements are not given with isoniazid therapy
22
Q

describe effects of pyridoxine deficiency

A
  • microcytic anemia: reduced heme synthesis as a result of reduced ALA synthase activity
  • peripheral neuropathy: due to reduced neurotransmitter formation
    • seizures may also occur
  • increased risk of cardiovascular disease (high levels of plasma homocysteine)
23
Q

describe the function of vitamin B12 (cobalamin) in the synthesis of methionine

A
  • required as a coenzyme for 2 reactions:
    • synthesis of methionine (methionine synthase)
  • this step also converts methyl-THF to THF; THF is the active form of folic acid
    • if there is vit. B12 deficiency, folate is trapped as methyl-THF (folate trap) which results in macrocytic anemia
24
Q

describe the function of vit. B12 (cobalamin) in the isomerization of methylmalonyl CoA

A
  • in vit. B12 deficiency, serum methylmalonate levels are high
    • high methylmalonate levels may be responsible for the neurological manifestations of vit. B12 deficiency
    • dietary vit. B12 supplementation is useful in patients with inherited methylmalonic aciduria
25
describe causes of vit. B12 deficiency
* vit. B12 is not present in plants and is derived from animal foods; **vegans have high risk of developing deficiency** * intrinsic factor (IF) produced by the gastric parietal cells is essential for vit. B12 absorption * parietal cell destruction = lack of IF, which leads to pernicious anemia * **IF-B12 complex is absorbed in the terminal ileum**
26
describe the functions of folic acid
* key role in 1-C metabolism * *THF receives 1-C from ser, gly, his* and transfers them to intermediates in purine and pyrimidine nucleotide synthesis * most cells receive folate in the form of methyl-THF; the conversion of methyl-THF to THF requires vit. B12 * otherwise, **folate trapping**
27
describe manifestations of folic acid deficiency
28
how to differentiate between folic and and B12 deficiency?
both have elevated homocysteine levels but **only B12 deficiency has increased methylmalonate levels as well**
29
there is an increased risk of _______ in the fetus with folic acid deficiency
there is an increased risk of **neural tube defects** in the fetus with folic acid deficiency folic acid supplements are recommended for all women at the time of conception and **during the 1st trimester**