B6,B9,B12 Flashcards

1
Q

Folate B9 folic acid

A
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2
Q

folate b9 active form body

A

tetrahydrofolate THF

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3
Q

folate b9 active form food

A

polyglutamate

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4
Q

folate b9 sources

A
  • Yeast, mushrooms, green vegetables, legumes, liver,
    fortified foods, citrus fruits – especially strawberries and
    oranges
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5
Q

Folate b9 enzyme that hydolyze it

A

conjugase

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6
Q

Folate b9 conjugase inhibitor

A

low zinc status, alcohol, inhibitors in foods

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7
Q

folate b9 function

A
  • Functions in single carbon transfers in:
  • Nucleic Acid Synthesis
  • dUMP converted to dTMP (required for DNA
    synthesis)
  • Carbon donator in purine synthesis
  • Essential for cell division
  • Amino Acid Metabolism
  • homocysteine converted to methionine
  • Glycine converted to serine
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8
Q

resynthesis of methionine from homocysteine

A
  • Methionine -> homocysteine
    Too much want to convert back to methionine
    -2 ways: either converting to something else
    (cystathionine) with use of VitB6 or go back
    to methionine w/ methionine synthase
    -Too much homocysteine = risk higher CVD
    -PLP to help homocysteine to cystathionine
    -1 methyl group difference in cystathionine to
    become methionine (methylcobalamine)
    Methylcobalamin (cobalamin is B12) to
    homocysteine
    -cobalamin left when become methionine
  • Cobalamin can get methyl group and
    become methylcobalamin from 5-methyl
    THF
    -Becomes THF = active form of folate
  • THF becomes 5,10 methylene THF
    -1 way direction, trapped in body
    *All other forms of folate can convert to each
    other as long as it is not in the form of
    5,10 methylene THF
    -THF used for glycine and serine
  • Cobalamin B12 saves the trapped form of
    folate in body
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9
Q

folate b9 deficiency

A

Megaloblastic Anemia
* immature red blood cells
* Due to decreased DNA synthesis and improper cell
division along with continued RNA production

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10
Q

folate b9 deficiency risk

A
  • Pregnancy
  • Birth defects highly
    correlated with folate
    deficiency
  • alcoholism
  • Elderly
  • Phenytoin users
    (anticonvulsant)
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11
Q

folate b9 toxicity

A
  • Supplementation may mask
    B12 deficiency while
    permitting neurological
    damage caused by B12
    deficiency
  • Megadoses may induce
    seizures in epileptics
  • UL: 1 mg/d from
    supplements and fortified
    foods
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12
Q

Folate b9 interactions

A

Vitamin B12: Methyl-
folate trap

  • Without B12, methyl group
    in N5 methyl THF cannot be
    removed
  • Zinc:
  • Folate may decrease zinc
    absorption
  • Zinc deficiency may
    decrease folate absorption
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13
Q

Folate b9 assesment

A
  • Plasma, serum, or RBC
    folate
  • Deoxyuridine suppression
    test (from dUMP to dTMP)
  • Plasma homocysteine

concentrations

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14
Q

cobalamin b12 sources

A

nature B12 is made by
microbes (ie. in
rumen and ileum of some
animals), so animal
products are the main
sources (MFP, egg, milk)

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15
Q

cobalamin b12 absorption

A

Mechanisms:
I. Intrinsic Factor mediated absorption
1) Intrinsic factor (IF, a glycoprotein) is synthesized in
the stomach.
2) B12 combines with r-protein stomach and
travels to small intestine
3) B12 releases R protein and complexes with IF
4) B12-IF is absorbed in the ileum
5) B12 is released once complex is in the enterocyte

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16
Q

cobalamin b12 function

A

Converts homocysteine to methionine by transfer of methyl
group from folate to homocysteine

  • Converts methylmalonyl CoA to succinyl CoA which can be
    used in energy metabolism
  • nucleic acid synthesis -> through
    methionine formation and possibly through reduction of
    ribonucleotides to deoxyribonucleotides
17
Q

cobalamin b12 deficiency

A

megaloblastic anemia

18
Q

cobalamin b12 deficiency symptoms

A
  • Large immature red blood
    cells, neuropathy, increased
    mean corpuscular volume
    (MCV)
  • Usually due to decreased
    absorption secondary to
    lack of IFas opposed to
    decreased intake, called
    pernicious anemia
19
Q

cobalamin b12 at risk groups

A
  • Elderly
  • Diseases/Surgery of the
    ileum
  • Alcoholic
  • Vegans
  • Stomach surgery recipients
20
Q

cobalamin b12 toxicity

A

none

21
Q

cobalamin b12 assessment

A
  • Serum B12
  • schilling test
  • Used to test B12
    absorption/presence of
    IF
  • inc plasma homocysteine

✽ Often done in conjunction
with folate assessment

22
Q

pyridoxine b6 coenzyme

A
  • PL, PM, PN, PLP, PMP, PNP
23
Q

pyridoxine b6 sources

A
  • Liver, nuts, bananas, legumes, meat, whole grains, salmon, sirloin steak, white meat chicken
24
Q

how is pyridoxine b6 metabolised to other forms

A

by phosphatase to most active form PLP

25
Q

pyridoxine b6 function

A

1) Amino acid metabolism

▪ Transamination coenzyme (ie. AST/GOT, ALT/GPT)
▪ Decarboxylation (ie. serotonin production)
▪ Transulfhydration/desulfhydration (ie. methionine to
cysteine or cysteine to pyruvate)
▪ Cleavage (ie. serine to glycine in folate metabolism)
2) Heme formation- with b6 and iron and makes red color of blood

3) niacin synthesis

4) Arachidonic acid production from lineoleate

5) Glycogenolysis (glycogen phosphorylase)

26
Q

pyridoxine b6 effects

A

coronary heart disease, premenstrual syndrome, and carpal tunnel syndrome

27
Q

pyridoxine b6 deficiency symptoms

A
  • Lethargy in adult
  • Seizures in infants
  • hypochromic/microcytic anemia
  • Depression
28
Q

pyridoxine b6 at risk groups

A
  • Breastfed infants of mothers with deficiency
  • Elderly
  • Alcoholics
  • Oral contraceptive users
29
Q

pyridoxine b6 assessment

A
  • plansme PLP
  • trasaminase activity
  • tryptophan load- b6 is required to convert to niacin
29
Q

B1
B2
B3
B5
B6
B7
B9
B12

A

Thiamin
Riboflavin
Niacin
Pantothenic Acid
Pyridoxine
Biotin
Folate
Cobalamin