Wednesday 16 June 2010

vitamin B

to a med student, knowing their B1, 2, 3, 6, 12 is as intrinsic as a preschooler knowing their A, B, Cs. sometimes the difference between an A grade and a B grade, is getting the right vitamin B type.



B1 thiamine
In thiamine pyrophosphate (TPP) a cofactor for:

  • Pyruvate DH (glycolysis)
  • Alpha ketoglutarate DH (TCA)
  • Transketolase (HMP)
  • Branched chained aa DH
     
At malnutrition or alcoholism (secondary malnutrition and malabsorption)

Impaired glucose breakdown leading to ATP depletion, so first organs affected are the brain and heart (highly aerobic tissues).

Wernicke-Korsakoff syndrome.
Wernicke:
  • confusion
  • opthalmoplegia,
  • ataxia
Korsakoff:
  • memory loss
  • confabulation
  • personality change
Beriberi:
§         wet beriberi (high output HF, dilated cardiomyopathy, edema)
§         dry beriberi (polyneuritis, symmetrical muscle atrophy)

mnemonic: ber1ber1
B2 riboflavin
Cofactor in oxidation and reduction (FADH2)
2 Cs:
  • Cheilosis
  • Corneal vascularization

mnemonic:
riboFlavin = FAD, FMN= 2 ATP
B3 niacin
  • Redox rxn (NAD+, NADP+)
  • Derived from tryptophan
  • Synthesis requires B6




*excess: facial flushing (seen at pharmacological doses of treating hyperlipidemia)
3 Ds of pellagra:
  • Dermatitis
  • Diarrhea
  • Dementia
Severe deficiency caused by:
1.      Hartnup’s disease (decreased tryptophan absorption)
2.      Malignant carcinoid syndrome (increased tryptophan metabolism)
3.      INH (decreased B6)

B5 pantothenate
Cofactor for acyl transfers and FA synthase
  • Dermatitis
  • Enteritis
  • Alopecia
  • Adrenal insufficiency
B6 pyridoxine
·        Required for synthesis of B3 from tryptophan
·        Converted to pyridoxal phosphate, a cofactor for:
«     transamination (eg: ALT, AST)
«     DC reactions
«     Glycogen phosphorylase
«     Cystathione synthesis
«     Heme synthesis


§         Convulsions
§         Hyperirritability
§         Peripheral neuropathy
§         Sideroblastic anemias

Deficiency can be caused by INH and OCPs.
B12 cobalamin
·        Cofactor for homocysteine methyltransferase and methylmalonyl COA mutase

(transfers CH3 group as methylcobalamin)
§         Macrocytic, megaloblastic anemia
§         Hypersegmented PMNs
§         Neuro symptoms such as paresthesias, subacute combined degeneration (abnormal myelin)
o Only vitamin stored (in liver). Other vitamin Bs are flushed out of the system
o Deficiency due to:
à      Pure vegan diet
à      Sprue
à      Enteritis
à      Diphyllobothrium latum
à      Lack of intrinsic factor (gastric bypass, pernicious anemia)
à      Absence of terminal ileum (Chron’s)

1 comment:

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