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chemical forms of b6
PLP, PL, PA
food sources
meat, fish: plp, pmp
plants: pnp, pn-glycoside
digestion absorption etc
plp,pnp etc needs to get dephosphorylated. alkaline phosphatase which is zinc dependent. pn-glycoside by glucosidase
absorption: all passive diffusion
transport: i newly absorped go to liver and get converted to plp. plp bound to albumin goes to tissues
storage: stored in muscles with gyocogen phosphorylase
excreted in urine as 4-PA
metabolic functions and roles
amino acid metabolism, neurotransmitter formation, heme formation, lipid metabolism

nutrient gene interactions
enzyme cystathione betasynthase requires b6. some defected ppl have lower enzyme activity. they have 10 fold higher plasma homocysteine
b6 deficiency
neurologic and dermatologic symptoms, microcytic anemia, inflammation, elevated homocysteine