The Vitamins 163
descriptor, with “pyridoxol” as the specifi c name for
the alcohol. The vitamers are metabolically intercon-
vertible and, as far as is known, they have equal bio-
logical activity; they are all converted in the body to
the metabolically active form, pyridoxal phosphate.
4-Pyridoxic acid is a biologically inactive end-product
of vitamin B 6 metabolism.
Absorption and metabolism
The phosphorylated vitamers are dephosphorylated
by membrane-bound alkaline phosphatase in the
intestinal mucosa; pyridoxal, pyridoxamine, and pyri-
doxine are all absorbed rapidly by passive diffusion.
Intestinal mucosal cells have pyridoxine kinase and
pyridoxine phosphate oxidase (Figure 8.11), so that
there is net accumulation of pyridoxal phosphate by
metabolic trapping. Much of the ingested pyridoxine
is released into the portal circulation as pyridoxal,
after dephosphorylation at the serosal surface. Unlike
other B vitamins, there seems to be no limit on the
amount of vitamin B 6 that is absorbed.
Most of the absorbed vitamin is taken up by the
liver by passive diffusion, followed by metabolic trap-
ping as phosphate esters, which do not cross cell
membranes, then oxidation to pyridoxal phosphate.
The liver exports both pyridoxal phosphate (bound
to albumin) and pyridoxal (which binds to both
albumin and hemoglobin). Free pyridoxal remaining
in the liver is rapidly oxidized to 4-pyridoxic acid,
which is the main excretory product.
Extrahepatic tissues take up pyridoxal and pyri-
doxal phosphate from the plasma. The phosphate is
N
H 2
C
HC O
HO
N
H 2
C
CH 2 OH
HO
N
H 2
C
H 2 C NH 2
HO
N
H 2
C
CH 2 OH
P O
O-
O-
O
N
H 2
C
HC
P O
O-
O-
O
N
H 2
C
CH 2 NH 2
P O
O-
O-
O
O
OH
CH 3
OH
CH 3
OH
CH 3
OH
CH 3
OH
CH 3
OH
CH 3
N
H 2
C
COO–
HO OH
CH 3
Kinase
Phosphatase
Kinase
Phosphatase
Kinase
Phosphatase
Oxidase
Oxidase
Transaminases Oxidase
Pyridoxine Pyridoxine phosphate
4-Pyridoxic acid Pyridoxal Pyridoxal phosphate
Pyridoxamine Pyridoxamine phosphate
Figure 8.11 Interconversion of the vitamin B 6 vitamers. Pyridoxal kinase (EC 2.7.1.38), pyridoxine phosphate oxidase (EC 1.1.1.65), pyridoxamine
phosphate oxidase (EC 1.4.3.5).