Gh. Aas et al., Blood appearance, metabolic transformation and plasma transport proteins of C-14-astaxanthin in Atlantic salmon (Salmo salar L.), FISH PHYS B, 21(4), 1999, pp. 325-334
The time of appearance in blood, and transport of astaxanthin, and cataboli
c transformation of astaxanthin to idoxanthin were investigated in Atlantic
salmon (Salmo salar) that had been force-fed a single dose of C-14-astaxan
thin. In addition to the LPs, a major protein, associated with radiolabeled
astaxanthin was detected. The maximum level of radiolabeled carotenoids in
blood was attained 30 h after administration of C-14-astaxanthin. Radioact
ive idoxanthin (combined 3',4'-cis and 3',4'- trans glycolic isomers of ido
xanthin) appeared after 6 h and a stable level was obtained after 18 h. LPD
P and LP, separated by ultracentrifugation, contained on average 89 and 11%
of the total radioactivity in plasma, respectively. During the 168 h exper
iment, maximum radioactivity in LP appeared after 22 h. Separation of plasm
a by ultracentrifugation on a discontinuous NaCl/KBr-gradient and an iodixa
nol-gradient confirmed that most of the radiolabeled carotenoids were prese
nt in the HDPF that did not contain LPs (58%), whereas HDL and LDL containe
d 36 and 6% of the radioactivity, respectively. Of the recovered radioactiv
ity, astaxanthin in the HDPF comprised 82%, idoxanthin 5% and unidentified
compounds 12%, whereas HDL contained 78% astaxanthin, 22% idoxanthin and no
unidentified compounds. Proteins from the fractions with the high density
and high radioactivity (iodixanol-gradient) were separated by PAGE under no
n-denaturing conditions and showed a radioactive band with parallel migrati
on length to BSA and salmon albumin. These results show that astaxanthin is
rapidly converted to idoxanthin and that the majority of astaxanthin in th
e plasma is associated with a protein other than LPs, presumably albumin. T
he identity of this protein requires verification.