Radiolabelled C-14 cylindrospermopsin (CYN) has been prepared and used to i
nvestigate the distribution and excretion of CYN in vivo in male Quackenbus
h mice. At a dose of 0.2 mg/kg (i.e., approx. median lethal dose) the follo
wing mean (SID) urinary and faecal recoveries (cumulative) were obtained, r
espectively: (0-6 hours, n = 4) 48.2 (29.3)%, 11.9 (21.4)%; (0-12 hours, n
= 12) 66.0 (27.1)%, 5.7 (5.6)%; (0-24 hours, n = 12) 68.4 (26.7)%, 8.5 (8.1
)%. Mean (SD) recoveries from livers at 6 hours were 20.6 (6.4)% (n = 4), a
t 48 hours 13.1 (7.7)% (n = 8), and 5-7 days were 2.1 (2.1)% (n = 8). A sub
stantial amount (up to 23%) can be retained in the liver for up to 48 hours
with a lesser amount retained in the kidneys. The excretion patterns show
substantial interindividual variability between predominantly faecal or uri
nary excretion, but these patterns are not related in any simple manner to
the outcome in terms of toxicity. There is at least one methanol-extractabl
e metabolite as well as a nonmethanol-extractable metabolite in the liver.
The methanol-extractable metabolite was not found in the kidney and is more
hydrophilic than CYN itself on reverse phase. (C) 2001 by John Wiley & Son
s, Inc.