Distribution of C-14 Cylindrospermopsin in vivo in the mouse

Citation
Rlg. Norris et al., Distribution of C-14 Cylindrospermopsin in vivo in the mouse, ENVIRON TOX, 16(6), 2001, pp. 498-505
Citations number
20
Categorie Soggetti
Environment/Ecology
Journal title
ENVIRONMENTAL TOXICOLOGY
ISSN journal
15204081 → ACNP
Volume
16
Issue
6
Year of publication
2001
Pages
498 - 505
Database
ISI
SICI code
1520-4081(200112)16:6<498:DOCCIV>2.0.ZU;2-X
Abstract
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.