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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Journal of Applied T...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Journal of Applied Toxicology
Article . 2002 . Peer-reviewed
License: Wiley Online Library User Agreement
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Lack of teratogenicity of microcystin‐LR in the mouse and toad

Authors: N, Chernoff; E S, Hunter; L L, Hall; M B, Rosen; C F, Brownie; D, Malarkey; M, Marr; +1 Authors

Lack of teratogenicity of microcystin‐LR in the mouse and toad

Abstract

AbstractMicrocystin‐LR (MC‐LR) is a cyanobacterial toxin generated by the organism Microcystis aeruginosa. Although the hepatotoxicity of this chemical has been characterized, the potential developmental toxicity in vertebrates has not been well studied. The purpose of this study was to elucidate the effects of this toxin on the in vivo and in vitro development of mammals and the development of an Anuran (toad). Initial acute toxicity experiments with female CD‐1 mice were accomplished with MC‐LR administered i.p. in saline. Lethality occurred at 128 and 160 µg kg −1 and histopathology revealed massive hepatic necrosis with diffuse hemorrhage. Developmental toxicity studies were done with MC‐LR administered i.p. for 2‐day periods: gestation days 7–8, 9–10 or 11–12. Doses used ranged from 2 to 128 µg kg−1. On gestation day 17, fetuses were weighed and analyzed for gross morphological and skeletal defects. No treatment‐related differences were seen in litter size, viability, weight or the incidence of anomalies. Groups of dams dosed with 32–128 µg kg−1 on gestation days 7–8, 9–10 or 11–12 were allowed to give birth and the growth and development of their pups were followed postnatally. There were no significant effects noted in the offspring of the treated dams. Neurulation‐staged CD‐1 mouse conceptuses were exposed to 50–1000 nM MC‐LR in whole embryo culture for 24 h. No significant increase in abnormalities or developmental delays was observed. Finally, exposure of the developing toad. Bufo arenarum was done from stage 17 (tail bud) for 10 days at concentrations of 1–20 mg l−1. No effect on morphological development or survival was noted in any exposed groups. These data indicate that microcystin does not appear to affect development adversely in the mouse (in vivo or in vitro) or the toad at the doses and exposure parameters used. Copyright © 2002 John Wiley & Sons, Ltd.

Keywords

Embryo, Nonmammalian, Microcystins, In Vitro Techniques, Cyanobacteria, Embryo, Mammalian, Peptides, Cyclic, Lethal Dose 50, Survival Rate, Mice, Maternal Exposure, Bufo arenarum, Toxicity Tests, Acute, Animals, Female, Marine Toxins, Enzyme Inhibitors

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
29
Top 10%
Top 10%
Top 10%
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