Neoplasia in Zebrafish (Danio rerio) Treated with N-methyl-N'nitro-N-nitrosoguanidine by Three Exposure Routes at ifferent Developmental Stages

Author:

Spitsbergen Jan M.1,Tsai Hsi-Wen2,Reddy Ashok3,Miller Tom2,Arbogast Dan2,Hendricks Jerry D.1,Bailey G.S.1

Affiliation:

1. Department of Environmental and Molecular Toxicology Oregon State University, Corvallis, Oregon 97331, Food Science and Technology, Oregon State University, Corvallis, Oregon 97331, Marine/Freshwater Biomedical Sciences Center, Oregon State University, Corvallis, Oregon 97331

2. Food Science and Technology, Oregon State University, Corvallis, Oregon 97331

3. Department of Environmental and Molecular Toxicology Oregon State University, Corvallis, Oregon 97331, Food Science and Technology, Oregon State University, Corvallis, Oregon 97331

Abstract

We exposed embryos (83 hours postfertilizaton) and fry (3 weeks posthatch) to N-methyl- N'-nitro- N-nitrosoguanidine (MNNG) by immersion in aqueous solutions of 0-10 ppm for 1 hour (embryo) or 0-2 ppm for 24 hours (fry). Zebrafish embryos were microinjected with MNNG at levels of 0 or 96 ng/egg. Diets containing 0-2,000 ppm MNNG were fed to juvenile zebrafish for 3 months beginning at 2 months posthatch. Fish were sampled for histopathologic study at 6-12 months after initiation of carcinogen exposure. Embryos and fry were both quite responsive to MNNG; however, juvenile zebrafish were remarkably refractory to MNNG-induced neoplasia. Principal target organs in zebrafish treated as embryos with MNNG were liver and testis, with hepatocellular adenoma the most prevalent hepatic neoplasm. A variety of mesenchymal neoplasms occurred in zebrafish following embryo exposure to MNNG, including chondroma, hemangioma, hemangiosarcoma, leiomyosarcoma, and rhabdomyosarcoma. Testis and blood vessels were primary target organs for MNNG following fry exposure, with seminoma, hemangioma, hemangiosarcoma, and various other epithelial and mesenchymal neoplasms occurring. The zebrafish is a responsive, cost-effective lower vertebrate model system in which to study mechanisms of carcinogenesis.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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