N-diethylnitrosamine mouse hepatotoxicity: Time-related effects on histology and oxidative stress

• Tipo: Artigo em Revista Científica Internacional
• Data: 2014

Autores

Nuno Paula Santos (Autor) Outra; Aura Colaço (Autor) Outra; Rui M. Gil da Costa (Autor) FEUP; Maria Manuel Oliveira (Autor) Outra; Francisco Peixoto (Autor) Outra; Paula Alexandra Oliveira (Autor) Outra

Revista

Título: Experimental and Toxicologic Pathology

Vol. 66 Nº 9-10

Páginas: 429-436

ISSN: 0940-2993

Editora: Urban und Fischer Verlag Jena

Indexação

ISI Web of Science

Scopus

Projetos Associados

UI0511 - PROJECTO ESTRATÉGICO - UI 511 - 2013-2014

Outras Informações

DOI: 10.1016/j.etp.2014.07.002

Abstract (EN): Animal models, namely mice, have been used to study chemically induced carcinogenesis due to their similarity to the histological and genetic features of human patients. Hepatocellular carcinoma (HCC) is a common malignancy with poor clinical outcome. The high incidence of HCC might be related to exposure to known risk factors, including carcinogenic compounds, such as N-nitrosamines, which cause DNA damage. N-nitrosamines affect cell mitochondrial metabolism, disturbing the balance between reactive oxygen species (ROS) and antioxidants, causing oxidative stress and DNA damage, potentially leading to carcinogenesis. This work addresses the progressive histological changes in the liver of Ndiethylnitrosamine (DEN)-exposed mice and its correlation with oxidative stress. Male ICR mice were randomly divided into five DEN-exposed and five matched control groups. DEN was IP administered, once a week, for eight consecutive weeks. Samples were taken 18 h after the last DEN injection (8 weeks post-exposure). The following sampling occurred at weeks 15th, 22nd, 29th and 36th after the first DEN injection. DEN resulted in early toxic lesions and, from week 29 onwards, in progressive proliferative lesions. Between 15 and 29 weeks, DEN-exposed animals showed significant changes in hepatic antioxidant (glutathione, glutathione reductase, and catalase) status (p < 0.05) compared with controls. These results point to an association between increased DEN-induced oxidative stress and the early histopathological alterations, suggesting that DEN disrupted the antioxidant defense mechanism, thereby triggering liver carcinogenesis.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 8