Use este identificador para citar ou linkar para este item: http://repositorio.ufc.br/handle/riufc/5608
Tipo: Artigo de Periódico
Título: In vivo growth-inhibition of Sarc oma 180 tumor by alginates from brown seaweed Sargassum vulgare
Autor(es): Sousa, Alessandra Paula Alves de
Torres, Márcia Rocha
Pessoa, Cláudia
Moraes Filho, Manoel Odorico de
Rocha Filho, Francisco Dário
Alves, Ana Paula Negreiros Nunes
Costa-Lotufo, Letícia Veras
Palavras-chave: Sarcoma 180;Feófitas
Data do documento: Mai-2007
Instituição/Editor/Publicador: Carbohydrate Polymers
Citação: SOUSA, A. P. A. de et al. In vivo growth-ingrowth-inhibition of Sarcoma 180 tumor by alginates from brown seaweed Sargassum vulgare. Carbohydrate Polymers, Barking, Inglaterra, v.69, n. 1, p. 7-13, maio, 2007.
Abstract: Previous studies had demonstrated that alginates from Sargassum sp. (Phaeophyta) showed a considerable activity against various murine tumors. The aim present study is to investigate the in vivo antitumor activity of two alginates (SVHV and SVLV) with di V erent viscosity extracted from brown seaweed Sargassum vulgare C. Agardh against Sarcoma 180 cells transplanted in mice. Both alginates inhibited growth of sarcoma 180. The oral route of administration was more e V ective for both alginates, leading to an inhibition of 51.8 and 74.8% for SVLV at the doses of 50 and 100 mg/m 2 /day, respectively, and of 66.2 and 88.8% for SVHV at the same doses. SVLV was 2.04 times more active after oral administration, while SVHV was 1.89, both at the dose of 100 mg/m 2 /day. Alginates-antitumor activity was related to the tumor proliferation rate inhibition, as observed by reduction of Ki67 staining in tumor of the treated-anima ls. The his- topathological analysis of liver and kidney showed that both organs were a V ected by SVHV and SVLV treatment. However, only SVLV led to acute tubular necrosis. Alginates cause the enlargement of the white pulp of the spleen of treated animals, suggesting t hat the observed antitumor activity could be related to alginates immunomodulatory properties.
URI: http://www.repositorio.ufc.br/handle/riufc/5608
ISSN: 0144-8617
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