Use este identificador para citar ou linkar para este item: http://repositorio.ufc.br/handle/riufc/19296
Tipo: Artigo de Periódico
Título: Alanyl-glutamine attenuates 5-fluorouracil-induced intestinal mucositis in apolipoprotein E-deficient mice
Autor(es): Araújo, C.V.
Lazzarotto, Cícera Regina
Aquino, Cristhyane Costa de
Figueiredo, Italo L.
Costa, Tiê Bezerra
Alves, L. A. de Oliveira
Ribeiro, Ronaldo A.
Bertolini, Luciana Relly
Lima, A. A. M.
Brito, Gerly A. C.
Oriá, Reinaldo do B.
Palavras-chave: Mucosite;Mucositis;Apoptose
Data do documento: Abr-2015
Instituição/Editor/Publicador: Brazilian journal of medical and biological research
Citação: ARAÚJO, C. V. et al. Alanyl-glutamine attenuates 5-fluorouracil-induced intestinal mucositis in apolipoprotein E-deficient mice. Brazilian journal of medical and biological research v. 48 n. 6, Ribeirão Preto, p. 493-501, apr., 2015.
Abstract: Apolipoprotein E (APOE=gene, apoE=protein) is a known factor regulating the inflammatory response that may have regenerative effects during tissue recovery from injury. We investigated whether apoE deficiency reduces the healing effect of alanyl-glutamine (Ala-Gln) treatment, a recognized gut-trophic nutrient, during tissue recovery after 5-FU-induced intestinal mucositis. APOE-knockout (APOE-/-) and wild-type (APOE+/+) C57BL6J male and female mice (N=86) were given either Ala-Gln (100 mM) or phosphate buffered saline (PBS) by gavage 3 days before and 5 days after a 5-fluorouracil (5-FU) challenge (450 mg/kg, via intraperitoneal injection). Mouse body weight was monitored daily. The 5-FU cytotoxic effect was evaluated by leukometry. Intestinal villus height, villus/crypt ratio, and villin expression were monitored to assess recovery of the intestinal absorptive surface area. Crypt length, mitotic, apoptotic, and necrotic crypt indexes, and quantitative real-time PCR for insulin-like growth factor-1 (IGF-1) and B-cell lymphoma 2 (Bcl-2) intestinal mRNA transcripts were used to evaluate intestinal epithelial cell turnover. 5-FU challenge caused significant weight loss and leukopenia (P<0.001) in both mouse strains, which was not improved by Ala-Gln. Villus blunting, crypt hyperplasia, and reduced villus/crypt ratio (P<0.05) were found in all 5-FU-challenged mice but not in PBS controls. Ala-Gln improved villus/crypt ratio, crypt length and mitotic index in all challenged mice, compared with PBS controls. Ala-Gln improved villus height only in APOE-/- mice. Crypt cell apoptosis and necrotic scores were increased in all mice challenged by 5-FU, compared with untreated controls. Those scores were significantly lower in Ala-Gln-treated APOE+/+ mice than in controls. Bcl-2 and IGF-1 mRNA transcripts were reduced only in the APOE-/--challenged mice. Altogether our findings suggest APOE-independent Ala-Gln regenerative effects after 5-FU challenge.
URI: http://www.repositorio.ufc.br/handle/riufc/19296
ISBN: On-line 1414-431X
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