Alanyl-glutamine attenuates 5-fluorouracil-induced intestinal mucositis in apolipoprotein E-deficient mice
Creators
- 1. Laboratório da Biologia da Cicatrização, Ontogenia e Nutrição de Tecidos, INCT - Instituto de Biomedicina do Semiárido Brasileiro, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, CE (Brazil)
- 2. Laboratório de Biologia Molecular e do Desenvolvimento, Universidade de Fortaleza, Fortaleza, CE (Brazil)
- 3. Laboratório da Inflamação e Câncer, INCT - Instituto de Biomedicina do Semiárido Brasileiro, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, CE (Brazil)
- 4. Laboratório de Doenças Infecciosas, INCT - Instituto de Biomedicina do Semiárido Brasileiro, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, CE (Brazil)
Description
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
Availability note (English)
Available from http://dx.doi.org/10.1590/1414-431X20144360; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470307Additional details
Identifiers
Publishing Information
- Journal Title
- Brazilian Journal of Medical and Biological Research
- Journal Volume
- 48
- Journal Issue
- 6
- Journal Page Range
- p. 493-501
- ISSN
- 0100-879X
INIS
- Country of Publication
- Brazil
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47006713
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- HEIGHT; INTRAPERITONEAL INJECTION; LEAD SULFIDES; LENGTH; MESSENGER-RNA; MICE; POLYMERASE CHAIN REACTION; SURFACE AREA; URACILS; WEIGHT
- Descriptors DEC
- ANIMALS; AZINES; CHALCOGENIDES; DIMENSIONS; GENE AMPLIFICATION; HETEROCYCLIC COMPOUNDS; HYDROXY COMPOUNDS; INJECTION; INTAKE; LEAD COMPOUNDS; MAMMALS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PYRIMIDINES; RNA; RODENTS; SULFIDES; SULFUR COMPOUNDS; SURFACE PROPERTIES; VERTEBRATES
Optional Information
- Notes
- PMCID: PMC4470307; PMID: 25945744; OAI: oai:pubmedcentral.nih.gov:4470307