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Sodium butyrate attenuates peritoneal fibroproliferative process in mice.
De Lazari, Marcela Guimarães Takahashi; Viana, Celso Tarso Rodrigues; Pereira, Luciana Xavier; Orellano, Laura Alejandra Ariza; Ulrich, Henning; Andrade, Silvia Passos; Campos, Paula Peixoto.
Affiliation
  • De Lazari MGT; Department of General Pathology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Viana CTR; Department of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, São Paulo, Brazil.
  • Pereira LX; Department of Experimental Pathology, Universidade Federal de São João del-Rei, Divinópolis, Minas Gerais, Brazil.
  • Orellano LAA; Department of Pathology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
  • Ulrich H; Department of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, São Paulo, Brazil.
  • Andrade SP; Department of Physiology and Biophysics, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Campos PP; Department of General Pathology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Exp Physiol ; 108(1): 146-157, 2023 01.
Article in En | MEDLINE | ID: mdl-36459573
NEW FINDINGS: What is the central question of this study? Peritoneal injury can result in a persistent fibroproliferative process in the abdominal cavity, causing pain and loss of function of internal organs. This study aimed to demonstrate the use of sodium butyrate (NaBu) as a potential agent to attenuate peritoneal fibrosis induced by a synthetic matrix. What is the main finding and its importance? Our findings provide the first evidence that NaBu attenuates the inflammatory, angiogenesis and fibrogenesis axes involved in the formation of peritoneal fibrovascular tissue, indicating the potential of this compound to ameliorate peritoneal fibrosis. ABSTRACT: The aim of this study was to identify the bio-efficacy of sodium butyrate (NaBu) on preventing the development of peritoneal fibrovascular tissue induced by implantation of a synthetic matrix in the abdominal cavity. Polyether-polyurethane sponge discs were implanted in the peritoneal cavity of mice, which were treated daily with oral administration of NaBu (100 mg/kg). Control animals received water (100 µl). After 7 days, the implants were removed for assessment of inflammatory, angiogenic and fibrogenic markers. Compared with control values, NaBu treatment decreased mast cell recruitment/activation, inflammatory enzyme activities, levels of pro-inflammatory cytokines, and the proteins p65 and p50 of the nuclear factor-κB pathway. Angiogenesis, as determined by haemoglobin content, vascular endothelial growth factor levels and the number of blood vessels in the implant, was reduced by the treatment. In NaBu-treated animals, the predominant collagen present in the abdominal fibrovascular tissue was thin collagen, whereas in control implants it was thick collagen. Transforming growth factor-ß1 levels were also lower in implants of treated animals. Sodium butyrate downregulated the inflammatory, angiogenesis and fibrogenesis axes of the fibroproliferative tissue induced by the intraperitoneal synthetic matrix. This compound has potential to control/regulate chronic inflammation and adverse healing processes in the abdominal cavity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peritoneal Fibrosis Type of study: Prognostic_studies Limits: Animals Language: En Journal: Exp Physiol Journal subject: FISIOLOGIA Year: 2023 Document type: Article Affiliation country: Brazil Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peritoneal Fibrosis Type of study: Prognostic_studies Limits: Animals Language: En Journal: Exp Physiol Journal subject: FISIOLOGIA Year: 2023 Document type: Article Affiliation country: Brazil Country of publication: United kingdom