| Literature DB >> 33098831 |
Elisa Feller Gonçalves da Silva1, Bruna Pasqualotto Costa2, Marcella Tornquist Nassr2, Bruno de Souza Basso2, Matheus Scherer Bastos2, Géssica Luana Antunes2, Camille Kirinus Reghelin2, Maria Claudia Rosa Garcia2, Vitor Giancarlo Schneider Levorse2, Leonardo Pfeiff Carlessi2, Krist Helen Antunes Fernandes3, Carine Raquel Richter Schmitz4, Gabriela Viegas Haute2, Carolina Luft2, Eliane Santarém5, Florencia María Barbé-Tuana6, Márcio Vinícius Fagundes Donadio2, Luiz Augusto Basso7, Pablo Machado7, Jarbas Rodrigues de Oliveira2.
Abstract
Potassium 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-olate (CPBMF65) is a potent inhibitor of the uridine phosphorylase 1 (UPP1) enzyme. Its non-ionized analog has already demonstrated biological properties by reducing adverse effects caused by the chemotherapeutic 5-fluorouracil (5-FU). In addition, it has been demonstrated that uridine inhibits inflammation and fibrosis in bleomycin lung injury, decreasing collagen production. The purpose of this study was to investigate the in vitro and in vivo effects of CPBMF65 on activated hepatic stellate cells (HSC) and on carbon tetrachloride-induced liver fibrosis in mice. After incubation with CPBMF65, decreased cell proliferation and phenotype reversion were observed in vitro. In addition, CPBMF65 promoted a protective effect on tetrachloride-induced liver fibrosis in mice, demonstrated by its antifibrotic and anti-inflammatory actions. The results of the present study indicate that the UPP1 inhibitor (CPBMF65) may have potential as a novel therapeutic agent for the treatment of liver fibrosis.Entities:
Keywords: Antifibrotic; Hepatic stellate cells; Liver fibrosis; Uridine phosphorylase 1
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Year: 2020 PMID: 33098831 DOI: 10.1016/j.ejphar.2020.173670
Source DB: PubMed Journal: Eur J Pharmacol ISSN: 0014-2999 Impact factor: 4.432