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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Vitamin D-3 supplementation alleviates chemically-induced cirrhosis-associated hepatocarcinogenesis

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Autor(es):
Goto, Renata L. [1] ; Tablas, Mariana B. [1] ; Prata, Gabriel B. [2] ; Espirito Santo, Sara G. [2] ; Fernandes, Ana Angelica H. [3] ; Cogliati, Bruno [4] ; Barbisan, Luis F. [1] ; Romualdo, Guilherme R. [2, 1]
Número total de Autores: 8
Afiliação do(s) autor(es):
[1] Sao Paulo State Univ UNESP, Biosci Inst, Dept Struct & Funct Biol, Botucatu, SP - Brazil
[2] Sao Paulo State Univ Unesp, Med Sch, Dept Pathol, Botucatu, SP - Brazil
[3] Sao Paulo State Univ UNESP, Biosci Inst, Dept Chem & Biol Sci, Botucatu, SP - Brazil
[4] Univ Sao Paulo, Dept Pathol, Sch Vet Med & Anim Sci, Sao Paulo, SP - Brazil
Número total de Afiliações: 4
Tipo de documento: Artigo Científico
Fonte: JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY; v. 215, JAN 2022.
Citações Web of Science: 0
Resumo

Vitamin D-3 (VD3) deficiency has been associated with increased risk for cirrhosis and hepatocellular carcinoma, a highly incident malignant neoplasia worldwide. On the other hand, VD3 supplementation has shown some beneficial effects in clinical studies and rodent models of chronic liver disease. However, preventive effects of dietary VD3 supplementation in cirrhosis-associated hepatocarcinogenesis is still unknow. To investigate this purpose, male Wistar rats submitted to a combined diethylnitrosamine- and thioacetamide-induced model were concomitantly supplemented with VD3 (5,000 and 10,000 IU/kg diet) for 25 weeks. Liver samples were collected for histological, biochemical and molecular analysis. Serum samples were used to measure 25-hydroxyvitamin D {[}25(OH)D] and alanine aminotransferase levels. Both VD3 interventions decreased hepatic collagen deposition and pro-inflammatory p65 protein levels, while increased hepatic antioxidant catalase and glutathione peroxidase activities and serum 25(OH)D, without a clear dose-response effect. Nonetheless, only the highest concentration of VD3 increased hepatic protein levels of VD receptor, while decreased the number of large preneoplastic glutathione-S-transferase- (>0.5 mm(2)) and keratin 8/18-positive lesions, as well the multiplicity of hepatocellular adenomas. Moreover, this intervention increased hepatic antioxidant Nrf2 protein levels and glutathione-S-transferase activity. In summary, dietary VD3 supplementation - in special the highest intervention - showed antifibrotic and antineoplastic properties in chemically-induced cirrhosis-associated hepatocarcinogenesis. The positive modulation of Nrf2 antioxidant axis may be mechanistically involved with these beneficial effects, and may guide future clinical studies. (AU)

Processo FAPESP: 12/03628-8 - Estudo da relação entre vitaminas e doenças crônicas: efeito da vitamina D na fibrose hepática e hepatocarcinogênese em ratos
Beneficiário:Luís Fernando Barbisan
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 12/03964-8 - Estudo da relação entre vitaminas e doenças crônicas: efeito da suplementação com vitamina D na fribrose hepática e hepatocarcinogênese em ratos
Beneficiário:Mariana Baptista Tablas
Modalidade de apoio: Bolsas no Brasil - Mestrado