Bergamot Polyphenols Improve Dyslipidemia and Pathophysiological Features in a Mouse Model of Non-Alcoholic Fatty Liver Disease

There is a need for continued drug development for nonalcoholic steatohepatitis (NASH). Bergamot is a plant whose fruit juice is enriched with flavonoids and phenolic compounds which improves dyslipidemia and markers of systemic inflammation in patients with Metabolic Syndrome. The aim of this study...

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Veröffentlicht in:Scientific reports 2020-02, Vol.10 (1), p.2565, Article 2565
Hauptverfasser: Musolino, Vincenzo, Gliozzi, Micaela, Scarano, Federica, Bosco, Francesca, Scicchitano, Miriam, Nucera, Saverio, Carresi, Cristina, Ruga, Stefano, Zito, Maria Caterina, Maiuolo, Jessica, Macrì, Roberta, Amodio, Nicola, Juli, Giada, Tassone, Pierfrancesco, Mollace, Rocco, Caffrey, Rebecca, Marioneaux, Jonathon, Walker, Ross, Ehrlich, James, Palma, Ernesto, Muscoli, Carolina, Bedossa, Pierre, Salvemini, Daniela, Mollace, Vincenzo, Sanyal, Arun J.
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Sprache:eng
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Zusammenfassung:There is a need for continued drug development for nonalcoholic steatohepatitis (NASH). Bergamot is a plant whose fruit juice is enriched with flavonoids and phenolic compounds which improves dyslipidemia and markers of systemic inflammation in patients with Metabolic Syndrome. The aim of this study was to perform a preclinical “proof of concept” study of Bergamot polyphenolic formulation (BPF99) for the treatment of NASH. A disease reversal study was performed in the diet-induced animal model of NAFLD (DIAMOND). Groups of 8 weeks old mice were randomly assigned to receive chow diet, high fat diet with sugar in drinking water (Western diet- WD). Mice on WD were further randomized to continue on WD gavaged with vehicle or continue on WD with additional gavage of BPF99 (50 mg/kg) after 16 weeks of diet. Mice were euthanized after 11 additional weeks. The primary endpoint was resolution of NASH. Secondary endpoints included changes in individual histological features, body weight, liver enzymes, dyslipidemia, markers of oxidative stress and molecular markers of disease activity and fibrosis. The results showed that BPF99 reduced ALT (mean 71.6 vs 44.6 IU/l, p 
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-020-59485-3