Author
Listed:
- Jessica Maiuolo
(Laboratory of Pharmaceutical Biology, IRC-FSH Center, Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Rocco Mollace
(San Raffaele Telematic University, 00163 Rome, Italy)
- Francesca Bosco
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Federica Scarano
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Francesca Oppedisano
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Saverio Nucera
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Stefano Ruga
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Lorenza Guarnieri
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Roberta Macri
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Irene Bava
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Cristina Carresi
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Micaela Gliozzi
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Vincenzo Musolino
(Laboratory of Pharmaceutical Biology, IRC-FSH Center, Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Antonio Cardamone
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Anna Rita Coppoletta
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Andrea Barillaro
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Virginia Simari
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy)
- Daniela Salvemini
(University of St. Luois, St. Louis, MO 63103, USA)
- Ernesto Palma
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy
These authors contributed equally to this work.)
- Vincenzo Mollace
(IRC-FSH Center Department of Health Sciences, University “Magna Græcia” of Catanzaro, 88100 Catanzaro, Italy
Nutramed S.c.a.r.l, Roccelletta di Borgia, 88021 Catanzaro, Italy
These authors contributed equally to this work.)
Abstract
Non-alcoholic fatty liver disease (NAFLD) is considered one of the leading causes of liver-related morbidity and mortality. NAFLD is a cluster of liver disorders that includes the accumulation of fat in the liver, insulin resistance, diffuse steatosis, lobular inflammation, fibrosis, cirrhosis and, in the latter stages, liver cancer. Due to the complexity of the disease and the multifactorial basis for the development of liver dysfunction, there is currently no unique drug treatment for NAFLD and the pharmacological options are inconclusive. In recent years, natural products have been studied for their potential beneficial effect in both preventing and treating fatty liver and its consequences in both local and systemic effects related to NAFLD. In particular, bergamot polyphenolic fraction (BPF), which is rich in natural polyphenols, and Cynara cardunculus wild type (which contains large quantities of sesquiterpenes, caffeic acid derivatives and luteolin) have both been investigated in both pre-clinical settings and clinical studies showing their effect in counteracting NAFLD-related health issues. In the present review we summarize the experimental and clinical evidence on the effect of BPF and Cynara extract alone or in their combination product (Bergacyn ® ) in NAFLD. In particular, data reported show that both extracts may synergize in counteracting the pathophysiological basis of NAFLD by inhibiting lipid accumulation in liver cells, oxidative stress and inflammation subsequent to liver syeatosis and, in the latter stages, liver fibrosis and tissue degeneration. Moreover, due to its powerful vasoprotective effect, the combination of BPF and Cynara extract (Bergacyn ® ) leads to improved endothelial dysfunction and cardioprotective response in both animal models of NAFLD, in veterinary medicine and in humans. Thus, supplementation with BPF and Cynara cardunculus extract and their combination product (Bergacyn ® ) represent a novel and potentially useful approach in preventing and treating NAFLD-associated complications.
Suggested Citation
Jessica Maiuolo & Rocco Mollace & Francesca Bosco & Federica Scarano & Francesca Oppedisano & Saverio Nucera & Stefano Ruga & Lorenza Guarnieri & Roberta Macri & Irene Bava & Cristina Carresi & Micael, 2023.
"The Phytochemical Synergistic Properties of Combination of Bergamot Polyphenolic Fraction and Cynara cardunculus Extract in Non-Alcoholic Fatty Liver Disease,"
Agriculture, MDPI, vol. 13(2), pages 1-19, January.
Handle:
RePEc:gam:jagris:v:13:y:2023:i:2:p:249-:d:1041920
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