Silybin and the liver: From basic research to clinical practice
Open accessAbstract
Herbal products are increasingly used, mainly in chronic liver disease. Extracts of milk thistle, Silymarin and silybin, are the most prescribed natural compounds, with different indications, but with no definitive results in terms of clinical efficacy. This review analyzes the available studies on the effects of the purified product silybin, both as a free and a conjugated molecule, on liver cells or on experimentally induced liver damage, and in patients with liver disease. We searched PUBMED for articles pertaining to the in vitro and in vivo effects of silybin, its antifibrotic, anti-inflammatory, and antioxidant properties, as well as its metabolic effects, combined with the authors' own knowledge of the literature. Results indicate that the bioavailability of silybin phytosome is higher than that of silymarin and is less influenced by liver damage; silybin does not show significant interactions with other drugs and at doses < 10 g/d has no significant side effects. Experimental studies have clearly demonstrated the antifibrotic, antioxidant and metabolic effects of silybin; previous human studies were insufficient for confirming the clinical efficacy in chronic liver disease, while ongoing clinical trials are promising. On the basis of literature data, silybin seems a promising drug for chronic liver disease.
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Silibinin inhibits formation of ROS by increasing tGSH, MnSOD, Catalase, and glutathione peroxidase levels in rat Kupffer cells, hepatocytes, HepG2 cells, and isolated rat hepatic mitochondria.
“Silibinin has shown to inhibit the formation of ROS by increasing tGSH, MnSOD, Catalase, and glutathione peroxidase levels in rat Kupffer cells, hepatocytes, HepG2 cells, and isolated rat hepatic mitochondria [46].”
From Intervention by picroside II on FFAs induced lipid accumulation and lipotoxicity in HepG2 cells (2021) · cites this paper as [46]
Besides picroside II, P. kurroa contains many other active compounds, including picroside I and apocynin, whose activities on other NAFLD targets have not been explored.
“Besides picroside II, there are many other active compounds present in P. kurroa. These include picroside I and apocynin whose activities have not been explored on other targets involved in pathogenesis of NAFLD such as insulin resistance, altered lipid metabolism, lipotoxicity, oxidative stress and inflammation, activation of immune cells, apoptosis, necrosis, fibrogenesis, and collagen turnover”
From Intervention by picroside II on FFAs induced lipid accumulation and lipotoxicity in HepG2 cells (2021) · cites this paper as [46]
Cited by
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Silymarin as a Natural Antioxidant: An Overview of the Current Evidence and Perspectives
Surai, P. (2015) · Antioxidants · doi:10.3390/antiox4010204 · Cited by 738 · see citing works
A randomized trial of silymarin for the treatment of nonalcoholic steatohepatitis
Wah Kheong, C., Nik Mustapha, N. R., & Mahadeva, S. (2017) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2017.04.016 · Cited by 264 · see citing works
Rizvi, S. A. A., Einstein, G. P., Tulp, O. L., Sainvil, F., & Branly, R. (2022) · Biomolecules · doi:10.3390/biom12101442 · Cited by 181 · see citing works
Intervention by picroside II on FFAs induced lipid accumulation and lipotoxicity in HepG2 cells
Dhami-Shah, H., Vaidya, R., Talwadekar, M., Shaw, E., Udipi, S., Kolthur-Seetharam, U., & Vaidya, A. D. B. (2021) · Journal of Ayurveda and Integrative Medicine · doi:10.1016/j.jaim.2021.04.007 · Cited by 15 · see citing works
“Silibinin has shown to inhibit the formation of ROS by increasing tGSH, MnSOD, Catalase, and glutathione peroxidase levels in rat Kupffer cells, hepatocytes, HepG2 cells, and isolated rat hepatic mitochondria [46].”
Background
- Authors
- Loguercio, C.
- Affiliations
- University of Campania "Luigi Vanvitelli" (IT)
- Corresponding author
- Loguercio, Carmela
- ORCID
- Loguercio, Carmela
- Venue
- World Journal of Gastroenterology
- Publisher
- Baishideng Publishing Group Inc.
- Published
- 2011
- Volume
- 17
- Issue
- 18
- Pages
- 2288
- ISSN
- 1007-9327 (ISSN-L)
- PMC
- PMC3098397
- OpenAlex
- W2153068313
- Cited by
- 375
- References
- 0
- Citations by year
- 2026: 17 · 2025: 25 · 2024: 25 · 2023: 23 · 2022: 27 · 2021: 26 · 2020: 22 · 2019: 34 · 2018: 29 · 2017: 34 · 2016: 23 · 2015: 29 · 2014: 23 · 2013: 22 · 2012: 16
- FWCI
- 16.90
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- World Journal of Gastroenterology (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion)
- Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli" (submittedVersion)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Silymarin and Mushroom Poisoning
- Health Sciences › Medicine › Complementary and alternative medicine › Nigella sativa pharmacological applications
- Health Sciences › Medicine › Complementary and alternative medicine › Medicinal plant effects and applications
- Keywords
- silibinin, silymarin, Silybum marianum, chronic liver disease, antifibrotic effect, antioxidant activity, anti-inflammatory activity, bioavailability, phytosomes, drug interactions, liver injury, herbal medicine
- MeSH terms
- Silybin, Antioxidants, Humans, Liver, Silymarin
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