Published online Jun 28, 2020. doi: 10.3748/wjg.v26.i24.3432
Peer-review started: March 4, 2020
First decision: April 12, 2020
Revised: April 24, 2020
Accepted: May 30, 2020
Article in press: May 30, 2020
Published online: June 28, 2020
Processing time: 115 Days and 23.1 Hours
Alcoholic liver disease (ALD) is a worldwide health problem with poor prognosis and limited efficacy of current treatments, resulting in major health and economic burdens on both individuals and the society. Many natural products have been shown to improve ALD due to their antioxidant activities.
Some parts of Hovenia dulcis (H. dulcis) provide health benefits. Nevertheless, the effects and mechanisms of H. dulcis seeds on ALD have not yet been fully elucidated.
The present study aimed to determine H. dulcis antioxidant activity, evaluate its effects against ALD, and investigate the related mechanisms via network pharmacology.
The antioxidant activity of H. dulcis seed was determined by both ferric-reducing antioxidant power (FRAP) and trolox equivalent antioxidant capacity (TEAC) assays. The total phenolic and flavonoid contents were determined by Folin–Ciocalteu method and aluminum chloride colorimetry, respectively, as well as polysaccharide by phenol-sulfuric acid method. The effects of H. dulcis seeds against alcoholic liver injury were investigated in mice with water extract pretreatment for 7 d followed by alcohol administration. Moreover, the mechanisms of action were explored with network pharmacology.
The results showed that H. dulcis seeds possessed strong antioxidant activity (245.11 ± 10.17 μmol Fe2+/g by FRAP, and 284.35 ± 23.57 μmol TE/g by TEAC, respectively), and contained remarkable phenols and flavonoids, as well as a few polysaccharides. H. dulcis seeds attenuated alcohol-induced oxidative liver injury, showing reduced serum alanine and aspartate aminotransferases, alkaline phosphatase and triglyceride, elevated hepatic glutathione, increased activities of superoxide dismutase and catalase, and reduced malondialdehyde as well as hepatic triglyceride. The results of network pharmacology analysis indicated that kaempferol, stigmasterol, and naringenin were the main bioactive compounds in H. dulcis seeds, and that modulating oxidative stress, inflammation, gut-derived products, and apoptosis were involved in the mechanisms of H. dulcis seeds’ protective effects on ALD.
The results of this study demonstrated that H. dulcis seeds could be a good natural antioxidant source with protective effects on oxidative diseases such as ALD.
The results of this study provide valid evidence for further application of the seeds of edible medicinal plant H. dulcis as nutraceuticals and pharmaceuticals to manage ALD.