Abstract

Alcohol Use Disorder (AUD) is one of leading external causes of mortality. Selenium-enriched Peanut Protein (SePP) is a type of Se compound present in Se-enriched plants. Our previous studies showed that SePP possesses potential therapeutic properties and could alleviate alcohol-induced AML-12 cytotoxicity. It spurred us to determine the underlying mechanisms and roles of SePP on gut microbiota. Here, ICR mice were fed either standard diet or ethanol (30%, v/v, 10 mL/kg bw/day) intragastric administration for 8 weeks. The intervention groups were divided into different doses of SePP groups and Se compounds groups, like Selenomethionine (SeMet) group, sodium selenite group. The composition of the gut microbiota was investigated by analyzing 16S rRNA gene sequences. Body weight, lipid metabolism markers, serum insulin and oxidative stress were assessed. Treatment with SePP at a certain dosage (25 μg/kg bw/day in Se) and SeMet reversed diversity loss and community alterations in the gut microbiota of the AUD group, as evidenced by an increased abundance of Firmicutes and decreased abundances of Bacteroidetes and Verrucomicrobia in AUD mice. SePP suppressed the relative abundance of the Rikenellaceae_RC9 gut group and increased those of Lachnospiraceae and Ruminococcaceae, which are associated with lipid metabolism and Short-Chain Fatty Acids (SCFAs) production. The study suggested that SePP has the potential to be used as a supplement for alleviating alcohol-induced liver damage.

Highlights

  • Alcohol Use Disorder (AUD), called alcohol addiction, is one of leading external causes of mortality (Satish, 2003)

  • After the interventions with Se compounds such as Selenium-enriched Peanut Protein (SePP), selenomethionine and sodium selenite with the same selenium concentration (25 μg Se/kg bw/day) (p

  • The results of this study show that supplement of SePP influenced the gut microbiota in AUD mice, which was associated with lipid metabolism and Short-Chain Fatty Acids (SCFAs) production

Read more

Summary

Introduction

Alcohol Use Disorder (AUD), called alcohol addiction, is one of leading external causes of mortality (Satish, 2003). Alcohol use disorder can lead to alcoholic liver toxicity, which is the leading risk of inflammation, fibrosis, or sclerosis of the liver and may even lead to cancer if left unchecked (Bajaj, 2019). The pathophysiological mechanisms of liver injury caused by alcohol still incompletely understood, which is always multifactorial (Stärkel and Schnabl, 2016). Among these factors, alcohol-induced immune responses, metabolic disturbance and inflammation seems to play a crucial role (Bajaj, 2019; Wang et al, 2020). A previous study (Satish, 2003) indicated chronic alcohol consumption result imbalance of the intestinal microbiota by changing the permeability of the intestinal mucosa

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call