Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice

The intestinal flora is recognized as a significant contributor to the immune system. In this research, the protective effects of oyster peptides on immune regulation and intestinal microbiota were investigated in mice treated with cyclophosphamide. The results showed that oyster peptides restored t...

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Published in:Marine Drugs
Main Authors: Xiang, Xing-Wei, Zheng, Hui-Zhen, Wang, Rui, Chen, Hui, Xiao, Jin-Xing, Zheng, Bin, Liu, Shu-Lai, Ding, Yu-Ting
Format: Text
Language:English
Published: MDPI 2021
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Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401037/
http://www.ncbi.nlm.nih.gov/pubmed/34436295
https://doi.org/10.3390/md19080456
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spelling ftpubmed:oai:pubmedcentral.nih.gov:8401037 2023-05-15T15:58:38+02:00 Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice Xiang, Xing-Wei Zheng, Hui-Zhen Wang, Rui Chen, Hui Xiao, Jin-Xing Zheng, Bin Liu, Shu-Lai Ding, Yu-Ting 2021-08-11 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401037/ http://www.ncbi.nlm.nih.gov/pubmed/34436295 https://doi.org/10.3390/md19080456 en eng MDPI http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401037/ http://www.ncbi.nlm.nih.gov/pubmed/34436295 http://dx.doi.org/10.3390/md19080456 © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). CC-BY Mar Drugs Article Text 2021 ftpubmed https://doi.org/10.3390/md19080456 2021-09-05T00:59:35Z The intestinal flora is recognized as a significant contributor to the immune system. In this research, the protective effects of oyster peptides on immune regulation and intestinal microbiota were investigated in mice treated with cyclophosphamide. The results showed that oyster peptides restored the indexes of thymus, spleen and liver, stimulated cytokines secretion and promoted the relative mRNA levels of Th1/Th2 cytokines (IL-2, IFN-γ, IL-4 and IL-10). The mRNA levels of Occludin, Claudin-1, ZO-1, and Mucin-2 were up-regulated, and the NF-κB signaling pathway was also activated after oyster peptides administration. Furthermore, oyster peptides treatment reduced the proportion of Firmicutes/Bacteroidetes, increased the relative abundance of Alistipes, Lactobacillus, Rikenell and the content of short-chain fatty acids, and reversed the composition of intestinal microflora similar to that of normal mice. In conclusion, oyster peptides effectively ameliorated cyclophosphamide-induced intestinal damage and modified gut microbiota structure in mice, and might be utilized as a beneficial ingredient in functional foods for immune regulation. Text Crassostrea gigas PubMed Central (PMC) Marine Drugs 19 8 456
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Article
spellingShingle Article
Xiang, Xing-Wei
Zheng, Hui-Zhen
Wang, Rui
Chen, Hui
Xiao, Jin-Xing
Zheng, Bin
Liu, Shu-Lai
Ding, Yu-Ting
Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice
topic_facet Article
description The intestinal flora is recognized as a significant contributor to the immune system. In this research, the protective effects of oyster peptides on immune regulation and intestinal microbiota were investigated in mice treated with cyclophosphamide. The results showed that oyster peptides restored the indexes of thymus, spleen and liver, stimulated cytokines secretion and promoted the relative mRNA levels of Th1/Th2 cytokines (IL-2, IFN-γ, IL-4 and IL-10). The mRNA levels of Occludin, Claudin-1, ZO-1, and Mucin-2 were up-regulated, and the NF-κB signaling pathway was also activated after oyster peptides administration. Furthermore, oyster peptides treatment reduced the proportion of Firmicutes/Bacteroidetes, increased the relative abundance of Alistipes, Lactobacillus, Rikenell and the content of short-chain fatty acids, and reversed the composition of intestinal microflora similar to that of normal mice. In conclusion, oyster peptides effectively ameliorated cyclophosphamide-induced intestinal damage and modified gut microbiota structure in mice, and might be utilized as a beneficial ingredient in functional foods for immune regulation.
format Text
author Xiang, Xing-Wei
Zheng, Hui-Zhen
Wang, Rui
Chen, Hui
Xiao, Jin-Xing
Zheng, Bin
Liu, Shu-Lai
Ding, Yu-Ting
author_facet Xiang, Xing-Wei
Zheng, Hui-Zhen
Wang, Rui
Chen, Hui
Xiao, Jin-Xing
Zheng, Bin
Liu, Shu-Lai
Ding, Yu-Ting
author_sort Xiang, Xing-Wei
title Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice
title_short Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice
title_full Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice
title_fullStr Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice
title_full_unstemmed Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice
title_sort ameliorative effects of peptides derived from oyster (crassostrea gigas) on immunomodulatory function and gut microbiota structure in cyclophosphamide-treated mice
publisher MDPI
publishDate 2021
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401037/
http://www.ncbi.nlm.nih.gov/pubmed/34436295
https://doi.org/10.3390/md19080456
genre Crassostrea gigas
genre_facet Crassostrea gigas
op_source Mar Drugs
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401037/
http://www.ncbi.nlm.nih.gov/pubmed/34436295
http://dx.doi.org/10.3390/md19080456
op_rights © 2021 by the authors.
https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
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