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: Xing-Wei Xiang, Hui-Zhen Zheng, Rui Wang, Hui Chen, Jin-Xing Xiao, Bin Zheng, Shu-Lai Liu, Yu-Ting Ding
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2021
Subjects:
Online Access:https://doi.org/10.3390/md19080456
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spelling ftmdpi:oai:mdpi.com:/1660-3397/19/8/456/ 2023-08-20T04:06:02+02:00 Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice Xing-Wei Xiang Hui-Zhen Zheng Rui Wang Hui Chen Jin-Xing Xiao Bin Zheng Shu-Lai Liu Yu-Ting Ding agris 2021-08-11 application/pdf https://doi.org/10.3390/md19080456 EN eng Multidisciplinary Digital Publishing Institute https://dx.doi.org/10.3390/md19080456 https://creativecommons.org/licenses/by/4.0/ Marine Drugs; Volume 19; Issue 8; Pages: 456 oyster ( Crassostrea gigas ) peptides cyclophosphamide immunomodulatory gut microbiota short-chain fatty acid Text 2021 ftmdpi https://doi.org/10.3390/md19080456 2023-08-01T02:24:27Z 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 MDPI Open Access Publishing Marine Drugs 19 8 456
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic oyster ( Crassostrea gigas )
peptides
cyclophosphamide
immunomodulatory
gut microbiota
short-chain fatty acid
spellingShingle oyster ( Crassostrea gigas )
peptides
cyclophosphamide
immunomodulatory
gut microbiota
short-chain fatty acid
Xing-Wei Xiang
Hui-Zhen Zheng
Rui Wang
Hui Chen
Jin-Xing Xiao
Bin Zheng
Shu-Lai Liu
Yu-Ting Ding
Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice
topic_facet oyster ( Crassostrea gigas )
peptides
cyclophosphamide
immunomodulatory
gut microbiota
short-chain fatty acid
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 Xing-Wei Xiang
Hui-Zhen Zheng
Rui Wang
Hui Chen
Jin-Xing Xiao
Bin Zheng
Shu-Lai Liu
Yu-Ting Ding
author_facet Xing-Wei Xiang
Hui-Zhen Zheng
Rui Wang
Hui Chen
Jin-Xing Xiao
Bin Zheng
Shu-Lai Liu
Yu-Ting Ding
author_sort Xing-Wei Xiang
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 Multidisciplinary Digital Publishing Institute
publishDate 2021
url https://doi.org/10.3390/md19080456
op_coverage agris
genre Crassostrea gigas
genre_facet Crassostrea gigas
op_source Marine Drugs; Volume 19; Issue 8; Pages: 456
op_relation https://dx.doi.org/10.3390/md19080456
op_rights https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.3390/md19080456
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