Nitrate ameliorates dextran sodium sulfate-induced colitis by regulating the homeostasis of the intestinal microbiota

Inflammatory bowel disease (IBD) involves chronic inflammation, loss of epithelial integrity, and gastrointestinal microbiota dysbiosis. Effective therapies for IBD have not been established. Accordingly, in this study, we evaluated the effects of inorganic nitrate, a potent nitric oxide (NO) donor...

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Veröffentlicht in:Free radical biology & medicine 2020-05, Vol.152, p.609-621
Hauptverfasser: Hu, Liang, Jin, Luyuan, Xia, Dengsheng, Zhang, Qian, Ma, Linsha, Zheng, Hui, Xu, Tiansong, Chang, Shimin, Li, Xiangchun, Xun, Zhe, Xu, Yipu, Zhang, Chunmei, Chen, Feng, Wang, Songlin
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container_title Free radical biology & medicine
container_volume 152
creator Hu, Liang
Jin, Luyuan
Xia, Dengsheng
Zhang, Qian
Ma, Linsha
Zheng, Hui
Xu, Tiansong
Chang, Shimin
Li, Xiangchun
Xun, Zhe
Xu, Yipu
Zhang, Chunmei
Chen, Feng
Wang, Songlin
description Inflammatory bowel disease (IBD) involves chronic inflammation, loss of epithelial integrity, and gastrointestinal microbiota dysbiosis. Effective therapies for IBD have not been established. Accordingly, in this study, we evaluated the effects of inorganic nitrate, a potent nitric oxide (NO) donor and microbiota regulator, in a mouse model of dextran sodium sulfate (DSS)-induced colitis. Mice were pretreated with NaNO3 (2 mM) in their drinking water for 5 days, and NaCl was used as a control. Feces were collected for microbiota analyses. The results showed that oral administration of dietary nitrate could maintained colon consistency, improved colon length, maintained body weight, decreased apoptosis in colon epithelial cells, and ameliorated inflammatory cell infiltration in both the colon and peripheral blood. Microbiota profiling revealed that nitrate regulated dysbiosis. Analysis of the top bacteria at the genus level showed that Bacteroidales_S24-7_group_unidentified, Lactobacillus, Bacteroides, and Prevotellaceae_UCG-001 decreased in the DSS group compared with that in the normal group, whereas Lactobacillus, Ruminococcaceae_UCG-014, and Prevotellaceae_UCG-001 were increased in the DSS + NaNO3 group compared with that in the DSS group. The enriched bacteria in the nitrate group included Gordonibacter, Ureaplasama, and Lachnospiraceae_UCG-006. Moreover, microbiota analysis revealed that nitrate could partially decrease the enriched metabolic pathways (p53 signaling pathway and colorectal cancer pathway) compared with that in the DSS and DSS + NaCl groups. Overall, these findings indicated that nitrate could ameliorate DSS-induced colitis by decreasing inflammation, reducing apoptosis, and regulating the microbiota by activation of the NO3−/NO2−/NO pathway. Nitrate might be a potential treatment for colitis patients in the future clinical application. Inflammatory bowel disease (IBD) which was characterized by impaired colon epithelium and dysbiosis of gut microbiome, has emerged as a public health challenge worldwide. Inorganic nitrate efficiently alleviated the symptoms of experimental mouse DSS induced colitis via activating the NO3−/NO2−/NO pathway. The potentially mechanism were via ameliorating inflammatory cell infiltration, regulating microbiota dysbiosis and restoring beneficial bacteria. [Display omitted] •We evaluated the effect of nitrate on DSS-induced colitis in mice.•Dietary nitrate ameliorated inflammatory cell infiltration in the colo
doi_str_mv 10.1016/j.freeradbiomed.2019.12.002
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Effective therapies for IBD have not been established. Accordingly, in this study, we evaluated the effects of inorganic nitrate, a potent nitric oxide (NO) donor and microbiota regulator, in a mouse model of dextran sodium sulfate (DSS)-induced colitis. Mice were pretreated with NaNO3 (2 mM) in their drinking water for 5 days, and NaCl was used as a control. Feces were collected for microbiota analyses. The results showed that oral administration of dietary nitrate could maintained colon consistency, improved colon length, maintained body weight, decreased apoptosis in colon epithelial cells, and ameliorated inflammatory cell infiltration in both the colon and peripheral blood. Microbiota profiling revealed that nitrate regulated dysbiosis. Analysis of the top bacteria at the genus level showed that Bacteroidales_S24-7_group_unidentified, Lactobacillus, Bacteroides, and Prevotellaceae_UCG-001 decreased in the DSS group compared with that in the normal group, whereas Lactobacillus, Ruminococcaceae_UCG-014, and Prevotellaceae_UCG-001 were increased in the DSS + NaNO3 group compared with that in the DSS group. The enriched bacteria in the nitrate group included Gordonibacter, Ureaplasama, and Lachnospiraceae_UCG-006. Moreover, microbiota analysis revealed that nitrate could partially decrease the enriched metabolic pathways (p53 signaling pathway and colorectal cancer pathway) compared with that in the DSS and DSS + NaCl groups. Overall, these findings indicated that nitrate could ameliorate DSS-induced colitis by decreasing inflammation, reducing apoptosis, and regulating the microbiota by activation of the NO3−/NO2−/NO pathway. Nitrate might be a potential treatment for colitis patients in the future clinical application. Inflammatory bowel disease (IBD) which was characterized by impaired colon epithelium and dysbiosis of gut microbiome, has emerged as a public health challenge worldwide. Inorganic nitrate efficiently alleviated the symptoms of experimental mouse DSS induced colitis via activating the NO3−/NO2−/NO pathway. The potentially mechanism were via ameliorating inflammatory cell infiltration, regulating microbiota dysbiosis and restoring beneficial bacteria. [Display omitted] •We evaluated the effect of nitrate on DSS-induced colitis in mice.•Dietary nitrate ameliorated inflammatory cell infiltration in the colon and PB.•Nitrate regulated microbiota dysbiosis and restored beneficial bacteria in the gut.•Nitrate ameliorated DSS-induced colitis by activation of the NO3−/NO2−/NO pathway.</description><identifier>ISSN: 0891-5849</identifier><identifier>EISSN: 1873-4596</identifier><identifier>DOI: 10.1016/j.freeradbiomed.2019.12.002</identifier><identifier>PMID: 31811920</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Colitis ; Epithelium apoptosis ; Inflammatory bowel disease ; Microbiota ; Nitrate/nitrite</subject><ispartof>Free radical biology &amp; medicine, 2020-05, Vol.152, p.609-621</ispartof><rights>2019 The Authors</rights><rights>Copyright © 2019 The Authors. Published by Elsevier Inc. 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Analysis of the top bacteria at the genus level showed that Bacteroidales_S24-7_group_unidentified, Lactobacillus, Bacteroides, and Prevotellaceae_UCG-001 decreased in the DSS group compared with that in the normal group, whereas Lactobacillus, Ruminococcaceae_UCG-014, and Prevotellaceae_UCG-001 were increased in the DSS + NaNO3 group compared with that in the DSS group. The enriched bacteria in the nitrate group included Gordonibacter, Ureaplasama, and Lachnospiraceae_UCG-006. Moreover, microbiota analysis revealed that nitrate could partially decrease the enriched metabolic pathways (p53 signaling pathway and colorectal cancer pathway) compared with that in the DSS and DSS + NaCl groups. Overall, these findings indicated that nitrate could ameliorate DSS-induced colitis by decreasing inflammation, reducing apoptosis, and regulating the microbiota by activation of the NO3−/NO2−/NO pathway. Nitrate might be a potential treatment for colitis patients in the future clinical application. Inflammatory bowel disease (IBD) which was characterized by impaired colon epithelium and dysbiosis of gut microbiome, has emerged as a public health challenge worldwide. Inorganic nitrate efficiently alleviated the symptoms of experimental mouse DSS induced colitis via activating the NO3−/NO2−/NO pathway. The potentially mechanism were via ameliorating inflammatory cell infiltration, regulating microbiota dysbiosis and restoring beneficial bacteria. [Display omitted] •We evaluated the effect of nitrate on DSS-induced colitis in mice.•Dietary nitrate ameliorated inflammatory cell infiltration in the colon and PB.•Nitrate regulated microbiota dysbiosis and restored beneficial bacteria in the gut.•Nitrate ameliorated DSS-induced colitis by activation of the NO3−/NO2−/NO pathway.</description><subject>Colitis</subject><subject>Epithelium apoptosis</subject><subject>Inflammatory bowel disease</subject><subject>Microbiota</subject><subject>Nitrate/nitrite</subject><issn>0891-5849</issn><issn>1873-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqNUE1P3TAQtBBVedD-BWSpFy4JXjvJi9VThfiSEL20Z8ux1-CnJKa2U8G_x-mDQ29cvNbszO7sEPINWA0MuvNd7SJi1HbwYUJbcwayBl4zxg_IBvqtqJpWdodkw3oJVds38ogcp7RjjDWt6D-TIwE9gORsQ5Z7n6POSPWEow_rN1GLzwWcaQrWLxNNy-gKXvnZLgYtNWH02Sc6vNCID8uos58faH5E-lgMhZR1Kt3g_kF-LhMLQY908iaGYjrrL-ST02PCr2_1hPy-uvx1cVPd_by-vfhxV5lGdLly1vUCuAbcMqGtwbbTrh3KHZ0csIMOeWN6aBsuOBcA5W2ts8YaIyVzgzghZ_u5TzH8WYoPNflkcBz1jGFJatVtRS95U6jf99TiMaWITj1FP-n4ooCpNXe1U__lrtbcFXBVci_q07dFy7D23rXvQRfC5Z6A5dy_HqNKxuNc4vQRTVY2-A8tegV2yp7i</recordid><startdate>20200520</startdate><enddate>20200520</enddate><creator>Hu, Liang</creator><creator>Jin, Luyuan</creator><creator>Xia, Dengsheng</creator><creator>Zhang, Qian</creator><creator>Ma, Linsha</creator><creator>Zheng, Hui</creator><creator>Xu, Tiansong</creator><creator>Chang, Shimin</creator><creator>Li, Xiangchun</creator><creator>Xun, Zhe</creator><creator>Xu, Yipu</creator><creator>Zhang, Chunmei</creator><creator>Chen, Feng</creator><creator>Wang, Songlin</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20200520</creationdate><title>Nitrate ameliorates dextran sodium sulfate-induced colitis by regulating the homeostasis of the intestinal microbiota</title><author>Hu, Liang ; Jin, Luyuan ; Xia, Dengsheng ; Zhang, Qian ; Ma, Linsha ; Zheng, Hui ; Xu, Tiansong ; Chang, Shimin ; Li, Xiangchun ; Xun, Zhe ; Xu, Yipu ; Zhang, Chunmei ; Chen, Feng ; Wang, Songlin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-fdf8312a1e703adce56af5b00069be616e24c815423223113225dfdcdcc990fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Colitis</topic><topic>Epithelium apoptosis</topic><topic>Inflammatory bowel disease</topic><topic>Microbiota</topic><topic>Nitrate/nitrite</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Liang</creatorcontrib><creatorcontrib>Jin, Luyuan</creatorcontrib><creatorcontrib>Xia, Dengsheng</creatorcontrib><creatorcontrib>Zhang, Qian</creatorcontrib><creatorcontrib>Ma, Linsha</creatorcontrib><creatorcontrib>Zheng, Hui</creatorcontrib><creatorcontrib>Xu, Tiansong</creatorcontrib><creatorcontrib>Chang, Shimin</creatorcontrib><creatorcontrib>Li, Xiangchun</creatorcontrib><creatorcontrib>Xun, Zhe</creatorcontrib><creatorcontrib>Xu, Yipu</creatorcontrib><creatorcontrib>Zhang, Chunmei</creatorcontrib><creatorcontrib>Chen, Feng</creatorcontrib><creatorcontrib>Wang, Songlin</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Free radical biology &amp; medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Liang</au><au>Jin, Luyuan</au><au>Xia, Dengsheng</au><au>Zhang, Qian</au><au>Ma, Linsha</au><au>Zheng, Hui</au><au>Xu, Tiansong</au><au>Chang, Shimin</au><au>Li, Xiangchun</au><au>Xun, Zhe</au><au>Xu, Yipu</au><au>Zhang, Chunmei</au><au>Chen, Feng</au><au>Wang, Songlin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitrate ameliorates dextran sodium sulfate-induced colitis by regulating the homeostasis of the intestinal microbiota</atitle><jtitle>Free radical biology &amp; medicine</jtitle><addtitle>Free Radic Biol Med</addtitle><date>2020-05-20</date><risdate>2020</risdate><volume>152</volume><spage>609</spage><epage>621</epage><pages>609-621</pages><issn>0891-5849</issn><eissn>1873-4596</eissn><abstract>Inflammatory bowel disease (IBD) involves chronic inflammation, loss of epithelial integrity, and gastrointestinal microbiota dysbiosis. Effective therapies for IBD have not been established. Accordingly, in this study, we evaluated the effects of inorganic nitrate, a potent nitric oxide (NO) donor and microbiota regulator, in a mouse model of dextran sodium sulfate (DSS)-induced colitis. Mice were pretreated with NaNO3 (2 mM) in their drinking water for 5 days, and NaCl was used as a control. Feces were collected for microbiota analyses. The results showed that oral administration of dietary nitrate could maintained colon consistency, improved colon length, maintained body weight, decreased apoptosis in colon epithelial cells, and ameliorated inflammatory cell infiltration in both the colon and peripheral blood. Microbiota profiling revealed that nitrate regulated dysbiosis. Analysis of the top bacteria at the genus level showed that Bacteroidales_S24-7_group_unidentified, Lactobacillus, Bacteroides, and Prevotellaceae_UCG-001 decreased in the DSS group compared with that in the normal group, whereas Lactobacillus, Ruminococcaceae_UCG-014, and Prevotellaceae_UCG-001 were increased in the DSS + NaNO3 group compared with that in the DSS group. The enriched bacteria in the nitrate group included Gordonibacter, Ureaplasama, and Lachnospiraceae_UCG-006. Moreover, microbiota analysis revealed that nitrate could partially decrease the enriched metabolic pathways (p53 signaling pathway and colorectal cancer pathway) compared with that in the DSS and DSS + NaCl groups. Overall, these findings indicated that nitrate could ameliorate DSS-induced colitis by decreasing inflammation, reducing apoptosis, and regulating the microbiota by activation of the NO3−/NO2−/NO pathway. Nitrate might be a potential treatment for colitis patients in the future clinical application. Inflammatory bowel disease (IBD) which was characterized by impaired colon epithelium and dysbiosis of gut microbiome, has emerged as a public health challenge worldwide. Inorganic nitrate efficiently alleviated the symptoms of experimental mouse DSS induced colitis via activating the NO3−/NO2−/NO pathway. The potentially mechanism were via ameliorating inflammatory cell infiltration, regulating microbiota dysbiosis and restoring beneficial bacteria. [Display omitted] •We evaluated the effect of nitrate on DSS-induced colitis in mice.•Dietary nitrate ameliorated inflammatory cell infiltration in the colon and PB.•Nitrate regulated microbiota dysbiosis and restored beneficial bacteria in the gut.•Nitrate ameliorated DSS-induced colitis by activation of the NO3−/NO2−/NO pathway.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31811920</pmid><doi>10.1016/j.freeradbiomed.2019.12.002</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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subjects Colitis
Epithelium apoptosis
Inflammatory bowel disease
Microbiota
Nitrate/nitrite
title Nitrate ameliorates dextran sodium sulfate-induced colitis by regulating the homeostasis of the intestinal microbiota
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