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Oral Exposure to Epoxiconazole Disturbed the Gut Micro-Environment and Metabolic Profiling in Male Mice
Epoxiconazole (EPX), a triazole fungicide, is widely used in agriculture to control pests and diseases. High residual and occupational exposure to EPX increases health risks, and evidence of potential harm to mammals remains to be added. In the present study, 6-week-old male mice were exposed to 10...
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Published in: | Metabolites 2023-04, Vol.13 (4), p.522 |
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description | Epoxiconazole (EPX), a triazole fungicide, is widely used in agriculture to control pests and diseases. High residual and occupational exposure to EPX increases health risks, and evidence of potential harm to mammals remains to be added. In the present study, 6-week-old male mice were exposed to 10 and 50 mg/kg bw EPX for 28 days. The results showed that EPX significantly increased the liver weights. EPX also decreased the mucus secretion of the colon and altered intestinal barrier function in mice including a reduced expression of some genes (
,
,
). Moreover, EPX altered the composition and abundance of gut microbiota in the colon of mice. The alpha diversity indices (Shannon, Simpson) in the gut microbiota increased after exposure to EPX for 28 days. Interestingly, EPX increased the ratio of
to
and the abundance of other harmful bacteria including
and
. Based on the untargeted metabolomic analysis, it was found that EPX altered the metabolic profiles of the liver in mice. KEGG analysis of differential metabolites revealed that EPX disrupted the pathway related to glycolipid metabolism, and the mRNA levels of related genes were also confirmed. In addition, the correlation analysis showed that the most altered harmful bacteria were associated with some significantly altered metabolites. The findings highlight that EPX exposure changed the micro-environment and lipid metabolism disturbance. These results also suggest that the potential toxicity of triazole fungicides to mammals cannot be ignored. |
doi_str_mv | 10.3390/metabo13040522 |
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,
,
). Moreover, EPX altered the composition and abundance of gut microbiota in the colon of mice. The alpha diversity indices (Shannon, Simpson) in the gut microbiota increased after exposure to EPX for 28 days. Interestingly, EPX increased the ratio of
to
and the abundance of other harmful bacteria including
and
. Based on the untargeted metabolomic analysis, it was found that EPX altered the metabolic profiles of the liver in mice. KEGG analysis of differential metabolites revealed that EPX disrupted the pathway related to glycolipid metabolism, and the mRNA levels of related genes were also confirmed. In addition, the correlation analysis showed that the most altered harmful bacteria were associated with some significantly altered metabolites. The findings highlight that EPX exposure changed the micro-environment and lipid metabolism disturbance. These results also suggest that the potential toxicity of triazole fungicides to mammals cannot be ignored.</description><identifier>ISSN: 2218-1989</identifier><identifier>EISSN: 2218-1989</identifier><identifier>DOI: 10.3390/metabo13040522</identifier><identifier>PMID: 37110180</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Animal experimentation ; Antibodies ; Cholesterol ; Colon ; Correlation analysis ; Digestive system ; Diversity indices ; Epoxiconazole ; Evaluation ; Fungicides ; Gastrointestinal tract ; Genes ; gut microbiota ; Health aspects ; intestinal barrier ; Intestinal microflora ; Laboratory animals ; Lipid metabolism ; Liver ; Metabolism ; Metabolites ; metabolome ; Metabolomics ; mice ; Microbiota ; Microbiota (Symbiotic organisms) ; mRNA ; Occupational exposure ; Pesticides ; Properties ; Sterols ; Toxicity ; Triazoles</subject><ispartof>Metabolites, 2023-04, Vol.13 (4), p.522</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. 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/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c552t-8dc4c8505bc81fc7a821b68b8bebe8b60f6a198fef2b83f537524deb39dd0703</citedby><cites>FETCH-LOGICAL-c552t-8dc4c8505bc81fc7a821b68b8bebe8b60f6a198fef2b83f537524deb39dd0703</cites><orcidid>0000-0003-4135-553X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2806581325/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2806581325?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37110180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weng, You</creatorcontrib><creatorcontrib>Xu, Ting</creatorcontrib><creatorcontrib>Wang, Caihong</creatorcontrib><creatorcontrib>Jin, Yuanxiang</creatorcontrib><title>Oral Exposure to Epoxiconazole Disturbed the Gut Micro-Environment and Metabolic Profiling in Male Mice</title><title>Metabolites</title><addtitle>Metabolites</addtitle><description>Epoxiconazole (EPX), a triazole fungicide, is widely used in agriculture to control pests and diseases. High residual and occupational exposure to EPX increases health risks, and evidence of potential harm to mammals remains to be added. In the present study, 6-week-old male mice were exposed to 10 and 50 mg/kg bw EPX for 28 days. The results showed that EPX significantly increased the liver weights. EPX also decreased the mucus secretion of the colon and altered intestinal barrier function in mice including a reduced expression of some genes (
,
,
). Moreover, EPX altered the composition and abundance of gut microbiota in the colon of mice. The alpha diversity indices (Shannon, Simpson) in the gut microbiota increased after exposure to EPX for 28 days. Interestingly, EPX increased the ratio of
to
and the abundance of other harmful bacteria including
and
. Based on the untargeted metabolomic analysis, it was found that EPX altered the metabolic profiles of the liver in mice. KEGG analysis of differential metabolites revealed that EPX disrupted the pathway related to glycolipid metabolism, and the mRNA levels of related genes were also confirmed. In addition, the correlation analysis showed that the most altered harmful bacteria were associated with some significantly altered metabolites. The findings highlight that EPX exposure changed the micro-environment and lipid metabolism disturbance. These results also suggest that the potential toxicity of triazole fungicides to mammals cannot be ignored.</description><subject>Animal experimentation</subject><subject>Antibodies</subject><subject>Cholesterol</subject><subject>Colon</subject><subject>Correlation analysis</subject><subject>Digestive system</subject><subject>Diversity indices</subject><subject>Epoxiconazole</subject><subject>Evaluation</subject><subject>Fungicides</subject><subject>Gastrointestinal tract</subject><subject>Genes</subject><subject>gut microbiota</subject><subject>Health aspects</subject><subject>intestinal barrier</subject><subject>Intestinal microflora</subject><subject>Laboratory animals</subject><subject>Lipid metabolism</subject><subject>Liver</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>metabolome</subject><subject>Metabolomics</subject><subject>mice</subject><subject>Microbiota</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>mRNA</subject><subject>Occupational exposure</subject><subject>Pesticides</subject><subject>Properties</subject><subject>Sterols</subject><subject>Toxicity</subject><subject>Triazoles</subject><issn>2218-1989</issn><issn>2218-1989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQhiMEolXplSOyxIVLir9iOydUlaVU6qocerf8Mdl6ldiLk1SFX4_TltJFtQ-27Hcee96ZqnpP8AljLf48wGRsIgxz3FD6qjqklKiatKp9_Wx_UB2P4xaXIXAjMXlbHTBJCCYKH1abq2x6tLrbpXHOgKaEVrt0F1yK5nfqAX0N4zRnCx5NN4DO5wmtg8upXsXbkFMcIE7IRI_W91_pg0M_cupCH-IGhYjWpjBKBLyr3nSmH-H4cT2qrr-trs--15dX5xdnp5e1axo61co77lSDG-sU6Zw0ihIrlFUWLCgrcCdMyamDjlrFuobJhnIPlrXeY4nZUXXxgPXJbPUuh8HkXzqZoO8PUt5ok6fgetDCC2k89pJyzFvsDIaWeFkOrXDc88L68sDazXYA70qqxas96P5NDDd6k251sZZzSmghfHok5PRzhnHSQxgd9L2JkOZRU4VlS5kgokg__ifdpjnHYtWiEo0ijDb_VJviqw6xS-Vht0D1qeRlMqGWZ09eUJXpYVgqC6U-8GJAqew4ZuiekiRYL52m9zutBHx4bs2T_G9fsT-Iy86i</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Weng, You</creator><creator>Xu, Ting</creator><creator>Wang, Caihong</creator><creator>Jin, Yuanxiang</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-4135-553X</orcidid></search><sort><creationdate>20230401</creationdate><title>Oral Exposure to Epoxiconazole Disturbed the Gut Micro-Environment and Metabolic Profiling in Male Mice</title><author>Weng, You ; Xu, Ting ; Wang, Caihong ; Jin, Yuanxiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c552t-8dc4c8505bc81fc7a821b68b8bebe8b60f6a198fef2b83f537524deb39dd0703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animal experimentation</topic><topic>Antibodies</topic><topic>Cholesterol</topic><topic>Colon</topic><topic>Correlation analysis</topic><topic>Digestive system</topic><topic>Diversity indices</topic><topic>Epoxiconazole</topic><topic>Evaluation</topic><topic>Fungicides</topic><topic>Gastrointestinal tract</topic><topic>Genes</topic><topic>gut microbiota</topic><topic>Health aspects</topic><topic>intestinal barrier</topic><topic>Intestinal microflora</topic><topic>Laboratory animals</topic><topic>Lipid metabolism</topic><topic>Liver</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>metabolome</topic><topic>Metabolomics</topic><topic>mice</topic><topic>Microbiota</topic><topic>Microbiota (Symbiotic organisms)</topic><topic>mRNA</topic><topic>Occupational exposure</topic><topic>Pesticides</topic><topic>Properties</topic><topic>Sterols</topic><topic>Toxicity</topic><topic>Triazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weng, You</creatorcontrib><creatorcontrib>Xu, Ting</creatorcontrib><creatorcontrib>Wang, Caihong</creatorcontrib><creatorcontrib>Jin, Yuanxiang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Metabolites</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weng, You</au><au>Xu, Ting</au><au>Wang, Caihong</au><au>Jin, Yuanxiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral Exposure to Epoxiconazole Disturbed the Gut Micro-Environment and Metabolic Profiling in Male Mice</atitle><jtitle>Metabolites</jtitle><addtitle>Metabolites</addtitle><date>2023-04-01</date><risdate>2023</risdate><volume>13</volume><issue>4</issue><spage>522</spage><pages>522-</pages><issn>2218-1989</issn><eissn>2218-1989</eissn><abstract>Epoxiconazole (EPX), a triazole fungicide, is widely used in agriculture to control pests and diseases. High residual and occupational exposure to EPX increases health risks, and evidence of potential harm to mammals remains to be added. In the present study, 6-week-old male mice were exposed to 10 and 50 mg/kg bw EPX for 28 days. The results showed that EPX significantly increased the liver weights. EPX also decreased the mucus secretion of the colon and altered intestinal barrier function in mice including a reduced expression of some genes (
,
,
). Moreover, EPX altered the composition and abundance of gut microbiota in the colon of mice. The alpha diversity indices (Shannon, Simpson) in the gut microbiota increased after exposure to EPX for 28 days. Interestingly, EPX increased the ratio of
to
and the abundance of other harmful bacteria including
and
. Based on the untargeted metabolomic analysis, it was found that EPX altered the metabolic profiles of the liver in mice. KEGG analysis of differential metabolites revealed that EPX disrupted the pathway related to glycolipid metabolism, and the mRNA levels of related genes were also confirmed. In addition, the correlation analysis showed that the most altered harmful bacteria were associated with some significantly altered metabolites. The findings highlight that EPX exposure changed the micro-environment and lipid metabolism disturbance. These results also suggest that the potential toxicity of triazole fungicides to mammals cannot be ignored.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37110180</pmid><doi>10.3390/metabo13040522</doi><orcidid>https://orcid.org/0000-0003-4135-553X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal experimentation Antibodies Cholesterol Colon Correlation analysis Digestive system Diversity indices Epoxiconazole Evaluation Fungicides Gastrointestinal tract Genes gut microbiota Health aspects intestinal barrier Intestinal microflora Laboratory animals Lipid metabolism Liver Metabolism Metabolites metabolome Metabolomics mice Microbiota Microbiota (Symbiotic organisms) mRNA Occupational exposure Pesticides Properties Sterols Toxicity Triazoles |
title | Oral Exposure to Epoxiconazole Disturbed the Gut Micro-Environment and Metabolic Profiling in Male Mice |
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