Coordinated action of a gut–liver pathway drives alcohol detoxification and consumption
Alcohol use disorder (AUD) affects millions of people worldwide, causing extensive morbidity and mortality with limited pharmacological treatments. The liver is considered as the principal site for the detoxification of ethanol metabolite, acetaldehyde (AcH), by aldehyde dehydrogenase 2 (ALDH2) and...
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Veröffentlicht in: | Nature metabolism 2024-07, Vol.6 (7), p.1380-1396 |
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creator | Fu, Yaojie Mackowiak, Bryan Lin, Yu-Hong Maccioni, Luca Lehner, Taylor Pan, Hongna Guan, Yukun Godlewski, Grzegorz Lu, Hongkun Chen, Cheng Wei, Shoupeng Feng, Dechun Paloczi, Janos Zhou, Huiping Pacher, Pal Zhang, Li Kunos, George Gao, Bin |
description | Alcohol use disorder (AUD) affects millions of people worldwide, causing extensive morbidity and mortality with limited pharmacological treatments. The liver is considered as the principal site for the detoxification of ethanol metabolite, acetaldehyde (AcH), by aldehyde dehydrogenase 2 (ALDH2) and as a target for AUD treatment, however, our recent data indicate that the liver only plays a partial role in clearing systemic AcH. Here we show that a liver–gut axis, rather than liver alone, synergistically drives systemic AcH clearance and voluntary alcohol drinking. Mechanistically, we find that after ethanol intake, a substantial proportion of AcH generated in the liver is excreted via the bile into the gastrointestinal tract where AcH is further metabolized by gut ALDH2. Modulating bile flow significantly affects serum AcH level and drinking behaviour. Thus, combined targeting of liver and gut ALDH2, and manipulation of bile flow and secretion are potential therapeutic strategies to treat AUD.
Fu, Mackowiak et al. show that cooperative action of the liver and the gut, rather than the liver alone, drives acetaldehyde clearance after alcohol consumption and modulates drinking behaviour. |
doi_str_mv | 10.1038/s42255-024-01063-2 |
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Fu, Mackowiak et al. show that cooperative action of the liver and the gut, rather than the liver alone, drives acetaldehyde clearance after alcohol consumption and modulates drinking behaviour.</description><identifier>ISSN: 2522-5812</identifier><identifier>EISSN: 2522-5812</identifier><identifier>DOI: 10.1038/s42255-024-01063-2</identifier><identifier>PMID: 38902331</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/443/319 ; 692/4020/2741 ; 692/4020/4021 ; 692/4020/4021/288 ; Biomedical and Life Sciences ; Life Sciences</subject><ispartof>Nature metabolism, 2024-07, Vol.6 (7), p.1380-1396</ispartof><rights>This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024</rights><rights>2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c277t-df62d1d3baafa1513510da81f56deb807e339dded5e393701b83b08eadbe705a3</citedby><cites>FETCH-LOGICAL-c277t-df62d1d3baafa1513510da81f56deb807e339dded5e393701b83b08eadbe705a3</cites><orcidid>0000-0001-7485-762X ; 0000-0001-9840-2013 ; 0000-0002-7700-7345 ; 0000-0002-0453-5008 ; 0009-0006-5411-6078 ; 0000-0002-0050-372X ; 0000-0001-7036-8108 ; 0009-0002-7008-2462 ; 0009-0000-7580-3340 ; 0000-0003-1788-4976 ; 0000-0002-0505-2972</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38902331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fu, Yaojie</creatorcontrib><creatorcontrib>Mackowiak, Bryan</creatorcontrib><creatorcontrib>Lin, Yu-Hong</creatorcontrib><creatorcontrib>Maccioni, Luca</creatorcontrib><creatorcontrib>Lehner, Taylor</creatorcontrib><creatorcontrib>Pan, Hongna</creatorcontrib><creatorcontrib>Guan, Yukun</creatorcontrib><creatorcontrib>Godlewski, Grzegorz</creatorcontrib><creatorcontrib>Lu, Hongkun</creatorcontrib><creatorcontrib>Chen, Cheng</creatorcontrib><creatorcontrib>Wei, Shoupeng</creatorcontrib><creatorcontrib>Feng, Dechun</creatorcontrib><creatorcontrib>Paloczi, Janos</creatorcontrib><creatorcontrib>Zhou, Huiping</creatorcontrib><creatorcontrib>Pacher, Pal</creatorcontrib><creatorcontrib>Zhang, Li</creatorcontrib><creatorcontrib>Kunos, George</creatorcontrib><creatorcontrib>Gao, Bin</creatorcontrib><title>Coordinated action of a gut–liver pathway drives alcohol detoxification and consumption</title><title>Nature metabolism</title><addtitle>Nat Metab</addtitle><addtitle>Nat Metab</addtitle><description>Alcohol use disorder (AUD) affects millions of people worldwide, causing extensive morbidity and mortality with limited pharmacological treatments. The liver is considered as the principal site for the detoxification of ethanol metabolite, acetaldehyde (AcH), by aldehyde dehydrogenase 2 (ALDH2) and as a target for AUD treatment, however, our recent data indicate that the liver only plays a partial role in clearing systemic AcH. Here we show that a liver–gut axis, rather than liver alone, synergistically drives systemic AcH clearance and voluntary alcohol drinking. Mechanistically, we find that after ethanol intake, a substantial proportion of AcH generated in the liver is excreted via the bile into the gastrointestinal tract where AcH is further metabolized by gut ALDH2. Modulating bile flow significantly affects serum AcH level and drinking behaviour. Thus, combined targeting of liver and gut ALDH2, and manipulation of bile flow and secretion are potential therapeutic strategies to treat AUD.
Fu, Mackowiak et al. show that cooperative action of the liver and the gut, rather than the liver alone, drives acetaldehyde clearance after alcohol consumption and modulates drinking behaviour.</description><subject>631/443/319</subject><subject>692/4020/2741</subject><subject>692/4020/4021</subject><subject>692/4020/4021/288</subject><subject>Biomedical and Life Sciences</subject><subject>Life Sciences</subject><issn>2522-5812</issn><issn>2522-5812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1OwzAQhS0EolXpBVggL9kExnbdOEtU8SdVYgMLVtYkdtpUSRzsBOiOO3BDTkL6A2LFauZp3nvSfIScMrhgINRlmHAuZQR8EgGDqYj4ARlyyXkkFeOHf_YBGYewAgDO2ITx5JgMhEqAC8GG5HnmnDdFja01FLO2cDV1OUW66Nqvj8-yeLWeNtgu33BNje9loFhmbulKamzr3ou8yHAbw9rQzNWhq5qNPiFHOZbBjvdzRJ5urh9nd9H84fZ-djWPMh7HbWTyKTfMiBQxRyaZkAwMKpbLqbGpgtgKkRhjjbQiETGwVIkUlEWT2hgkihE53_U23r10NrS6KkJmyxJr67qgBcSgRDJVrLfynTXzLgRvc934okK_1gz0hqreUdU9Vb2lqnkfOtv3d2llzW_kh2FvEDtD6E_1wnq9cp2v-5__q_0GPcaE2A</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Fu, Yaojie</creator><creator>Mackowiak, Bryan</creator><creator>Lin, Yu-Hong</creator><creator>Maccioni, Luca</creator><creator>Lehner, Taylor</creator><creator>Pan, Hongna</creator><creator>Guan, Yukun</creator><creator>Godlewski, Grzegorz</creator><creator>Lu, Hongkun</creator><creator>Chen, Cheng</creator><creator>Wei, Shoupeng</creator><creator>Feng, Dechun</creator><creator>Paloczi, Janos</creator><creator>Zhou, Huiping</creator><creator>Pacher, Pal</creator><creator>Zhang, Li</creator><creator>Kunos, George</creator><creator>Gao, Bin</creator><general>Nature Publishing Group UK</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7485-762X</orcidid><orcidid>https://orcid.org/0000-0001-9840-2013</orcidid><orcidid>https://orcid.org/0000-0002-7700-7345</orcidid><orcidid>https://orcid.org/0000-0002-0453-5008</orcidid><orcidid>https://orcid.org/0009-0006-5411-6078</orcidid><orcidid>https://orcid.org/0000-0002-0050-372X</orcidid><orcidid>https://orcid.org/0000-0001-7036-8108</orcidid><orcidid>https://orcid.org/0009-0002-7008-2462</orcidid><orcidid>https://orcid.org/0009-0000-7580-3340</orcidid><orcidid>https://orcid.org/0000-0003-1788-4976</orcidid><orcidid>https://orcid.org/0000-0002-0505-2972</orcidid></search><sort><creationdate>20240701</creationdate><title>Coordinated action of a gut–liver pathway drives alcohol detoxification and consumption</title><author>Fu, Yaojie ; 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The liver is considered as the principal site for the detoxification of ethanol metabolite, acetaldehyde (AcH), by aldehyde dehydrogenase 2 (ALDH2) and as a target for AUD treatment, however, our recent data indicate that the liver only plays a partial role in clearing systemic AcH. Here we show that a liver–gut axis, rather than liver alone, synergistically drives systemic AcH clearance and voluntary alcohol drinking. Mechanistically, we find that after ethanol intake, a substantial proportion of AcH generated in the liver is excreted via the bile into the gastrointestinal tract where AcH is further metabolized by gut ALDH2. Modulating bile flow significantly affects serum AcH level and drinking behaviour. Thus, combined targeting of liver and gut ALDH2, and manipulation of bile flow and secretion are potential therapeutic strategies to treat AUD.
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title | Coordinated action of a gut–liver pathway drives alcohol detoxification and consumption |
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