Loading…
Limonin, an AMPK Activator, Inhibits Hepatic Lipid Accumulation in High Fat Diet Fed Mice
NAFLD is the most prevalent liver disease in human history. The treatment is still limited yet. In the current study, we reported that limonin inhibited hepatic lipid accumulation and fatty acid synthesis in HFD fed mice. Using AMPK inhibitor and AMPK deficient , we revealed the effect was dependent...
Saved in:
Published in: | Frontiers in pharmacology 2022-01, Vol.13, p.833705-833705 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c465t-e8f17d5c7b05803a17ca1f8fffdaab054f1fc5e6316d31170952cbad0ed11c7a3 |
---|---|
cites | cdi_FETCH-LOGICAL-c465t-e8f17d5c7b05803a17ca1f8fffdaab054f1fc5e6316d31170952cbad0ed11c7a3 |
container_end_page | 833705 |
container_issue | |
container_start_page | 833705 |
container_title | Frontiers in pharmacology |
container_volume | 13 |
creator | Wang, Si-Wei Lan, Tian Chen, Hang-Fei Sheng, Hao Xu, Chun-Yi Xu, Li-Feng Zheng, Fang Zhang, Feng |
description | NAFLD is the most prevalent liver disease in human history. The treatment is still limited yet. In the current study, we reported that limonin inhibited hepatic lipid accumulation and fatty acid synthesis in HFD fed mice. Using AMPK inhibitor and AMPK deficient
, we revealed the effect was dependent on the activation of AMPK. We found that limonin activated AMPK through inhibition of cellular energy metabolism and increasing ADP:ATP ratio. Furthermore, the treatment of limonin induced AMPK mediated suppression of the transcriptional activity of SREBP1/2. Our study suggests that limonin may a promising therapeutic agent for the treatment of NAFLD. |
doi_str_mv | 10.3389/fphar.2022.833705 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_8a95095c2b4547f1a667af4bae1b0481</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_8a95095c2b4547f1a667af4bae1b0481</doaj_id><sourcerecordid>2627479985</sourcerecordid><originalsourceid>FETCH-LOGICAL-c465t-e8f17d5c7b05803a17ca1f8fffdaab054f1fc5e6316d31170952cbad0ed11c7a3</originalsourceid><addsrcrecordid>eNpVkUFv1DAQhSMEolXpD-CCfOTQ3XpiO7YvSKuWZVdsBQc4cLImjr3rKomDk1Ti3-N226r1xdbze9-M9IriI9AlY0pf-uGAaVnSslwqxiQVb4pTqCq20ArKty_eJ8X5ON7SfJjWrOLvixMmgNOqhNPizy50sQ_9BcGerG5-ficrO4U7nGK6INv-EOowjWTjBpyCJbswhCY77NzNbVZiT0JPNmF_IGucyHVwE1m7htwE6z4U7zy2ozt_vM-K3-uvv642i92Pb9ur1W5heSWmhVMeZCOsrKlQlCFIi-CV975BzBr34K1wFYOqYQCSalHaGhvqGgArkZ0V2yO3iXhrhhQ6TP9MxGAehJj2BlNevnVGoRY5b8uaCy49YFVJ9LxGBzXlCjLry5E1zHXnGuv6KWH7Cvr6pw8Hs493RinQQvMM-PwISPHv7MbJdGG0rm2xd3EeTVmVkkutlchWOFptiuOYnH8eA9TcN2weGjb3DZtjwznz6eV-z4mnPtl_SgeiAw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2627479985</pqid></control><display><type>article</type><title>Limonin, an AMPK Activator, Inhibits Hepatic Lipid Accumulation in High Fat Diet Fed Mice</title><source>PubMed Central Free</source><creator>Wang, Si-Wei ; Lan, Tian ; Chen, Hang-Fei ; Sheng, Hao ; Xu, Chun-Yi ; Xu, Li-Feng ; Zheng, Fang ; Zhang, Feng</creator><creatorcontrib>Wang, Si-Wei ; Lan, Tian ; Chen, Hang-Fei ; Sheng, Hao ; Xu, Chun-Yi ; Xu, Li-Feng ; Zheng, Fang ; Zhang, Feng</creatorcontrib><description>NAFLD is the most prevalent liver disease in human history. The treatment is still limited yet. In the current study, we reported that limonin inhibited hepatic lipid accumulation and fatty acid synthesis in HFD fed mice. Using AMPK inhibitor and AMPK deficient
, we revealed the effect was dependent on the activation of AMPK. We found that limonin activated AMPK through inhibition of cellular energy metabolism and increasing ADP:ATP ratio. Furthermore, the treatment of limonin induced AMPK mediated suppression of the transcriptional activity of SREBP1/2. Our study suggests that limonin may a promising therapeutic agent for the treatment of NAFLD.</description><identifier>ISSN: 1663-9812</identifier><identifier>EISSN: 1663-9812</identifier><identifier>DOI: 10.3389/fphar.2022.833705</identifier><identifier>PMID: 35140621</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>AMPK ; limonin ; lipid accumulation ; NAFLD ; Pharmacology ; SREBP</subject><ispartof>Frontiers in pharmacology, 2022-01, Vol.13, p.833705-833705</ispartof><rights>Copyright © 2022 Wang, Lan, Chen, Sheng, Xu, Xu, Zheng and Zhang.</rights><rights>Copyright © 2022 Wang, Lan, Chen, Sheng, Xu, Xu, Zheng and Zhang. 2022 Wang, Lan, Chen, Sheng, Xu, Xu, Zheng and Zhang</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-e8f17d5c7b05803a17ca1f8fffdaab054f1fc5e6316d31170952cbad0ed11c7a3</citedby><cites>FETCH-LOGICAL-c465t-e8f17d5c7b05803a17ca1f8fffdaab054f1fc5e6316d31170952cbad0ed11c7a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819594/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819594/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35140621$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Si-Wei</creatorcontrib><creatorcontrib>Lan, Tian</creatorcontrib><creatorcontrib>Chen, Hang-Fei</creatorcontrib><creatorcontrib>Sheng, Hao</creatorcontrib><creatorcontrib>Xu, Chun-Yi</creatorcontrib><creatorcontrib>Xu, Li-Feng</creatorcontrib><creatorcontrib>Zheng, Fang</creatorcontrib><creatorcontrib>Zhang, Feng</creatorcontrib><title>Limonin, an AMPK Activator, Inhibits Hepatic Lipid Accumulation in High Fat Diet Fed Mice</title><title>Frontiers in pharmacology</title><addtitle>Front Pharmacol</addtitle><description>NAFLD is the most prevalent liver disease in human history. The treatment is still limited yet. In the current study, we reported that limonin inhibited hepatic lipid accumulation and fatty acid synthesis in HFD fed mice. Using AMPK inhibitor and AMPK deficient
, we revealed the effect was dependent on the activation of AMPK. We found that limonin activated AMPK through inhibition of cellular energy metabolism and increasing ADP:ATP ratio. Furthermore, the treatment of limonin induced AMPK mediated suppression of the transcriptional activity of SREBP1/2. Our study suggests that limonin may a promising therapeutic agent for the treatment of NAFLD.</description><subject>AMPK</subject><subject>limonin</subject><subject>lipid accumulation</subject><subject>NAFLD</subject><subject>Pharmacology</subject><subject>SREBP</subject><issn>1663-9812</issn><issn>1663-9812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkUFv1DAQhSMEolXpD-CCfOTQ3XpiO7YvSKuWZVdsBQc4cLImjr3rKomDk1Ti3-N226r1xdbze9-M9IriI9AlY0pf-uGAaVnSslwqxiQVb4pTqCq20ArKty_eJ8X5ON7SfJjWrOLvixMmgNOqhNPizy50sQ_9BcGerG5-ficrO4U7nGK6INv-EOowjWTjBpyCJbswhCY77NzNbVZiT0JPNmF_IGucyHVwE1m7htwE6z4U7zy2ozt_vM-K3-uvv642i92Pb9ur1W5heSWmhVMeZCOsrKlQlCFIi-CV975BzBr34K1wFYOqYQCSalHaGhvqGgArkZ0V2yO3iXhrhhQ6TP9MxGAehJj2BlNevnVGoRY5b8uaCy49YFVJ9LxGBzXlCjLry5E1zHXnGuv6KWH7Cvr6pw8Hs493RinQQvMM-PwISPHv7MbJdGG0rm2xd3EeTVmVkkutlchWOFptiuOYnH8eA9TcN2weGjb3DZtjwznz6eV-z4mnPtl_SgeiAw</recordid><startdate>20220124</startdate><enddate>20220124</enddate><creator>Wang, Si-Wei</creator><creator>Lan, Tian</creator><creator>Chen, Hang-Fei</creator><creator>Sheng, Hao</creator><creator>Xu, Chun-Yi</creator><creator>Xu, Li-Feng</creator><creator>Zheng, Fang</creator><creator>Zhang, Feng</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220124</creationdate><title>Limonin, an AMPK Activator, Inhibits Hepatic Lipid Accumulation in High Fat Diet Fed Mice</title><author>Wang, Si-Wei ; Lan, Tian ; Chen, Hang-Fei ; Sheng, Hao ; Xu, Chun-Yi ; Xu, Li-Feng ; Zheng, Fang ; Zhang, Feng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-e8f17d5c7b05803a17ca1f8fffdaab054f1fc5e6316d31170952cbad0ed11c7a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>AMPK</topic><topic>limonin</topic><topic>lipid accumulation</topic><topic>NAFLD</topic><topic>Pharmacology</topic><topic>SREBP</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Si-Wei</creatorcontrib><creatorcontrib>Lan, Tian</creatorcontrib><creatorcontrib>Chen, Hang-Fei</creatorcontrib><creatorcontrib>Sheng, Hao</creatorcontrib><creatorcontrib>Xu, Chun-Yi</creatorcontrib><creatorcontrib>Xu, Li-Feng</creatorcontrib><creatorcontrib>Zheng, Fang</creatorcontrib><creatorcontrib>Zhang, Feng</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Frontiers in pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Si-Wei</au><au>Lan, Tian</au><au>Chen, Hang-Fei</au><au>Sheng, Hao</au><au>Xu, Chun-Yi</au><au>Xu, Li-Feng</au><au>Zheng, Fang</au><au>Zhang, Feng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Limonin, an AMPK Activator, Inhibits Hepatic Lipid Accumulation in High Fat Diet Fed Mice</atitle><jtitle>Frontiers in pharmacology</jtitle><addtitle>Front Pharmacol</addtitle><date>2022-01-24</date><risdate>2022</risdate><volume>13</volume><spage>833705</spage><epage>833705</epage><pages>833705-833705</pages><issn>1663-9812</issn><eissn>1663-9812</eissn><abstract>NAFLD is the most prevalent liver disease in human history. The treatment is still limited yet. In the current study, we reported that limonin inhibited hepatic lipid accumulation and fatty acid synthesis in HFD fed mice. Using AMPK inhibitor and AMPK deficient
, we revealed the effect was dependent on the activation of AMPK. We found that limonin activated AMPK through inhibition of cellular energy metabolism and increasing ADP:ATP ratio. Furthermore, the treatment of limonin induced AMPK mediated suppression of the transcriptional activity of SREBP1/2. Our study suggests that limonin may a promising therapeutic agent for the treatment of NAFLD.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>35140621</pmid><doi>10.3389/fphar.2022.833705</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1663-9812 |
ispartof | Frontiers in pharmacology, 2022-01, Vol.13, p.833705-833705 |
issn | 1663-9812 1663-9812 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_8a95095c2b4547f1a667af4bae1b0481 |
source | PubMed Central Free |
subjects | AMPK limonin lipid accumulation NAFLD Pharmacology SREBP |
title | Limonin, an AMPK Activator, Inhibits Hepatic Lipid Accumulation in High Fat Diet Fed Mice |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T03%3A53%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Limonin,%20an%20AMPK%20Activator,%20Inhibits%20Hepatic%20Lipid%20Accumulation%20in%20High%20Fat%20Diet%20Fed%20Mice&rft.jtitle=Frontiers%20in%20pharmacology&rft.au=Wang,%20Si-Wei&rft.date=2022-01-24&rft.volume=13&rft.spage=833705&rft.epage=833705&rft.pages=833705-833705&rft.issn=1663-9812&rft.eissn=1663-9812&rft_id=info:doi/10.3389/fphar.2022.833705&rft_dat=%3Cproquest_doaj_%3E2627479985%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c465t-e8f17d5c7b05803a17ca1f8fffdaab054f1fc5e6316d31170952cbad0ed11c7a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2627479985&rft_id=info:pmid/35140621&rfr_iscdi=true |