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The combination of dapagliflozin and statins ameliorates renal injury through attenuating the activation of inflammasome‐mediated autophagy in insulin‐resistant rats
Long‐term use of a high‐fat diet with high‐fructose (HFF) intake could promote insulin resistance and induce lipid accumulation leading to kidney injury possibly via impairment of the autophagy process and enhancement of the inflammasome pathway. We investigated whether dapagliflozin as a monotherap...
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Published in: | Journal of biochemical and molecular toxicology 2022-04, Vol.36 (4), p.e22978-n/a |
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creator | Thongnak, Laongdao Pengrattanachot, Nattavadee Promsan, Sasivimon Phengpol, Nichakorn Sutthasupha, Prempree Chatsudthipong, Varanuj Lungkaphin, Anusorn |
description | Long‐term use of a high‐fat diet with high‐fructose (HFF) intake could promote insulin resistance and induce lipid accumulation leading to kidney injury possibly via impairment of the autophagy process and enhancement of the inflammasome pathway. We investigated whether dapagliflozin as a monotherapy or combined with atorvastatin could restore kidney autophagy impairment and reduce inflammasome activation associated with kidney injury induced by HFF consumption. Male Wistar rats were given an HFF for 16 weeks and then treated with dapagliflozin with or without atorvastatin for 4 weeks. Impaired glucose tolerance, dyslipidemia, renal lipid accumulation along with impaired renal autophagy and activated inflammasome pathway promoted renal injury were exhibited in HFF rats. Dapagliflozin with or without atorvastatin treatment could partially restore disrupted metabolic parameters and reduce kidney injury. In particular, the combination treatment group showed significant amelioration of inflammasome activation and autophagy impairment. In conclusion, the combination therapy of dapagliflozin and atorvastatin has a positive effect on renal injury associated with autophagy and inflammasome activation induced by HFF in insulin‐resistant rats. This study is the first report demonstrating the underlying mechanism associated with a combination treatment of dapagliflozin and atorvastatin on autophagy and inflammasome pathways in an insulin‐resistant condition. Therefore, dapagliflozin in combination with atorvastatin may be a further preventive or therapeutic strategy for chronic kidney disease in an insulin‐resistant or diabetic condition. |
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We investigated whether dapagliflozin as a monotherapy or combined with atorvastatin could restore kidney autophagy impairment and reduce inflammasome activation associated with kidney injury induced by HFF consumption. Male Wistar rats were given an HFF for 16 weeks and then treated with dapagliflozin with or without atorvastatin for 4 weeks. Impaired glucose tolerance, dyslipidemia, renal lipid accumulation along with impaired renal autophagy and activated inflammasome pathway promoted renal injury were exhibited in HFF rats. Dapagliflozin with or without atorvastatin treatment could partially restore disrupted metabolic parameters and reduce kidney injury. In particular, the combination treatment group showed significant amelioration of inflammasome activation and autophagy impairment. In conclusion, the combination therapy of dapagliflozin and atorvastatin has a positive effect on renal injury associated with autophagy and inflammasome activation induced by HFF in insulin‐resistant rats. This study is the first report demonstrating the underlying mechanism associated with a combination treatment of dapagliflozin and atorvastatin on autophagy and inflammasome pathways in an insulin‐resistant condition. Therefore, dapagliflozin in combination with atorvastatin may be a further preventive or therapeutic strategy for chronic kidney disease in an insulin‐resistant or diabetic condition.</description><identifier>ISSN: 1095-6670</identifier><identifier>EISSN: 1099-0461</identifier><identifier>DOI: 10.1002/jbt.22978</identifier><identifier>PMID: 34939712</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Accumulation ; Antidiabetics ; Atorvastatin ; Autophagy ; dapagliflozin ; Diabetes mellitus ; Dyslipidemia ; Glucose tolerance ; High fat diet ; Impairment ; inflammasome ; Inflammasomes ; Injury prevention ; Insulin ; Insulin resistance ; Kidney diseases ; Kidneys ; Lipids ; Rodents ; Statins</subject><ispartof>Journal of biochemical and molecular toxicology, 2022-04, Vol.36 (4), p.e22978-n/a</ispartof><rights>2021 Wiley Periodicals LLC</rights><rights>2021 Wiley Periodicals LLC.</rights><rights>2022 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-7a95f4c68141b3c4e5845818f46a1f6a94ae89e5fade57011596135ed1c978c43</citedby><cites>FETCH-LOGICAL-c3538-7a95f4c68141b3c4e5845818f46a1f6a94ae89e5fade57011596135ed1c978c43</cites><orcidid>0000-0003-4522-0026</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/34939712$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thongnak, Laongdao</creatorcontrib><creatorcontrib>Pengrattanachot, Nattavadee</creatorcontrib><creatorcontrib>Promsan, Sasivimon</creatorcontrib><creatorcontrib>Phengpol, Nichakorn</creatorcontrib><creatorcontrib>Sutthasupha, Prempree</creatorcontrib><creatorcontrib>Chatsudthipong, Varanuj</creatorcontrib><creatorcontrib>Lungkaphin, Anusorn</creatorcontrib><title>The combination of dapagliflozin and statins ameliorates renal injury through attenuating the activation of inflammasome‐mediated autophagy in insulin‐resistant rats</title><title>Journal of biochemical and molecular toxicology</title><addtitle>J Biochem Mol Toxicol</addtitle><description>Long‐term use of a high‐fat diet with high‐fructose (HFF) intake could promote insulin resistance and induce lipid accumulation leading to kidney injury possibly via impairment of the autophagy process and enhancement of the inflammasome pathway. We investigated whether dapagliflozin as a monotherapy or combined with atorvastatin could restore kidney autophagy impairment and reduce inflammasome activation associated with kidney injury induced by HFF consumption. Male Wistar rats were given an HFF for 16 weeks and then treated with dapagliflozin with or without atorvastatin for 4 weeks. Impaired glucose tolerance, dyslipidemia, renal lipid accumulation along with impaired renal autophagy and activated inflammasome pathway promoted renal injury were exhibited in HFF rats. Dapagliflozin with or without atorvastatin treatment could partially restore disrupted metabolic parameters and reduce kidney injury. In particular, the combination treatment group showed significant amelioration of inflammasome activation and autophagy impairment. In conclusion, the combination therapy of dapagliflozin and atorvastatin has a positive effect on renal injury associated with autophagy and inflammasome activation induced by HFF in insulin‐resistant rats. This study is the first report demonstrating the underlying mechanism associated with a combination treatment of dapagliflozin and atorvastatin on autophagy and inflammasome pathways in an insulin‐resistant condition. Therefore, dapagliflozin in combination with atorvastatin may be a further preventive or therapeutic strategy for chronic kidney disease in an insulin‐resistant or diabetic condition.</description><subject>Accumulation</subject><subject>Antidiabetics</subject><subject>Atorvastatin</subject><subject>Autophagy</subject><subject>dapagliflozin</subject><subject>Diabetes mellitus</subject><subject>Dyslipidemia</subject><subject>Glucose tolerance</subject><subject>High fat diet</subject><subject>Impairment</subject><subject>inflammasome</subject><subject>Inflammasomes</subject><subject>Injury prevention</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Kidney diseases</subject><subject>Kidneys</subject><subject>Lipids</subject><subject>Rodents</subject><subject>Statins</subject><issn>1095-6670</issn><issn>1099-0461</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kctu1DAUhiNERS-w4AWQJTZ0kdaO7SReQsWlVSU2wzo6kxzPeOTYgy-gYcUj8Bq8Fk-Cp9N2gYRkyZbPp-9I_19VLxm9YJQ2l5tlumga1fVPqhNGlaqpaNnTu7es27ajx9VpjBtKqVSdfFYdc6G46lhzUv1erJGMfl4aB8l4R7wmE2xhZY22_odxBNxEYipDFwnMaI0PkDCSgA4sMW6Tw46kdfB5tSaQErq8h1flDwmMyXx7FBunLcwzRD_jn5-_ZpxMUU0EcvLbNax2hSgnZmtcmQeMpmx2iZSN8Xl1pMFGfHF_n1VfPrxfXH2qbz9_vL56e1uPXPK-7kBJLca2Z4It-ShQ9kL2rNeiBaZbUAKwVyg1TCg7yphULeMSJzaWAEfBz6o3B-82-K8ZYxpmE0e0Fhz6HIem4I3ifbdHX_-DbnwOJZY9JWnDlaBdoc4P1Bh8jAH1sA1mhrAbGB32_Q2lv-Guv8K-ujfmZYnnkXworACXB-C7sbj7v2m4ebc4KP8CUd-qqw</recordid><startdate>202204</startdate><enddate>202204</enddate><creator>Thongnak, Laongdao</creator><creator>Pengrattanachot, Nattavadee</creator><creator>Promsan, Sasivimon</creator><creator>Phengpol, Nichakorn</creator><creator>Sutthasupha, Prempree</creator><creator>Chatsudthipong, Varanuj</creator><creator>Lungkaphin, Anusorn</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4522-0026</orcidid></search><sort><creationdate>202204</creationdate><title>The combination of dapagliflozin and statins ameliorates renal injury through attenuating the activation of inflammasome‐mediated autophagy in insulin‐resistant rats</title><author>Thongnak, Laongdao ; Pengrattanachot, Nattavadee ; Promsan, Sasivimon ; Phengpol, Nichakorn ; Sutthasupha, Prempree ; Chatsudthipong, Varanuj ; Lungkaphin, Anusorn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-7a95f4c68141b3c4e5845818f46a1f6a94ae89e5fade57011596135ed1c978c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Accumulation</topic><topic>Antidiabetics</topic><topic>Atorvastatin</topic><topic>Autophagy</topic><topic>dapagliflozin</topic><topic>Diabetes mellitus</topic><topic>Dyslipidemia</topic><topic>Glucose tolerance</topic><topic>High fat diet</topic><topic>Impairment</topic><topic>inflammasome</topic><topic>Inflammasomes</topic><topic>Injury prevention</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Kidney diseases</topic><topic>Kidneys</topic><topic>Lipids</topic><topic>Rodents</topic><topic>Statins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thongnak, Laongdao</creatorcontrib><creatorcontrib>Pengrattanachot, Nattavadee</creatorcontrib><creatorcontrib>Promsan, Sasivimon</creatorcontrib><creatorcontrib>Phengpol, Nichakorn</creatorcontrib><creatorcontrib>Sutthasupha, Prempree</creatorcontrib><creatorcontrib>Chatsudthipong, Varanuj</creatorcontrib><creatorcontrib>Lungkaphin, Anusorn</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biochemical and molecular toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thongnak, Laongdao</au><au>Pengrattanachot, Nattavadee</au><au>Promsan, Sasivimon</au><au>Phengpol, Nichakorn</au><au>Sutthasupha, Prempree</au><au>Chatsudthipong, Varanuj</au><au>Lungkaphin, Anusorn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The combination of dapagliflozin and statins ameliorates renal injury through attenuating the activation of inflammasome‐mediated autophagy in insulin‐resistant rats</atitle><jtitle>Journal of biochemical and molecular toxicology</jtitle><addtitle>J Biochem Mol Toxicol</addtitle><date>2022-04</date><risdate>2022</risdate><volume>36</volume><issue>4</issue><spage>e22978</spage><epage>n/a</epage><pages>e22978-n/a</pages><issn>1095-6670</issn><eissn>1099-0461</eissn><abstract>Long‐term use of a high‐fat diet with high‐fructose (HFF) intake could promote insulin resistance and induce lipid accumulation leading to kidney injury possibly via impairment of the autophagy process and enhancement of the inflammasome pathway. We investigated whether dapagliflozin as a monotherapy or combined with atorvastatin could restore kidney autophagy impairment and reduce inflammasome activation associated with kidney injury induced by HFF consumption. Male Wistar rats were given an HFF for 16 weeks and then treated with dapagliflozin with or without atorvastatin for 4 weeks. Impaired glucose tolerance, dyslipidemia, renal lipid accumulation along with impaired renal autophagy and activated inflammasome pathway promoted renal injury were exhibited in HFF rats. Dapagliflozin with or without atorvastatin treatment could partially restore disrupted metabolic parameters and reduce kidney injury. In particular, the combination treatment group showed significant amelioration of inflammasome activation and autophagy impairment. In conclusion, the combination therapy of dapagliflozin and atorvastatin has a positive effect on renal injury associated with autophagy and inflammasome activation induced by HFF in insulin‐resistant rats. This study is the first report demonstrating the underlying mechanism associated with a combination treatment of dapagliflozin and atorvastatin on autophagy and inflammasome pathways in an insulin‐resistant condition. Therefore, dapagliflozin in combination with atorvastatin may be a further preventive or therapeutic strategy for chronic kidney disease in an insulin‐resistant or diabetic condition.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34939712</pmid><doi>10.1002/jbt.22978</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4522-0026</orcidid></addata></record> |
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subjects | Accumulation Antidiabetics Atorvastatin Autophagy dapagliflozin Diabetes mellitus Dyslipidemia Glucose tolerance High fat diet Impairment inflammasome Inflammasomes Injury prevention Insulin Insulin resistance Kidney diseases Kidneys Lipids Rodents Statins |
title | The combination of dapagliflozin and statins ameliorates renal injury through attenuating the activation of inflammasome‐mediated autophagy in insulin‐resistant rats |
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