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Liraglutide improves adipose tissue remodeling and mitochondrial dynamics in a visceral obesity model induced by a high-fat diet
Central obesity is characterized by visceral adipose tissue (VAT) expansion, considered one of the main risk factors for metabolic complications. In recent years, new drugs have been studied for obesity treatment. Liraglutide (LGT), a GLP-1 agonist, decreases body weight, however, several mechanisms...
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Published in: | Current research in pharmacology and drug discovery 2024-01, Vol.6, p.100185, Article 100185 |
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creator | Touceda, Vanessa Fontana Estevez, Florencia Cacciagiú, Leonardo Finocchietto, Paola Bustos, Romina Vidal, Agustina Berg, Gabriela Morales, Celina González, Germán E. Miksztowicz, Veronica |
description | Central obesity is characterized by visceral adipose tissue (VAT) expansion, considered one of the main risk factors for metabolic complications. In recent years, new drugs have been studied for obesity treatment. Liraglutide (LGT), a GLP-1 agonist, decreases body weight, however, several mechanisms of action on VAT are still unknown.
to study the effect of LGT on factors associated with VAT remodeling and mitochondrial dynamics in mice fed a high-fat diet (HFD).
C57BL/6 mice were divided into Control (C) and HFD. After 15 weeks of feeding, each group was subdivided according to LGT administration for 5 weeks: C, C + LGT, HFD, and HFD + LGT. In epididymal AT (EAT) we evaluated histological and mitochondrial characteristics, vascularity, gelatinase activity (MMPs), and galectin-3 expression.
HFD presented larger adipocytes (p |
doi_str_mv | 10.1016/j.crphar.2024.100185 |
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to study the effect of LGT on factors associated with VAT remodeling and mitochondrial dynamics in mice fed a high-fat diet (HFD).
C57BL/6 mice were divided into Control (C) and HFD. After 15 weeks of feeding, each group was subdivided according to LGT administration for 5 weeks: C, C + LGT, HFD, and HFD + LGT. In epididymal AT (EAT) we evaluated histological and mitochondrial characteristics, vascularity, gelatinase activity (MMPs), and galectin-3 expression.
HFD presented larger adipocytes (p < 0.05), and lower vascular density and MMP-9 activity (p < 0.01) than C, while a major number of smaller adipocytes (p < 0.05) and an increase in vascularity (p < 0.001) and MMP-9 activity (p < 0.01) was observed in HFD + LGT. Collagen content was higher (p < 0.05) in EAT from HFD and decreased in HFD + LGT. In C, C + LGT, and HFD + LGT, mitochondria were predominantly tubular-shaped while in HFD mitochondria were mostly spherical (p < 0.001).
LGT positively influences VAT behavior by modulating gelatinase activity, enhancing vascularization, and improving adipocyte histological characteristics. Additionally, LGT improves mitochondrial dynamics, a process that would favor VAT functionality.
[Display omitted]
•Liraglutide improves histological characteristics of expanded adipose tissue.•An increase in vascularity and gelatinase activity was produced by liraglutide.•Collagen interstitial content decreases with liraglutide in visceral obesity.•Liraglutide promotes an increase in tubular-shaped mitochondria.]]></description><identifier>ISSN: 2590-2571</identifier><identifier>EISSN: 2590-2571</identifier><identifier>DOI: 10.1016/j.crphar.2024.100185</identifier><identifier>PMID: 38846009</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Liraglutide ; Metalloproteinase ; Vascular density ; Visceral adipose tissue</subject><ispartof>Current research in pharmacology and drug discovery, 2024-01, Vol.6, p.100185, Article 100185</ispartof><rights>2024 The Authors</rights><rights>2024 The Authors.</rights><rights>2024 The Authors 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3945-abd06cb94fcea527ba8da9fa28339bcc7f200703b1966b38b623dc0cdc1b68f33</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/PMC11153889/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2590257124000129$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3549,27924,27925,45780,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38846009$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Touceda, Vanessa</creatorcontrib><creatorcontrib>Fontana Estevez, Florencia</creatorcontrib><creatorcontrib>Cacciagiú, Leonardo</creatorcontrib><creatorcontrib>Finocchietto, Paola</creatorcontrib><creatorcontrib>Bustos, Romina</creatorcontrib><creatorcontrib>Vidal, Agustina</creatorcontrib><creatorcontrib>Berg, Gabriela</creatorcontrib><creatorcontrib>Morales, Celina</creatorcontrib><creatorcontrib>González, Germán E.</creatorcontrib><creatorcontrib>Miksztowicz, Veronica</creatorcontrib><title>Liraglutide improves adipose tissue remodeling and mitochondrial dynamics in a visceral obesity model induced by a high-fat diet</title><title>Current research in pharmacology and drug discovery</title><addtitle>Curr Res Pharmacol Drug Discov</addtitle><description><![CDATA[Central obesity is characterized by visceral adipose tissue (VAT) expansion, considered one of the main risk factors for metabolic complications. In recent years, new drugs have been studied for obesity treatment. Liraglutide (LGT), a GLP-1 agonist, decreases body weight, however, several mechanisms of action on VAT are still unknown.
to study the effect of LGT on factors associated with VAT remodeling and mitochondrial dynamics in mice fed a high-fat diet (HFD).
C57BL/6 mice were divided into Control (C) and HFD. After 15 weeks of feeding, each group was subdivided according to LGT administration for 5 weeks: C, C + LGT, HFD, and HFD + LGT. In epididymal AT (EAT) we evaluated histological and mitochondrial characteristics, vascularity, gelatinase activity (MMPs), and galectin-3 expression.
HFD presented larger adipocytes (p < 0.05), and lower vascular density and MMP-9 activity (p < 0.01) than C, while a major number of smaller adipocytes (p < 0.05) and an increase in vascularity (p < 0.001) and MMP-9 activity (p < 0.01) was observed in HFD + LGT. Collagen content was higher (p < 0.05) in EAT from HFD and decreased in HFD + LGT. In C, C + LGT, and HFD + LGT, mitochondria were predominantly tubular-shaped while in HFD mitochondria were mostly spherical (p < 0.001).
LGT positively influences VAT behavior by modulating gelatinase activity, enhancing vascularization, and improving adipocyte histological characteristics. Additionally, LGT improves mitochondrial dynamics, a process that would favor VAT functionality.
[Display omitted]
•Liraglutide improves histological characteristics of expanded adipose tissue.•An increase in vascularity and gelatinase activity was produced by liraglutide.•Collagen interstitial content decreases with liraglutide in visceral obesity.•Liraglutide promotes an increase in tubular-shaped mitochondria.]]></description><subject>Liraglutide</subject><subject>Metalloproteinase</subject><subject>Vascular density</subject><subject>Visceral adipose tissue</subject><issn>2590-2571</issn><issn>2590-2571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9Uk1vEzEUXCEQrUr_AUI-cknq77UvIFQBrRSJC5yt549NHO2ug70bKTd-Ok63VO2Fk633ZubZ86Zp3hO8JpjIm_3a5cMO8ppiymsJEyVeNZdUaLyioiWvn90vmutS9hhj2mqOpXrbXDCluMRYXzZ_NjHDtp-n6AOKwyGnYygIfDykEtAUS5kDymFIPvRx3CIYPRrilNwujT5H6JE_jTBEV1AcEaBjLC7kWk42lDid0AOz9vzsgkf2VDG7uN2tOpiQj2F617zpoC_h-vG8an59-_rz9m61-fH9_vbLZuWY5mIF1mPprOadCyBoa0F50B1QxZi2zrUdxbjFzBItpWXKSsq8w847YqXqGLtq7hddn2BvDjkOkE8mQTQPhZS3BvIUXR8Mp-ABhFKUCC6IUxyYY5jLtpWdYG3V-rxoHWY7BO_CONUvvxB92RnjzmzT0RBCRPVeV4WPjwo5_Z5DmcxwNq7vYQxpLoZhKbTimskK5QvU5VRKDt3THILNOQxmb5YwmHMYzBKGSvvw_I1PpH-rr4BPCyBU148xZFNcDGPdUszBTdWW-P8JfwEn8soI</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Touceda, Vanessa</creator><creator>Fontana Estevez, Florencia</creator><creator>Cacciagiú, Leonardo</creator><creator>Finocchietto, Paola</creator><creator>Bustos, Romina</creator><creator>Vidal, Agustina</creator><creator>Berg, Gabriela</creator><creator>Morales, Celina</creator><creator>González, Germán E.</creator><creator>Miksztowicz, Veronica</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20240101</creationdate><title>Liraglutide improves adipose tissue remodeling and mitochondrial dynamics in a visceral obesity model induced by a high-fat diet</title><author>Touceda, Vanessa ; Fontana Estevez, Florencia ; Cacciagiú, Leonardo ; Finocchietto, Paola ; Bustos, Romina ; Vidal, Agustina ; Berg, Gabriela ; Morales, Celina ; González, Germán E. ; Miksztowicz, Veronica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3945-abd06cb94fcea527ba8da9fa28339bcc7f200703b1966b38b623dc0cdc1b68f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Liraglutide</topic><topic>Metalloproteinase</topic><topic>Vascular density</topic><topic>Visceral adipose tissue</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Touceda, Vanessa</creatorcontrib><creatorcontrib>Fontana Estevez, Florencia</creatorcontrib><creatorcontrib>Cacciagiú, Leonardo</creatorcontrib><creatorcontrib>Finocchietto, Paola</creatorcontrib><creatorcontrib>Bustos, Romina</creatorcontrib><creatorcontrib>Vidal, Agustina</creatorcontrib><creatorcontrib>Berg, Gabriela</creatorcontrib><creatorcontrib>Morales, Celina</creatorcontrib><creatorcontrib>González, Germán E.</creatorcontrib><creatorcontrib>Miksztowicz, Veronica</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Current research in pharmacology and drug discovery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Touceda, Vanessa</au><au>Fontana Estevez, Florencia</au><au>Cacciagiú, Leonardo</au><au>Finocchietto, Paola</au><au>Bustos, Romina</au><au>Vidal, Agustina</au><au>Berg, Gabriela</au><au>Morales, Celina</au><au>González, Germán E.</au><au>Miksztowicz, Veronica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liraglutide improves adipose tissue remodeling and mitochondrial dynamics in a visceral obesity model induced by a high-fat diet</atitle><jtitle>Current research in pharmacology and drug discovery</jtitle><addtitle>Curr Res Pharmacol Drug Discov</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>6</volume><spage>100185</spage><pages>100185-</pages><artnum>100185</artnum><issn>2590-2571</issn><eissn>2590-2571</eissn><abstract><![CDATA[Central obesity is characterized by visceral adipose tissue (VAT) expansion, considered one of the main risk factors for metabolic complications. In recent years, new drugs have been studied for obesity treatment. Liraglutide (LGT), a GLP-1 agonist, decreases body weight, however, several mechanisms of action on VAT are still unknown.
to study the effect of LGT on factors associated with VAT remodeling and mitochondrial dynamics in mice fed a high-fat diet (HFD).
C57BL/6 mice were divided into Control (C) and HFD. After 15 weeks of feeding, each group was subdivided according to LGT administration for 5 weeks: C, C + LGT, HFD, and HFD + LGT. In epididymal AT (EAT) we evaluated histological and mitochondrial characteristics, vascularity, gelatinase activity (MMPs), and galectin-3 expression.
HFD presented larger adipocytes (p < 0.05), and lower vascular density and MMP-9 activity (p < 0.01) than C, while a major number of smaller adipocytes (p < 0.05) and an increase in vascularity (p < 0.001) and MMP-9 activity (p < 0.01) was observed in HFD + LGT. Collagen content was higher (p < 0.05) in EAT from HFD and decreased in HFD + LGT. In C, C + LGT, and HFD + LGT, mitochondria were predominantly tubular-shaped while in HFD mitochondria were mostly spherical (p < 0.001).
LGT positively influences VAT behavior by modulating gelatinase activity, enhancing vascularization, and improving adipocyte histological characteristics. Additionally, LGT improves mitochondrial dynamics, a process that would favor VAT functionality.
[Display omitted]
•Liraglutide improves histological characteristics of expanded adipose tissue.•An increase in vascularity and gelatinase activity was produced by liraglutide.•Collagen interstitial content decreases with liraglutide in visceral obesity.•Liraglutide promotes an increase in tubular-shaped mitochondria.]]></abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38846009</pmid><doi>10.1016/j.crphar.2024.100185</doi><oa>free_for_read</oa></addata></record> |
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subjects | Liraglutide Metalloproteinase Vascular density Visceral adipose tissue |
title | Liraglutide improves adipose tissue remodeling and mitochondrial dynamics in a visceral obesity model induced by a high-fat diet |
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