Illudins C2 and C3 Stimulate Lipolysis in 3T3-L1 Adipocytes and Suppress Adipogenesis in 3T3-L1 Preadipocytes
The secondary metabolites illudins C2 (1) and C3 (2), obtained from the culture broth of Coprinus atramentarius, have been shown to possess antimicrobial activity. In the present study, we discovered novel biological activities of 1 and 2 in lipolysis of differentiated 3T3-L1 adipocytes and adipogen...
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Veröffentlicht in: | Journal of natural products (Washington, D.C.) D.C.), 2014-04, Vol.77 (4), p.744-750 |
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creator | Kim, Sun-Ok Sakchaisri, Krisada Asami, Yukihiro Ryoo, In-Ja Choo, Soo-Jin Yoo, Ick-Dong Soung, Nak-Kyun Kim, Young Sang Jang, Jae-Hyuk Kim, Bo Yeon Ahn, Jong Seog |
description | The secondary metabolites illudins C2 (1) and C3 (2), obtained from the culture broth of Coprinus atramentarius, have been shown to possess antimicrobial activity. In the present study, we discovered novel biological activities of 1 and 2 in lipolysis of differentiated 3T3-L1 adipocytes and adipogenesis of 3T3-L1 preadipocytes. Compounds 1 and 2 exhibit a dose-dependent increase in glycerol release and thereby reduce intracellular lipid accumulation. The stimulatory effects of 1 and 2 on lipolysis are prevented by cAMP-dependent protein kinase (PKA) and extracellular signal-regulated kinase (ERK) inhibitors. Compounds 1 and 2 down-regulated perilipin and also affected the mRNA and protein levels of adipose triglyceride lipase (ATGL) and hormone-sensitive lipase (HSL). However, 1 and 2 treatment leads to a significant increase in PKA-mediated phosphorylation of HSL at S563 and S660. In addition, 1 and 2 treatment in 3T3-L1 preadipocytes induces down-regulation of the critical transcription factors, CCAAT/enhancer binding protein α and β (C/EBPα and C/EBPβ), and peroxisome proliferator activated receptor γ (PPARγ), which are required for adipogenesis, and accordingly inhibits adipogenesis. These results suggest that 1 and 2 might be useful for treating obesity due to their modulatory effects on fat by affecting adipocyte differentiation and fat mobilization. |
doi_str_mv | 10.1021/np400520a |
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In the present study, we discovered novel biological activities of 1 and 2 in lipolysis of differentiated 3T3-L1 adipocytes and adipogenesis of 3T3-L1 preadipocytes. Compounds 1 and 2 exhibit a dose-dependent increase in glycerol release and thereby reduce intracellular lipid accumulation. The stimulatory effects of 1 and 2 on lipolysis are prevented by cAMP-dependent protein kinase (PKA) and extracellular signal-regulated kinase (ERK) inhibitors. Compounds 1 and 2 down-regulated perilipin and also affected the mRNA and protein levels of adipose triglyceride lipase (ATGL) and hormone-sensitive lipase (HSL). However, 1 and 2 treatment leads to a significant increase in PKA-mediated phosphorylation of HSL at S563 and S660. In addition, 1 and 2 treatment in 3T3-L1 preadipocytes induces down-regulation of the critical transcription factors, CCAAT/enhancer binding protein α and β (C/EBPα and C/EBPβ), and peroxisome proliferator activated receptor γ (PPARγ), which are required for adipogenesis, and accordingly inhibits adipogenesis. These results suggest that 1 and 2 might be useful for treating obesity due to their modulatory effects on fat by affecting adipocyte differentiation and fat mobilization.</description><identifier>ISSN: 0163-3864</identifier><identifier>EISSN: 1520-6025</identifier><identifier>DOI: 10.1021/np400520a</identifier><identifier>PMID: 24597820</identifier><language>eng</language><publisher>United States: American Chemical Society and American Society of Pharmacognosy</publisher><subject>3T3-L1 Cells ; Adipocytes - drug effects ; Adipocytes - metabolism ; Adipogenesis - drug effects ; Adipogenesis - physiology ; Animals ; CCAAT-Enhancer-Binding Protein-alpha ; CCAAT-Enhancer-Binding Protein-beta - drug effects ; Coprinus - chemistry ; Cyclic AMP-Dependent Protein Kinases - metabolism ; Dose-Response Relationship, Drug ; Extracellular Signal-Regulated MAP Kinases - metabolism ; Glycerol - analysis ; Glycerol - metabolism ; Lipase - analysis ; Lipase - metabolism ; Lipolysis - drug effects ; Lipolysis - physiology ; Mice ; Molecular Structure ; Obesity - drug therapy ; PPAR gamma - metabolism ; Sesquiterpenes - chemistry ; Sesquiterpenes - isolation & purification ; Sesquiterpenes - pharmacology</subject><ispartof>Journal of natural products (Washington, D.C.), 2014-04, Vol.77 (4), p.744-750</ispartof><rights>Copyright © 2014 American Chemical Society and American Society of Pharmacognosy</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/np400520a$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/np400520a$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,27055,27903,27904,56717,56767</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24597820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Sun-Ok</creatorcontrib><creatorcontrib>Sakchaisri, Krisada</creatorcontrib><creatorcontrib>Asami, Yukihiro</creatorcontrib><creatorcontrib>Ryoo, In-Ja</creatorcontrib><creatorcontrib>Choo, Soo-Jin</creatorcontrib><creatorcontrib>Yoo, Ick-Dong</creatorcontrib><creatorcontrib>Soung, Nak-Kyun</creatorcontrib><creatorcontrib>Kim, Young Sang</creatorcontrib><creatorcontrib>Jang, Jae-Hyuk</creatorcontrib><creatorcontrib>Kim, Bo Yeon</creatorcontrib><creatorcontrib>Ahn, Jong Seog</creatorcontrib><title>Illudins C2 and C3 Stimulate Lipolysis in 3T3-L1 Adipocytes and Suppress Adipogenesis in 3T3-L1 Preadipocytes</title><title>Journal of natural products (Washington, D.C.)</title><addtitle>J. Nat. Prod</addtitle><description>The secondary metabolites illudins C2 (1) and C3 (2), obtained from the culture broth of Coprinus atramentarius, have been shown to possess antimicrobial activity. In the present study, we discovered novel biological activities of 1 and 2 in lipolysis of differentiated 3T3-L1 adipocytes and adipogenesis of 3T3-L1 preadipocytes. Compounds 1 and 2 exhibit a dose-dependent increase in glycerol release and thereby reduce intracellular lipid accumulation. The stimulatory effects of 1 and 2 on lipolysis are prevented by cAMP-dependent protein kinase (PKA) and extracellular signal-regulated kinase (ERK) inhibitors. Compounds 1 and 2 down-regulated perilipin and also affected the mRNA and protein levels of adipose triglyceride lipase (ATGL) and hormone-sensitive lipase (HSL). However, 1 and 2 treatment leads to a significant increase in PKA-mediated phosphorylation of HSL at S563 and S660. In addition, 1 and 2 treatment in 3T3-L1 preadipocytes induces down-regulation of the critical transcription factors, CCAAT/enhancer binding protein α and β (C/EBPα and C/EBPβ), and peroxisome proliferator activated receptor γ (PPARγ), which are required for adipogenesis, and accordingly inhibits adipogenesis. These results suggest that 1 and 2 might be useful for treating obesity due to their modulatory effects on fat by affecting adipocyte differentiation and fat mobilization.</description><subject>3T3-L1 Cells</subject><subject>Adipocytes - drug effects</subject><subject>Adipocytes - metabolism</subject><subject>Adipogenesis - drug effects</subject><subject>Adipogenesis - physiology</subject><subject>Animals</subject><subject>CCAAT-Enhancer-Binding Protein-alpha</subject><subject>CCAAT-Enhancer-Binding Protein-beta - drug effects</subject><subject>Coprinus - chemistry</subject><subject>Cyclic AMP-Dependent Protein Kinases - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Extracellular Signal-Regulated MAP Kinases - metabolism</subject><subject>Glycerol - analysis</subject><subject>Glycerol - metabolism</subject><subject>Lipase - analysis</subject><subject>Lipase - metabolism</subject><subject>Lipolysis - drug effects</subject><subject>Lipolysis - physiology</subject><subject>Mice</subject><subject>Molecular Structure</subject><subject>Obesity - drug therapy</subject><subject>PPAR gamma - metabolism</subject><subject>Sesquiterpenes - chemistry</subject><subject>Sesquiterpenes - isolation & purification</subject><subject>Sesquiterpenes - pharmacology</subject><issn>0163-3864</issn><issn>1520-6025</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtLxDAUhYMozji68A9INoKb6k3Sps1yGHxBQWHGdbhpEunQl027mH9vdcYBVwcO37lcPkKuGdwz4Oyh6WKAhAOekDmbMpLAk1MyByZFJDIZz8hFCFsAEKCSczLjcaLSjMOc1K9VNdqyCXTFKTaWrgRdD2U9Vjg4mpddW-1CGWjZULERUc7o0k5lsRtc-OXXY9f1LoR9_-ka9x9_7x0eF5fkzGMV3NUhF-Tj6XGzeonyt-fX1TKPkHM-RKkx3ipbWCy8V1IglxlnzBuFaGziFPjMGGskt5hl3njgacwYepg8pAbFgtzt73Z9-zW6MOi6DIWrKmxcOwbNEqa45JKpCb05oKOpndVdX9bY7_Sfogm43QNYBL1tx76ZPtcM9I96fVQvvgH3xHMQ</recordid><startdate>20140425</startdate><enddate>20140425</enddate><creator>Kim, Sun-Ok</creator><creator>Sakchaisri, Krisada</creator><creator>Asami, Yukihiro</creator><creator>Ryoo, In-Ja</creator><creator>Choo, Soo-Jin</creator><creator>Yoo, Ick-Dong</creator><creator>Soung, Nak-Kyun</creator><creator>Kim, Young Sang</creator><creator>Jang, Jae-Hyuk</creator><creator>Kim, Bo Yeon</creator><creator>Ahn, Jong Seog</creator><general>American Chemical Society and American Society of Pharmacognosy</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20140425</creationdate><title>Illudins C2 and C3 Stimulate Lipolysis in 3T3-L1 Adipocytes and Suppress Adipogenesis in 3T3-L1 Preadipocytes</title><author>Kim, Sun-Ok ; Sakchaisri, Krisada ; Asami, Yukihiro ; Ryoo, In-Ja ; Choo, Soo-Jin ; Yoo, Ick-Dong ; Soung, Nak-Kyun ; Kim, Young Sang ; Jang, Jae-Hyuk ; Kim, Bo Yeon ; Ahn, Jong Seog</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a222t-7bbfd9dcdacff963a268211fb9aabd5e90f8bbdb62da88fbf027411af04007ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>3T3-L1 Cells</topic><topic>Adipocytes - drug effects</topic><topic>Adipocytes - metabolism</topic><topic>Adipogenesis - drug effects</topic><topic>Adipogenesis - physiology</topic><topic>Animals</topic><topic>CCAAT-Enhancer-Binding Protein-alpha</topic><topic>CCAAT-Enhancer-Binding Protein-beta - drug effects</topic><topic>Coprinus - chemistry</topic><topic>Cyclic AMP-Dependent Protein Kinases - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Extracellular Signal-Regulated MAP Kinases - metabolism</topic><topic>Glycerol - analysis</topic><topic>Glycerol - metabolism</topic><topic>Lipase - analysis</topic><topic>Lipase - metabolism</topic><topic>Lipolysis - drug effects</topic><topic>Lipolysis - physiology</topic><topic>Mice</topic><topic>Molecular Structure</topic><topic>Obesity - drug therapy</topic><topic>PPAR gamma - metabolism</topic><topic>Sesquiterpenes - chemistry</topic><topic>Sesquiterpenes - isolation & purification</topic><topic>Sesquiterpenes - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Sun-Ok</creatorcontrib><creatorcontrib>Sakchaisri, Krisada</creatorcontrib><creatorcontrib>Asami, Yukihiro</creatorcontrib><creatorcontrib>Ryoo, In-Ja</creatorcontrib><creatorcontrib>Choo, Soo-Jin</creatorcontrib><creatorcontrib>Yoo, Ick-Dong</creatorcontrib><creatorcontrib>Soung, Nak-Kyun</creatorcontrib><creatorcontrib>Kim, Young Sang</creatorcontrib><creatorcontrib>Jang, Jae-Hyuk</creatorcontrib><creatorcontrib>Kim, Bo Yeon</creatorcontrib><creatorcontrib>Ahn, Jong Seog</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of natural products (Washington, D.C.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Sun-Ok</au><au>Sakchaisri, Krisada</au><au>Asami, Yukihiro</au><au>Ryoo, In-Ja</au><au>Choo, Soo-Jin</au><au>Yoo, Ick-Dong</au><au>Soung, Nak-Kyun</au><au>Kim, Young Sang</au><au>Jang, Jae-Hyuk</au><au>Kim, Bo Yeon</au><au>Ahn, Jong Seog</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Illudins C2 and C3 Stimulate Lipolysis in 3T3-L1 Adipocytes and Suppress Adipogenesis in 3T3-L1 Preadipocytes</atitle><jtitle>Journal of natural products (Washington, D.C.)</jtitle><addtitle>J. Nat. Prod</addtitle><date>2014-04-25</date><risdate>2014</risdate><volume>77</volume><issue>4</issue><spage>744</spage><epage>750</epage><pages>744-750</pages><issn>0163-3864</issn><eissn>1520-6025</eissn><abstract>The secondary metabolites illudins C2 (1) and C3 (2), obtained from the culture broth of Coprinus atramentarius, have been shown to possess antimicrobial activity. In the present study, we discovered novel biological activities of 1 and 2 in lipolysis of differentiated 3T3-L1 adipocytes and adipogenesis of 3T3-L1 preadipocytes. Compounds 1 and 2 exhibit a dose-dependent increase in glycerol release and thereby reduce intracellular lipid accumulation. The stimulatory effects of 1 and 2 on lipolysis are prevented by cAMP-dependent protein kinase (PKA) and extracellular signal-regulated kinase (ERK) inhibitors. Compounds 1 and 2 down-regulated perilipin and also affected the mRNA and protein levels of adipose triglyceride lipase (ATGL) and hormone-sensitive lipase (HSL). However, 1 and 2 treatment leads to a significant increase in PKA-mediated phosphorylation of HSL at S563 and S660. In addition, 1 and 2 treatment in 3T3-L1 preadipocytes induces down-regulation of the critical transcription factors, CCAAT/enhancer binding protein α and β (C/EBPα and C/EBPβ), and peroxisome proliferator activated receptor γ (PPARγ), which are required for adipogenesis, and accordingly inhibits adipogenesis. These results suggest that 1 and 2 might be useful for treating obesity due to their modulatory effects on fat by affecting adipocyte differentiation and fat mobilization.</abstract><cop>United States</cop><pub>American Chemical Society and American Society of Pharmacognosy</pub><pmid>24597820</pmid><doi>10.1021/np400520a</doi><tpages>7</tpages></addata></record> |
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subjects | 3T3-L1 Cells Adipocytes - drug effects Adipocytes - metabolism Adipogenesis - drug effects Adipogenesis - physiology Animals CCAAT-Enhancer-Binding Protein-alpha CCAAT-Enhancer-Binding Protein-beta - drug effects Coprinus - chemistry Cyclic AMP-Dependent Protein Kinases - metabolism Dose-Response Relationship, Drug Extracellular Signal-Regulated MAP Kinases - metabolism Glycerol - analysis Glycerol - metabolism Lipase - analysis Lipase - metabolism Lipolysis - drug effects Lipolysis - physiology Mice Molecular Structure Obesity - drug therapy PPAR gamma - metabolism Sesquiterpenes - chemistry Sesquiterpenes - isolation & purification Sesquiterpenes - pharmacology |
title | Illudins C2 and C3 Stimulate Lipolysis in 3T3-L1 Adipocytes and Suppress Adipogenesis in 3T3-L1 Preadipocytes |
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