Inhibitory effects of Aster spathulifolius extract on adipogenesis and lipid accumulation in 3T3-L1 preadipocytes

Objectives Aster spathulifolius Maxim (AS), known for its anti‐viral and anti‐allergic activity, is also known to reduce body weight gain in high fat diet‐induced obese rats. But its molecular mechanism of the anti‐obesity effects is still unclear. So, we investigated the inhibitory effect of AS ext...

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Veröffentlicht in:Journal of pharmacy and pharmacology 2016-01, Vol.68 (1), p.107-118
Hauptverfasser: Kim, Sa-Jic, Choung, Se-Young
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description Objectives Aster spathulifolius Maxim (AS), known for its anti‐viral and anti‐allergic activity, is also known to reduce body weight gain in high fat diet‐induced obese rats. But its molecular mechanism of the anti‐obesity effects is still unclear. So, we investigated the inhibitory effect of AS extract (ASE) on adipogenesis and lipid accumulation to determine the underlying cellular molecular mechanism. Methods To perform this study, the contents of intracellular triglyceride were analysed. Real‐time polymerase chain reaction and Western blotting were carried out to investigate the expression of adipogenic transcriptional factors. Key findings ASE showed the suppression of adipogenic differentiation and the considerable reduction of the lipid accumulation in 3T3‐L1 cells. Especially, ASE inhibited the early stage of differentiation via the downregulation of C/EBP‐β and C/EBP‐δ, which are early adipogenic factors. Major adipogenic factors, such as PPAR‐γ and C/EBP‐α, were also subsequently inhibited. These findings were supported by Oil Red O staining and intracellular triglyceride levels. A molecular mechanism liking the effect of ASE was identified through the activation of AMPKα pathway. ASE increased protein levels of phosphorylated AMPKα and phosphorylated ACC. Conclusions ASE showed anti‐adipogenic and anti‐lipogenic effects through the regulation of adipogenic factors and AMPKα pathway.
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But its molecular mechanism of the anti‐obesity effects is still unclear. So, we investigated the inhibitory effect of AS extract (ASE) on adipogenesis and lipid accumulation to determine the underlying cellular molecular mechanism. Methods To perform this study, the contents of intracellular triglyceride were analysed. Real‐time polymerase chain reaction and Western blotting were carried out to investigate the expression of adipogenic transcriptional factors. Key findings ASE showed the suppression of adipogenic differentiation and the considerable reduction of the lipid accumulation in 3T3‐L1 cells. Especially, ASE inhibited the early stage of differentiation via the downregulation of C/EBP‐β and C/EBP‐δ, which are early adipogenic factors. Major adipogenic factors, such as PPAR‐γ and C/EBP‐α, were also subsequently inhibited. These findings were supported by Oil Red O staining and intracellular triglyceride levels. A molecular mechanism liking the effect of ASE was identified through the activation of AMPKα pathway. ASE increased protein levels of phosphorylated AMPKα and phosphorylated ACC. Conclusions ASE showed anti‐adipogenic and anti‐lipogenic effects through the regulation of adipogenic factors and AMPKα pathway.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1111/jphp.12485</identifier><identifier>PMID: 26471469</identifier><identifier>CODEN: JPPMAB</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>3T3-L1 Cells ; Adipocytes - drug effects ; Adipocytes - metabolism ; adipogenesis ; Adipogenesis - drug effects ; AMPKα ; Animals ; Aster Plant - chemistry ; Aster spathulifolius maxim ; CCAAT-Enhancer-Binding Protein-alpha - metabolism ; Cell Differentiation - drug effects ; Cell Line ; Down-Regulation - drug effects ; Lipid Metabolism - drug effects ; Lipids ; Mice ; Obesity - drug therapy ; Obesity - metabolism ; Phosphorylation - drug effects ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; PPAR gamma - metabolism ; PPAR-γ ; Rodents ; Signal Transduction - drug effects ; Studies ; Triglycerides - metabolism</subject><ispartof>Journal of pharmacy and pharmacology, 2016-01, Vol.68 (1), p.107-118</ispartof><rights>2015 Royal Pharmaceutical Society</rights><rights>2015 Royal Pharmaceutical Society.</rights><rights>Copyright © 2016 Royal Pharmaceutical Society</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://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjphp.12485$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjphp.12485$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26471469$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Sa-Jic</creatorcontrib><creatorcontrib>Choung, Se-Young</creatorcontrib><title>Inhibitory effects of Aster spathulifolius extract on adipogenesis and lipid accumulation in 3T3-L1 preadipocytes</title><title>Journal of pharmacy and pharmacology</title><addtitle>J Pharm Pharmacol</addtitle><description>Objectives Aster spathulifolius Maxim (AS), known for its anti‐viral and anti‐allergic activity, is also known to reduce body weight gain in high fat diet‐induced obese rats. But its molecular mechanism of the anti‐obesity effects is still unclear. So, we investigated the inhibitory effect of AS extract (ASE) on adipogenesis and lipid accumulation to determine the underlying cellular molecular mechanism. Methods To perform this study, the contents of intracellular triglyceride were analysed. Real‐time polymerase chain reaction and Western blotting were carried out to investigate the expression of adipogenic transcriptional factors. Key findings ASE showed the suppression of adipogenic differentiation and the considerable reduction of the lipid accumulation in 3T3‐L1 cells. Especially, ASE inhibited the early stage of differentiation via the downregulation of C/EBP‐β and C/EBP‐δ, which are early adipogenic factors. Major adipogenic factors, such as PPAR‐γ and C/EBP‐α, were also subsequently inhibited. These findings were supported by Oil Red O staining and intracellular triglyceride levels. A molecular mechanism liking the effect of ASE was identified through the activation of AMPKα pathway. ASE increased protein levels of phosphorylated AMPKα and phosphorylated ACC. Conclusions ASE showed anti‐adipogenic and anti‐lipogenic effects through the regulation of adipogenic factors and AMPKα pathway.</description><subject>3T3-L1 Cells</subject><subject>Adipocytes - drug effects</subject><subject>Adipocytes - metabolism</subject><subject>adipogenesis</subject><subject>Adipogenesis - drug effects</subject><subject>AMPKα</subject><subject>Animals</subject><subject>Aster Plant - chemistry</subject><subject>Aster spathulifolius maxim</subject><subject>CCAAT-Enhancer-Binding Protein-alpha - metabolism</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Line</subject><subject>Down-Regulation - drug effects</subject><subject>Lipid Metabolism - drug effects</subject><subject>Lipids</subject><subject>Mice</subject><subject>Obesity - drug therapy</subject><subject>Obesity - metabolism</subject><subject>Phosphorylation - drug effects</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>PPAR gamma - metabolism</subject><subject>PPAR-γ</subject><subject>Rodents</subject><subject>Signal Transduction - drug effects</subject><subject>Studies</subject><subject>Triglycerides - metabolism</subject><issn>0022-3573</issn><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUFv1DAQhS1ERbeFCz8AWeLSS1qPHdubY1VBW7SFHhYhcbEcZ8x6ySap7ajdf9_sbumBucxI873R6D1CPgI7h6ku1sNqOAdezuUbMuOs5IUGOX9LZoxxXgipxTE5SWnNGNNKqXfkmKtSQ6mqGXm47VahDrmPW4reo8uJ9p5epoyRpsHm1dgG37dhTBSfcrQu076jtglD_wc7TCFR2zW0DUNoqHVu3IytzWFiQkfFUhQLoEPEvcBtM6b35MjbNuGHl35Kfn79sry6KRY_rm-vLhdFEJLLAh16W3NRC2gAFDSqkVhXNXDvvBDWWcsBGg6q8ly4uSxRoq5l5QX3daPEKTk73B1i_zBiymYTksO2tR32YzKg50xyLiRM6Of_0HU_xm76bqJkJaDSekd9eqHGeoONGWLY2Lg1_8ycADgAj6HF7esemNnFZHYxmX1M5tv9zf1-mjTFQRMmx59eNTb-NUoLLc2v79dmSnOx_C3vzJ14BlVzlao</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Kim, Sa-Jic</creator><creator>Choung, Se-Young</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QP</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>201601</creationdate><title>Inhibitory effects of Aster spathulifolius extract on adipogenesis and lipid accumulation in 3T3-L1 preadipocytes</title><author>Kim, Sa-Jic ; Choung, Se-Young</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3525-ecefab23b31d1161d6d5eb9b12fcf33acaa211d2169f23c854e5e7b59f32fbd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>3T3-L1 Cells</topic><topic>Adipocytes - drug effects</topic><topic>Adipocytes - metabolism</topic><topic>adipogenesis</topic><topic>Adipogenesis - drug effects</topic><topic>AMPKα</topic><topic>Animals</topic><topic>Aster Plant - chemistry</topic><topic>Aster spathulifolius maxim</topic><topic>CCAAT-Enhancer-Binding Protein-alpha - metabolism</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Line</topic><topic>Down-Regulation - drug effects</topic><topic>Lipid Metabolism - drug effects</topic><topic>Lipids</topic><topic>Mice</topic><topic>Obesity - drug therapy</topic><topic>Obesity - metabolism</topic><topic>Phosphorylation - drug effects</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>PPAR gamma - metabolism</topic><topic>PPAR-γ</topic><topic>Rodents</topic><topic>Signal Transduction - drug effects</topic><topic>Studies</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Sa-Jic</creatorcontrib><creatorcontrib>Choung, Se-Young</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Calcium &amp; 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But its molecular mechanism of the anti‐obesity effects is still unclear. So, we investigated the inhibitory effect of AS extract (ASE) on adipogenesis and lipid accumulation to determine the underlying cellular molecular mechanism. Methods To perform this study, the contents of intracellular triglyceride were analysed. Real‐time polymerase chain reaction and Western blotting were carried out to investigate the expression of adipogenic transcriptional factors. Key findings ASE showed the suppression of adipogenic differentiation and the considerable reduction of the lipid accumulation in 3T3‐L1 cells. Especially, ASE inhibited the early stage of differentiation via the downregulation of C/EBP‐β and C/EBP‐δ, which are early adipogenic factors. Major adipogenic factors, such as PPAR‐γ and C/EBP‐α, were also subsequently inhibited. These findings were supported by Oil Red O staining and intracellular triglyceride levels. A molecular mechanism liking the effect of ASE was identified through the activation of AMPKα pathway. ASE increased protein levels of phosphorylated AMPKα and phosphorylated ACC. Conclusions ASE showed anti‐adipogenic and anti‐lipogenic effects through the regulation of adipogenic factors and AMPKα pathway.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26471469</pmid><doi>10.1111/jphp.12485</doi><tpages>12</tpages></addata></record>
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subjects 3T3-L1 Cells
Adipocytes - drug effects
Adipocytes - metabolism
adipogenesis
Adipogenesis - drug effects
AMPKα
Animals
Aster Plant - chemistry
Aster spathulifolius maxim
CCAAT-Enhancer-Binding Protein-alpha - metabolism
Cell Differentiation - drug effects
Cell Line
Down-Regulation - drug effects
Lipid Metabolism - drug effects
Lipids
Mice
Obesity - drug therapy
Obesity - metabolism
Phosphorylation - drug effects
Plant Extracts - chemistry
Plant Extracts - pharmacology
PPAR gamma - metabolism
PPAR-γ
Rodents
Signal Transduction - drug effects
Studies
Triglycerides - metabolism
title Inhibitory effects of Aster spathulifolius extract on adipogenesis and lipid accumulation in 3T3-L1 preadipocytes
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