Accelerated BDNF expression in visceral white adipose tissues following high‐fat diet feeding in mice
Brain‐derived neurotrophic factor (BDNF) is expressed in the white adipose tissues (WATs), and the expression increases during high‐fat diet (HFD) feeding, implicating its role in obesity. Here, we focused on BDNF expression in epididymal WAT (eWAT), a visceral adipose tissue, in mice. During 2 week...
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Veröffentlicht in: | Genes to cells : devoted to molecular & cellular mechanisms 2024-11, Vol.29 (11), p.1077-1084 |
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description | Brain‐derived neurotrophic factor (BDNF) is expressed in the white adipose tissues (WATs), and the expression increases during high‐fat diet (HFD) feeding, implicating its role in obesity. Here, we focused on BDNF expression in epididymal WAT (eWAT), a visceral adipose tissue, in mice. During 2 weeks of HFD feeding, Bdnf mRNA expression in eWAT slightly increased, but a robust increase was observed after 8 weeks of HFD feeding. This upregulation of Bdnf mRNA was correlated with significant induction of hypoxia‐inducible factor 1α (Hif1α) and platelet‐derived growth factor subunit B (Pdgfb) mRNA in eWAT following 8 weeks of HFD feeding. Furthermore, the increased expression of the M1 macrophage markers was strongly correlated with the elevation of Bdnf mRNA in the eWAT. Notably, 8 weeks of HFD feeding significantly elevated Tnfα mRNA expression in eWAT, while no such induction was observed in inguinal WAT (iWAT). In contrast, the expression of Adipoq (adiponectin), implicated in improved insulin sensitivity and anti‐inflammatory effects, was significantly upregulated in iWAT, but not in eWAT. Thus, our study may show the role of BDNF in eWAT in obesity models, potentially contributing to the pathological state of visceral adipose tissues.
A robust induction of brain‐derived neurotrophic factor mRNA expression was observed particularly in epididymal white adipose tissue of mice fed with high‐fat diet for 8 weeks. |
doi_str_mv | 10.1111/gtc.13162 |
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A robust induction of brain‐derived neurotrophic factor mRNA expression was observed particularly in epididymal white adipose tissue of mice fed with high‐fat diet for 8 weeks.</description><identifier>ISSN: 1356-9597</identifier><identifier>ISSN: 1365-2443</identifier><identifier>EISSN: 1365-2443</identifier><identifier>DOI: 10.1111/gtc.13162</identifier><identifier>PMID: 39278976</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adiponectin ; Adiponectin - genetics ; Adiponectin - metabolism ; Adipose tissue ; Adipose Tissue, White - metabolism ; Animals ; BDNF ; Brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - genetics ; Brain-Derived Neurotrophic Factor - metabolism ; Diet, High-Fat - adverse effects ; epididymal white adipose tissue ; Feeding ; Gene expression ; High fat diet ; Hypoxia ; Hypoxia-Inducible Factor 1, alpha Subunit - genetics ; Hypoxia-Inducible Factor 1, alpha Subunit - metabolism ; Intra-Abdominal Fat - metabolism ; Macrophages ; Male ; Mice ; Mice, Inbred C57BL ; Obesity ; Obesity - genetics ; Obesity - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; visceral adipose tissue</subject><ispartof>Genes to cells : devoted to molecular & cellular mechanisms, 2024-11, Vol.29 (11), p.1077-1084</ispartof><rights>2024 Molecular Biology Society of Japan and John Wiley & Sons Australia, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2432-89c79480c29400069d560bbc3f8c4a47baf2d3e5405bf142efbb1f33d3854f6b3</cites><orcidid>0000-0002-6807-8707</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fgtc.13162$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fgtc.13162$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39278976$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sakata, Kurumi</creatorcontrib><creatorcontrib>Fukuchi, Mamoru</creatorcontrib><title>Accelerated BDNF expression in visceral white adipose tissues following high‐fat diet feeding in mice</title><title>Genes to cells : devoted to molecular & cellular mechanisms</title><addtitle>Genes Cells</addtitle><description>Brain‐derived neurotrophic factor (BDNF) is expressed in the white adipose tissues (WATs), and the expression increases during high‐fat diet (HFD) feeding, implicating its role in obesity. Here, we focused on BDNF expression in epididymal WAT (eWAT), a visceral adipose tissue, in mice. During 2 weeks of HFD feeding, Bdnf mRNA expression in eWAT slightly increased, but a robust increase was observed after 8 weeks of HFD feeding. This upregulation of Bdnf mRNA was correlated with significant induction of hypoxia‐inducible factor 1α (Hif1α) and platelet‐derived growth factor subunit B (Pdgfb) mRNA in eWAT following 8 weeks of HFD feeding. Furthermore, the increased expression of the M1 macrophage markers was strongly correlated with the elevation of Bdnf mRNA in the eWAT. Notably, 8 weeks of HFD feeding significantly elevated Tnfα mRNA expression in eWAT, while no such induction was observed in inguinal WAT (iWAT). In contrast, the expression of Adipoq (adiponectin), implicated in improved insulin sensitivity and anti‐inflammatory effects, was significantly upregulated in iWAT, but not in eWAT. Thus, our study may show the role of BDNF in eWAT in obesity models, potentially contributing to the pathological state of visceral adipose tissues.
A robust induction of brain‐derived neurotrophic factor mRNA expression was observed particularly in epididymal white adipose tissue of mice fed with high‐fat diet for 8 weeks.</description><subject>Adiponectin</subject><subject>Adiponectin - genetics</subject><subject>Adiponectin - metabolism</subject><subject>Adipose tissue</subject><subject>Adipose Tissue, White - metabolism</subject><subject>Animals</subject><subject>BDNF</subject><subject>Brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - genetics</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Diet, High-Fat - adverse effects</subject><subject>epididymal white adipose tissue</subject><subject>Feeding</subject><subject>Gene expression</subject><subject>High fat diet</subject><subject>Hypoxia</subject><subject>Hypoxia-Inducible Factor 1, alpha Subunit - genetics</subject><subject>Hypoxia-Inducible Factor 1, alpha Subunit - metabolism</subject><subject>Intra-Abdominal Fat - metabolism</subject><subject>Macrophages</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Obesity</subject><subject>Obesity - genetics</subject><subject>Obesity - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>visceral adipose tissue</subject><issn>1356-9597</issn><issn>1365-2443</issn><issn>1365-2443</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE9PwjAYhxujEUQPfgHTxIseBv27rUdEQROiFzwvW_cWSsaG6xC5-RH8jH4Si6AHE3tp875Pnvz6Q-icki71pzdtdJdyGrID1KY8lAETgh9u3zIMlFRRC504NyeEckbkMWpxxaJYRWEbTftaQwF12kCOb24fhxjeljU4Z6sS2xK_Wqf9tsDrmW0Ap7ldVg5wY51bgcOmKopqbcspntnp7PP9w6QNzi002ADk27l3LKyGU3Rk0sLB2f7uoOfh3WRwH4yfRg-D_jjQTHAWxEpHSsREMyUIIaHKZUiyTHMTa5GKKEsNyzlIQWRmqGBgsowaznMeS2HCjHfQ1c67rKsXn7BJFtsfFEVaQrVyCadECkWVDD16-QedV6u69Ok8xUTMRSwiT13vKF1XztVgkmVtF2m9SShJtu0nvv3ku33PXuyNq2wB-S_5U7cHejtgbQvY_G9KRpPBTvkFCJiO1g</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Sakata, Kurumi</creator><creator>Fukuchi, Mamoru</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6807-8707</orcidid></search><sort><creationdate>202411</creationdate><title>Accelerated BDNF expression in visceral white adipose tissues following high‐fat diet feeding in mice</title><author>Sakata, Kurumi ; Fukuchi, Mamoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2432-89c79480c29400069d560bbc3f8c4a47baf2d3e5405bf142efbb1f33d3854f6b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adiponectin</topic><topic>Adiponectin - genetics</topic><topic>Adiponectin - metabolism</topic><topic>Adipose tissue</topic><topic>Adipose Tissue, White - metabolism</topic><topic>Animals</topic><topic>BDNF</topic><topic>Brain-derived neurotrophic factor</topic><topic>Brain-Derived Neurotrophic Factor - genetics</topic><topic>Brain-Derived Neurotrophic Factor - metabolism</topic><topic>Diet, High-Fat - adverse effects</topic><topic>epididymal white adipose tissue</topic><topic>Feeding</topic><topic>Gene expression</topic><topic>High fat diet</topic><topic>Hypoxia</topic><topic>Hypoxia-Inducible Factor 1, alpha Subunit - genetics</topic><topic>Hypoxia-Inducible Factor 1, alpha Subunit - metabolism</topic><topic>Intra-Abdominal Fat - metabolism</topic><topic>Macrophages</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Obesity</topic><topic>Obesity - genetics</topic><topic>Obesity - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>visceral adipose tissue</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sakata, Kurumi</creatorcontrib><creatorcontrib>Fukuchi, Mamoru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Genes to cells : devoted to molecular & cellular mechanisms</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sakata, Kurumi</au><au>Fukuchi, Mamoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Accelerated BDNF expression in visceral white adipose tissues following high‐fat diet feeding in mice</atitle><jtitle>Genes to cells : devoted to molecular & cellular mechanisms</jtitle><addtitle>Genes Cells</addtitle><date>2024-11</date><risdate>2024</risdate><volume>29</volume><issue>11</issue><spage>1077</spage><epage>1084</epage><pages>1077-1084</pages><issn>1356-9597</issn><issn>1365-2443</issn><eissn>1365-2443</eissn><abstract>Brain‐derived neurotrophic factor (BDNF) is expressed in the white adipose tissues (WATs), and the expression increases during high‐fat diet (HFD) feeding, implicating its role in obesity. Here, we focused on BDNF expression in epididymal WAT (eWAT), a visceral adipose tissue, in mice. During 2 weeks of HFD feeding, Bdnf mRNA expression in eWAT slightly increased, but a robust increase was observed after 8 weeks of HFD feeding. This upregulation of Bdnf mRNA was correlated with significant induction of hypoxia‐inducible factor 1α (Hif1α) and platelet‐derived growth factor subunit B (Pdgfb) mRNA in eWAT following 8 weeks of HFD feeding. Furthermore, the increased expression of the M1 macrophage markers was strongly correlated with the elevation of Bdnf mRNA in the eWAT. Notably, 8 weeks of HFD feeding significantly elevated Tnfα mRNA expression in eWAT, while no such induction was observed in inguinal WAT (iWAT). In contrast, the expression of Adipoq (adiponectin), implicated in improved insulin sensitivity and anti‐inflammatory effects, was significantly upregulated in iWAT, but not in eWAT. Thus, our study may show the role of BDNF in eWAT in obesity models, potentially contributing to the pathological state of visceral adipose tissues.
A robust induction of brain‐derived neurotrophic factor mRNA expression was observed particularly in epididymal white adipose tissue of mice fed with high‐fat diet for 8 weeks.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>39278976</pmid><doi>10.1111/gtc.13162</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-6807-8707</orcidid></addata></record> |
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subjects | Adiponectin Adiponectin - genetics Adiponectin - metabolism Adipose tissue Adipose Tissue, White - metabolism Animals BDNF Brain-derived neurotrophic factor Brain-Derived Neurotrophic Factor - genetics Brain-Derived Neurotrophic Factor - metabolism Diet, High-Fat - adverse effects epididymal white adipose tissue Feeding Gene expression High fat diet Hypoxia Hypoxia-Inducible Factor 1, alpha Subunit - genetics Hypoxia-Inducible Factor 1, alpha Subunit - metabolism Intra-Abdominal Fat - metabolism Macrophages Male Mice Mice, Inbred C57BL Obesity Obesity - genetics Obesity - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism visceral adipose tissue |
title | Accelerated BDNF expression in visceral white adipose tissues following high‐fat diet feeding in mice |
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