Adipokine zinc‐α2‐glycoprotein regulated by growth hormone and linked to insulin sensitivity

Objective Hypertrophic obesity is associated with impaired insulin sensitivity and lipid‐mobilizing activity of zinc‐α2‐glycoprotein. Adipose tissue (AT) of growth hormone (GH) ‐deficient patients is characterized by extreme adipocyte hypertrophy due to defects in AT lipid metabolism. It was hypothe...

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Veröffentlicht in:Obesity (Silver Spring, Md.) Md.), 2015-02, Vol.23 (2), p.322-328
Hauptverfasser: Balaz, Miroslav, Ukropcova, Barbara, Kurdiova, Timea, Gajdosechova, Lucia, Vlcek, Miroslav, Janakova, Zuzana, Fedeles, Jozef, Pura, Mikulas, Gasperikova, Daniela, Smith, Steven R., Tkacova, Ruzena, Klimes, Iwar, Payer, Juraj, Wolfrum, Christian, Ukropec, Jozef
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container_end_page 328
container_issue 2
container_start_page 322
container_title Obesity (Silver Spring, Md.)
container_volume 23
creator Balaz, Miroslav
Ukropcova, Barbara
Kurdiova, Timea
Gajdosechova, Lucia
Vlcek, Miroslav
Janakova, Zuzana
Fedeles, Jozef
Pura, Mikulas
Gasperikova, Daniela
Smith, Steven R.
Tkacova, Ruzena
Klimes, Iwar
Payer, Juraj
Wolfrum, Christian
Ukropec, Jozef
description Objective Hypertrophic obesity is associated with impaired insulin sensitivity and lipid‐mobilizing activity of zinc‐α2‐glycoprotein. Adipose tissue (AT) of growth hormone (GH) ‐deficient patients is characterized by extreme adipocyte hypertrophy due to defects in AT lipid metabolism. It was hypothesized that zinc‐α2‐glycoprotein is regulated by GH and mediates some of its beneficial effects in AT. Methods AT from patients with GH deficiency and individuals with obesity‐related GH deficit was obtained before and after 5‐year and 24‐month GH supplementation therapy. GH action was tested in primary human adipocytes. Relationships of GH and zinc‐α2‐glycoprotein with adipocyte size and insulin sensitivity were evaluated in nondiabetic patients with noncancerous cachexia and hypertrophic obesity. Results AT in GH‐deficient adults displayed a substantial reduction of zinc‐α2‐glycoprotein. GH therapy normalized AT zinc‐α2‐glycoprotein. Obesity‐related relative GH deficit was associated with almost 80% reduction of zinc‐α2‐glycoprotein mRNA in AT. GH increased zinc‐α2‐glycoprotein mRNA in both AT of obese men and primary human adipocytes. Interdependence of GH and zinc‐α2‐glycoprotein in regulating AT morphology and metabolic phenotype was evident from their relationship with adipocyte size and AT‐specific and whole‐body insulin sensitivity. Conclusions The results demonstrate that GH is involved in regulation of AT zinc‐α2‐glycoprotein; however, the molecular mechanism linking GH and zinc‐α2‐glycoprotein in AT is yet unknown.
doi_str_mv 10.1002/oby.20856
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Adipose tissue (AT) of growth hormone (GH) ‐deficient patients is characterized by extreme adipocyte hypertrophy due to defects in AT lipid metabolism. It was hypothesized that zinc‐α2‐glycoprotein is regulated by GH and mediates some of its beneficial effects in AT. Methods AT from patients with GH deficiency and individuals with obesity‐related GH deficit was obtained before and after 5‐year and 24‐month GH supplementation therapy. GH action was tested in primary human adipocytes. Relationships of GH and zinc‐α2‐glycoprotein with adipocyte size and insulin sensitivity were evaluated in nondiabetic patients with noncancerous cachexia and hypertrophic obesity. Results AT in GH‐deficient adults displayed a substantial reduction of zinc‐α2‐glycoprotein. GH therapy normalized AT zinc‐α2‐glycoprotein. Obesity‐related relative GH deficit was associated with almost 80% reduction of zinc‐α2‐glycoprotein mRNA in AT. GH increased zinc‐α2‐glycoprotein mRNA in both AT of obese men and primary human adipocytes. Interdependence of GH and zinc‐α2‐glycoprotein in regulating AT morphology and metabolic phenotype was evident from their relationship with adipocyte size and AT‐specific and whole‐body insulin sensitivity. Conclusions The results demonstrate that GH is involved in regulation of AT zinc‐α2‐glycoprotein; however, the molecular mechanism linking GH and zinc‐α2‐glycoprotein in AT is yet unknown.</description><identifier>ISSN: 1930-7381</identifier><identifier>EISSN: 1930-739X</identifier><identifier>DOI: 10.1002/oby.20856</identifier><identifier>PMID: 25098857</identifier><language>eng</language><publisher>United States</publisher><subject>Adipocytes - drug effects ; Adipocytes - metabolism ; Adipose Tissue - drug effects ; Adipose Tissue - metabolism ; Administration, Oral ; Adult ; Aged ; Case-Control Studies ; Cohort Studies ; Dietary Supplements ; Female ; Human Growth Hormone - administration &amp; dosage ; Human Growth Hormone - deficiency ; Human Growth Hormone - pharmacology ; Humans ; Lipid Metabolism ; Male ; Middle Aged ; Obesity - metabolism ; Seminal Plasma Proteins - metabolism</subject><ispartof>Obesity (Silver Spring, Md.), 2015-02, Vol.23 (2), p.322-328</ispartof><rights>2014 The Obesity Society</rights><rights>2014 The Obesity Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2066-6c42ec77167022f02660353a933e0321d8146598c0a9b905fe7366ec74a2a6db3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Foby.20856$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Foby.20856$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,1432,27922,27923,45572,45573,46407,46831</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25098857$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Balaz, Miroslav</creatorcontrib><creatorcontrib>Ukropcova, Barbara</creatorcontrib><creatorcontrib>Kurdiova, Timea</creatorcontrib><creatorcontrib>Gajdosechova, Lucia</creatorcontrib><creatorcontrib>Vlcek, Miroslav</creatorcontrib><creatorcontrib>Janakova, Zuzana</creatorcontrib><creatorcontrib>Fedeles, Jozef</creatorcontrib><creatorcontrib>Pura, Mikulas</creatorcontrib><creatorcontrib>Gasperikova, Daniela</creatorcontrib><creatorcontrib>Smith, Steven R.</creatorcontrib><creatorcontrib>Tkacova, Ruzena</creatorcontrib><creatorcontrib>Klimes, Iwar</creatorcontrib><creatorcontrib>Payer, Juraj</creatorcontrib><creatorcontrib>Wolfrum, Christian</creatorcontrib><creatorcontrib>Ukropec, Jozef</creatorcontrib><title>Adipokine zinc‐α2‐glycoprotein regulated by growth hormone and linked to insulin sensitivity</title><title>Obesity (Silver Spring, Md.)</title><addtitle>Obesity (Silver Spring)</addtitle><description>Objective Hypertrophic obesity is associated with impaired insulin sensitivity and lipid‐mobilizing activity of zinc‐α2‐glycoprotein. Adipose tissue (AT) of growth hormone (GH) ‐deficient patients is characterized by extreme adipocyte hypertrophy due to defects in AT lipid metabolism. It was hypothesized that zinc‐α2‐glycoprotein is regulated by GH and mediates some of its beneficial effects in AT. Methods AT from patients with GH deficiency and individuals with obesity‐related GH deficit was obtained before and after 5‐year and 24‐month GH supplementation therapy. GH action was tested in primary human adipocytes. Relationships of GH and zinc‐α2‐glycoprotein with adipocyte size and insulin sensitivity were evaluated in nondiabetic patients with noncancerous cachexia and hypertrophic obesity. Results AT in GH‐deficient adults displayed a substantial reduction of zinc‐α2‐glycoprotein. GH therapy normalized AT zinc‐α2‐glycoprotein. Obesity‐related relative GH deficit was associated with almost 80% reduction of zinc‐α2‐glycoprotein mRNA in AT. GH increased zinc‐α2‐glycoprotein mRNA in both AT of obese men and primary human adipocytes. Interdependence of GH and zinc‐α2‐glycoprotein in regulating AT morphology and metabolic phenotype was evident from their relationship with adipocyte size and AT‐specific and whole‐body insulin sensitivity. Conclusions The results demonstrate that GH is involved in regulation of AT zinc‐α2‐glycoprotein; however, the molecular mechanism linking GH and zinc‐α2‐glycoprotein in AT is yet unknown.</description><subject>Adipocytes - drug effects</subject><subject>Adipocytes - metabolism</subject><subject>Adipose Tissue - drug effects</subject><subject>Adipose Tissue - metabolism</subject><subject>Administration, Oral</subject><subject>Adult</subject><subject>Aged</subject><subject>Case-Control Studies</subject><subject>Cohort Studies</subject><subject>Dietary Supplements</subject><subject>Female</subject><subject>Human Growth Hormone - administration &amp; dosage</subject><subject>Human Growth Hormone - deficiency</subject><subject>Human Growth Hormone - pharmacology</subject><subject>Humans</subject><subject>Lipid Metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Obesity - metabolism</subject><subject>Seminal Plasma Proteins - metabolism</subject><issn>1930-7381</issn><issn>1930-739X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1OwzAQhS0EoqWw4ALISzZpx3biOMtS8SdV6gYkWEVO4ramqV3ihCqsOAJX4SIcgpNg2tLN_Oh9bzR6CJ0T6BMAOrBZ26cgIn6AuiRhEMQseTrcz4J00IlzLwAhh4gcow6NIBEiirtIDgu9sgttFH7XJv_5-Pz-or7Oyja3q8rWShtcqVlTyloVOGvxrLLreo7ntlpa75KmwKU2Cy_WFmvjGr9hp4zTtX7TdXuKjqaydOps13vo8eb6YXQXjCe396PhOMgpcB7wPKQqj2PCY6B0CpRzYBGTCWMKGCWFICGPEpGDTLIEoqmKGefeEUoqeZGxHrrc3vVfvzbK1elSu1yVpTTKNi4lPKIhpUJQj17s0CZbqiJdVXopqzb9j8UDgy2w1qVq9zqB9C_v1OedbvJOJ1fPm4H9ArHVdUA</recordid><startdate>201502</startdate><enddate>201502</enddate><creator>Balaz, Miroslav</creator><creator>Ukropcova, Barbara</creator><creator>Kurdiova, Timea</creator><creator>Gajdosechova, Lucia</creator><creator>Vlcek, Miroslav</creator><creator>Janakova, Zuzana</creator><creator>Fedeles, Jozef</creator><creator>Pura, Mikulas</creator><creator>Gasperikova, Daniela</creator><creator>Smith, Steven R.</creator><creator>Tkacova, Ruzena</creator><creator>Klimes, Iwar</creator><creator>Payer, Juraj</creator><creator>Wolfrum, Christian</creator><creator>Ukropec, Jozef</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201502</creationdate><title>Adipokine zinc‐α2‐glycoprotein regulated by growth hormone and linked to insulin sensitivity</title><author>Balaz, Miroslav ; Ukropcova, Barbara ; Kurdiova, Timea ; Gajdosechova, Lucia ; Vlcek, Miroslav ; Janakova, Zuzana ; Fedeles, Jozef ; Pura, Mikulas ; Gasperikova, Daniela ; Smith, Steven R. ; Tkacova, Ruzena ; Klimes, Iwar ; Payer, Juraj ; Wolfrum, Christian ; Ukropec, Jozef</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2066-6c42ec77167022f02660353a933e0321d8146598c0a9b905fe7366ec74a2a6db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adipocytes - drug effects</topic><topic>Adipocytes - metabolism</topic><topic>Adipose Tissue - drug effects</topic><topic>Adipose Tissue - metabolism</topic><topic>Administration, Oral</topic><topic>Adult</topic><topic>Aged</topic><topic>Case-Control Studies</topic><topic>Cohort Studies</topic><topic>Dietary Supplements</topic><topic>Female</topic><topic>Human Growth Hormone - administration &amp; dosage</topic><topic>Human Growth Hormone - deficiency</topic><topic>Human Growth Hormone - pharmacology</topic><topic>Humans</topic><topic>Lipid Metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Obesity - metabolism</topic><topic>Seminal Plasma Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Balaz, Miroslav</creatorcontrib><creatorcontrib>Ukropcova, Barbara</creatorcontrib><creatorcontrib>Kurdiova, Timea</creatorcontrib><creatorcontrib>Gajdosechova, Lucia</creatorcontrib><creatorcontrib>Vlcek, Miroslav</creatorcontrib><creatorcontrib>Janakova, Zuzana</creatorcontrib><creatorcontrib>Fedeles, Jozef</creatorcontrib><creatorcontrib>Pura, Mikulas</creatorcontrib><creatorcontrib>Gasperikova, Daniela</creatorcontrib><creatorcontrib>Smith, Steven R.</creatorcontrib><creatorcontrib>Tkacova, Ruzena</creatorcontrib><creatorcontrib>Klimes, Iwar</creatorcontrib><creatorcontrib>Payer, Juraj</creatorcontrib><creatorcontrib>Wolfrum, Christian</creatorcontrib><creatorcontrib>Ukropec, Jozef</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>Obesity (Silver Spring, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Balaz, Miroslav</au><au>Ukropcova, Barbara</au><au>Kurdiova, Timea</au><au>Gajdosechova, Lucia</au><au>Vlcek, Miroslav</au><au>Janakova, Zuzana</au><au>Fedeles, Jozef</au><au>Pura, Mikulas</au><au>Gasperikova, Daniela</au><au>Smith, Steven R.</au><au>Tkacova, Ruzena</au><au>Klimes, Iwar</au><au>Payer, Juraj</au><au>Wolfrum, Christian</au><au>Ukropec, Jozef</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adipokine zinc‐α2‐glycoprotein regulated by growth hormone and linked to insulin sensitivity</atitle><jtitle>Obesity (Silver Spring, Md.)</jtitle><addtitle>Obesity (Silver Spring)</addtitle><date>2015-02</date><risdate>2015</risdate><volume>23</volume><issue>2</issue><spage>322</spage><epage>328</epage><pages>322-328</pages><issn>1930-7381</issn><eissn>1930-739X</eissn><abstract>Objective Hypertrophic obesity is associated with impaired insulin sensitivity and lipid‐mobilizing activity of zinc‐α2‐glycoprotein. Adipose tissue (AT) of growth hormone (GH) ‐deficient patients is characterized by extreme adipocyte hypertrophy due to defects in AT lipid metabolism. It was hypothesized that zinc‐α2‐glycoprotein is regulated by GH and mediates some of its beneficial effects in AT. Methods AT from patients with GH deficiency and individuals with obesity‐related GH deficit was obtained before and after 5‐year and 24‐month GH supplementation therapy. GH action was tested in primary human adipocytes. Relationships of GH and zinc‐α2‐glycoprotein with adipocyte size and insulin sensitivity were evaluated in nondiabetic patients with noncancerous cachexia and hypertrophic obesity. Results AT in GH‐deficient adults displayed a substantial reduction of zinc‐α2‐glycoprotein. GH therapy normalized AT zinc‐α2‐glycoprotein. Obesity‐related relative GH deficit was associated with almost 80% reduction of zinc‐α2‐glycoprotein mRNA in AT. GH increased zinc‐α2‐glycoprotein mRNA in both AT of obese men and primary human adipocytes. Interdependence of GH and zinc‐α2‐glycoprotein in regulating AT morphology and metabolic phenotype was evident from their relationship with adipocyte size and AT‐specific and whole‐body insulin sensitivity. Conclusions The results demonstrate that GH is involved in regulation of AT zinc‐α2‐glycoprotein; however, the molecular mechanism linking GH and zinc‐α2‐glycoprotein in AT is yet unknown.</abstract><cop>United States</cop><pmid>25098857</pmid><doi>10.1002/oby.20856</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Wiley Free Content; Wiley Online Library All Journals
subjects Adipocytes - drug effects
Adipocytes - metabolism
Adipose Tissue - drug effects
Adipose Tissue - metabolism
Administration, Oral
Adult
Aged
Case-Control Studies
Cohort Studies
Dietary Supplements
Female
Human Growth Hormone - administration & dosage
Human Growth Hormone - deficiency
Human Growth Hormone - pharmacology
Humans
Lipid Metabolism
Male
Middle Aged
Obesity - metabolism
Seminal Plasma Proteins - metabolism
title Adipokine zinc‐α2‐glycoprotein regulated by growth hormone and linked to insulin sensitivity
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