The role of the novel adipocyte-derived hormone adiponectin in human disease

Adiponectin, also called GBP-28, apM1, AdipoQ and Acrp30, is a novel adipose tIssue-specific protein that has structural homology to collagen VIII and X and complement factor C1q, and that circulates in human plasma at high levels. It is one of the physiologically active polypeptides secreted by adi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of endocrinology 2003-03, Vol.148 (3), p.293-300
Hauptverfasser: DIEZ, Juan J, IGLESIAS, Pedro
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 300
container_issue 3
container_start_page 293
container_title European journal of endocrinology
container_volume 148
creator DIEZ, Juan J
IGLESIAS, Pedro
description Adiponectin, also called GBP-28, apM1, AdipoQ and Acrp30, is a novel adipose tIssue-specific protein that has structural homology to collagen VIII and X and complement factor C1q, and that circulates in human plasma at high levels. It is one of the physiologically active polypeptides secreted by adipose tIssue, whose multiple functions have started to be understood in the last few Years.A reduction in adiponectin expression is associated with insulin resistance in some animal models. Administration of adiponectin has been accompanied by a reduction in plasma glucose and an increase in insulin sensitivity. In addition, thiazolidinediones, drugs that enhance insulin sensitivity through stimulation of the peroxisome proliferator-activated receptor-gamma, increase plasma adiponectin and mRNA levels in mice. On the other hand, this adipocyte protein seems to play a protective role in experimental models of vascular injury. In humans, adiponectin levels are inversely related to the degree of adiposity and positively associated with insulin sensitivity both in healthy subjects and in diabetic patients. Plasma adiponectin levels have been reported to be decreased in some insulin-resistant states, such as obesity and type 2 diabetes mellitus, and also in patients with coronary artery disease. On the contrary, chronic renal failure, type 1 diabetes and anorexia nervosa are associated with increased plasma adiponectin levels. Concentrations of plasma adiponectin have been shown to correlate negatively with glucose, insulin, triglyceride levels and body mass index, and positively with high-density lipoprotein-cholesterol levels and insulin-stimulated glucose disposal. Weight loss and therapy with thiazolidinediones increased endogenous adiponectin production in humans. Adiponectin increases insulin sensitivity by increasing tIssue fat oxidation, resulting in reduced circulating fatty acid levels and reduced intracellular triglyceride contents in liver and muscle. This protein also suppresses the expression of adhesion molecules in vascular endothelial cells and cytokine production from macrophages, thus inhibiting the inflammatory processes that occur during the early phases of atherosclerosis. In view of these data, it is possible that hypoadiponectinemia may play a role in the development of atherosclerotic vascular disease. In summary, the ability of adiponectin to increase insulin sensitivity in conjunction with its anti-inflammatory and anti-atherogenic propertie
doi_str_mv 10.1530/eje.0.1480293
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73074644</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73074644</sourcerecordid><originalsourceid>FETCH-LOGICAL-c453t-157d4285d5c7f753fff2cb410df436138e81e9f9b6e3498b2a90c2dd4bbfbb513</originalsourceid><addsrcrecordid>eNpFkE1Lw0AQhhdRbK0evUouekvdzWy-jlL8goCXCt7CfszSlCRbd5NC_70rCRQG5oF5eGFeQu4ZXbMU6DPucR2QFzQp4YIsGc_LOCvg55IsaUF5zDMOC3Lj_Z5SFphekwVLMsYyWi5Jtd1h5GyLkTXRELi3R2wjoZuDVacBY42uOaKOdtZ1tsfp0qMamj4Ksxs70Ue68Sg83pIrI1qPd_Neke-31-3mI66-3j83L1WseApDzNJc86RIdapyk6dgjEmU5IxqwyFjUGDBsDSlzBB4WchElFQlWnMpjZQpgxV5mnIPzv6O6Ie6a7zCthU92tHXOdA8vM2DGE-ictZ7h6Y-uKYT7lQzWv_XV4f66oBTfcF_mINH2aE-23NfQXicBeGVaI0TvWr82eMZMEgA_gA26Hhd</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73074644</pqid></control><display><type>article</type><title>The role of the novel adipocyte-derived hormone adiponectin in human disease</title><source>MEDLINE</source><source>Oxford Academic Journals (OUP)</source><creator>DIEZ, Juan J ; IGLESIAS, Pedro</creator><creatorcontrib>DIEZ, Juan J ; IGLESIAS, Pedro</creatorcontrib><description>Adiponectin, also called GBP-28, apM1, AdipoQ and Acrp30, is a novel adipose tIssue-specific protein that has structural homology to collagen VIII and X and complement factor C1q, and that circulates in human plasma at high levels. It is one of the physiologically active polypeptides secreted by adipose tIssue, whose multiple functions have started to be understood in the last few Years.A reduction in adiponectin expression is associated with insulin resistance in some animal models. Administration of adiponectin has been accompanied by a reduction in plasma glucose and an increase in insulin sensitivity. In addition, thiazolidinediones, drugs that enhance insulin sensitivity through stimulation of the peroxisome proliferator-activated receptor-gamma, increase plasma adiponectin and mRNA levels in mice. On the other hand, this adipocyte protein seems to play a protective role in experimental models of vascular injury. In humans, adiponectin levels are inversely related to the degree of adiposity and positively associated with insulin sensitivity both in healthy subjects and in diabetic patients. Plasma adiponectin levels have been reported to be decreased in some insulin-resistant states, such as obesity and type 2 diabetes mellitus, and also in patients with coronary artery disease. On the contrary, chronic renal failure, type 1 diabetes and anorexia nervosa are associated with increased plasma adiponectin levels. Concentrations of plasma adiponectin have been shown to correlate negatively with glucose, insulin, triglyceride levels and body mass index, and positively with high-density lipoprotein-cholesterol levels and insulin-stimulated glucose disposal. Weight loss and therapy with thiazolidinediones increased endogenous adiponectin production in humans. Adiponectin increases insulin sensitivity by increasing tIssue fat oxidation, resulting in reduced circulating fatty acid levels and reduced intracellular triglyceride contents in liver and muscle. This protein also suppresses the expression of adhesion molecules in vascular endothelial cells and cytokine production from macrophages, thus inhibiting the inflammatory processes that occur during the early phases of atherosclerosis. In view of these data, it is possible that hypoadiponectinemia may play a role in the development of atherosclerotic vascular disease. In summary, the ability of adiponectin to increase insulin sensitivity in conjunction with its anti-inflammatory and anti-atherogenic properties have made this novel adipocytokine a promising therapeutic tool for the future, with potential applications in states associated with low plasma adiponectin levels.</description><identifier>ISSN: 0804-4643</identifier><identifier>EISSN: 1479-683X</identifier><identifier>DOI: 10.1530/eje.0.1480293</identifier><identifier>PMID: 12611609</identifier><language>eng</language><publisher>Colchester: Portland Press</publisher><subject>Adipocytes - physiology ; Adiponectin ; Adipose Tissue - physiology ; Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Humans ; Intercellular Signaling Peptides and Proteins ; Proteins - pharmacology ; Proteins - physiology ; Proteins - therapeutic use ; Vertebrates: skin, associated glands, phaneres, light organs, various exocrine glands (salt gland, uropygial gland...), adipose tissue, connective tissue</subject><ispartof>European journal of endocrinology, 2003-03, Vol.148 (3), p.293-300</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-157d4285d5c7f753fff2cb410df436138e81e9f9b6e3498b2a90c2dd4bbfbb513</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14631323$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12611609$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DIEZ, Juan J</creatorcontrib><creatorcontrib>IGLESIAS, Pedro</creatorcontrib><title>The role of the novel adipocyte-derived hormone adiponectin in human disease</title><title>European journal of endocrinology</title><addtitle>Eur J Endocrinol</addtitle><description>Adiponectin, also called GBP-28, apM1, AdipoQ and Acrp30, is a novel adipose tIssue-specific protein that has structural homology to collagen VIII and X and complement factor C1q, and that circulates in human plasma at high levels. It is one of the physiologically active polypeptides secreted by adipose tIssue, whose multiple functions have started to be understood in the last few Years.A reduction in adiponectin expression is associated with insulin resistance in some animal models. Administration of adiponectin has been accompanied by a reduction in plasma glucose and an increase in insulin sensitivity. In addition, thiazolidinediones, drugs that enhance insulin sensitivity through stimulation of the peroxisome proliferator-activated receptor-gamma, increase plasma adiponectin and mRNA levels in mice. On the other hand, this adipocyte protein seems to play a protective role in experimental models of vascular injury. In humans, adiponectin levels are inversely related to the degree of adiposity and positively associated with insulin sensitivity both in healthy subjects and in diabetic patients. Plasma adiponectin levels have been reported to be decreased in some insulin-resistant states, such as obesity and type 2 diabetes mellitus, and also in patients with coronary artery disease. On the contrary, chronic renal failure, type 1 diabetes and anorexia nervosa are associated with increased plasma adiponectin levels. Concentrations of plasma adiponectin have been shown to correlate negatively with glucose, insulin, triglyceride levels and body mass index, and positively with high-density lipoprotein-cholesterol levels and insulin-stimulated glucose disposal. Weight loss and therapy with thiazolidinediones increased endogenous adiponectin production in humans. Adiponectin increases insulin sensitivity by increasing tIssue fat oxidation, resulting in reduced circulating fatty acid levels and reduced intracellular triglyceride contents in liver and muscle. This protein also suppresses the expression of adhesion molecules in vascular endothelial cells and cytokine production from macrophages, thus inhibiting the inflammatory processes that occur during the early phases of atherosclerosis. In view of these data, it is possible that hypoadiponectinemia may play a role in the development of atherosclerotic vascular disease. In summary, the ability of adiponectin to increase insulin sensitivity in conjunction with its anti-inflammatory and anti-atherogenic properties have made this novel adipocytokine a promising therapeutic tool for the future, with potential applications in states associated with low plasma adiponectin levels.</description><subject>Adipocytes - physiology</subject><subject>Adiponectin</subject><subject>Adipose Tissue - physiology</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins</subject><subject>Proteins - pharmacology</subject><subject>Proteins - physiology</subject><subject>Proteins - therapeutic use</subject><subject>Vertebrates: skin, associated glands, phaneres, light organs, various exocrine glands (salt gland, uropygial gland...), adipose tissue, connective tissue</subject><issn>0804-4643</issn><issn>1479-683X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1Lw0AQhhdRbK0evUouekvdzWy-jlL8goCXCt7CfszSlCRbd5NC_70rCRQG5oF5eGFeQu4ZXbMU6DPucR2QFzQp4YIsGc_LOCvg55IsaUF5zDMOC3Lj_Z5SFphekwVLMsYyWi5Jtd1h5GyLkTXRELi3R2wjoZuDVacBY42uOaKOdtZ1tsfp0qMamj4Ksxs70Ue68Sg83pIrI1qPd_Neke-31-3mI66-3j83L1WseApDzNJc86RIdapyk6dgjEmU5IxqwyFjUGDBsDSlzBB4WchElFQlWnMpjZQpgxV5mnIPzv6O6Ie6a7zCthU92tHXOdA8vM2DGE-ictZ7h6Y-uKYT7lQzWv_XV4f66oBTfcF_mINH2aE-23NfQXicBeGVaI0TvWr82eMZMEgA_gA26Hhd</recordid><startdate>20030301</startdate><enddate>20030301</enddate><creator>DIEZ, Juan J</creator><creator>IGLESIAS, Pedro</creator><general>Portland Press</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20030301</creationdate><title>The role of the novel adipocyte-derived hormone adiponectin in human disease</title><author>DIEZ, Juan J ; IGLESIAS, Pedro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-157d4285d5c7f753fff2cb410df436138e81e9f9b6e3498b2a90c2dd4bbfbb513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adipocytes - physiology</topic><topic>Adiponectin</topic><topic>Adipose Tissue - physiology</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins</topic><topic>Proteins - pharmacology</topic><topic>Proteins - physiology</topic><topic>Proteins - therapeutic use</topic><topic>Vertebrates: skin, associated glands, phaneres, light organs, various exocrine glands (salt gland, uropygial gland...), adipose tissue, connective tissue</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DIEZ, Juan J</creatorcontrib><creatorcontrib>IGLESIAS, Pedro</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DIEZ, Juan J</au><au>IGLESIAS, Pedro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of the novel adipocyte-derived hormone adiponectin in human disease</atitle><jtitle>European journal of endocrinology</jtitle><addtitle>Eur J Endocrinol</addtitle><date>2003-03-01</date><risdate>2003</risdate><volume>148</volume><issue>3</issue><spage>293</spage><epage>300</epage><pages>293-300</pages><issn>0804-4643</issn><eissn>1479-683X</eissn><abstract>Adiponectin, also called GBP-28, apM1, AdipoQ and Acrp30, is a novel adipose tIssue-specific protein that has structural homology to collagen VIII and X and complement factor C1q, and that circulates in human plasma at high levels. It is one of the physiologically active polypeptides secreted by adipose tIssue, whose multiple functions have started to be understood in the last few Years.A reduction in adiponectin expression is associated with insulin resistance in some animal models. Administration of adiponectin has been accompanied by a reduction in plasma glucose and an increase in insulin sensitivity. In addition, thiazolidinediones, drugs that enhance insulin sensitivity through stimulation of the peroxisome proliferator-activated receptor-gamma, increase plasma adiponectin and mRNA levels in mice. On the other hand, this adipocyte protein seems to play a protective role in experimental models of vascular injury. In humans, adiponectin levels are inversely related to the degree of adiposity and positively associated with insulin sensitivity both in healthy subjects and in diabetic patients. Plasma adiponectin levels have been reported to be decreased in some insulin-resistant states, such as obesity and type 2 diabetes mellitus, and also in patients with coronary artery disease. On the contrary, chronic renal failure, type 1 diabetes and anorexia nervosa are associated with increased plasma adiponectin levels. Concentrations of plasma adiponectin have been shown to correlate negatively with glucose, insulin, triglyceride levels and body mass index, and positively with high-density lipoprotein-cholesterol levels and insulin-stimulated glucose disposal. Weight loss and therapy with thiazolidinediones increased endogenous adiponectin production in humans. Adiponectin increases insulin sensitivity by increasing tIssue fat oxidation, resulting in reduced circulating fatty acid levels and reduced intracellular triglyceride contents in liver and muscle. This protein also suppresses the expression of adhesion molecules in vascular endothelial cells and cytokine production from macrophages, thus inhibiting the inflammatory processes that occur during the early phases of atherosclerosis. In view of these data, it is possible that hypoadiponectinemia may play a role in the development of atherosclerotic vascular disease. In summary, the ability of adiponectin to increase insulin sensitivity in conjunction with its anti-inflammatory and anti-atherogenic properties have made this novel adipocytokine a promising therapeutic tool for the future, with potential applications in states associated with low plasma adiponectin levels.</abstract><cop>Colchester</cop><pub>Portland Press</pub><pmid>12611609</pmid><doi>10.1530/eje.0.1480293</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0804-4643
ispartof European journal of endocrinology, 2003-03, Vol.148 (3), p.293-300
issn 0804-4643
1479-683X
language eng
recordid cdi_proquest_miscellaneous_73074644
source MEDLINE; Oxford Academic Journals (OUP)
subjects Adipocytes - physiology
Adiponectin
Adipose Tissue - physiology
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Humans
Intercellular Signaling Peptides and Proteins
Proteins - pharmacology
Proteins - physiology
Proteins - therapeutic use
Vertebrates: skin, associated glands, phaneres, light organs, various exocrine glands (salt gland, uropygial gland...), adipose tissue, connective tissue
title The role of the novel adipocyte-derived hormone adiponectin in human disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T13%3A50%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20role%20of%20the%20novel%20adipocyte-derived%20hormone%20adiponectin%20in%20human%20disease&rft.jtitle=European%20journal%20of%20endocrinology&rft.au=DIEZ,%20Juan%20J&rft.date=2003-03-01&rft.volume=148&rft.issue=3&rft.spage=293&rft.epage=300&rft.pages=293-300&rft.issn=0804-4643&rft.eissn=1479-683X&rft_id=info:doi/10.1530/eje.0.1480293&rft_dat=%3Cproquest_cross%3E73074644%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=73074644&rft_id=info:pmid/12611609&rfr_iscdi=true