Ghrelin regulation of glucose metabolism
•Ghrelin exerts broad pharmacological effects on systems metabolism.•Ghrelin regulates glucose metabolism and insulin secretion in a variety of species.•Ghrelin inhibition has pharmacological potential for the treatment of T2DM. The a 28-amino acid peptide ghrelin was discovered in 1999 as a growth...
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Veröffentlicht in: | Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2018-02, Vol.100, p.236-242 |
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description | •Ghrelin exerts broad pharmacological effects on systems metabolism.•Ghrelin regulates glucose metabolism and insulin secretion in a variety of species.•Ghrelin inhibition has pharmacological potential for the treatment of T2DM.
The a 28-amino acid peptide ghrelin was discovered in 1999 as a growth hormone (GH) releasing peptide. Soon after its discovery, ghrelin was found to increase body weight and adiposity by acting on the hypothalamic melanocortinergic system. Subsequently, ghrelin was found to exert a series of metabolic effects, overall testifying ghrelin a pleiotropic nature of broad pharmacological interest. Ghrelin acts through the growth hormone secretagogue-receptor (GHS-R), a seven transmembrane G protein-coupled receptor with high expression in the anterior pituitary, pancreatic islets, thyroid gland, heart and various regions of the brain. Among ghrelins numerous metabolic effects are the most prominent the stimulation of appetite via activation of orexigenic hypothalamic neurocircuits and the food-intake independent stimulation of lipogenesis, which both together lead to an increase in body weight and adiposity. Ghrelin effects beyond the regulation of appetite and GH secretion include the regulation of gut motility, sleep-wake rhythm, taste sensation, reward seeking behaviour, and the regulation of glucose metabolism. The latter received recently increasing recognition because pharmacological inhibition of ghrelin signaling might be of therapeutic value to improve insuin resistance and type 2 diabetes. In this review we highlight the multifaceted nature of ghrelin and summarize its glucoregulatory action and discuss the pharmacological value of ghrelin pathway inhibition for the treatment of glucose intolerance and type 2 diabetes. |
doi_str_mv | 10.1016/j.peptides.2017.12.015 |
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The a 28-amino acid peptide ghrelin was discovered in 1999 as a growth hormone (GH) releasing peptide. Soon after its discovery, ghrelin was found to increase body weight and adiposity by acting on the hypothalamic melanocortinergic system. Subsequently, ghrelin was found to exert a series of metabolic effects, overall testifying ghrelin a pleiotropic nature of broad pharmacological interest. Ghrelin acts through the growth hormone secretagogue-receptor (GHS-R), a seven transmembrane G protein-coupled receptor with high expression in the anterior pituitary, pancreatic islets, thyroid gland, heart and various regions of the brain. Among ghrelins numerous metabolic effects are the most prominent the stimulation of appetite via activation of orexigenic hypothalamic neurocircuits and the food-intake independent stimulation of lipogenesis, which both together lead to an increase in body weight and adiposity. Ghrelin effects beyond the regulation of appetite and GH secretion include the regulation of gut motility, sleep-wake rhythm, taste sensation, reward seeking behaviour, and the regulation of glucose metabolism. The latter received recently increasing recognition because pharmacological inhibition of ghrelin signaling might be of therapeutic value to improve insuin resistance and type 2 diabetes. In this review we highlight the multifaceted nature of ghrelin and summarize its glucoregulatory action and discuss the pharmacological value of ghrelin pathway inhibition for the treatment of glucose intolerance and type 2 diabetes.</description><identifier>ISSN: 0196-9781</identifier><identifier>EISSN: 1873-5169</identifier><identifier>DOI: 10.1016/j.peptides.2017.12.015</identifier><identifier>PMID: 29412824</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Carbohydrate Metabolism - drug effects ; Diabetes ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes Mellitus, Type 2 - metabolism ; Diabetes Mellitus, Type 2 - pathology ; Diet-induced obesity ; Eating - drug effects ; Ghrelin ; Ghrelin - metabolism ; Ghrelin - therapeutic use ; Glucose - metabolism ; Humans ; Insulin sensitivity ; Receptors, Ghrelin - genetics ; Receptors, Ghrelin - metabolism ; Signal Transduction - drug effects</subject><ispartof>Peptides (New York, N.Y. : 1980), 2018-02, Vol.100, p.236-242</ispartof><rights>2017 The Author(s)</rights><rights>Copyright © 2017 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><rights>2017 The Author(s) 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-592c6306b38997a6e248e43fcbf6a953a517bead55dc41e1ef7c83e212b655193</citedby><cites>FETCH-LOGICAL-c471t-592c6306b38997a6e248e43fcbf6a953a517bead55dc41e1ef7c83e212b655193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.peptides.2017.12.015$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29412824$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Poher, Anne-Laure</creatorcontrib><creatorcontrib>Tschöp, Matthias H.</creatorcontrib><creatorcontrib>Müller, Timo D.</creatorcontrib><title>Ghrelin regulation of glucose metabolism</title><title>Peptides (New York, N.Y. : 1980)</title><addtitle>Peptides</addtitle><description>•Ghrelin exerts broad pharmacological effects on systems metabolism.•Ghrelin regulates glucose metabolism and insulin secretion in a variety of species.•Ghrelin inhibition has pharmacological potential for the treatment of T2DM.
The a 28-amino acid peptide ghrelin was discovered in 1999 as a growth hormone (GH) releasing peptide. Soon after its discovery, ghrelin was found to increase body weight and adiposity by acting on the hypothalamic melanocortinergic system. Subsequently, ghrelin was found to exert a series of metabolic effects, overall testifying ghrelin a pleiotropic nature of broad pharmacological interest. Ghrelin acts through the growth hormone secretagogue-receptor (GHS-R), a seven transmembrane G protein-coupled receptor with high expression in the anterior pituitary, pancreatic islets, thyroid gland, heart and various regions of the brain. Among ghrelins numerous metabolic effects are the most prominent the stimulation of appetite via activation of orexigenic hypothalamic neurocircuits and the food-intake independent stimulation of lipogenesis, which both together lead to an increase in body weight and adiposity. Ghrelin effects beyond the regulation of appetite and GH secretion include the regulation of gut motility, sleep-wake rhythm, taste sensation, reward seeking behaviour, and the regulation of glucose metabolism. The latter received recently increasing recognition because pharmacological inhibition of ghrelin signaling might be of therapeutic value to improve insuin resistance and type 2 diabetes. In this review we highlight the multifaceted nature of ghrelin and summarize its glucoregulatory action and discuss the pharmacological value of ghrelin pathway inhibition for the treatment of glucose intolerance and type 2 diabetes.</description><subject>Carbohydrate Metabolism - drug effects</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Diabetes Mellitus, Type 2 - pathology</subject><subject>Diet-induced obesity</subject><subject>Eating - drug effects</subject><subject>Ghrelin</subject><subject>Ghrelin - metabolism</subject><subject>Ghrelin - therapeutic use</subject><subject>Glucose - metabolism</subject><subject>Humans</subject><subject>Insulin sensitivity</subject><subject>Receptors, Ghrelin - genetics</subject><subject>Receptors, Ghrelin - metabolism</subject><subject>Signal Transduction - drug effects</subject><issn>0196-9781</issn><issn>1873-5169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhi0EoqXwF6qOXRJ8TuzYCwIhviQkFpgtx7kUV0lc7KQS_55UpQgmphvued87PYTMgaZAQVyu0w1ueldhTBmFIgWWUuBHZAqyyBIOQh2TKQUlElVImJCzGNeU0jxX8pRMmMqBSZZPyfLhPWDjukXA1dCY3vlu4evFqhmsj7hosTelb1xsz8lJbZqIF99zRt7u715vH5Pnl4en25vnxOYF9AlXzIqMijKTShVGIMsl5llty1oYxTPDoSjRVJxXNgcErAsrM2TASsE5qGxGrva9m6FssbLY9cE0ehNca8Kn9sbpv5vOveuV32ouKZccxoLld0HwHwPGXrcuWmwa06EfogallJC0ADaiYo_a4GMMWP-cAap3mvVaHzTrnWYNTI-ax-D895M_sYPXEbjeAziq2joMOlqHncXKBbS9rrz778YX1uySdg</recordid><startdate>201802</startdate><enddate>201802</enddate><creator>Poher, Anne-Laure</creator><creator>Tschöp, Matthias H.</creator><creator>Müller, Timo D.</creator><general>Elsevier Inc</general><general>Elsevier Science Inc</general><scope>6I.</scope><scope>AAFTH</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><scope>5PM</scope></search><sort><creationdate>201802</creationdate><title>Ghrelin regulation of glucose metabolism</title><author>Poher, Anne-Laure ; Tschöp, Matthias H. ; Müller, Timo D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-592c6306b38997a6e248e43fcbf6a953a517bead55dc41e1ef7c83e212b655193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Carbohydrate Metabolism - drug effects</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Diabetes Mellitus, Type 2 - pathology</topic><topic>Diet-induced obesity</topic><topic>Eating - drug effects</topic><topic>Ghrelin</topic><topic>Ghrelin - metabolism</topic><topic>Ghrelin - therapeutic use</topic><topic>Glucose - metabolism</topic><topic>Humans</topic><topic>Insulin sensitivity</topic><topic>Receptors, Ghrelin - genetics</topic><topic>Receptors, Ghrelin - metabolism</topic><topic>Signal Transduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poher, Anne-Laure</creatorcontrib><creatorcontrib>Tschöp, Matthias H.</creatorcontrib><creatorcontrib>Müller, Timo D.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Peptides (New York, N.Y. : 1980)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poher, Anne-Laure</au><au>Tschöp, Matthias H.</au><au>Müller, Timo D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ghrelin regulation of glucose metabolism</atitle><jtitle>Peptides (New York, N.Y. : 1980)</jtitle><addtitle>Peptides</addtitle><date>2018-02</date><risdate>2018</risdate><volume>100</volume><spage>236</spage><epage>242</epage><pages>236-242</pages><issn>0196-9781</issn><eissn>1873-5169</eissn><abstract>•Ghrelin exerts broad pharmacological effects on systems metabolism.•Ghrelin regulates glucose metabolism and insulin secretion in a variety of species.•Ghrelin inhibition has pharmacological potential for the treatment of T2DM.
The a 28-amino acid peptide ghrelin was discovered in 1999 as a growth hormone (GH) releasing peptide. Soon after its discovery, ghrelin was found to increase body weight and adiposity by acting on the hypothalamic melanocortinergic system. Subsequently, ghrelin was found to exert a series of metabolic effects, overall testifying ghrelin a pleiotropic nature of broad pharmacological interest. Ghrelin acts through the growth hormone secretagogue-receptor (GHS-R), a seven transmembrane G protein-coupled receptor with high expression in the anterior pituitary, pancreatic islets, thyroid gland, heart and various regions of the brain. Among ghrelins numerous metabolic effects are the most prominent the stimulation of appetite via activation of orexigenic hypothalamic neurocircuits and the food-intake independent stimulation of lipogenesis, which both together lead to an increase in body weight and adiposity. Ghrelin effects beyond the regulation of appetite and GH secretion include the regulation of gut motility, sleep-wake rhythm, taste sensation, reward seeking behaviour, and the regulation of glucose metabolism. The latter received recently increasing recognition because pharmacological inhibition of ghrelin signaling might be of therapeutic value to improve insuin resistance and type 2 diabetes. In this review we highlight the multifaceted nature of ghrelin and summarize its glucoregulatory action and discuss the pharmacological value of ghrelin pathway inhibition for the treatment of glucose intolerance and type 2 diabetes.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29412824</pmid><doi>10.1016/j.peptides.2017.12.015</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Carbohydrate Metabolism - drug effects Diabetes Diabetes Mellitus, Type 2 - drug therapy Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - pathology Diet-induced obesity Eating - drug effects Ghrelin Ghrelin - metabolism Ghrelin - therapeutic use Glucose - metabolism Humans Insulin sensitivity Receptors, Ghrelin - genetics Receptors, Ghrelin - metabolism Signal Transduction - drug effects |
title | Ghrelin regulation of glucose metabolism |
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