The hypothalamic RFamide, QRFP, increases feeding and locomotor activity: The role of Gpr103 and orexin receptors
Here we show that central administration of pyroglutamylated arginine-phenylamine-amide peptide (QRFP/26RFa) increases both food intake and locomotor activity, without any significant effect on energy expenditure, thermogenesis or reward. Germline knock out of either of the mouse QRFP receptor ortho...
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description | Here we show that central administration of pyroglutamylated arginine-phenylamine-amide peptide (QRFP/26RFa) increases both food intake and locomotor activity, without any significant effect on energy expenditure, thermogenesis or reward. Germline knock out of either of the mouse QRFP receptor orthologs, Gpr103a and Gpr103b, did not produce a metabolic phenotype. However, both receptors are required for the effect of centrally administered QRFP to increase feeding and locomotor activity. As central injection of QRFP activated orexin/hypocretin neurons in the lateral hypothalamus, we compared the action of QRFP and orexin on behaviour. Both peptides increased arousal and locomotor activity. However, while orexin increased consummatory behaviour, QRFP also affected other appetitive behaviours. Furthermore, the feeding but not the locomotor response to QRFP, was blocked by co-administration of an orexin receptor 1 antagonist. These results suggest that QRFP agonism induces both appetitive and consummatory behaviour, but only the latter is dependent on orexin/hypocretin receptor signalling. |
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Germline knock out of either of the mouse QRFP receptor orthologs, Gpr103a and Gpr103b, did not produce a metabolic phenotype. However, both receptors are required for the effect of centrally administered QRFP to increase feeding and locomotor activity. As central injection of QRFP activated orexin/hypocretin neurons in the lateral hypothalamus, we compared the action of QRFP and orexin on behaviour. Both peptides increased arousal and locomotor activity. However, while orexin increased consummatory behaviour, QRFP also affected other appetitive behaviours. Furthermore, the feeding but not the locomotor response to QRFP, was blocked by co-administration of an orexin receptor 1 antagonist. These results suggest that QRFP agonism induces both appetitive and consummatory behaviour, but only the latter is dependent on orexin/hypocretin receptor signalling.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0275604</identifier><identifier>PMID: 36251705</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Analysis ; Appetite ; Arousal ; Binding sites ; Biology and Life Sciences ; Body fat ; Consummatory behavior ; Energy ; Energy expenditure ; Feeding ; Feeding behavior ; Food ; Food habits ; Food intake ; Genes ; Genotype & phenotype ; Health aspects ; Hypothalamus ; Hypothalamus (lateral) ; Laboratory animals ; Locomotor activity ; Medicine and Health Sciences ; Metabolism ; Neuropeptides ; Orexin receptors ; Orexins ; Peptides ; Phenotypes ; Receptors ; Reinforcement ; Social Sciences ; Thermogenesis</subject><ispartof>PloS one, 2022-10, Vol.17 (10), p.e0275604-e0275604</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Cook et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 Cook et al 2022 Cook et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c669t-adea503e254c112653a0a75cc4d3d7c5fda7345936b6b183d4642943c65afaa53</citedby><cites>FETCH-LOGICAL-c669t-adea503e254c112653a0a75cc4d3d7c5fda7345936b6b183d4642943c65afaa53</cites><orcidid>0000-0001-5318-5473</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576062/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576062/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids></links><search><contributor>Aguila, Marcia B.</contributor><creatorcontrib>Cook, Chris</creatorcontrib><creatorcontrib>Nunn, Nicolas</creatorcontrib><creatorcontrib>Worth, Amy A</creatorcontrib><creatorcontrib>Bechtold, David A</creatorcontrib><creatorcontrib>Suter, Todd</creatorcontrib><creatorcontrib>Gackeheimer, Susan</creatorcontrib><creatorcontrib>Foltz, Lisa</creatorcontrib><creatorcontrib>Emmerson, Paul J</creatorcontrib><creatorcontrib>Statnick, Michael A</creatorcontrib><creatorcontrib>Luckman, Simon M</creatorcontrib><title>The hypothalamic RFamide, QRFP, increases feeding and locomotor activity: The role of Gpr103 and orexin receptors</title><title>PloS one</title><description>Here we show that central administration of pyroglutamylated arginine-phenylamine-amide peptide (QRFP/26RFa) increases both food intake and locomotor activity, without any significant effect on energy expenditure, thermogenesis or reward. Germline knock out of either of the mouse QRFP receptor orthologs, Gpr103a and Gpr103b, did not produce a metabolic phenotype. However, both receptors are required for the effect of centrally administered QRFP to increase feeding and locomotor activity. As central injection of QRFP activated orexin/hypocretin neurons in the lateral hypothalamus, we compared the action of QRFP and orexin on behaviour. Both peptides increased arousal and locomotor activity. However, while orexin increased consummatory behaviour, QRFP also affected other appetitive behaviours. Furthermore, the feeding but not the locomotor response to QRFP, was blocked by co-administration of an orexin receptor 1 antagonist. These results suggest that QRFP agonism induces both appetitive and consummatory behaviour, but only the latter is dependent on orexin/hypocretin receptor signalling.</description><subject>Analysis</subject><subject>Appetite</subject><subject>Arousal</subject><subject>Binding sites</subject><subject>Biology and Life Sciences</subject><subject>Body fat</subject><subject>Consummatory behavior</subject><subject>Energy</subject><subject>Energy expenditure</subject><subject>Feeding</subject><subject>Feeding behavior</subject><subject>Food</subject><subject>Food habits</subject><subject>Food intake</subject><subject>Genes</subject><subject>Genotype & phenotype</subject><subject>Health aspects</subject><subject>Hypothalamus</subject><subject>Hypothalamus (lateral)</subject><subject>Laboratory animals</subject><subject>Locomotor activity</subject><subject>Medicine and Health Sciences</subject><subject>Metabolism</subject><subject>Neuropeptides</subject><subject>Orexin 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hypothalamic RFamide, QRFP, increases feeding and locomotor activity: The role of Gpr103 and orexin receptors</title><author>Cook, Chris ; Nunn, Nicolas ; Worth, Amy A ; Bechtold, David A ; Suter, Todd ; Gackeheimer, Susan ; Foltz, Lisa ; Emmerson, Paul J ; Statnick, Michael A ; Luckman, Simon M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c669t-adea503e254c112653a0a75cc4d3d7c5fda7345936b6b183d4642943c65afaa53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analysis</topic><topic>Appetite</topic><topic>Arousal</topic><topic>Binding sites</topic><topic>Biology and Life Sciences</topic><topic>Body fat</topic><topic>Consummatory behavior</topic><topic>Energy</topic><topic>Energy expenditure</topic><topic>Feeding</topic><topic>Feeding behavior</topic><topic>Food</topic><topic>Food habits</topic><topic>Food intake</topic><topic>Genes</topic><topic>Genotype & phenotype</topic><topic>Health aspects</topic><topic>Hypothalamus</topic><topic>Hypothalamus (lateral)</topic><topic>Laboratory animals</topic><topic>Locomotor activity</topic><topic>Medicine and Health Sciences</topic><topic>Metabolism</topic><topic>Neuropeptides</topic><topic>Orexin receptors</topic><topic>Orexins</topic><topic>Peptides</topic><topic>Phenotypes</topic><topic>Receptors</topic><topic>Reinforcement</topic><topic>Social Sciences</topic><topic>Thermogenesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cook, Chris</creatorcontrib><creatorcontrib>Nunn, Nicolas</creatorcontrib><creatorcontrib>Worth, Amy A</creatorcontrib><creatorcontrib>Bechtold, David A</creatorcontrib><creatorcontrib>Suter, Todd</creatorcontrib><creatorcontrib>Gackeheimer, Susan</creatorcontrib><creatorcontrib>Foltz, Lisa</creatorcontrib><creatorcontrib>Emmerson, Paul J</creatorcontrib><creatorcontrib>Statnick, Michael 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of Gpr103 and orexin receptors</atitle><jtitle>PloS one</jtitle><date>2022-10-17</date><risdate>2022</risdate><volume>17</volume><issue>10</issue><spage>e0275604</spage><epage>e0275604</epage><pages>e0275604-e0275604</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Here we show that central administration of pyroglutamylated arginine-phenylamine-amide peptide (QRFP/26RFa) increases both food intake and locomotor activity, without any significant effect on energy expenditure, thermogenesis or reward. Germline knock out of either of the mouse QRFP receptor orthologs, Gpr103a and Gpr103b, did not produce a metabolic phenotype. However, both receptors are required for the effect of centrally administered QRFP to increase feeding and locomotor activity. As central injection of QRFP activated orexin/hypocretin neurons in the lateral hypothalamus, we compared the action of QRFP and orexin on behaviour. Both peptides increased arousal and locomotor activity. However, while orexin increased consummatory behaviour, QRFP also affected other appetitive behaviours. Furthermore, the feeding but not the locomotor response to QRFP, was blocked by co-administration of an orexin receptor 1 antagonist. These results suggest that QRFP agonism induces both appetitive and consummatory behaviour, but only the latter is dependent on orexin/hypocretin receptor signalling.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>36251705</pmid><doi>10.1371/journal.pone.0275604</doi><tpages>e0275604</tpages><orcidid>https://orcid.org/0000-0001-5318-5473</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Appetite Arousal Binding sites Biology and Life Sciences Body fat Consummatory behavior Energy Energy expenditure Feeding Feeding behavior Food Food habits Food intake Genes Genotype & phenotype Health aspects Hypothalamus Hypothalamus (lateral) Laboratory animals Locomotor activity Medicine and Health Sciences Metabolism Neuropeptides Orexin receptors Orexins Peptides Phenotypes Receptors Reinforcement Social Sciences Thermogenesis |
title | The hypothalamic RFamide, QRFP, increases feeding and locomotor activity: The role of Gpr103 and orexin receptors |
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