Regulation of hypothalamic proopiomelanocortin mRNA by leptin in ob/ob mice

The hormone leptin acts on the brain to regulate feeding, metabolism, and reproduction; however, its cellular targets and molecular mechanisms of action remain to be fully elucidated. The melanocortins, which are derived from the precursor proopiomelanocortin (POMC), are also implicated in the physi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Endocrinology (Philadelphia) 1997-11, Vol.138 (11), p.5063-5066
Hauptverfasser: Thornton, J E, Cheung, C C, Clifton, D K, Steiner, R A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 5066
container_issue 11
container_start_page 5063
container_title Endocrinology (Philadelphia)
container_volume 138
creator Thornton, J E
Cheung, C C
Clifton, D K
Steiner, R A
description The hormone leptin acts on the brain to regulate feeding, metabolism, and reproduction; however, its cellular targets and molecular mechanisms of action remain to be fully elucidated. The melanocortins, which are derived from the precursor proopiomelanocortin (POMC), are also implicated in the physiological regulation of body weight. POMC-containing neurons express the leptin receptor, and thus it is conceivable that the POMC gene itself may be part of the signaling pathway involved in leptin's action on the brain. Using in situ hybridization and computerized image analysis, we tested the hypothesis that the POMC gene is a target for regulation by leptin by comparing cellular levels of POMC mRNA in the hypothalamus among groups of leptin-deficient (ob/ob) mice, leptin-treated ob/ob mice, and wild-type controls. POMC mRNA levels were significantly reduced throughout the arcuate nucleus in vehicle-treated ob/ob mice relative to wild-type controls, whereas POMC mRNA levels in leptin-treated ob/ob mice were indistinguishable from wild-type controls. These observations suggest that one or more products of POMC serve as an integrative link between leptin and the central mechanisms governing body weight regulation and reproduction.
doi_str_mv 10.1210/en.138.11.5063
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_79361206</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>79361206</sourcerecordid><originalsourceid>FETCH-LOGICAL-c289t-d9a2705bc3bf870897d9035d318f90e693812ae04f1afb92d95804019a70b8663</originalsourceid><addsrcrecordid>eNotj01LxDAYhHNQ1nX16k3IyVu775ukTXJcFr9wUVj0XJI2dSttU5v20H9vFwsDw8DDMEPIHUKMDGHr2hi5ihHjBFJ-QdYAyCPJmLwi1yH8zFEIwVdkpblQTOCavB3d91ibofIt9SU9TZ0fTqY2TZXTrve-q3zjatP63PdD1dLm-L6jdqK1685xlrdbb-nMuxtyWZo6uNvFN-Tr6fFz_xIdPp5f97tDlDOlh6jQhklIbM5tqSQoLQsNPCk4qlKDSzVXyIwDUaIprWaFThQIQG0kWJWmfEMe_nvngb-jC0PWVCF39TzT-TFkUvMUGZzB-wUcbeOKrOurxvRTtrznf6HbWQ0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79361206</pqid></control><display><type>article</type><title>Regulation of hypothalamic proopiomelanocortin mRNA by leptin in ob/ob mice</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Thornton, J E ; Cheung, C C ; Clifton, D K ; Steiner, R A</creator><creatorcontrib>Thornton, J E ; Cheung, C C ; Clifton, D K ; Steiner, R A</creatorcontrib><description>The hormone leptin acts on the brain to regulate feeding, metabolism, and reproduction; however, its cellular targets and molecular mechanisms of action remain to be fully elucidated. The melanocortins, which are derived from the precursor proopiomelanocortin (POMC), are also implicated in the physiological regulation of body weight. POMC-containing neurons express the leptin receptor, and thus it is conceivable that the POMC gene itself may be part of the signaling pathway involved in leptin's action on the brain. Using in situ hybridization and computerized image analysis, we tested the hypothesis that the POMC gene is a target for regulation by leptin by comparing cellular levels of POMC mRNA in the hypothalamus among groups of leptin-deficient (ob/ob) mice, leptin-treated ob/ob mice, and wild-type controls. POMC mRNA levels were significantly reduced throughout the arcuate nucleus in vehicle-treated ob/ob mice relative to wild-type controls, whereas POMC mRNA levels in leptin-treated ob/ob mice were indistinguishable from wild-type controls. These observations suggest that one or more products of POMC serve as an integrative link between leptin and the central mechanisms governing body weight regulation and reproduction.</description><identifier>ISSN: 0013-7227</identifier><identifier>DOI: 10.1210/en.138.11.5063</identifier><identifier>PMID: 9348241</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Cell Count ; Eating - drug effects ; Hypothalamus - metabolism ; Hypothalamus - pathology ; Leptin ; Male ; Mice ; Mice, Mutant Strains - genetics ; Neurons - metabolism ; Neurons - pathology ; Obesity - genetics ; Obesity - metabolism ; Obesity - pathology ; Pro-Opiomelanocortin - genetics ; Proteins - genetics ; Proteins - metabolism ; Proteins - pharmacology ; RNA, Messenger - metabolism</subject><ispartof>Endocrinology (Philadelphia), 1997-11, Vol.138 (11), p.5063-5066</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c289t-d9a2705bc3bf870897d9035d318f90e693812ae04f1afb92d95804019a70b8663</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9348241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thornton, J E</creatorcontrib><creatorcontrib>Cheung, C C</creatorcontrib><creatorcontrib>Clifton, D K</creatorcontrib><creatorcontrib>Steiner, R A</creatorcontrib><title>Regulation of hypothalamic proopiomelanocortin mRNA by leptin in ob/ob mice</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>The hormone leptin acts on the brain to regulate feeding, metabolism, and reproduction; however, its cellular targets and molecular mechanisms of action remain to be fully elucidated. The melanocortins, which are derived from the precursor proopiomelanocortin (POMC), are also implicated in the physiological regulation of body weight. POMC-containing neurons express the leptin receptor, and thus it is conceivable that the POMC gene itself may be part of the signaling pathway involved in leptin's action on the brain. Using in situ hybridization and computerized image analysis, we tested the hypothesis that the POMC gene is a target for regulation by leptin by comparing cellular levels of POMC mRNA in the hypothalamus among groups of leptin-deficient (ob/ob) mice, leptin-treated ob/ob mice, and wild-type controls. POMC mRNA levels were significantly reduced throughout the arcuate nucleus in vehicle-treated ob/ob mice relative to wild-type controls, whereas POMC mRNA levels in leptin-treated ob/ob mice were indistinguishable from wild-type controls. These observations suggest that one or more products of POMC serve as an integrative link between leptin and the central mechanisms governing body weight regulation and reproduction.</description><subject>Animals</subject><subject>Cell Count</subject><subject>Eating - drug effects</subject><subject>Hypothalamus - metabolism</subject><subject>Hypothalamus - pathology</subject><subject>Leptin</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Mutant Strains - genetics</subject><subject>Neurons - metabolism</subject><subject>Neurons - pathology</subject><subject>Obesity - genetics</subject><subject>Obesity - metabolism</subject><subject>Obesity - pathology</subject><subject>Pro-Opiomelanocortin - genetics</subject><subject>Proteins - genetics</subject><subject>Proteins - metabolism</subject><subject>Proteins - pharmacology</subject><subject>RNA, Messenger - metabolism</subject><issn>0013-7227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotj01LxDAYhHNQ1nX16k3IyVu775ukTXJcFr9wUVj0XJI2dSttU5v20H9vFwsDw8DDMEPIHUKMDGHr2hi5ihHjBFJ-QdYAyCPJmLwi1yH8zFEIwVdkpblQTOCavB3d91ibofIt9SU9TZ0fTqY2TZXTrve-q3zjatP63PdD1dLm-L6jdqK1685xlrdbb-nMuxtyWZo6uNvFN-Tr6fFz_xIdPp5f97tDlDOlh6jQhklIbM5tqSQoLQsNPCk4qlKDSzVXyIwDUaIprWaFThQIQG0kWJWmfEMe_nvngb-jC0PWVCF39TzT-TFkUvMUGZzB-wUcbeOKrOurxvRTtrznf6HbWQ0</recordid><startdate>199711</startdate><enddate>199711</enddate><creator>Thornton, J E</creator><creator>Cheung, C C</creator><creator>Clifton, D K</creator><creator>Steiner, R A</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>199711</creationdate><title>Regulation of hypothalamic proopiomelanocortin mRNA by leptin in ob/ob mice</title><author>Thornton, J E ; Cheung, C C ; Clifton, D K ; Steiner, R A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c289t-d9a2705bc3bf870897d9035d318f90e693812ae04f1afb92d95804019a70b8663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Cell Count</topic><topic>Eating - drug effects</topic><topic>Hypothalamus - metabolism</topic><topic>Hypothalamus - pathology</topic><topic>Leptin</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Mutant Strains - genetics</topic><topic>Neurons - metabolism</topic><topic>Neurons - pathology</topic><topic>Obesity - genetics</topic><topic>Obesity - metabolism</topic><topic>Obesity - pathology</topic><topic>Pro-Opiomelanocortin - genetics</topic><topic>Proteins - genetics</topic><topic>Proteins - metabolism</topic><topic>Proteins - pharmacology</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thornton, J E</creatorcontrib><creatorcontrib>Cheung, C C</creatorcontrib><creatorcontrib>Clifton, D K</creatorcontrib><creatorcontrib>Steiner, R A</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>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thornton, J E</au><au>Cheung, C C</au><au>Clifton, D K</au><au>Steiner, R A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of hypothalamic proopiomelanocortin mRNA by leptin in ob/ob mice</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>1997-11</date><risdate>1997</risdate><volume>138</volume><issue>11</issue><spage>5063</spage><epage>5066</epage><pages>5063-5066</pages><issn>0013-7227</issn><abstract>The hormone leptin acts on the brain to regulate feeding, metabolism, and reproduction; however, its cellular targets and molecular mechanisms of action remain to be fully elucidated. The melanocortins, which are derived from the precursor proopiomelanocortin (POMC), are also implicated in the physiological regulation of body weight. POMC-containing neurons express the leptin receptor, and thus it is conceivable that the POMC gene itself may be part of the signaling pathway involved in leptin's action on the brain. Using in situ hybridization and computerized image analysis, we tested the hypothesis that the POMC gene is a target for regulation by leptin by comparing cellular levels of POMC mRNA in the hypothalamus among groups of leptin-deficient (ob/ob) mice, leptin-treated ob/ob mice, and wild-type controls. POMC mRNA levels were significantly reduced throughout the arcuate nucleus in vehicle-treated ob/ob mice relative to wild-type controls, whereas POMC mRNA levels in leptin-treated ob/ob mice were indistinguishable from wild-type controls. These observations suggest that one or more products of POMC serve as an integrative link between leptin and the central mechanisms governing body weight regulation and reproduction.</abstract><cop>United States</cop><pmid>9348241</pmid><doi>10.1210/en.138.11.5063</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0013-7227
ispartof Endocrinology (Philadelphia), 1997-11, Vol.138 (11), p.5063-5066
issn 0013-7227
language eng
recordid cdi_proquest_miscellaneous_79361206
source Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Animals
Cell Count
Eating - drug effects
Hypothalamus - metabolism
Hypothalamus - pathology
Leptin
Male
Mice
Mice, Mutant Strains - genetics
Neurons - metabolism
Neurons - pathology
Obesity - genetics
Obesity - metabolism
Obesity - pathology
Pro-Opiomelanocortin - genetics
Proteins - genetics
Proteins - metabolism
Proteins - pharmacology
RNA, Messenger - metabolism
title Regulation of hypothalamic proopiomelanocortin mRNA by leptin in ob/ob mice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T17%3A53%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regulation%20of%20hypothalamic%20proopiomelanocortin%20mRNA%20by%20leptin%20in%20ob/ob%20mice&rft.jtitle=Endocrinology%20(Philadelphia)&rft.au=Thornton,%20J%20E&rft.date=1997-11&rft.volume=138&rft.issue=11&rft.spage=5063&rft.epage=5066&rft.pages=5063-5066&rft.issn=0013-7227&rft_id=info:doi/10.1210/en.138.11.5063&rft_dat=%3Cproquest_pubme%3E79361206%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=79361206&rft_id=info:pmid/9348241&rfr_iscdi=true