Leptin coordinates efferent sympathetic outflow to the white adipose tissue through the midbrain centrally-projecting Edinger-Westphal nucleus in male rats
The centrally-projecting Edinger-Westphal nucleus (EWcp) hosts a large population of neurons expressing urocortin 1 (Ucn1) and about half of these neurons also express the leptin receptor (LepRb). Previously, we have shown that the peripheral adiposity hormone leptin signaling energy surfeit modulat...
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Veröffentlicht in: | Neuropharmacology 2022-03, Vol.205, p.108898-108898, Article 108898 |
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creator | Xu, Lu Füredi, Nóra Lutter, Christoph Geenen, Bram Pétervári, Erika Balaskó, Márta Dénes, Ádám Kovács, Krisztina J. Gaszner, Balázs Kozicz, Tamás |
description | The centrally-projecting Edinger-Westphal nucleus (EWcp) hosts a large population of neurons expressing urocortin 1 (Ucn1) and about half of these neurons also express the leptin receptor (LepRb). Previously, we have shown that the peripheral adiposity hormone leptin signaling energy surfeit modulates EWcp neurons' activity. Here, we hypothesized that Ucn1/LepRb neurons in the EWcp would act as a crucial neuronal node in the brain-white adipose tissue (WAT) axis modulating efferent sympathetic outflow to the WAT. We showed that leptin bound to neurons of the EWcp stimulated STAT3 phosphorylation, and increased Ucn1-production in a time-dependent manner. Besides, retrograde transneuronal tract-tracing using pseudorabies virus (PRV) identified EWcp Ucn1 neurons connected to WAT. Interestingly, reducing EWcp Ucn1 contents by ablating EWcp LepRb-positive neurons with leptin-saporin, did not affect food intake and body weight gain, but substantially (+26%) increased WAT weight accompanied by a higher plasma leptin level and changed plasma lipid profile. We also found that ablation of EWcp Ucn1/LepRb neurons resulted in lower respiratory quotient and oxygen consumption one week after surgery, but was comparable to sham values after 3 and 5 weeks of surgery. Taken together, we report that EWcp/LepRb/Ucn1 neurons not only respond to leptin signaling but also control WAT size and fat metabolism without altering food intake. These data suggest the existence of a EWcp-WAT circuitry allowing an organism to recruit fuels without being able to eat in situations such as the fight-or-flight response.
[Display omitted]
•Leptin bound to EWcp stimulates STAT3 phosphorylation and urocortin 1 production.•Pseudorabies virus labeling proves that EWcp Ucn1 neurons are connected to WAT.•EWcp Ucn1 neuron ablation increases WAT weight and plasma leptin level.•EWcp Ucn1 neuron loss reduces respiratory quotient and oxygen consumption. |
doi_str_mv | 10.1016/j.neuropharm.2021.108898 |
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[Display omitted]
•Leptin bound to EWcp stimulates STAT3 phosphorylation and urocortin 1 production.•Pseudorabies virus labeling proves that EWcp Ucn1 neurons are connected to WAT.•EWcp Ucn1 neuron ablation increases WAT weight and plasma leptin level.•EWcp Ucn1 neuron loss reduces respiratory quotient and oxygen consumption.</description><identifier>ISSN: 0028-3908</identifier><identifier>EISSN: 1873-7064</identifier><identifier>DOI: 10.1016/j.neuropharm.2021.108898</identifier><identifier>PMID: 34861283</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adipose Tissue, White - metabolism ; Animals ; Edinger-Westphal Nucleus - metabolism ; Energy metabolism ; Herpesvirus 1, Suid ; Leptin - metabolism ; Leptin receptor ; Male ; Pseudorabies virus ; Rats ; Receptors, Leptin - metabolism ; STAT3 ; STAT3 Transcription Factor - metabolism ; Sympathetic Nervous System - metabolism ; Urocortin 1 ; Urocortins - metabolism</subject><ispartof>Neuropharmacology, 2022-03, Vol.205, p.108898-108898, Article 108898</ispartof><rights>2021 The Authors</rights><rights>Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-53878af3766722a82f08b3baacffc8bccfb0e6656a8d6f3416abb9dc79e09ef83</citedby><cites>FETCH-LOGICAL-c424t-53878af3766722a82f08b3baacffc8bccfb0e6656a8d6f3416abb9dc79e09ef83</cites><orcidid>0000-0003-2830-2732 ; 0000-0001-7838-3097 ; 0000-0001-6915-4364</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuropharm.2021.108898$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34861283$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Lu</creatorcontrib><creatorcontrib>Füredi, Nóra</creatorcontrib><creatorcontrib>Lutter, Christoph</creatorcontrib><creatorcontrib>Geenen, Bram</creatorcontrib><creatorcontrib>Pétervári, Erika</creatorcontrib><creatorcontrib>Balaskó, Márta</creatorcontrib><creatorcontrib>Dénes, Ádám</creatorcontrib><creatorcontrib>Kovács, Krisztina J.</creatorcontrib><creatorcontrib>Gaszner, Balázs</creatorcontrib><creatorcontrib>Kozicz, Tamás</creatorcontrib><title>Leptin coordinates efferent sympathetic outflow to the white adipose tissue through the midbrain centrally-projecting Edinger-Westphal nucleus in male rats</title><title>Neuropharmacology</title><addtitle>Neuropharmacology</addtitle><description>The centrally-projecting Edinger-Westphal nucleus (EWcp) hosts a large population of neurons expressing urocortin 1 (Ucn1) and about half of these neurons also express the leptin receptor (LepRb). Previously, we have shown that the peripheral adiposity hormone leptin signaling energy surfeit modulates EWcp neurons' activity. Here, we hypothesized that Ucn1/LepRb neurons in the EWcp would act as a crucial neuronal node in the brain-white adipose tissue (WAT) axis modulating efferent sympathetic outflow to the WAT. We showed that leptin bound to neurons of the EWcp stimulated STAT3 phosphorylation, and increased Ucn1-production in a time-dependent manner. Besides, retrograde transneuronal tract-tracing using pseudorabies virus (PRV) identified EWcp Ucn1 neurons connected to WAT. Interestingly, reducing EWcp Ucn1 contents by ablating EWcp LepRb-positive neurons with leptin-saporin, did not affect food intake and body weight gain, but substantially (+26%) increased WAT weight accompanied by a higher plasma leptin level and changed plasma lipid profile. We also found that ablation of EWcp Ucn1/LepRb neurons resulted in lower respiratory quotient and oxygen consumption one week after surgery, but was comparable to sham values after 3 and 5 weeks of surgery. Taken together, we report that EWcp/LepRb/Ucn1 neurons not only respond to leptin signaling but also control WAT size and fat metabolism without altering food intake. These data suggest the existence of a EWcp-WAT circuitry allowing an organism to recruit fuels without being able to eat in situations such as the fight-or-flight response.
[Display omitted]
•Leptin bound to EWcp stimulates STAT3 phosphorylation and urocortin 1 production.•Pseudorabies virus labeling proves that EWcp Ucn1 neurons are connected to WAT.•EWcp Ucn1 neuron ablation increases WAT weight and plasma leptin level.•EWcp Ucn1 neuron loss reduces respiratory quotient and oxygen consumption.</description><subject>Adipose Tissue, White - metabolism</subject><subject>Animals</subject><subject>Edinger-Westphal Nucleus - metabolism</subject><subject>Energy metabolism</subject><subject>Herpesvirus 1, Suid</subject><subject>Leptin - metabolism</subject><subject>Leptin receptor</subject><subject>Male</subject><subject>Pseudorabies virus</subject><subject>Rats</subject><subject>Receptors, Leptin - metabolism</subject><subject>STAT3</subject><subject>STAT3 Transcription Factor - metabolism</subject><subject>Sympathetic Nervous System - metabolism</subject><subject>Urocortin 1</subject><subject>Urocortins - metabolism</subject><issn>0028-3908</issn><issn>1873-7064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUcuO0zAUtRCI6Qz8AvKSTTp-pI6zhNEMIFViA2JpOc5148qJgx-M-i38LC4dYMnqSlfncc89CGFKtpRQcXvcLlBiWCcd5y0jjNa1lL18hjZUdrzpiGifow0hTDa8J_IKXad0JIS0ksqX6Iq3UlAm-Qb93MOa3YJNCHF0i86QMFgLEZaM02ledZ4gO4NDydaHR5wDrhv8OLkMWI9uDQlwdimVOqYYymH6DZjdOER9Vq5KUXt_atYYjmCq2wHfV68DxOYbpFxTeLwU46EkXAmz9oCjzukVemG1T_D6ad6grw_3X-4-NvvPHz7dvds3pmVtbnZcdlJb3gnRMaYls0QOfNDaWGvkYIwdCAixE1qOwvKWCj0M_Wi6HkgPVvIb9PaiWw_8XupFanbJgPd6gVCSYoKInu2IoBUqL1ATQ0oRrFqjm3U8KUrUuRp1VP-qUedq1KWaSn3z5FKGGca_xD9dVMD7CwBq1h8OokrGwWJgdLG-TY3B_d_lFzosqu0</recordid><startdate>20220301</startdate><enddate>20220301</enddate><creator>Xu, Lu</creator><creator>Füredi, Nóra</creator><creator>Lutter, Christoph</creator><creator>Geenen, Bram</creator><creator>Pétervári, Erika</creator><creator>Balaskó, Márta</creator><creator>Dénes, Ádám</creator><creator>Kovács, Krisztina J.</creator><creator>Gaszner, Balázs</creator><creator>Kozicz, Tamás</creator><general>Elsevier Ltd</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><orcidid>https://orcid.org/0000-0003-2830-2732</orcidid><orcidid>https://orcid.org/0000-0001-7838-3097</orcidid><orcidid>https://orcid.org/0000-0001-6915-4364</orcidid></search><sort><creationdate>20220301</creationdate><title>Leptin coordinates efferent sympathetic outflow to the white adipose tissue through the midbrain centrally-projecting Edinger-Westphal nucleus in male rats</title><author>Xu, Lu ; Füredi, Nóra ; Lutter, Christoph ; Geenen, Bram ; Pétervári, Erika ; Balaskó, Márta ; Dénes, Ádám ; Kovács, Krisztina J. ; Gaszner, Balázs ; Kozicz, Tamás</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-53878af3766722a82f08b3baacffc8bccfb0e6656a8d6f3416abb9dc79e09ef83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adipose Tissue, White - metabolism</topic><topic>Animals</topic><topic>Edinger-Westphal Nucleus - metabolism</topic><topic>Energy metabolism</topic><topic>Herpesvirus 1, Suid</topic><topic>Leptin - metabolism</topic><topic>Leptin receptor</topic><topic>Male</topic><topic>Pseudorabies virus</topic><topic>Rats</topic><topic>Receptors, Leptin - metabolism</topic><topic>STAT3</topic><topic>STAT3 Transcription Factor - metabolism</topic><topic>Sympathetic Nervous System - metabolism</topic><topic>Urocortin 1</topic><topic>Urocortins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Lu</creatorcontrib><creatorcontrib>Füredi, Nóra</creatorcontrib><creatorcontrib>Lutter, Christoph</creatorcontrib><creatorcontrib>Geenen, Bram</creatorcontrib><creatorcontrib>Pétervári, Erika</creatorcontrib><creatorcontrib>Balaskó, Márta</creatorcontrib><creatorcontrib>Dénes, Ádám</creatorcontrib><creatorcontrib>Kovács, Krisztina J.</creatorcontrib><creatorcontrib>Gaszner, Balázs</creatorcontrib><creatorcontrib>Kozicz, Tamás</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><jtitle>Neuropharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Lu</au><au>Füredi, Nóra</au><au>Lutter, Christoph</au><au>Geenen, Bram</au><au>Pétervári, Erika</au><au>Balaskó, Márta</au><au>Dénes, Ádám</au><au>Kovács, Krisztina J.</au><au>Gaszner, Balázs</au><au>Kozicz, Tamás</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leptin coordinates efferent sympathetic outflow to the white adipose tissue through the midbrain centrally-projecting Edinger-Westphal nucleus in male rats</atitle><jtitle>Neuropharmacology</jtitle><addtitle>Neuropharmacology</addtitle><date>2022-03-01</date><risdate>2022</risdate><volume>205</volume><spage>108898</spage><epage>108898</epage><pages>108898-108898</pages><artnum>108898</artnum><issn>0028-3908</issn><eissn>1873-7064</eissn><abstract>The centrally-projecting Edinger-Westphal nucleus (EWcp) hosts a large population of neurons expressing urocortin 1 (Ucn1) and about half of these neurons also express the leptin receptor (LepRb). Previously, we have shown that the peripheral adiposity hormone leptin signaling energy surfeit modulates EWcp neurons' activity. Here, we hypothesized that Ucn1/LepRb neurons in the EWcp would act as a crucial neuronal node in the brain-white adipose tissue (WAT) axis modulating efferent sympathetic outflow to the WAT. We showed that leptin bound to neurons of the EWcp stimulated STAT3 phosphorylation, and increased Ucn1-production in a time-dependent manner. Besides, retrograde transneuronal tract-tracing using pseudorabies virus (PRV) identified EWcp Ucn1 neurons connected to WAT. Interestingly, reducing EWcp Ucn1 contents by ablating EWcp LepRb-positive neurons with leptin-saporin, did not affect food intake and body weight gain, but substantially (+26%) increased WAT weight accompanied by a higher plasma leptin level and changed plasma lipid profile. We also found that ablation of EWcp Ucn1/LepRb neurons resulted in lower respiratory quotient and oxygen consumption one week after surgery, but was comparable to sham values after 3 and 5 weeks of surgery. Taken together, we report that EWcp/LepRb/Ucn1 neurons not only respond to leptin signaling but also control WAT size and fat metabolism without altering food intake. These data suggest the existence of a EWcp-WAT circuitry allowing an organism to recruit fuels without being able to eat in situations such as the fight-or-flight response.
[Display omitted]
•Leptin bound to EWcp stimulates STAT3 phosphorylation and urocortin 1 production.•Pseudorabies virus labeling proves that EWcp Ucn1 neurons are connected to WAT.•EWcp Ucn1 neuron ablation increases WAT weight and plasma leptin level.•EWcp Ucn1 neuron loss reduces respiratory quotient and oxygen consumption.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>34861283</pmid><doi>10.1016/j.neuropharm.2021.108898</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2830-2732</orcidid><orcidid>https://orcid.org/0000-0001-7838-3097</orcidid><orcidid>https://orcid.org/0000-0001-6915-4364</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adipose Tissue, White - metabolism Animals Edinger-Westphal Nucleus - metabolism Energy metabolism Herpesvirus 1, Suid Leptin - metabolism Leptin receptor Male Pseudorabies virus Rats Receptors, Leptin - metabolism STAT3 STAT3 Transcription Factor - metabolism Sympathetic Nervous System - metabolism Urocortin 1 Urocortins - metabolism |
title | Leptin coordinates efferent sympathetic outflow to the white adipose tissue through the midbrain centrally-projecting Edinger-Westphal nucleus in male rats |
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