Suprachiasmatic Nucleus Interaction with the Arcuate Nucleus; Essential for Organizing Physiological Rhythms
The suprachiasmatic nucleus (SCN) is generally considered the master clock, independently driving all circadian rhythms. We recently demonstrated the SCN receives metabolic and cardiovascular feedback adeptly altering its neuronal activity. In the present study, we show that microcuts effectively re...
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description | The suprachiasmatic nucleus (SCN) is generally considered the master clock, independently driving all circadian rhythms. We recently demonstrated the SCN receives metabolic and cardiovascular feedback adeptly altering its neuronal activity. In the present study, we show that microcuts effectively removing SCN-arcuate nucleus (ARC) interconnectivity in Wistar rats result in a loss of rhythmicity in locomotor activity, corticosterone levels, and body temperature in constant dark (DD) conditions. Elimination of these reciprocal connections did not affect SCN clock gene rhythmicity but did cause the ARC to desynchronize. Moreover, unilateral SCN lesions with contralateral retrochiasmatic microcuts resulted in identical arrhythmicity, proving that for the expression of physiological rhythms this reciprocal SCN-ARC interaction is essential. The unaltered SCN c-Fos expression following glucose administration in disconnected animals as compared to a significant decrease in controls demonstrates the importance of the ARC as metabolic modulator of SCN neuronal activity. Together, these results indicate that the SCN is more than an autonomous clock, and forms an essential component of a larger network controlling homeostasis. The present novel findings illustrate how an imbalance between SCN and ARC communication through circadian disruption could be involved in the etiology of metabolic disorders. |
doi_str_mv | 10.1523/ENEURO.0028-17.2017 |
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We recently demonstrated the SCN receives metabolic and cardiovascular feedback adeptly altering its neuronal activity. In the present study, we show that microcuts effectively removing SCN-arcuate nucleus (ARC) interconnectivity in Wistar rats result in a loss of rhythmicity in locomotor activity, corticosterone levels, and body temperature in constant dark (DD) conditions. Elimination of these reciprocal connections did not affect SCN clock gene rhythmicity but did cause the ARC to desynchronize. Moreover, unilateral SCN lesions with contralateral retrochiasmatic microcuts resulted in identical arrhythmicity, proving that for the expression of physiological rhythms this reciprocal SCN-ARC interaction is essential. The unaltered SCN c-Fos expression following glucose administration in disconnected animals as compared to a significant decrease in controls demonstrates the importance of the ARC as metabolic modulator of SCN neuronal activity. Together, these results indicate that the SCN is more than an autonomous clock, and forms an essential component of a larger network controlling homeostasis. The present novel findings illustrate how an imbalance between SCN and ARC communication through circadian disruption could be involved in the etiology of metabolic disorders.</description><identifier>ISSN: 2373-2822</identifier><identifier>EISSN: 2373-2822</identifier><identifier>DOI: 10.1523/ENEURO.0028-17.2017</identifier><identifier>PMID: 28374011</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Animals ; Arcuate Nucleus of Hypothalamus - pathology ; Arcuate Nucleus of Hypothalamus - physiology ; Arcuate Nucleus of Hypothalamus - physiopathology ; Body Temperature - physiology ; Circadian Rhythm - physiology ; Corticosterone - metabolism ; Glucose - administration & dosage ; Glucose - metabolism ; Liver - metabolism ; Models, Animal ; Motor Activity - physiology ; Neural Pathways - physiology ; Neural Pathways - physiopathology ; Neurons - metabolism ; Neurons - pathology ; New Research ; Period Circadian Proteins - metabolism ; Proto-Oncogene Proteins c-fos - metabolism ; Rats, Wistar ; Suprachiasmatic Nucleus - pathology ; Suprachiasmatic Nucleus - physiology ; Suprachiasmatic Nucleus - physiopathology</subject><ispartof>eNeuro, 2017-03, Vol.4 (2), p.ENEURO.0028-17.2017</ispartof><rights>Copyright © 2017 Buijs et al. 2017 Buijs et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-fd1d146796d5621dd73eb28e7f9811fb2ce569a39aab0ea9c33636c8db9b6b6e3</citedby><cites>FETCH-LOGICAL-c405t-fd1d146796d5621dd73eb28e7f9811fb2ce569a39aab0ea9c33636c8db9b6b6e3</cites><orcidid>0000-0001-6362-7968 ; 0000-0003-3894-4632 ; 0000-0002-5932-9148 ; 0000-0001-9606-8453 ; 0000-0002-2974-7875</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/PMC5364589/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364589/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28374011$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Buijs, Frederik N</creatorcontrib><creatorcontrib>Guzmán-Ruiz, Mara</creatorcontrib><creatorcontrib>León-Mercado, Luis</creatorcontrib><creatorcontrib>Basualdo, Mari Carmen</creatorcontrib><creatorcontrib>Escobar, Carolina</creatorcontrib><creatorcontrib>Kalsbeek, Andries</creatorcontrib><creatorcontrib>Buijs, Ruud M</creatorcontrib><title>Suprachiasmatic Nucleus Interaction with the Arcuate Nucleus; Essential for Organizing Physiological Rhythms</title><title>eNeuro</title><addtitle>eNeuro</addtitle><description>The suprachiasmatic nucleus (SCN) is generally considered the master clock, independently driving all circadian rhythms. We recently demonstrated the SCN receives metabolic and cardiovascular feedback adeptly altering its neuronal activity. In the present study, we show that microcuts effectively removing SCN-arcuate nucleus (ARC) interconnectivity in Wistar rats result in a loss of rhythmicity in locomotor activity, corticosterone levels, and body temperature in constant dark (DD) conditions. Elimination of these reciprocal connections did not affect SCN clock gene rhythmicity but did cause the ARC to desynchronize. Moreover, unilateral SCN lesions with contralateral retrochiasmatic microcuts resulted in identical arrhythmicity, proving that for the expression of physiological rhythms this reciprocal SCN-ARC interaction is essential. The unaltered SCN c-Fos expression following glucose administration in disconnected animals as compared to a significant decrease in controls demonstrates the importance of the ARC as metabolic modulator of SCN neuronal activity. Together, these results indicate that the SCN is more than an autonomous clock, and forms an essential component of a larger network controlling homeostasis. The present novel findings illustrate how an imbalance between SCN and ARC communication through circadian disruption could be involved in the etiology of metabolic disorders.</description><subject>Animals</subject><subject>Arcuate Nucleus of Hypothalamus - pathology</subject><subject>Arcuate Nucleus of Hypothalamus - physiology</subject><subject>Arcuate Nucleus of Hypothalamus - physiopathology</subject><subject>Body Temperature - physiology</subject><subject>Circadian Rhythm - physiology</subject><subject>Corticosterone - metabolism</subject><subject>Glucose - administration & dosage</subject><subject>Glucose - metabolism</subject><subject>Liver - metabolism</subject><subject>Models, Animal</subject><subject>Motor Activity - physiology</subject><subject>Neural Pathways - physiology</subject><subject>Neural Pathways - physiopathology</subject><subject>Neurons - metabolism</subject><subject>Neurons - pathology</subject><subject>New Research</subject><subject>Period Circadian Proteins - metabolism</subject><subject>Proto-Oncogene Proteins c-fos - metabolism</subject><subject>Rats, Wistar</subject><subject>Suprachiasmatic Nucleus - pathology</subject><subject>Suprachiasmatic Nucleus - physiology</subject><subject>Suprachiasmatic Nucleus - physiopathology</subject><issn>2373-2822</issn><issn>2373-2822</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV9r2zAUxUVZWUrXTzAoetyLU13JlmQGg1LSNVCa0j_PQpblWMO2MkneSD_9HNKE7uleOOeee-CH0Fcgcygou1o8LF6fVnNCqMxAzCkBcYLOKBMso5LSTx_2GbqI8RchBDgVIOEzmlHJRE4AzlD3PG6CNq3TsdfJGfwwms6OES-HZCchOT_gvy61OLUWXwcz6mQPpu94EaMdktMdbnzAq7DWg3tzwxo_ttvofOfXzkziU7tNbR-_oNNGd9FevM9z9Hq7eLm5y-5XP5c31_eZyUmRsqaGGnIuSl4XnEJdC2YrKq1oSgnQVNTYgpealVpXxOrSMMYZN7KuyopX3LJz9GOfuxmr3tZmqhh0pzbB9TpslddO_a8MrlVr_0cVjOeFLKeAb-8Bwf8ebUyqd9HYrtOD9WNUIGUOgkwlJyvbW03wMQbbHN8AUTtUao9K7VApEGqHarq6_NjweHMAw_4BpgOTWg</recordid><startdate>20170301</startdate><enddate>20170301</enddate><creator>Buijs, Frederik N</creator><creator>Guzmán-Ruiz, Mara</creator><creator>León-Mercado, Luis</creator><creator>Basualdo, Mari Carmen</creator><creator>Escobar, Carolina</creator><creator>Kalsbeek, Andries</creator><creator>Buijs, Ruud M</creator><general>Society for Neuroscience</general><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><orcidid>https://orcid.org/0000-0001-6362-7968</orcidid><orcidid>https://orcid.org/0000-0003-3894-4632</orcidid><orcidid>https://orcid.org/0000-0002-5932-9148</orcidid><orcidid>https://orcid.org/0000-0001-9606-8453</orcidid><orcidid>https://orcid.org/0000-0002-2974-7875</orcidid></search><sort><creationdate>20170301</creationdate><title>Suprachiasmatic Nucleus Interaction with the Arcuate Nucleus; Essential for Organizing Physiological Rhythms</title><author>Buijs, Frederik N ; Guzmán-Ruiz, Mara ; León-Mercado, Luis ; Basualdo, Mari Carmen ; Escobar, Carolina ; Kalsbeek, Andries ; Buijs, Ruud M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-fd1d146796d5621dd73eb28e7f9811fb2ce569a39aab0ea9c33636c8db9b6b6e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Arcuate Nucleus of Hypothalamus - pathology</topic><topic>Arcuate Nucleus of Hypothalamus - physiology</topic><topic>Arcuate Nucleus of Hypothalamus - physiopathology</topic><topic>Body Temperature - physiology</topic><topic>Circadian Rhythm - physiology</topic><topic>Corticosterone - metabolism</topic><topic>Glucose - administration & dosage</topic><topic>Glucose - metabolism</topic><topic>Liver - metabolism</topic><topic>Models, Animal</topic><topic>Motor Activity - physiology</topic><topic>Neural Pathways - physiology</topic><topic>Neural Pathways - physiopathology</topic><topic>Neurons - metabolism</topic><topic>Neurons - pathology</topic><topic>New Research</topic><topic>Period Circadian Proteins - metabolism</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>Rats, Wistar</topic><topic>Suprachiasmatic Nucleus - pathology</topic><topic>Suprachiasmatic Nucleus - physiology</topic><topic>Suprachiasmatic Nucleus - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Buijs, Frederik N</creatorcontrib><creatorcontrib>Guzmán-Ruiz, Mara</creatorcontrib><creatorcontrib>León-Mercado, Luis</creatorcontrib><creatorcontrib>Basualdo, Mari Carmen</creatorcontrib><creatorcontrib>Escobar, Carolina</creatorcontrib><creatorcontrib>Kalsbeek, Andries</creatorcontrib><creatorcontrib>Buijs, Ruud M</creatorcontrib><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>eNeuro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Buijs, Frederik N</au><au>Guzmán-Ruiz, Mara</au><au>León-Mercado, Luis</au><au>Basualdo, Mari Carmen</au><au>Escobar, Carolina</au><au>Kalsbeek, Andries</au><au>Buijs, Ruud M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suprachiasmatic Nucleus Interaction with the Arcuate Nucleus; Essential for Organizing Physiological Rhythms</atitle><jtitle>eNeuro</jtitle><addtitle>eNeuro</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>4</volume><issue>2</issue><spage>ENEURO.0028-17.2017</spage><pages>ENEURO.0028-17.2017-</pages><issn>2373-2822</issn><eissn>2373-2822</eissn><abstract>The suprachiasmatic nucleus (SCN) is generally considered the master clock, independently driving all circadian rhythms. We recently demonstrated the SCN receives metabolic and cardiovascular feedback adeptly altering its neuronal activity. In the present study, we show that microcuts effectively removing SCN-arcuate nucleus (ARC) interconnectivity in Wistar rats result in a loss of rhythmicity in locomotor activity, corticosterone levels, and body temperature in constant dark (DD) conditions. Elimination of these reciprocal connections did not affect SCN clock gene rhythmicity but did cause the ARC to desynchronize. Moreover, unilateral SCN lesions with contralateral retrochiasmatic microcuts resulted in identical arrhythmicity, proving that for the expression of physiological rhythms this reciprocal SCN-ARC interaction is essential. The unaltered SCN c-Fos expression following glucose administration in disconnected animals as compared to a significant decrease in controls demonstrates the importance of the ARC as metabolic modulator of SCN neuronal activity. Together, these results indicate that the SCN is more than an autonomous clock, and forms an essential component of a larger network controlling homeostasis. The present novel findings illustrate how an imbalance between SCN and ARC communication through circadian disruption could be involved in the etiology of metabolic disorders.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>28374011</pmid><doi>10.1523/ENEURO.0028-17.2017</doi><orcidid>https://orcid.org/0000-0001-6362-7968</orcidid><orcidid>https://orcid.org/0000-0003-3894-4632</orcidid><orcidid>https://orcid.org/0000-0002-5932-9148</orcidid><orcidid>https://orcid.org/0000-0001-9606-8453</orcidid><orcidid>https://orcid.org/0000-0002-2974-7875</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Arcuate Nucleus of Hypothalamus - pathology Arcuate Nucleus of Hypothalamus - physiology Arcuate Nucleus of Hypothalamus - physiopathology Body Temperature - physiology Circadian Rhythm - physiology Corticosterone - metabolism Glucose - administration & dosage Glucose - metabolism Liver - metabolism Models, Animal Motor Activity - physiology Neural Pathways - physiology Neural Pathways - physiopathology Neurons - metabolism Neurons - pathology New Research Period Circadian Proteins - metabolism Proto-Oncogene Proteins c-fos - metabolism Rats, Wistar Suprachiasmatic Nucleus - pathology Suprachiasmatic Nucleus - physiology Suprachiasmatic Nucleus - physiopathology |
title | Suprachiasmatic Nucleus Interaction with the Arcuate Nucleus; Essential for Organizing Physiological Rhythms |
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