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Multi-transcriptional profiling of melanin-concentrating hormone and orexin-containing neurons
1.Melanin-concentrating hormone (MCH) and orexin-containing neurons participate in hypothalamic circuits that control energy homeostasis. While these two systems have projections to widespread target areas within the central nervous system, little is known about intrinsic characteristics and the mol...
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Published in: | Cellular and molecular neurobiology 2005-12, Vol.25 (8), p.1209-1223 |
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description | 1.Melanin-concentrating hormone (MCH) and orexin-containing neurons participate in hypothalamic circuits that control energy homeostasis. While these two systems have projections to widespread target areas within the central nervous system, little is known about intrinsic characteristics and the molecular composition of both the MCH and orexin neurons themselves. 2. By a combinatory approach of quantitative immunocytochemical identification and analysis with laser microdissection and semi-quantitative Real-time RT-PCR, here we present multi-transcriptional profiling of MCH and orexin neurons in the rat lateral hypothalamus. 3. Immunocytochemical analysis showed that orexin peptide expression was increased after fasting both during the activity and resting period of rats, whereas MCH peptide content was only clearly upregulated at resting phase. Subsequent transcriptional profiling showed distinct expression patterns of MCH, orexin and cocaine-amphetamine regulated transcript (CART) between MCH and orexin neurons. A low expression level of dynorphin was found both in MCH and orexin neurons. Receptor expression profiles, reflecting interaction with neuropeptide Y, melanocortins, leptin, glucocorticoids and GABA, showed approximately similar expression patterns among the MCH and orexin neuronal systems. Expression of glutamate- and GABA-markers revealed a possible contributory role of both glutamate and GABA in functional output of MCH and orexin neurons. 4. This method allowed differential screening at mRNA level after immunocytochemical neuron identification and analysis in heterogeneous brain regions, which can further specify functioning of the individual neurons. With respect to MCH and orexin neurons, this study emphasizes that these neurons are targets for stimulatory and inhibitory signals from other brain regions including the arcuate nucleus and the general circulation. Additionally, both glutamate and GABA appear to be involved in MCH and orexin neuronal functioning related to feeding and regulation of the energy balance. |
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While these two systems have projections to widespread target areas within the central nervous system, little is known about intrinsic characteristics and the molecular composition of both the MCH and orexin neurons themselves. 2. By a combinatory approach of quantitative immunocytochemical identification and analysis with laser microdissection and semi-quantitative Real-time RT-PCR, here we present multi-transcriptional profiling of MCH and orexin neurons in the rat lateral hypothalamus. 3. Immunocytochemical analysis showed that orexin peptide expression was increased after fasting both during the activity and resting period of rats, whereas MCH peptide content was only clearly upregulated at resting phase. Subsequent transcriptional profiling showed distinct expression patterns of MCH, orexin and cocaine-amphetamine regulated transcript (CART) between MCH and orexin neurons. A low expression level of dynorphin was found both in MCH and orexin neurons. Receptor expression profiles, reflecting interaction with neuropeptide Y, melanocortins, leptin, glucocorticoids and GABA, showed approximately similar expression patterns among the MCH and orexin neuronal systems. Expression of glutamate- and GABA-markers revealed a possible contributory role of both glutamate and GABA in functional output of MCH and orexin neurons. 4. This method allowed differential screening at mRNA level after immunocytochemical neuron identification and analysis in heterogeneous brain regions, which can further specify functioning of the individual neurons. With respect to MCH and orexin neurons, this study emphasizes that these neurons are targets for stimulatory and inhibitory signals from other brain regions including the arcuate nucleus and the general circulation. Additionally, both glutamate and GABA appear to be involved in MCH and orexin neuronal functioning related to feeding and regulation of the energy balance.</description><identifier>ISSN: 0272-4340</identifier><identifier>EISSN: 1573-6830</identifier><identifier>DOI: 10.1007/s10571-005-8184-8</identifier><identifier>PMID: 16388333</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Amphetamines ; Animals ; Appetite Regulation - physiology ; Arcuate nucleus ; Brain ; Central nervous system ; Circadian Rhythm - physiology ; Cocaine ; Dynorphin ; Energy balance ; Food Deprivation - physiology ; gamma-Aminobutyric Acid - metabolism ; Gene Expression Profiling - methods ; Glucocorticoids ; Glutamic Acid - metabolism ; Homeostasis ; Hormones - metabolism ; Hypothalamic Area, Lateral - cytology ; Hypothalamic Area, Lateral - metabolism ; Hypothalamic Hormones - genetics ; Hypothalamic Hormones - metabolism ; Hypothalamus (lateral) ; Immunohistochemistry ; Intracellular Signaling Peptides and Proteins - genetics ; Intracellular Signaling Peptides and Proteins - metabolism ; Leptin ; Male ; Melanin ; Melanin-concentrating hormone ; Melanins - genetics ; Melanins - metabolism ; Microdissection - methods ; Motor Activity - physiology ; Nerve Tissue Proteins - genetics ; Nerve Tissue Proteins - metabolism ; Neural Pathways - cytology ; Neural Pathways - metabolism ; Neurons ; Neurons - cytology ; Neurons - metabolism ; Neuropeptide Y ; Neuropeptides - genetics ; Neuropeptides - metabolism ; Orexin Receptors ; Orexins ; Peptides ; Pituitary Hormones - genetics ; Pituitary Hormones - metabolism ; Rats ; Rats, Wistar ; Receptors, G-Protein-Coupled ; Receptors, Neuropeptide - metabolism ; Receptors, Pituitary Hormone - metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - analysis ; RNA, Messenger - genetics ; Transcription ; Up-Regulation - physiology ; γ-Aminobutyric acid</subject><ispartof>Cellular and molecular neurobiology, 2005-12, Vol.25 (8), p.1209-1223</ispartof><rights>Springer Science + Business Media, Inc. 2005.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-7a3035b8f877ad9898fbda974f4bf7cd26640dfa88040bcc4ea5084a356743e3</citedby><cites>FETCH-LOGICAL-c424t-7a3035b8f877ad9898fbda974f4bf7cd26640dfa88040bcc4ea5084a356743e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16388333$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harthoorn, Lucien F</creatorcontrib><creatorcontrib>Sañé, Arseni</creatorcontrib><creatorcontrib>Nethe, Micha</creatorcontrib><creatorcontrib>Van Heerikhuize, Joop J</creatorcontrib><title>Multi-transcriptional profiling of melanin-concentrating hormone and orexin-containing neurons</title><title>Cellular and molecular neurobiology</title><addtitle>Cell Mol Neurobiol</addtitle><description>1.Melanin-concentrating hormone (MCH) and orexin-containing neurons participate in hypothalamic circuits that control energy homeostasis. While these two systems have projections to widespread target areas within the central nervous system, little is known about intrinsic characteristics and the molecular composition of both the MCH and orexin neurons themselves. 2. By a combinatory approach of quantitative immunocytochemical identification and analysis with laser microdissection and semi-quantitative Real-time RT-PCR, here we present multi-transcriptional profiling of MCH and orexin neurons in the rat lateral hypothalamus. 3. Immunocytochemical analysis showed that orexin peptide expression was increased after fasting both during the activity and resting period of rats, whereas MCH peptide content was only clearly upregulated at resting phase. Subsequent transcriptional profiling showed distinct expression patterns of MCH, orexin and cocaine-amphetamine regulated transcript (CART) between MCH and orexin neurons. A low expression level of dynorphin was found both in MCH and orexin neurons. Receptor expression profiles, reflecting interaction with neuropeptide Y, melanocortins, leptin, glucocorticoids and GABA, showed approximately similar expression patterns among the MCH and orexin neuronal systems. Expression of glutamate- and GABA-markers revealed a possible contributory role of both glutamate and GABA in functional output of MCH and orexin neurons. 4. This method allowed differential screening at mRNA level after immunocytochemical neuron identification and analysis in heterogeneous brain regions, which can further specify functioning of the individual neurons. With respect to MCH and orexin neurons, this study emphasizes that these neurons are targets for stimulatory and inhibitory signals from other brain regions including the arcuate nucleus and the general circulation. Additionally, both glutamate and GABA appear to be involved in MCH and orexin neuronal functioning related to feeding and regulation of the energy balance.</description><subject>Amphetamines</subject><subject>Animals</subject><subject>Appetite Regulation - physiology</subject><subject>Arcuate nucleus</subject><subject>Brain</subject><subject>Central nervous system</subject><subject>Circadian Rhythm - physiology</subject><subject>Cocaine</subject><subject>Dynorphin</subject><subject>Energy balance</subject><subject>Food Deprivation - physiology</subject><subject>gamma-Aminobutyric Acid - metabolism</subject><subject>Gene Expression Profiling - methods</subject><subject>Glucocorticoids</subject><subject>Glutamic Acid - metabolism</subject><subject>Homeostasis</subject><subject>Hormones - metabolism</subject><subject>Hypothalamic Area, Lateral - cytology</subject><subject>Hypothalamic Area, Lateral - metabolism</subject><subject>Hypothalamic Hormones - genetics</subject><subject>Hypothalamic Hormones - metabolism</subject><subject>Hypothalamus (lateral)</subject><subject>Immunohistochemistry</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Leptin</subject><subject>Male</subject><subject>Melanin</subject><subject>Melanin-concentrating hormone</subject><subject>Melanins - genetics</subject><subject>Melanins - metabolism</subject><subject>Microdissection - methods</subject><subject>Motor Activity - physiology</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neural Pathways - cytology</subject><subject>Neural Pathways - metabolism</subject><subject>Neurons</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Neuropeptide Y</subject><subject>Neuropeptides - genetics</subject><subject>Neuropeptides - metabolism</subject><subject>Orexin Receptors</subject><subject>Orexins</subject><subject>Peptides</subject><subject>Pituitary Hormones - genetics</subject><subject>Pituitary Hormones - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, G-Protein-Coupled</subject><subject>Receptors, Neuropeptide - metabolism</subject><subject>Receptors, Pituitary Hormone - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - genetics</subject><subject>Transcription</subject><subject>Up-Regulation - physiology</subject><subject>γ-Aminobutyric acid</subject><issn>0272-4340</issn><issn>1573-6830</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkUtLxDAUhYMoOj5-gBspCO6iN03aJEsRX6C4cW1I00QjbTImLei_N-MMCG5c3cX9zuFwDkLHBM4JAL_IBBpOMECDBREMiy20IA2nuBUUttECal5jRhnsof2c3wFAFnYX7ZGWCkEpXaCXx3mYPJ6SDtkkv5x8DHqolik6P_jwWkVXjXbQwQdsYjA2FHRaPd5iGmOwlQ59FZP9XAOT9mH1DXZOMeRDtOP0kO3R5h6g55vr56s7_PB0e391-YANq9mEuaZAm044wbnupZDCdb2WnDnWOW76um0Z9E4LAQw6Y5jVDQimadNyRi09QGdr25L7Y7Z5UqPPxg4lt41zVq0EJllp5j-QyJo3VMoCnv4B3-OcSjVZ_YRpCRV1ociaMinmnKxTy-RHnb4UAbWaSK0nUqV2tZpIiaI52TjP3Wj7X8VmE_oNeMSNgQ</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>Harthoorn, Lucien F</creator><creator>Sañé, Arseni</creator><creator>Nethe, Micha</creator><creator>Van Heerikhuize, Joop J</creator><general>Springer Nature B.V</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20051201</creationdate><title>Multi-transcriptional profiling of melanin-concentrating hormone and orexin-containing neurons</title><author>Harthoorn, Lucien F ; Sañé, Arseni ; Nethe, Micha ; Van Heerikhuize, Joop J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-7a3035b8f877ad9898fbda974f4bf7cd26640dfa88040bcc4ea5084a356743e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Amphetamines</topic><topic>Animals</topic><topic>Appetite Regulation - physiology</topic><topic>Arcuate nucleus</topic><topic>Brain</topic><topic>Central nervous system</topic><topic>Circadian Rhythm - physiology</topic><topic>Cocaine</topic><topic>Dynorphin</topic><topic>Energy balance</topic><topic>Food Deprivation - physiology</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>Gene Expression Profiling - methods</topic><topic>Glucocorticoids</topic><topic>Glutamic Acid - metabolism</topic><topic>Homeostasis</topic><topic>Hormones - metabolism</topic><topic>Hypothalamic Area, Lateral - cytology</topic><topic>Hypothalamic Area, Lateral - metabolism</topic><topic>Hypothalamic Hormones - genetics</topic><topic>Hypothalamic Hormones - metabolism</topic><topic>Hypothalamus (lateral)</topic><topic>Immunohistochemistry</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Leptin</topic><topic>Male</topic><topic>Melanin</topic><topic>Melanin-concentrating hormone</topic><topic>Melanins - genetics</topic><topic>Melanins - metabolism</topic><topic>Microdissection - methods</topic><topic>Motor Activity - physiology</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neural Pathways - cytology</topic><topic>Neural Pathways - metabolism</topic><topic>Neurons</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>Neuropeptide Y</topic><topic>Neuropeptides - genetics</topic><topic>Neuropeptides - metabolism</topic><topic>Orexin Receptors</topic><topic>Orexins</topic><topic>Peptides</topic><topic>Pituitary Hormones - genetics</topic><topic>Pituitary Hormones - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, G-Protein-Coupled</topic><topic>Receptors, Neuropeptide - metabolism</topic><topic>Receptors, Pituitary Hormone - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - genetics</topic><topic>Transcription</topic><topic>Up-Regulation - physiology</topic><topic>γ-Aminobutyric acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harthoorn, Lucien F</creatorcontrib><creatorcontrib>Sañé, Arseni</creatorcontrib><creatorcontrib>Nethe, Micha</creatorcontrib><creatorcontrib>Van Heerikhuize, Joop J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular and molecular neurobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harthoorn, Lucien F</au><au>Sañé, Arseni</au><au>Nethe, Micha</au><au>Van Heerikhuize, Joop J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multi-transcriptional profiling of melanin-concentrating hormone and orexin-containing neurons</atitle><jtitle>Cellular and molecular neurobiology</jtitle><addtitle>Cell Mol Neurobiol</addtitle><date>2005-12-01</date><risdate>2005</risdate><volume>25</volume><issue>8</issue><spage>1209</spage><epage>1223</epage><pages>1209-1223</pages><issn>0272-4340</issn><eissn>1573-6830</eissn><abstract>1.Melanin-concentrating hormone (MCH) and orexin-containing neurons participate in hypothalamic circuits that control energy homeostasis. While these two systems have projections to widespread target areas within the central nervous system, little is known about intrinsic characteristics and the molecular composition of both the MCH and orexin neurons themselves. 2. By a combinatory approach of quantitative immunocytochemical identification and analysis with laser microdissection and semi-quantitative Real-time RT-PCR, here we present multi-transcriptional profiling of MCH and orexin neurons in the rat lateral hypothalamus. 3. Immunocytochemical analysis showed that orexin peptide expression was increased after fasting both during the activity and resting period of rats, whereas MCH peptide content was only clearly upregulated at resting phase. Subsequent transcriptional profiling showed distinct expression patterns of MCH, orexin and cocaine-amphetamine regulated transcript (CART) between MCH and orexin neurons. A low expression level of dynorphin was found both in MCH and orexin neurons. Receptor expression profiles, reflecting interaction with neuropeptide Y, melanocortins, leptin, glucocorticoids and GABA, showed approximately similar expression patterns among the MCH and orexin neuronal systems. Expression of glutamate- and GABA-markers revealed a possible contributory role of both glutamate and GABA in functional output of MCH and orexin neurons. 4. This method allowed differential screening at mRNA level after immunocytochemical neuron identification and analysis in heterogeneous brain regions, which can further specify functioning of the individual neurons. With respect to MCH and orexin neurons, this study emphasizes that these neurons are targets for stimulatory and inhibitory signals from other brain regions including the arcuate nucleus and the general circulation. Additionally, both glutamate and GABA appear to be involved in MCH and orexin neuronal functioning related to feeding and regulation of the energy balance.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>16388333</pmid><doi>10.1007/s10571-005-8184-8</doi><tpages>15</tpages></addata></record> |
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subjects | Amphetamines Animals Appetite Regulation - physiology Arcuate nucleus Brain Central nervous system Circadian Rhythm - physiology Cocaine Dynorphin Energy balance Food Deprivation - physiology gamma-Aminobutyric Acid - metabolism Gene Expression Profiling - methods Glucocorticoids Glutamic Acid - metabolism Homeostasis Hormones - metabolism Hypothalamic Area, Lateral - cytology Hypothalamic Area, Lateral - metabolism Hypothalamic Hormones - genetics Hypothalamic Hormones - metabolism Hypothalamus (lateral) Immunohistochemistry Intracellular Signaling Peptides and Proteins - genetics Intracellular Signaling Peptides and Proteins - metabolism Leptin Male Melanin Melanin-concentrating hormone Melanins - genetics Melanins - metabolism Microdissection - methods Motor Activity - physiology Nerve Tissue Proteins - genetics Nerve Tissue Proteins - metabolism Neural Pathways - cytology Neural Pathways - metabolism Neurons Neurons - cytology Neurons - metabolism Neuropeptide Y Neuropeptides - genetics Neuropeptides - metabolism Orexin Receptors Orexins Peptides Pituitary Hormones - genetics Pituitary Hormones - metabolism Rats Rats, Wistar Receptors, G-Protein-Coupled Receptors, Neuropeptide - metabolism Receptors, Pituitary Hormone - metabolism Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - analysis RNA, Messenger - genetics Transcription Up-Regulation - physiology γ-Aminobutyric acid |
title | Multi-transcriptional profiling of melanin-concentrating hormone and orexin-containing neurons |
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