Hypothalamic Orexin Stimulates Feeding-Associated Glucose Utilization in Skeletal Muscle via Sympathetic Nervous System
Hypothalamic neurons containing orexin (hypocretin) are activated during motivated behaviors and active waking. We show that injection of orexin-A into the ventromedial hypothalamus (VMH) of mice or rats increased glucose uptake and promoted insulin-induced glucose uptake and glycogen synthesis in s...
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Veröffentlicht in: | Cell metabolism 2009-12, Vol.10 (6), p.466-480 |
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creator | Shiuchi, Tetsuya Haque, Mohammad Shahidul Okamoto, Shiki Inoue, Tsuyoshi Kageyama, Haruaki Lee, Suni Toda, Chitoku Suzuki, Atsushi Bachman, Eric S. Kim, Young-Bum Sakurai, Takashi Yanagisawa, Masashi Shioda, Seiji Imoto, Keiji Minokoshi, Yasuhiko |
description | Hypothalamic neurons containing orexin (hypocretin) are activated during motivated behaviors and active waking. We show that injection of orexin-A into the ventromedial hypothalamus (VMH) of mice or rats increased glucose uptake and promoted insulin-induced glucose uptake and glycogen synthesis in skeletal muscle, but not in white adipose tissue, by activating the sympathetic nervous system. These effects of orexin were blunted in mice lacking β-adrenergic receptors but were restored by forced expression of the β2-adrenergic receptor in both myocytes and nonmyocyte cells of skeletal muscle. Orexin neurons are activated by conditioned sweet tasting and directly excite VMH neurons, thereby increasing muscle glucose metabolism and its insulin sensitivity. Orexin and its receptor in VMH thus play a key role in the regulation of muscle glucose metabolism associated with highly motivated behavior by activating muscle sympathetic nerves and β2-adrenergic signaling. |
doi_str_mv | 10.1016/j.cmet.2009.09.013 |
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We show that injection of orexin-A into the ventromedial hypothalamus (VMH) of mice or rats increased glucose uptake and promoted insulin-induced glucose uptake and glycogen synthesis in skeletal muscle, but not in white adipose tissue, by activating the sympathetic nervous system. These effects of orexin were blunted in mice lacking β-adrenergic receptors but were restored by forced expression of the β2-adrenergic receptor in both myocytes and nonmyocyte cells of skeletal muscle. Orexin neurons are activated by conditioned sweet tasting and directly excite VMH neurons, thereby increasing muscle glucose metabolism and its insulin sensitivity. Orexin and its receptor in VMH thus play a key role in the regulation of muscle glucose metabolism associated with highly motivated behavior by activating muscle sympathetic nerves and β2-adrenergic signaling.</description><identifier>ISSN: 1550-4131</identifier><identifier>EISSN: 1932-7420</identifier><identifier>DOI: 10.1016/j.cmet.2009.09.013</identifier><identifier>PMID: 19945404</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adipose Tissue, White - metabolism ; Animals ; Feeding Behavior - physiology ; Glucose - metabolism ; Glycogen - biosynthesis ; HUMDISEASE ; Insulin - metabolism ; Intracellular Signaling Peptides and Proteins - metabolism ; Intracellular Signaling Peptides and Proteins - pharmacology ; Male ; Mice ; Motivation - physiology ; Muscle, Skeletal - metabolism ; Neuropeptides - metabolism ; Neuropeptides - pharmacology ; Orexin Receptors ; Orexins ; Rats ; Receptors, Adrenergic, beta - metabolism ; Receptors, G-Protein-Coupled - metabolism ; Receptors, Neuropeptide - metabolism ; Sympathetic Nervous System - metabolism ; Sympathomimetics - metabolism ; Sympathomimetics - pharmacology ; Ventromedial Hypothalamic Nucleus - drug effects ; Ventromedial Hypothalamic Nucleus - physiology</subject><ispartof>Cell metabolism, 2009-12, Vol.10 (6), p.466-480</ispartof><rights>2009 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c496t-483e8699c1498bab7f95ce0358e5bda2e6dc55cf7982dc3e1f28a34ed7d13e73</citedby><cites>FETCH-LOGICAL-c496t-483e8699c1498bab7f95ce0358e5bda2e6dc55cf7982dc3e1f28a34ed7d13e73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S155041310900309X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19945404$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shiuchi, Tetsuya</creatorcontrib><creatorcontrib>Haque, Mohammad Shahidul</creatorcontrib><creatorcontrib>Okamoto, Shiki</creatorcontrib><creatorcontrib>Inoue, Tsuyoshi</creatorcontrib><creatorcontrib>Kageyama, Haruaki</creatorcontrib><creatorcontrib>Lee, Suni</creatorcontrib><creatorcontrib>Toda, Chitoku</creatorcontrib><creatorcontrib>Suzuki, Atsushi</creatorcontrib><creatorcontrib>Bachman, Eric S.</creatorcontrib><creatorcontrib>Kim, Young-Bum</creatorcontrib><creatorcontrib>Sakurai, Takashi</creatorcontrib><creatorcontrib>Yanagisawa, Masashi</creatorcontrib><creatorcontrib>Shioda, Seiji</creatorcontrib><creatorcontrib>Imoto, Keiji</creatorcontrib><creatorcontrib>Minokoshi, Yasuhiko</creatorcontrib><title>Hypothalamic Orexin Stimulates Feeding-Associated Glucose Utilization in Skeletal Muscle via Sympathetic Nervous System</title><title>Cell metabolism</title><addtitle>Cell Metab</addtitle><description>Hypothalamic neurons containing orexin (hypocretin) are activated during motivated behaviors and active waking. We show that injection of orexin-A into the ventromedial hypothalamus (VMH) of mice or rats increased glucose uptake and promoted insulin-induced glucose uptake and glycogen synthesis in skeletal muscle, but not in white adipose tissue, by activating the sympathetic nervous system. These effects of orexin were blunted in mice lacking β-adrenergic receptors but were restored by forced expression of the β2-adrenergic receptor in both myocytes and nonmyocyte cells of skeletal muscle. Orexin neurons are activated by conditioned sweet tasting and directly excite VMH neurons, thereby increasing muscle glucose metabolism and its insulin sensitivity. Orexin and its receptor in VMH thus play a key role in the regulation of muscle glucose metabolism associated with highly motivated behavior by activating muscle sympathetic nerves and β2-adrenergic signaling.</description><subject>Adipose Tissue, White - metabolism</subject><subject>Animals</subject><subject>Feeding Behavior - physiology</subject><subject>Glucose - metabolism</subject><subject>Glycogen - biosynthesis</subject><subject>HUMDISEASE</subject><subject>Insulin - metabolism</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Intracellular Signaling Peptides and Proteins - pharmacology</subject><subject>Male</subject><subject>Mice</subject><subject>Motivation - physiology</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Neuropeptides - metabolism</subject><subject>Neuropeptides - pharmacology</subject><subject>Orexin Receptors</subject><subject>Orexins</subject><subject>Rats</subject><subject>Receptors, Adrenergic, beta - metabolism</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Receptors, Neuropeptide - metabolism</subject><subject>Sympathetic Nervous System - metabolism</subject><subject>Sympathomimetics - metabolism</subject><subject>Sympathomimetics - pharmacology</subject><subject>Ventromedial Hypothalamic Nucleus - drug effects</subject><subject>Ventromedial Hypothalamic Nucleus - physiology</subject><issn>1550-4131</issn><issn>1932-7420</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1qGzEUhUVoiPPTF-iiaNWuxpFG0swIugmhSQppsrC7FrJ0p5armXEljRPn6avBhu4CFyQu3zlczkHoEyVzSmh1vZmbDtK8JETOp6HsBJ1Tycqi5iX5kP9CkIJTRmfoIsYNIaxikp2hGZWSC074OXp52G-HtNZed87g5wCvrseL5LrR6wQR3wFY1_8ubmIcjMsri-_9aIYI-Fdy3r3p5IYeT6I_4CFpj3-O0XjAO6fxYt9tdVpDyt5PEHbDGPMuJuiu0GmrfYSPx_cSLe--L28fisfn-x-3N4-F4bJKBW8YNJWUhnLZrPSqbqUwQJhoQKysLqGyRgjT1rIprWFA27LRjIOtLWVQs0v09WC7DcPfEWJSnYsGvNc95GNUzaZISMUz-eVdsqS0ElUtMlgeQBOGGAO0ahtcp8NeUaKmXtRGTb2oqRc1DWVZ9PnoPq46sP8lxyIy8O0AQA5j5yCoaBz0JqcfwCRlB_ee_z-8QKFZ</recordid><startdate>20091202</startdate><enddate>20091202</enddate><creator>Shiuchi, Tetsuya</creator><creator>Haque, Mohammad Shahidul</creator><creator>Okamoto, Shiki</creator><creator>Inoue, Tsuyoshi</creator><creator>Kageyama, Haruaki</creator><creator>Lee, Suni</creator><creator>Toda, Chitoku</creator><creator>Suzuki, Atsushi</creator><creator>Bachman, Eric S.</creator><creator>Kim, Young-Bum</creator><creator>Sakurai, Takashi</creator><creator>Yanagisawa, Masashi</creator><creator>Shioda, Seiji</creator><creator>Imoto, Keiji</creator><creator>Minokoshi, Yasuhiko</creator><general>Elsevier Inc</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20091202</creationdate><title>Hypothalamic Orexin Stimulates Feeding-Associated Glucose Utilization in Skeletal Muscle via Sympathetic Nervous System</title><author>Shiuchi, Tetsuya ; Haque, Mohammad Shahidul ; Okamoto, Shiki ; Inoue, Tsuyoshi ; Kageyama, Haruaki ; Lee, Suni ; Toda, Chitoku ; Suzuki, Atsushi ; Bachman, Eric S. ; Kim, Young-Bum ; Sakurai, Takashi ; Yanagisawa, Masashi ; Shioda, Seiji ; Imoto, Keiji ; Minokoshi, Yasuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-483e8699c1498bab7f95ce0358e5bda2e6dc55cf7982dc3e1f28a34ed7d13e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adipose Tissue, White - metabolism</topic><topic>Animals</topic><topic>Feeding Behavior - physiology</topic><topic>Glucose - metabolism</topic><topic>Glycogen - biosynthesis</topic><topic>HUMDISEASE</topic><topic>Insulin - metabolism</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Intracellular Signaling Peptides and Proteins - pharmacology</topic><topic>Male</topic><topic>Mice</topic><topic>Motivation - physiology</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Neuropeptides - metabolism</topic><topic>Neuropeptides - pharmacology</topic><topic>Orexin Receptors</topic><topic>Orexins</topic><topic>Rats</topic><topic>Receptors, Adrenergic, beta - metabolism</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Receptors, Neuropeptide - metabolism</topic><topic>Sympathetic Nervous System - metabolism</topic><topic>Sympathomimetics - metabolism</topic><topic>Sympathomimetics - pharmacology</topic><topic>Ventromedial Hypothalamic Nucleus - drug effects</topic><topic>Ventromedial Hypothalamic Nucleus - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shiuchi, Tetsuya</creatorcontrib><creatorcontrib>Haque, Mohammad Shahidul</creatorcontrib><creatorcontrib>Okamoto, Shiki</creatorcontrib><creatorcontrib>Inoue, Tsuyoshi</creatorcontrib><creatorcontrib>Kageyama, Haruaki</creatorcontrib><creatorcontrib>Lee, Suni</creatorcontrib><creatorcontrib>Toda, Chitoku</creatorcontrib><creatorcontrib>Suzuki, Atsushi</creatorcontrib><creatorcontrib>Bachman, Eric S.</creatorcontrib><creatorcontrib>Kim, Young-Bum</creatorcontrib><creatorcontrib>Sakurai, Takashi</creatorcontrib><creatorcontrib>Yanagisawa, Masashi</creatorcontrib><creatorcontrib>Shioda, Seiji</creatorcontrib><creatorcontrib>Imoto, Keiji</creatorcontrib><creatorcontrib>Minokoshi, Yasuhiko</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cell metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shiuchi, Tetsuya</au><au>Haque, Mohammad Shahidul</au><au>Okamoto, Shiki</au><au>Inoue, Tsuyoshi</au><au>Kageyama, Haruaki</au><au>Lee, Suni</au><au>Toda, Chitoku</au><au>Suzuki, Atsushi</au><au>Bachman, Eric S.</au><au>Kim, Young-Bum</au><au>Sakurai, Takashi</au><au>Yanagisawa, Masashi</au><au>Shioda, Seiji</au><au>Imoto, Keiji</au><au>Minokoshi, Yasuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypothalamic Orexin Stimulates Feeding-Associated Glucose Utilization in Skeletal Muscle via Sympathetic Nervous System</atitle><jtitle>Cell metabolism</jtitle><addtitle>Cell Metab</addtitle><date>2009-12-02</date><risdate>2009</risdate><volume>10</volume><issue>6</issue><spage>466</spage><epage>480</epage><pages>466-480</pages><issn>1550-4131</issn><eissn>1932-7420</eissn><abstract>Hypothalamic neurons containing orexin (hypocretin) are activated during motivated behaviors and active waking. We show that injection of orexin-A into the ventromedial hypothalamus (VMH) of mice or rats increased glucose uptake and promoted insulin-induced glucose uptake and glycogen synthesis in skeletal muscle, but not in white adipose tissue, by activating the sympathetic nervous system. These effects of orexin were blunted in mice lacking β-adrenergic receptors but were restored by forced expression of the β2-adrenergic receptor in both myocytes and nonmyocyte cells of skeletal muscle. Orexin neurons are activated by conditioned sweet tasting and directly excite VMH neurons, thereby increasing muscle glucose metabolism and its insulin sensitivity. Orexin and its receptor in VMH thus play a key role in the regulation of muscle glucose metabolism associated with highly motivated behavior by activating muscle sympathetic nerves and β2-adrenergic signaling.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19945404</pmid><doi>10.1016/j.cmet.2009.09.013</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adipose Tissue, White - metabolism Animals Feeding Behavior - physiology Glucose - metabolism Glycogen - biosynthesis HUMDISEASE Insulin - metabolism Intracellular Signaling Peptides and Proteins - metabolism Intracellular Signaling Peptides and Proteins - pharmacology Male Mice Motivation - physiology Muscle, Skeletal - metabolism Neuropeptides - metabolism Neuropeptides - pharmacology Orexin Receptors Orexins Rats Receptors, Adrenergic, beta - metabolism Receptors, G-Protein-Coupled - metabolism Receptors, Neuropeptide - metabolism Sympathetic Nervous System - metabolism Sympathomimetics - metabolism Sympathomimetics - pharmacology Ventromedial Hypothalamic Nucleus - drug effects Ventromedial Hypothalamic Nucleus - physiology |
title | Hypothalamic Orexin Stimulates Feeding-Associated Glucose Utilization in Skeletal Muscle via Sympathetic Nervous System |
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