Source:http://linkedlifedata.com/resource/pubmed/id/15220198
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2004-6-28
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pubmed:abstractText |
Many metabolic factors affect the secretion of insulin from beta-cells and glucagon from alpha-cells of the islets of Langerhans to regulate blood glucose. Somatostatin from delta-cells, considered a local inhibitor of islet function, reduces insulin and glucagon secretion by activating somatostatin receptors in islet cells. Somatostatin secretion from delta-cells is increased by high glucose via glucose metabolism in a similar way to insulin secretion from beta-cells. However, it is unknown how low glucose triggers somatostatin secretion. Because L-glutamate is cosecreted with glucagon from alpha-cells under low-glucose conditions and acts as a primary intercellular messenger, we hypothesized that glutamate signaling triggers the secretion of somatostatin. In this study, we showed that delta-cells express GluR4c-flip, a newly identified splicing variant of GluR4, an (RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type ionotropic glutamate receptor of rat. After treatment with L-glutamate, AMPA, or kainate, secretion of somatostatin from isolated islets was significantly stimulated under low-glucose conditions. The glutamate-dependent somatostatin secretion was Ca(2+) dependent and blocked by 6-cyano-7-nitroquinoxaline-2,3-dione. Somatostatin in turn inhibited the secretion of L-glutamate and glucagon from alpha-cells. These results indicate that L-glutamate triggers somatostatin secretion from delta-cells by way of the GluR4c-flip receptor under low-glucose conditions. The released somatostatin may complete the feedback inhibition of alpha-cells. Thus, alpha- and delta-cells may communicate with each other through L-glutamate and somatostatin signaling.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Excitatory Amino Acid Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Glucagon,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Hormones,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, AMPA,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Glutamate,
http://linkedlifedata.com/resource/pubmed/chemical/Somatostatin,
http://linkedlifedata.com/resource/pubmed/chemical/glutamate receptor ionotropic...
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0012-1797
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pubmed:author |
pubmed-author:EchigoNorikoN,
pubmed-author:HayashiMitsukoM,
pubmed-author:KohDuk-SuDS,
pubmed-author:MorimotoRiyoR,
pubmed-author:MoritaMitsuhiroM,
pubmed-author:MoriyamaYoshinoriY,
pubmed-author:MuroyamaAkikoA,
pubmed-author:UeharaShunsukeS,
pubmed-author:YamamotoAkitsuguA,
pubmed-author:YatsushiroShoukiS
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pubmed:issnType |
Print
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1743-53
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15220198-Animals,
pubmed-meshheading:15220198-Culture Techniques,
pubmed-meshheading:15220198-Excitatory Amino Acid Antagonists,
pubmed-meshheading:15220198-Glucagon,
pubmed-meshheading:15220198-Glutamic Acid,
pubmed-meshheading:15220198-Hormones,
pubmed-meshheading:15220198-Islets of Langerhans,
pubmed-meshheading:15220198-Male,
pubmed-meshheading:15220198-Rats,
pubmed-meshheading:15220198-Rats, Wistar,
pubmed-meshheading:15220198-Receptors, AMPA,
pubmed-meshheading:15220198-Receptors, Glutamate,
pubmed-meshheading:15220198-Somatostatin
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pubmed:year |
2004
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pubmed:articleTitle |
A novel variant of ionotropic glutamate receptor regulates somatostatin secretion from delta-cells of islets of Langerhans.
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pubmed:affiliation |
Department of Biochemistry, Faculty of Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan. moriyama@pheasant.pharm.okayama-u.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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