Isolation and molecular characterization of porcine calcitonin gene-related peptide (CGRP) and its endocrine effects in the porcine pancreas
The aim of this study was to investigate the possible role of porcine calcitonin gene-related peptide (CGRP) in the regulation of the endocrine porcine pancreas. Initially, we isolated and purified CGRP from extracts of porcine adrenal glands and pancreases. A single molecular form of the peptide wa...
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Veröffentlicht in: | Pancreas 1998-03, Vol.16 (2), p.195-204 |
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description | The aim of this study was to investigate the possible role of porcine calcitonin gene-related peptide (CGRP) in the regulation of the endocrine porcine pancreas. Initially, we isolated and purified CGRP from extracts of porcine adrenal glands and pancreases. A single molecular form of the peptide was found in the two tissues. The adrenal peptide was sequenced and found to differ from human alpha-CGRP at six positions and from human beta-CGRP at three positions. By immunohistochemistry, CGRP was found in nerve fibers in the pancreatic ganglia. A synthetic replica of the porcine peptide was infused at different dose levels (10(-10), 10(-9), and 10(-8) M) into isolated perfused porcine pancreata. With 5 mmol/L glucose in the perfusate. CGRP at 10(-10) and 10(-9) M increased insulin and glucagon secretion, whereas significant decreases were observed with 10(-8) M. Somatostatin secretion was increased significantly by 10(-8) M CGRP. In immunoneutralization studies (n = 6) using a high-affinity somatostatin antibody, the inhibitory effect of CGRP at 10(-8) M was reversed to a significant stimulation of insulin and glucagon secretion. Insulin secretion in response to square-wave increases in glucose concentration to 11 mM was inhibited dose dependently by CGRP; at 10(-8) M the insulin output decreased by 72+/-9% (n = 6). The present results indicate that CGRP may be involved in the regulation of insulin and glucagon secretion from the porcine pancreas. |
doi_str_mv | 10.1097/00006676-199803000-00014 |
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N ; BERSANI, M ; SCHMIDT, P ; THIM, L ; KOFOD, H ; JØRGENSEN, P. N ; POULSEN, S. S ; HOLST, J. J</creator><creatorcontrib>RASMUSSEN, T. N ; BERSANI, M ; SCHMIDT, P ; THIM, L ; KOFOD, H ; JØRGENSEN, P. N ; POULSEN, S. S ; HOLST, J. J</creatorcontrib><description>The aim of this study was to investigate the possible role of porcine calcitonin gene-related peptide (CGRP) in the regulation of the endocrine porcine pancreas. Initially, we isolated and purified CGRP from extracts of porcine adrenal glands and pancreases. A single molecular form of the peptide was found in the two tissues. The adrenal peptide was sequenced and found to differ from human alpha-CGRP at six positions and from human beta-CGRP at three positions. By immunohistochemistry, CGRP was found in nerve fibers in the pancreatic ganglia. A synthetic replica of the porcine peptide was infused at different dose levels (10(-10), 10(-9), and 10(-8) M) into isolated perfused porcine pancreata. With 5 mmol/L glucose in the perfusate. CGRP at 10(-10) and 10(-9) M increased insulin and glucagon secretion, whereas significant decreases were observed with 10(-8) M. Somatostatin secretion was increased significantly by 10(-8) M CGRP. In immunoneutralization studies (n = 6) using a high-affinity somatostatin antibody, the inhibitory effect of CGRP at 10(-8) M was reversed to a significant stimulation of insulin and glucagon secretion. Insulin secretion in response to square-wave increases in glucose concentration to 11 mM was inhibited dose dependently by CGRP; at 10(-8) M the insulin output decreased by 72+/-9% (n = 6). The present results indicate that CGRP may be involved in the regulation of insulin and glucagon secretion from the porcine pancreas.</description><identifier>ISSN: 0885-3177</identifier><identifier>EISSN: 1536-4828</identifier><identifier>DOI: 10.1097/00006676-199803000-00014</identifier><identifier>PMID: 9510144</identifier><identifier>CODEN: PANCE4</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adrenal Glands - chemistry ; Amino Acid Sequence ; Animals ; Antibodies - pharmacology ; Biological and medical sciences ; Calcitonin Gene-Related Peptide - genetics ; Calcitonin Gene-Related Peptide - isolation & purification ; Calcitonin Gene-Related Peptide - pharmacology ; Endocrine pancreas ; Fundamental and applied biological sciences. Psychology ; Glucagon - metabolism ; Hormones. Régulation ; Humans ; Immunohistochemistry ; Insulin - metabolism ; Insulin Secretion ; Islets of Langerhans - drug effects ; Islets of Langerhans - metabolism ; Molecular Sequence Data ; Nerve Fibers - chemistry ; Pancreas - chemistry ; Pancreas - drug effects ; Pancreas - innervation ; Sequence Homology ; Somatostatin - antagonists & inhibitors ; Somatostatin - metabolism ; Swine ; Vertebrates: endocrinology</subject><ispartof>Pancreas, 1998-03, Vol.16 (2), p.195-204</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-8502413a9418bac3de60be15ea8658c536c7e0f9a6b515f6395b7619f9c44a603</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2157756$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9510144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RASMUSSEN, T. N</creatorcontrib><creatorcontrib>BERSANI, M</creatorcontrib><creatorcontrib>SCHMIDT, P</creatorcontrib><creatorcontrib>THIM, L</creatorcontrib><creatorcontrib>KOFOD, H</creatorcontrib><creatorcontrib>JØRGENSEN, P. N</creatorcontrib><creatorcontrib>POULSEN, S. S</creatorcontrib><creatorcontrib>HOLST, J. J</creatorcontrib><title>Isolation and molecular characterization of porcine calcitonin gene-related peptide (CGRP) and its endocrine effects in the porcine pancreas</title><title>Pancreas</title><addtitle>Pancreas</addtitle><description>The aim of this study was to investigate the possible role of porcine calcitonin gene-related peptide (CGRP) in the regulation of the endocrine porcine pancreas. Initially, we isolated and purified CGRP from extracts of porcine adrenal glands and pancreases. A single molecular form of the peptide was found in the two tissues. The adrenal peptide was sequenced and found to differ from human alpha-CGRP at six positions and from human beta-CGRP at three positions. By immunohistochemistry, CGRP was found in nerve fibers in the pancreatic ganglia. A synthetic replica of the porcine peptide was infused at different dose levels (10(-10), 10(-9), and 10(-8) M) into isolated perfused porcine pancreata. With 5 mmol/L glucose in the perfusate. CGRP at 10(-10) and 10(-9) M increased insulin and glucagon secretion, whereas significant decreases were observed with 10(-8) M. Somatostatin secretion was increased significantly by 10(-8) M CGRP. In immunoneutralization studies (n = 6) using a high-affinity somatostatin antibody, the inhibitory effect of CGRP at 10(-8) M was reversed to a significant stimulation of insulin and glucagon secretion. Insulin secretion in response to square-wave increases in glucose concentration to 11 mM was inhibited dose dependently by CGRP; at 10(-8) M the insulin output decreased by 72+/-9% (n = 6). The present results indicate that CGRP may be involved in the regulation of insulin and glucagon secretion from the porcine pancreas.</description><subject>Adrenal Glands - chemistry</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antibodies - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Calcitonin Gene-Related Peptide - genetics</subject><subject>Calcitonin Gene-Related Peptide - isolation & purification</subject><subject>Calcitonin Gene-Related Peptide - pharmacology</subject><subject>Endocrine pancreas</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucagon - metabolism</subject><subject>Hormones. Régulation</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Insulin - metabolism</subject><subject>Insulin Secretion</subject><subject>Islets of Langerhans - drug effects</subject><subject>Islets of Langerhans - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Nerve Fibers - chemistry</subject><subject>Pancreas - chemistry</subject><subject>Pancreas - drug effects</subject><subject>Pancreas - innervation</subject><subject>Sequence Homology</subject><subject>Somatostatin - antagonists & inhibitors</subject><subject>Somatostatin - metabolism</subject><subject>Swine</subject><subject>Vertebrates: endocrinology</subject><issn>0885-3177</issn><issn>1536-4828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UcuKFDEUDaKM7egnCFmI6KI0t1N5LaXRcWBAEV0Xt1I3TqQ6KZPqxfgNfrSZ6bYDIdycR8g5jHEQ70A48160pbXRHThnhWxT1zb0j9gGlNRdb7f2MdsIa1UnwZin7FmtvxrDSOUu2IVT0Nj9hv29rnnGNebEMU18n2fyhxkL97dY0K9U4p8jnANfcvExEfc4-7jmFBP_SYm6Qs2CJr7QssaJ-Jvd1bevbx8M41o5pSn7ci-kEMi3myZcb-nst2DyhbA-Z08CzpVenM5L9uPTx--7z93Nl6vr3Yebzktt184qse1BouvBjujlRFqMBIrQamV9-783JIJDPSpQQUunRqPBBef7HrWQl-z10Xcp-feB6jrsY_U0z5goH-pgnJEAYBvRHom-5FoLhWEpcY_lbgAx3Bcx_C9iOBcxPBTRpC9PbxzGPU1n4Sn5hr864VhbnqG0DGI907agjFFa_gMO7pG9</recordid><startdate>19980301</startdate><enddate>19980301</enddate><creator>RASMUSSEN, T. N</creator><creator>BERSANI, M</creator><creator>SCHMIDT, P</creator><creator>THIM, L</creator><creator>KOFOD, H</creator><creator>JØRGENSEN, P. N</creator><creator>POULSEN, S. S</creator><creator>HOLST, J. J</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</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></search><sort><creationdate>19980301</creationdate><title>Isolation and molecular characterization of porcine calcitonin gene-related peptide (CGRP) and its endocrine effects in the porcine pancreas</title><author>RASMUSSEN, T. N ; BERSANI, M ; SCHMIDT, P ; THIM, L ; KOFOD, H ; JØRGENSEN, P. N ; POULSEN, S. S ; HOLST, J. J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-8502413a9418bac3de60be15ea8658c536c7e0f9a6b515f6395b7619f9c44a603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adrenal Glands - chemistry</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Antibodies - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Calcitonin Gene-Related Peptide - genetics</topic><topic>Calcitonin Gene-Related Peptide - isolation & purification</topic><topic>Calcitonin Gene-Related Peptide - pharmacology</topic><topic>Endocrine pancreas</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucagon - metabolism</topic><topic>Hormones. Régulation</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Insulin - metabolism</topic><topic>Insulin Secretion</topic><topic>Islets of Langerhans - drug effects</topic><topic>Islets of Langerhans - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Nerve Fibers - chemistry</topic><topic>Pancreas - chemistry</topic><topic>Pancreas - drug effects</topic><topic>Pancreas - innervation</topic><topic>Sequence Homology</topic><topic>Somatostatin - antagonists & inhibitors</topic><topic>Somatostatin - metabolism</topic><topic>Swine</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RASMUSSEN, T. N</creatorcontrib><creatorcontrib>BERSANI, M</creatorcontrib><creatorcontrib>SCHMIDT, P</creatorcontrib><creatorcontrib>THIM, L</creatorcontrib><creatorcontrib>KOFOD, H</creatorcontrib><creatorcontrib>JØRGENSEN, P. N</creatorcontrib><creatorcontrib>POULSEN, S. S</creatorcontrib><creatorcontrib>HOLST, J. J</creatorcontrib><collection>Pascal-Francis</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>Pancreas</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RASMUSSEN, T. N</au><au>BERSANI, M</au><au>SCHMIDT, P</au><au>THIM, L</au><au>KOFOD, H</au><au>JØRGENSEN, P. N</au><au>POULSEN, S. S</au><au>HOLST, J. J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation and molecular characterization of porcine calcitonin gene-related peptide (CGRP) and its endocrine effects in the porcine pancreas</atitle><jtitle>Pancreas</jtitle><addtitle>Pancreas</addtitle><date>1998-03-01</date><risdate>1998</risdate><volume>16</volume><issue>2</issue><spage>195</spage><epage>204</epage><pages>195-204</pages><issn>0885-3177</issn><eissn>1536-4828</eissn><coden>PANCE4</coden><abstract>The aim of this study was to investigate the possible role of porcine calcitonin gene-related peptide (CGRP) in the regulation of the endocrine porcine pancreas. Initially, we isolated and purified CGRP from extracts of porcine adrenal glands and pancreases. A single molecular form of the peptide was found in the two tissues. The adrenal peptide was sequenced and found to differ from human alpha-CGRP at six positions and from human beta-CGRP at three positions. By immunohistochemistry, CGRP was found in nerve fibers in the pancreatic ganglia. A synthetic replica of the porcine peptide was infused at different dose levels (10(-10), 10(-9), and 10(-8) M) into isolated perfused porcine pancreata. With 5 mmol/L glucose in the perfusate. CGRP at 10(-10) and 10(-9) M increased insulin and glucagon secretion, whereas significant decreases were observed with 10(-8) M. Somatostatin secretion was increased significantly by 10(-8) M CGRP. In immunoneutralization studies (n = 6) using a high-affinity somatostatin antibody, the inhibitory effect of CGRP at 10(-8) M was reversed to a significant stimulation of insulin and glucagon secretion. Insulin secretion in response to square-wave increases in glucose concentration to 11 mM was inhibited dose dependently by CGRP; at 10(-8) M the insulin output decreased by 72+/-9% (n = 6). The present results indicate that CGRP may be involved in the regulation of insulin and glucagon secretion from the porcine pancreas.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>9510144</pmid><doi>10.1097/00006676-199803000-00014</doi><tpages>10</tpages></addata></record> |
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subjects | Adrenal Glands - chemistry Amino Acid Sequence Animals Antibodies - pharmacology Biological and medical sciences Calcitonin Gene-Related Peptide - genetics Calcitonin Gene-Related Peptide - isolation & purification Calcitonin Gene-Related Peptide - pharmacology Endocrine pancreas Fundamental and applied biological sciences. Psychology Glucagon - metabolism Hormones. Régulation Humans Immunohistochemistry Insulin - metabolism Insulin Secretion Islets of Langerhans - drug effects Islets of Langerhans - metabolism Molecular Sequence Data Nerve Fibers - chemistry Pancreas - chemistry Pancreas - drug effects Pancreas - innervation Sequence Homology Somatostatin - antagonists & inhibitors Somatostatin - metabolism Swine Vertebrates: endocrinology |
title | Isolation and molecular characterization of porcine calcitonin gene-related peptide (CGRP) and its endocrine effects in the porcine pancreas |
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