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Increased intestinal non-substance P tachykinin concentrations in malignant midgut carcinoid disease
Background: Diarrhoea is an important feature of the carcinoid syndrome, and various agents which may be released from carcinoid tumours have been considered to contribute pathophysiologically. The aim of the present study was to determine luminal concentrations of possible chemical mediators in an...
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Published in: | Journal of gastroenterology and hepatology 1999-05, Vol.14 (5), p.500-507 |
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creator | Makridis, Charlie Theodorsson, Elvar Åkerström, Göran Öberg, Kjell Knutson, Lars |
description | Background: Diarrhoea is an important feature of the carcinoid syndrome, and various agents which may be released from carcinoid tumours have been considered to contribute pathophysiologically. The aim of the present study was to determine luminal concentrations of possible chemical mediators in an uninvolved small intestinal segment using a two‐balloon six‐channel tube in nine patients with malignant midgut carcinoid disease.
Methods: All patients were treated with interferon and/or octreotide to alleviate the most severe flush. Ion transport was measured during luminal perfusion and luminal perfusate concentrations of calcitonin gene‐related peptide, neurotensin, prostaglandin E (PGE)2, neuropeptide Y, somatostatin, vasoactive intestinal polypeptide, substance P and other tachykinins (neurokinin A, neurokinin B, neuropeptide K, eledoisin) were determined by separate assays.
Results: Carcinoid patients showed decreased absorption of Cl–, Na+, K+ and water and increased luminal content of non‐substance P tachykinins to 424.5 fmol/cm per h, compared with 255.5 fmol/cm per h in control subjects. There were also increased luminal concentrations of PGE2, commonly claimed as a more general mediator of diarrhoea.
Conclusions: The observed increase in intestinal tachykinins may involve extended activity from tachykinin‐containing intrinsic neurones in the enteric nervous system, contributing to enhanced intestinal motility and secretory diarrhoea in patients with carcinoid syndrome. |
doi_str_mv | 10.1046/j.1440-1746.1999.01888.x |
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Methods: All patients were treated with interferon and/or octreotide to alleviate the most severe flush. Ion transport was measured during luminal perfusion and luminal perfusate concentrations of calcitonin gene‐related peptide, neurotensin, prostaglandin E (PGE)2, neuropeptide Y, somatostatin, vasoactive intestinal polypeptide, substance P and other tachykinins (neurokinin A, neurokinin B, neuropeptide K, eledoisin) were determined by separate assays.
Results: Carcinoid patients showed decreased absorption of Cl–, Na+, K+ and water and increased luminal content of non‐substance P tachykinins to 424.5 fmol/cm per h, compared with 255.5 fmol/cm per h in control subjects. There were also increased luminal concentrations of PGE2, commonly claimed as a more general mediator of diarrhoea.
Conclusions: The observed increase in intestinal tachykinins may involve extended activity from tachykinin‐containing intrinsic neurones in the enteric nervous system, contributing to enhanced intestinal motility and secretory diarrhoea in patients with carcinoid syndrome.</description><identifier>ISSN: 0815-9319</identifier><identifier>EISSN: 1440-1746</identifier><identifier>DOI: 10.1046/j.1440-1746.1999.01888.x</identifier><identifier>PMID: 10355517</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Science Pty</publisher><subject>Adult ; Aged ; Biogenic Amines - metabolism ; Biological and medical sciences ; Biomarkers, Tumor - metabolism ; carcinoid disease ; Carcinoid Tumor - physiopathology ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Ileal Neoplasms - physiopathology ; Intestine, Small - metabolism ; ion transport ; Male ; Malignant Carcinoid Syndrome - metabolism ; Medical sciences ; Middle Aged ; Neuropeptides - metabolism ; Perfusion ; prostaglandins ; Radioimmunoassay ; segmental intestinal perfusion ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; tachykinins ; Tachykinins - metabolism ; Tumors</subject><ispartof>Journal of gastroenterology and hepatology, 1999-05, Vol.14 (5), p.500-507</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4328-5d3e5c3f5f619c6e2a78cdc46b505d3a39b2e94b994a34ceaa7e7529faca3f133</citedby><cites>FETCH-LOGICAL-c4328-5d3e5c3f5f619c6e2a78cdc46b505d3a39b2e94b994a34ceaa7e7529faca3f133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1788837$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10355517$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Makridis, Charlie</creatorcontrib><creatorcontrib>Theodorsson, Elvar</creatorcontrib><creatorcontrib>Åkerström, Göran</creatorcontrib><creatorcontrib>Öberg, Kjell</creatorcontrib><creatorcontrib>Knutson, Lars</creatorcontrib><title>Increased intestinal non-substance P tachykinin concentrations in malignant midgut carcinoid disease</title><title>Journal of gastroenterology and hepatology</title><addtitle>J Gastroenterol Hepatol</addtitle><description>Background: Diarrhoea is an important feature of the carcinoid syndrome, and various agents which may be released from carcinoid tumours have been considered to contribute pathophysiologically. The aim of the present study was to determine luminal concentrations of possible chemical mediators in an uninvolved small intestinal segment using a two‐balloon six‐channel tube in nine patients with malignant midgut carcinoid disease.
Methods: All patients were treated with interferon and/or octreotide to alleviate the most severe flush. Ion transport was measured during luminal perfusion and luminal perfusate concentrations of calcitonin gene‐related peptide, neurotensin, prostaglandin E (PGE)2, neuropeptide Y, somatostatin, vasoactive intestinal polypeptide, substance P and other tachykinins (neurokinin A, neurokinin B, neuropeptide K, eledoisin) were determined by separate assays.
Results: Carcinoid patients showed decreased absorption of Cl–, Na+, K+ and water and increased luminal content of non‐substance P tachykinins to 424.5 fmol/cm per h, compared with 255.5 fmol/cm per h in control subjects. There were also increased luminal concentrations of PGE2, commonly claimed as a more general mediator of diarrhoea.
Conclusions: The observed increase in intestinal tachykinins may involve extended activity from tachykinin‐containing intrinsic neurones in the enteric nervous system, contributing to enhanced intestinal motility and secretory diarrhoea in patients with carcinoid syndrome.</description><subject>Adult</subject><subject>Aged</subject><subject>Biogenic Amines - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>carcinoid disease</subject><subject>Carcinoid Tumor - physiopathology</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Ileal Neoplasms - physiopathology</subject><subject>Intestine, Small - metabolism</subject><subject>ion transport</subject><subject>Male</subject><subject>Malignant Carcinoid Syndrome - metabolism</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neuropeptides - metabolism</subject><subject>Perfusion</subject><subject>prostaglandins</subject><subject>Radioimmunoassay</subject><subject>segmental intestinal perfusion</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>tachykinins</subject><subject>Tachykinins - metabolism</subject><subject>Tumors</subject><issn>0815-9319</issn><issn>1440-1746</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqNkM-P1CAUx4nRuOPqv2A4GG-tMEApBw-60Zk16-ph_HEjr5SuzLZ0BRpn_nupnaweDQfIe5_ve-GDEKakpIRXr_Yl5ZwUVPKqpEqpktC6rsvDA7S6bzxEK1JTUShG1Rl6EuOeEMKJFI_RGSVMCEHlCrWX3gQL0bbY-WRjch567EdfxKmJCbyx-DNOYH4cb513Hpsxl3wKkNzoYw7hAXp348EnPLj2ZkrYQDDOj67FrYvz7KfoUQd9tM9O9zn68v7d7mJbXH3aXF68uSoMZ-u6EC2zwrBOdBVVprJrkLVpDa8aQXIPmGrWVvFGKQ6MGwsgrRRr1YEB1lHGztHLZe5dGH9O-TN6cNHYvgdvxynqSsl8OMlgvYAmjDEG2-m74AYIR02Jng3rvZ5F6lmkng3rP4b1IUefn3ZMzWDbf4KL0gy8OAEQDfRdyA5d_MvJPIfN2OsF--V6e_zv_frDZju_cr5Y8i4me7jPQ7jVlWRS6G_XG_326_a7-ri71jv2G1RHqLc</recordid><startdate>199905</startdate><enddate>199905</enddate><creator>Makridis, Charlie</creator><creator>Theodorsson, Elvar</creator><creator>Åkerström, Göran</creator><creator>Öberg, Kjell</creator><creator>Knutson, Lars</creator><general>Blackwell Science Pty</general><general>Blackwell Science</general><scope>BSCLL</scope><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>199905</creationdate><title>Increased intestinal non-substance P tachykinin concentrations in malignant midgut carcinoid disease</title><author>Makridis, Charlie ; Theodorsson, Elvar ; Åkerström, Göran ; Öberg, Kjell ; Knutson, Lars</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4328-5d3e5c3f5f619c6e2a78cdc46b505d3a39b2e94b994a34ceaa7e7529faca3f133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biogenic Amines - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>carcinoid disease</topic><topic>Carcinoid Tumor - physiopathology</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Ileal Neoplasms - physiopathology</topic><topic>Intestine, Small - metabolism</topic><topic>ion transport</topic><topic>Male</topic><topic>Malignant Carcinoid Syndrome - metabolism</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neuropeptides - metabolism</topic><topic>Perfusion</topic><topic>prostaglandins</topic><topic>Radioimmunoassay</topic><topic>segmental intestinal perfusion</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>tachykinins</topic><topic>Tachykinins - metabolism</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Makridis, Charlie</creatorcontrib><creatorcontrib>Theodorsson, Elvar</creatorcontrib><creatorcontrib>Åkerström, Göran</creatorcontrib><creatorcontrib>Öberg, Kjell</creatorcontrib><creatorcontrib>Knutson, Lars</creatorcontrib><collection>Istex</collection><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>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Makridis, Charlie</au><au>Theodorsson, Elvar</au><au>Åkerström, Göran</au><au>Öberg, Kjell</au><au>Knutson, Lars</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased intestinal non-substance P tachykinin concentrations in malignant midgut carcinoid disease</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>1999-05</date><risdate>1999</risdate><volume>14</volume><issue>5</issue><spage>500</spage><epage>507</epage><pages>500-507</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background: Diarrhoea is an important feature of the carcinoid syndrome, and various agents which may be released from carcinoid tumours have been considered to contribute pathophysiologically. The aim of the present study was to determine luminal concentrations of possible chemical mediators in an uninvolved small intestinal segment using a two‐balloon six‐channel tube in nine patients with malignant midgut carcinoid disease.
Methods: All patients were treated with interferon and/or octreotide to alleviate the most severe flush. Ion transport was measured during luminal perfusion and luminal perfusate concentrations of calcitonin gene‐related peptide, neurotensin, prostaglandin E (PGE)2, neuropeptide Y, somatostatin, vasoactive intestinal polypeptide, substance P and other tachykinins (neurokinin A, neurokinin B, neuropeptide K, eledoisin) were determined by separate assays.
Results: Carcinoid patients showed decreased absorption of Cl–, Na+, K+ and water and increased luminal content of non‐substance P tachykinins to 424.5 fmol/cm per h, compared with 255.5 fmol/cm per h in control subjects. There were also increased luminal concentrations of PGE2, commonly claimed as a more general mediator of diarrhoea.
Conclusions: The observed increase in intestinal tachykinins may involve extended activity from tachykinin‐containing intrinsic neurones in the enteric nervous system, contributing to enhanced intestinal motility and secretory diarrhoea in patients with carcinoid syndrome.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Science Pty</pub><pmid>10355517</pmid><doi>10.1046/j.1440-1746.1999.01888.x</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Aged Biogenic Amines - metabolism Biological and medical sciences Biomarkers, Tumor - metabolism carcinoid disease Carcinoid Tumor - physiopathology Female Gastroenterology. Liver. Pancreas. Abdomen Humans Ileal Neoplasms - physiopathology Intestine, Small - metabolism ion transport Male Malignant Carcinoid Syndrome - metabolism Medical sciences Middle Aged Neuropeptides - metabolism Perfusion prostaglandins Radioimmunoassay segmental intestinal perfusion Stomach. Duodenum. Small intestine. Colon. Rectum. Anus tachykinins Tachykinins - metabolism Tumors |
title | Increased intestinal non-substance P tachykinin concentrations in malignant midgut carcinoid disease |
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