Regulation of pancreatic secretion by vagal nerve during short-term duct occlusion in conscious rats

The basal exocrine secretion of the pancreas is maintained at a constant level in conscious rats. We examined the changes in basal secretion with respect to the effect of various time periods of pancreatic duct occlusion (PDL). Male Wistar rats were prepared with cannulae that separately drained bil...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pancreas 2000, Vol.20 (1), p.94-101
Hauptverfasser: SUZUKI, S, KANAI, S, MIYASAKA, K, JIMI, A, FUNAKOSHI, A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 101
container_issue 1
container_start_page 94
container_title Pancreas
container_volume 20
creator SUZUKI, S
KANAI, S
MIYASAKA, K
JIMI, A
FUNAKOSHI, A
description The basal exocrine secretion of the pancreas is maintained at a constant level in conscious rats. We examined the changes in basal secretion with respect to the effect of various time periods of pancreatic duct occlusion (PDL). Male Wistar rats were prepared with cannulae that separately drained bile and pancreatic juice as well as with a duodenal cannula. Rats were placed in restraint cages, and experiments were conducted without anesthesia 4 days after the operation. Cholecystokinin (CCK) release was artificially prevented by the continuous infusion of bile with trypsin into the duodenal lumen throughout the experimental period to avoid the modification of pancreatic response by CCK. After 2-h basal collection, a pancreatic secretion was interrupted for 0.5-4 h, and then the collection of pancreatic juice was initiated again for an additional 2-4.5 h. The pancreatic secretion after the reopening of the 0.5-to 3-h PDL was comparable to basal secretion levels. However, protein secretion was significantly inhibited after the removal of 4-h PDL. Both vagotomy and capsaicin treatment abolished this inhibition, and the protein secretion after 1-h PDL in vagotomized rats increased 1.5-fold high compared with the basal value. These observations indicate that protein secretion was ceased during PDL via vagal nerve, and this may be a self-protective mechanism.
doi_str_mv 10.1097/00006676-200001000-00013
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70835823</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70835823</sourcerecordid><originalsourceid>FETCH-LOGICAL-c369t-f39257967d9fc2e23df8fa0a722a12cd7d9c2c820b8f17c623477f5a42dffdf03</originalsourceid><addsrcrecordid>eNpNkNtKAzEQhoMotlZfQXIh3kVz6CbZSymeoCCIXod0ktSV7W5Ndgt9e7NtPQTCTH6-ScKHEGb0htFS3dK8pFSS8KFjeZOhiiM0ZoWQZKq5PkZjqnVBBFNqhM5S-syEEkV5ikaMSkGFLsfIvfplX9uuahvcBry2DUSfj4CTz90uX2zxxi5tjRsfNx67PlbNEqePNnak83GVE-hwC1D3aeCrBkPbJKjaPuFou3SOToKtk7841Al6f7h_mz2R-cvj8-xuTkDIsiNBlLxQpVSuDMA9Fy7oYKlVnFvGweUcOGhOFzowBZKLqVKhsFPuQnCBigm63t-7ju1X71NnVlUCX9e28fkvRlEtCs1FBvUehNimFH0w61itbNwaRs1g2PwYNr-Gzc5wHr08vNEvVt79G9wrzcDVAbAJbB1iVlqlP45LKakQ3_w-hNQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70835823</pqid></control><display><type>article</type><title>Regulation of pancreatic secretion by vagal nerve during short-term duct occlusion in conscious rats</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><creator>SUZUKI, S ; KANAI, S ; MIYASAKA, K ; JIMI, A ; FUNAKOSHI, A</creator><creatorcontrib>SUZUKI, S ; KANAI, S ; MIYASAKA, K ; JIMI, A ; FUNAKOSHI, A</creatorcontrib><description>The basal exocrine secretion of the pancreas is maintained at a constant level in conscious rats. We examined the changes in basal secretion with respect to the effect of various time periods of pancreatic duct occlusion (PDL). Male Wistar rats were prepared with cannulae that separately drained bile and pancreatic juice as well as with a duodenal cannula. Rats were placed in restraint cages, and experiments were conducted without anesthesia 4 days after the operation. Cholecystokinin (CCK) release was artificially prevented by the continuous infusion of bile with trypsin into the duodenal lumen throughout the experimental period to avoid the modification of pancreatic response by CCK. After 2-h basal collection, a pancreatic secretion was interrupted for 0.5-4 h, and then the collection of pancreatic juice was initiated again for an additional 2-4.5 h. The pancreatic secretion after the reopening of the 0.5-to 3-h PDL was comparable to basal secretion levels. However, protein secretion was significantly inhibited after the removal of 4-h PDL. Both vagotomy and capsaicin treatment abolished this inhibition, and the protein secretion after 1-h PDL in vagotomized rats increased 1.5-fold high compared with the basal value. These observations indicate that protein secretion was ceased during PDL via vagal nerve, and this may be a self-protective mechanism.</description><identifier>ISSN: 0885-3177</identifier><identifier>EISSN: 1536-4828</identifier><identifier>DOI: 10.1097/00006676-200001000-00013</identifier><identifier>PMID: 10630389</identifier><identifier>CODEN: PANCE4</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams &amp; Wilkins</publisher><subject>Afferent Pathways - physiology ; Animals ; Bile - physiology ; Biological and medical sciences ; Capsaicin - pharmacology ; Cholecystokinin - physiology ; Consciousness ; Constriction ; Duodenum ; Gastroenterology. Liver. Pancreas. Abdomen ; Male ; Medical sciences ; Other diseases. Semiology ; Pancreas - metabolism ; Pancreatic Ducts - physiopathology ; Pancreatic Juice - metabolism ; Rats ; Rats, Wistar ; Secretory Rate ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Trypsin - pharmacology ; Trypsin - physiology ; Vagotomy ; Vagus Nerve - physiology</subject><ispartof>Pancreas, 2000, Vol.20 (1), p.94-101</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-f39257967d9fc2e23df8fa0a722a12cd7d9c2c820b8f17c623477f5a42dffdf03</citedby><cites>FETCH-LOGICAL-c369t-f39257967d9fc2e23df8fa0a722a12cd7d9c2c820b8f17c623477f5a42dffdf03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1266603$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10630389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SUZUKI, S</creatorcontrib><creatorcontrib>KANAI, S</creatorcontrib><creatorcontrib>MIYASAKA, K</creatorcontrib><creatorcontrib>JIMI, A</creatorcontrib><creatorcontrib>FUNAKOSHI, A</creatorcontrib><title>Regulation of pancreatic secretion by vagal nerve during short-term duct occlusion in conscious rats</title><title>Pancreas</title><addtitle>Pancreas</addtitle><description>The basal exocrine secretion of the pancreas is maintained at a constant level in conscious rats. We examined the changes in basal secretion with respect to the effect of various time periods of pancreatic duct occlusion (PDL). Male Wistar rats were prepared with cannulae that separately drained bile and pancreatic juice as well as with a duodenal cannula. Rats were placed in restraint cages, and experiments were conducted without anesthesia 4 days after the operation. Cholecystokinin (CCK) release was artificially prevented by the continuous infusion of bile with trypsin into the duodenal lumen throughout the experimental period to avoid the modification of pancreatic response by CCK. After 2-h basal collection, a pancreatic secretion was interrupted for 0.5-4 h, and then the collection of pancreatic juice was initiated again for an additional 2-4.5 h. The pancreatic secretion after the reopening of the 0.5-to 3-h PDL was comparable to basal secretion levels. However, protein secretion was significantly inhibited after the removal of 4-h PDL. Both vagotomy and capsaicin treatment abolished this inhibition, and the protein secretion after 1-h PDL in vagotomized rats increased 1.5-fold high compared with the basal value. These observations indicate that protein secretion was ceased during PDL via vagal nerve, and this may be a self-protective mechanism.</description><subject>Afferent Pathways - physiology</subject><subject>Animals</subject><subject>Bile - physiology</subject><subject>Biological and medical sciences</subject><subject>Capsaicin - pharmacology</subject><subject>Cholecystokinin - physiology</subject><subject>Consciousness</subject><subject>Constriction</subject><subject>Duodenum</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Pancreas - metabolism</subject><subject>Pancreatic Ducts - physiopathology</subject><subject>Pancreatic Juice - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Secretory Rate</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Trypsin - pharmacology</subject><subject>Trypsin - physiology</subject><subject>Vagotomy</subject><subject>Vagus Nerve - physiology</subject><issn>0885-3177</issn><issn>1536-4828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkNtKAzEQhoMotlZfQXIh3kVz6CbZSymeoCCIXod0ktSV7W5Ndgt9e7NtPQTCTH6-ScKHEGb0htFS3dK8pFSS8KFjeZOhiiM0ZoWQZKq5PkZjqnVBBFNqhM5S-syEEkV5ikaMSkGFLsfIvfplX9uuahvcBry2DUSfj4CTz90uX2zxxi5tjRsfNx67PlbNEqePNnak83GVE-hwC1D3aeCrBkPbJKjaPuFou3SOToKtk7841Al6f7h_mz2R-cvj8-xuTkDIsiNBlLxQpVSuDMA9Fy7oYKlVnFvGweUcOGhOFzowBZKLqVKhsFPuQnCBigm63t-7ju1X71NnVlUCX9e28fkvRlEtCs1FBvUehNimFH0w61itbNwaRs1g2PwYNr-Gzc5wHr08vNEvVt79G9wrzcDVAbAJbB1iVlqlP45LKakQ3_w-hNQ</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>SUZUKI, S</creator><creator>KANAI, S</creator><creator>MIYASAKA, K</creator><creator>JIMI, A</creator><creator>FUNAKOSHI, A</creator><general>Lippincott Williams &amp; 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>2000</creationdate><title>Regulation of pancreatic secretion by vagal nerve during short-term duct occlusion in conscious rats</title><author>SUZUKI, S ; KANAI, S ; MIYASAKA, K ; JIMI, A ; FUNAKOSHI, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-f39257967d9fc2e23df8fa0a722a12cd7d9c2c820b8f17c623477f5a42dffdf03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Afferent Pathways - physiology</topic><topic>Animals</topic><topic>Bile - physiology</topic><topic>Biological and medical sciences</topic><topic>Capsaicin - pharmacology</topic><topic>Cholecystokinin - physiology</topic><topic>Consciousness</topic><topic>Constriction</topic><topic>Duodenum</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><topic>Pancreas - metabolism</topic><topic>Pancreatic Ducts - physiopathology</topic><topic>Pancreatic Juice - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Secretory Rate</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Trypsin - pharmacology</topic><topic>Trypsin - physiology</topic><topic>Vagotomy</topic><topic>Vagus Nerve - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SUZUKI, S</creatorcontrib><creatorcontrib>KANAI, S</creatorcontrib><creatorcontrib>MIYASAKA, K</creatorcontrib><creatorcontrib>JIMI, A</creatorcontrib><creatorcontrib>FUNAKOSHI, A</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>SUZUKI, S</au><au>KANAI, S</au><au>MIYASAKA, K</au><au>JIMI, A</au><au>FUNAKOSHI, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of pancreatic secretion by vagal nerve during short-term duct occlusion in conscious rats</atitle><jtitle>Pancreas</jtitle><addtitle>Pancreas</addtitle><date>2000</date><risdate>2000</risdate><volume>20</volume><issue>1</issue><spage>94</spage><epage>101</epage><pages>94-101</pages><issn>0885-3177</issn><eissn>1536-4828</eissn><coden>PANCE4</coden><abstract>The basal exocrine secretion of the pancreas is maintained at a constant level in conscious rats. We examined the changes in basal secretion with respect to the effect of various time periods of pancreatic duct occlusion (PDL). Male Wistar rats were prepared with cannulae that separately drained bile and pancreatic juice as well as with a duodenal cannula. Rats were placed in restraint cages, and experiments were conducted without anesthesia 4 days after the operation. Cholecystokinin (CCK) release was artificially prevented by the continuous infusion of bile with trypsin into the duodenal lumen throughout the experimental period to avoid the modification of pancreatic response by CCK. After 2-h basal collection, a pancreatic secretion was interrupted for 0.5-4 h, and then the collection of pancreatic juice was initiated again for an additional 2-4.5 h. The pancreatic secretion after the reopening of the 0.5-to 3-h PDL was comparable to basal secretion levels. However, protein secretion was significantly inhibited after the removal of 4-h PDL. Both vagotomy and capsaicin treatment abolished this inhibition, and the protein secretion after 1-h PDL in vagotomized rats increased 1.5-fold high compared with the basal value. These observations indicate that protein secretion was ceased during PDL via vagal nerve, and this may be a self-protective mechanism.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>10630389</pmid><doi>10.1097/00006676-200001000-00013</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0885-3177
ispartof Pancreas, 2000, Vol.20 (1), p.94-101
issn 0885-3177
1536-4828
language eng
recordid cdi_proquest_miscellaneous_70835823
source MEDLINE; Journals@Ovid Complete
subjects Afferent Pathways - physiology
Animals
Bile - physiology
Biological and medical sciences
Capsaicin - pharmacology
Cholecystokinin - physiology
Consciousness
Constriction
Duodenum
Gastroenterology. Liver. Pancreas. Abdomen
Male
Medical sciences
Other diseases. Semiology
Pancreas - metabolism
Pancreatic Ducts - physiopathology
Pancreatic Juice - metabolism
Rats
Rats, Wistar
Secretory Rate
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Trypsin - pharmacology
Trypsin - physiology
Vagotomy
Vagus Nerve - physiology
title Regulation of pancreatic secretion by vagal nerve during short-term duct occlusion in conscious rats
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T12%3A38%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regulation%20of%20pancreatic%20secretion%20by%20vagal%20nerve%20during%20short-term%20duct%20occlusion%20in%20conscious%20rats&rft.jtitle=Pancreas&rft.au=SUZUKI,%20S&rft.date=2000&rft.volume=20&rft.issue=1&rft.spage=94&rft.epage=101&rft.pages=94-101&rft.issn=0885-3177&rft.eissn=1536-4828&rft.coden=PANCE4&rft_id=info:doi/10.1097/00006676-200001000-00013&rft_dat=%3Cproquest_cross%3E70835823%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70835823&rft_id=info:pmid/10630389&rfr_iscdi=true