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...
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Veröffentlicht in: | Pancreas 2000, Vol.20 (1), p.94-101 |
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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 |
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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 & 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. 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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 & 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 & Wilkins</pub><pmid>10630389</pmid><doi>10.1097/00006676-200001000-00013</doi><tpages>8</tpages></addata></record> |
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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 |
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