Neural mechanisms involved in the delay of gastric emptying and gastrointestinal transit of liquid after thoracic spinal cord transection in awake rats

Spinal cord transection (SCT) delays gastric emptying (GE), and intestinal and gastrointestinal (GI) transit of liquid in awake rats. This study evaluates the neural mechanisms involved in this phenomenon. Male Wistar rats ( N=147) were fasted for 16 h and had the left jugular vein cannulated follow...

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Veröffentlicht in:Autonomic neuroscience 2001-02, Vol.87 (1), p.52-58
Hauptverfasser: de Assis Aquino Gondim, Francisco, Leite Rodrigues, Cleonisio, Ronaldo Vasconcelos da Graça, José, Duarte Camurça, Flávio, Menezes Piancó de Alencar, Hamilton, Aguiar dos Santos, Armenio, Hélio Rola, Francisco
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creator de Assis Aquino Gondim, Francisco
Leite Rodrigues, Cleonisio
Ronaldo Vasconcelos da Graça, José
Duarte Camurça, Flávio
Menezes Piancó de Alencar, Hamilton
Aguiar dos Santos, Armenio
Hélio Rola, Francisco
description Spinal cord transection (SCT) delays gastric emptying (GE), and intestinal and gastrointestinal (GI) transit of liquid in awake rats. This study evaluates the neural mechanisms involved in this phenomenon. Male Wistar rats ( N=147) were fasted for 16 h and had the left jugular vein cannulated followed by laminectomy or laminectomy+complete SCT between T 4 and T 5 vertebrae. The next day, a test meal (1.5 ml of a phenol red solution, 0.5 mg/ml in 5% glucose) was administered by gavage feeding and 10 min later cervical dislocation was performed. Dye recovery in the stomach, and proximal, mid and distal small intestine was determined by spectrophotometry. SCT inhibited GE and GI transit since it increased gastric recovery by 71.3% and decreased mid small intestine recovery by 100% ( P
doi_str_mv 10.1016/S1566-0702(00)00261-7
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This study evaluates the neural mechanisms involved in this phenomenon. Male Wistar rats ( N=147) were fasted for 16 h and had the left jugular vein cannulated followed by laminectomy or laminectomy+complete SCT between T 4 and T 5 vertebrae. The next day, a test meal (1.5 ml of a phenol red solution, 0.5 mg/ml in 5% glucose) was administered by gavage feeding and 10 min later cervical dislocation was performed. Dye recovery in the stomach, and proximal, mid and distal small intestine was determined by spectrophotometry. SCT inhibited GE and GI transit since it increased gastric recovery by 71.3% and decreased mid small intestine recovery by 100% ( P&lt;0.05). Subdiaphragmatic vagotomy, celiac ganglionectomy+section of the splanchnic nerves, i.v. hexamethonium (20 mg/kg) or yohimbine (3 mg/kg) prevented the development of the SCT effect on GE and GI transit. Pretreatment with i.v. naloxone (2 mg/kg), l-NAME (3 mg/kg) or propranolol (2 mg/kg) was ineffective. Bilateral adrenalectomy or guanethidine (10 mg/kg) increased the magnitude of the GE inhibition, while i.v. prazosin (1 mg/kg) or atropine (0.5 mg/kg) decreased the magnitude but did not abolish the GE inhibition. 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This study evaluates the neural mechanisms involved in this phenomenon. Male Wistar rats ( N=147) were fasted for 16 h and had the left jugular vein cannulated followed by laminectomy or laminectomy+complete SCT between T 4 and T 5 vertebrae. The next day, a test meal (1.5 ml of a phenol red solution, 0.5 mg/ml in 5% glucose) was administered by gavage feeding and 10 min later cervical dislocation was performed. Dye recovery in the stomach, and proximal, mid and distal small intestine was determined by spectrophotometry. SCT inhibited GE and GI transit since it increased gastric recovery by 71.3% and decreased mid small intestine recovery by 100% ( P&lt;0.05). Subdiaphragmatic vagotomy, celiac ganglionectomy+section of the splanchnic nerves, i.v. hexamethonium (20 mg/kg) or yohimbine (3 mg/kg) prevented the development of the SCT effect on GE and GI transit. Pretreatment with i.v. naloxone (2 mg/kg), l-NAME (3 mg/kg) or propranolol (2 mg/kg) was ineffective. 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Psychology</topic><topic>Ganglia, Sympathetic - physiology</topic><topic>Ganglia, Sympathetic - surgery</topic><topic>Ganglionectomy - adverse effects</topic><topic>Gastric emptying</topic><topic>Gastric Emptying - drug effects</topic><topic>Gastric Emptying - physiology</topic><topic>Gastrointestinal Diseases - drug therapy</topic><topic>Gastrointestinal Diseases - etiology</topic><topic>Gastrointestinal Diseases - physiopathology</topic><topic>Gastrointestinal motility</topic><topic>Gastrointestinal Motility - drug effects</topic><topic>Gastrointestinal Motility - physiology</topic><topic>Indicators and Reagents - pharmacokinetics</topic><topic>Male</topic><topic>Phenolsulfonphthalein - pharmacokinetics</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Spinal Cord - pathology</topic><topic>Spinal Cord - physiopathology</topic><topic>Spinal Cord Injuries - complications</topic><topic>Spinal cord injury</topic><topic>Splanchnic Nerves - physiology</topic><topic>Splanchnic Nerves - surgery</topic><topic>Stomach</topic><topic>Sympathectomy - adverse effects</topic><topic>Thoracic Vertebrae</topic><topic>Time Factors</topic><topic>Vagotomy - adverse effects</topic><topic>Vagus nerve</topic><topic>Vertebrates: digestive system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Assis Aquino Gondim, Francisco</creatorcontrib><creatorcontrib>Leite Rodrigues, Cleonisio</creatorcontrib><creatorcontrib>Ronaldo Vasconcelos da Graça, José</creatorcontrib><creatorcontrib>Duarte Camurça, Flávio</creatorcontrib><creatorcontrib>Menezes Piancó de Alencar, Hamilton</creatorcontrib><creatorcontrib>Aguiar dos Santos, Armenio</creatorcontrib><creatorcontrib>Hélio Rola, Francisco</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>Autonomic neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Assis Aquino Gondim, Francisco</au><au>Leite Rodrigues, Cleonisio</au><au>Ronaldo Vasconcelos da Graça, José</au><au>Duarte Camurça, Flávio</au><au>Menezes Piancó de Alencar, Hamilton</au><au>Aguiar dos Santos, Armenio</au><au>Hélio Rola, Francisco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neural mechanisms involved in the delay of gastric emptying and gastrointestinal transit of liquid after thoracic spinal cord transection in awake rats</atitle><jtitle>Autonomic neuroscience</jtitle><addtitle>Auton Neurosci</addtitle><date>2001-02-20</date><risdate>2001</risdate><volume>87</volume><issue>1</issue><spage>52</spage><epage>58</epage><pages>52-58</pages><issn>1566-0702</issn><eissn>1872-7484</eissn><abstract>Spinal cord transection (SCT) delays gastric emptying (GE), and intestinal and gastrointestinal (GI) transit of liquid in awake rats. This study evaluates the neural mechanisms involved in this phenomenon. Male Wistar rats ( N=147) were fasted for 16 h and had the left jugular vein cannulated followed by laminectomy or laminectomy+complete SCT between T 4 and T 5 vertebrae. The next day, a test meal (1.5 ml of a phenol red solution, 0.5 mg/ml in 5% glucose) was administered by gavage feeding and 10 min later cervical dislocation was performed. Dye recovery in the stomach, and proximal, mid and distal small intestine was determined by spectrophotometry. SCT inhibited GE and GI transit since it increased gastric recovery by 71.3% and decreased mid small intestine recovery by 100% ( P&lt;0.05). Subdiaphragmatic vagotomy, celiac ganglionectomy+section of the splanchnic nerves, i.v. hexamethonium (20 mg/kg) or yohimbine (3 mg/kg) prevented the development of the SCT effect on GE and GI transit. Pretreatment with i.v. naloxone (2 mg/kg), l-NAME (3 mg/kg) or propranolol (2 mg/kg) was ineffective. Bilateral adrenalectomy or guanethidine (10 mg/kg) increased the magnitude of the GE inhibition, while i.v. prazosin (1 mg/kg) or atropine (0.5 mg/kg) decreased the magnitude but did not abolish the GE inhibition. In summary, the inhibition of GI motility observed 1 day after thoracic SCT in awake rats seems to involve vagal and possibly splanchnic pathways.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>11280307</pmid><doi>10.1016/S1566-0702(00)00261-7</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Autonomic Nervous System - drug effects
Autonomic Nervous System - pathology
Autonomic Nervous System - physiopathology
Biological and medical sciences
Cardiovascular Physiological Phenomena - drug effects
Celiac ganglion
Digestive System - drug effects
Digestive System - innervation
Digestive System Physiological Phenomena
Fundamental and applied biological sciences. Psychology
Ganglia, Sympathetic - physiology
Ganglia, Sympathetic - surgery
Ganglionectomy - adverse effects
Gastric emptying
Gastric Emptying - drug effects
Gastric Emptying - physiology
Gastrointestinal Diseases - drug therapy
Gastrointestinal Diseases - etiology
Gastrointestinal Diseases - physiopathology
Gastrointestinal motility
Gastrointestinal Motility - drug effects
Gastrointestinal Motility - physiology
Indicators and Reagents - pharmacokinetics
Male
Phenolsulfonphthalein - pharmacokinetics
Rats
Rats, Wistar
Spinal Cord - pathology
Spinal Cord - physiopathology
Spinal Cord Injuries - complications
Spinal cord injury
Splanchnic Nerves - physiology
Splanchnic Nerves - surgery
Stomach
Sympathectomy - adverse effects
Thoracic Vertebrae
Time Factors
Vagotomy - adverse effects
Vagus nerve
Vertebrates: digestive system
title Neural mechanisms involved in the delay of gastric emptying and gastrointestinal transit of liquid after thoracic spinal cord transection in awake rats
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