A simple method to investigate the inhibitory effects of drugs on gastric emptying in the mouse in vivo
Introduction: The aim was to develop a simple method to study modification of gastric motility in the mouse in vivo. Methods: Mice were fed a hydrated diet in which the fluid content of standard laboratory chow was increased by adding water. Gastric emptying was assessed at specified times following...
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Veröffentlicht in: | Journal of pharmacological and toxicological methods 2001-05, Vol.45 (3), p.235-240 |
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description | Introduction: The aim was to develop a simple method to study modification of gastric motility in the mouse in vivo. Methods: Mice were fed a hydrated diet in which the fluid content of standard laboratory chow was increased by adding water. Gastric emptying was assessed at specified times following a 1-h treatment period with orally administered pharmacological agents. Results: We demonstrated consistent and progressive gastric emptying over a 4-h period, stomach content being decreased from 7.52±0.90 at time zero to 2.80±0.25 mg/g body weight after 4 h. Results demonstrated typical effects of inhibitory agents (atropine and morphine) and showed inhibitory effects of three potassium channel opening agents, pinacidil, cromakalim, and SDZ PCO400: the residue remaining in the stomach was increased by 3.66±0.84, 6.56±1.35, and 5.68±1.33 mg/g body weight respectively 1 h after treatment with 10 mg/kg of these agents, compared to vehicle controls. Discussion: The inhibitory activity observed correlated well with previous studies on the effects of potassium channel opening agents on mouse gastrointestinal motility in vivo and in vitro. The present model may thus be of value in the pharmacological investigation of gastrointestinal motility owing to cost and convenience advantages, together with the possibility of its application to studies using transgenic animals. |
doi_str_mv | 10.1016/S1056-8719(01)00155-1 |
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Methods: Mice were fed a hydrated diet in which the fluid content of standard laboratory chow was increased by adding water. Gastric emptying was assessed at specified times following a 1-h treatment period with orally administered pharmacological agents. Results: We demonstrated consistent and progressive gastric emptying over a 4-h period, stomach content being decreased from 7.52±0.90 at time zero to 2.80±0.25 mg/g body weight after 4 h. Results demonstrated typical effects of inhibitory agents (atropine and morphine) and showed inhibitory effects of three potassium channel opening agents, pinacidil, cromakalim, and SDZ PCO400: the residue remaining in the stomach was increased by 3.66±0.84, 6.56±1.35, and 5.68±1.33 mg/g body weight respectively 1 h after treatment with 10 mg/kg of these agents, compared to vehicle controls. Discussion: The inhibitory activity observed correlated well with previous studies on the effects of potassium channel opening agents on mouse gastrointestinal motility in vivo and in vitro. The present model may thus be of value in the pharmacological investigation of gastrointestinal motility owing to cost and convenience advantages, together with the possibility of its application to studies using transgenic animals.</description><identifier>ISSN: 1056-8719</identifier><identifier>EISSN: 1873-488X</identifier><identifier>DOI: 10.1016/S1056-8719(01)00155-1</identifier><identifier>PMID: 11755388</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Administration, Oral ; Animal Feed ; Animals ; Atropine - toxicity ; Benzopyrans - toxicity ; Carbachol - toxicity ; Cromakalim - toxicity ; Cyclopentanes - toxicity ; Dose-Response Relationship, Drug ; Gastric emptying ; Gastric Emptying - drug effects ; Gastric Emptying - physiology ; Inhibition of gastric motility ; Male ; Methods ; Metoclopramide - toxicity ; Mice ; Mice, Inbred Strains ; Morphine - toxicity ; Mouse ; Organ Size - drug effects ; Pinacidil - toxicity ; Potassium Channel Blockers - administration & dosage ; Potassium Channel Blockers - toxicity ; Potassium channel openers ; Stomach ; Stomach - drug effects ; Stomach - pathology ; Toxicology - methods</subject><ispartof>Journal of pharmacological and toxicological methods, 2001-05, Vol.45 (3), p.235-240</ispartof><rights>2002 Elsevier Science Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-231c48c8ba292e7b0bdfab60e40f910ce5e664933c38849a92787cff89e113943</citedby><cites>FETCH-LOGICAL-c392t-231c48c8ba292e7b0bdfab60e40f910ce5e664933c38849a92787cff89e113943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S1056-8719(01)00155-1$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11755388$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yeung, Chi-Kong</creatorcontrib><creatorcontrib>McCurrie, Janice R.</creatorcontrib><creatorcontrib>Wood, Diana</creatorcontrib><title>A simple method to investigate the inhibitory effects of drugs on gastric emptying in the mouse in vivo</title><title>Journal of pharmacological and toxicological methods</title><addtitle>J Pharmacol Toxicol Methods</addtitle><description>Introduction: The aim was to develop a simple method to study modification of gastric motility in the mouse in vivo. Methods: Mice were fed a hydrated diet in which the fluid content of standard laboratory chow was increased by adding water. Gastric emptying was assessed at specified times following a 1-h treatment period with orally administered pharmacological agents. Results: We demonstrated consistent and progressive gastric emptying over a 4-h period, stomach content being decreased from 7.52±0.90 at time zero to 2.80±0.25 mg/g body weight after 4 h. Results demonstrated typical effects of inhibitory agents (atropine and morphine) and showed inhibitory effects of three potassium channel opening agents, pinacidil, cromakalim, and SDZ PCO400: the residue remaining in the stomach was increased by 3.66±0.84, 6.56±1.35, and 5.68±1.33 mg/g body weight respectively 1 h after treatment with 10 mg/kg of these agents, compared to vehicle controls. Discussion: The inhibitory activity observed correlated well with previous studies on the effects of potassium channel opening agents on mouse gastrointestinal motility in vivo and in vitro. The present model may thus be of value in the pharmacological investigation of gastrointestinal motility owing to cost and convenience advantages, together with the possibility of its application to studies using transgenic animals.</description><subject>Administration, Oral</subject><subject>Animal Feed</subject><subject>Animals</subject><subject>Atropine - toxicity</subject><subject>Benzopyrans - toxicity</subject><subject>Carbachol - toxicity</subject><subject>Cromakalim - toxicity</subject><subject>Cyclopentanes - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Gastric emptying</subject><subject>Gastric Emptying - drug effects</subject><subject>Gastric Emptying - physiology</subject><subject>Inhibition of gastric motility</subject><subject>Male</subject><subject>Methods</subject><subject>Metoclopramide - toxicity</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Morphine - toxicity</subject><subject>Mouse</subject><subject>Organ Size - drug effects</subject><subject>Pinacidil - toxicity</subject><subject>Potassium Channel Blockers - administration & dosage</subject><subject>Potassium Channel Blockers - toxicity</subject><subject>Potassium channel openers</subject><subject>Stomach</subject><subject>Stomach - drug effects</subject><subject>Stomach - pathology</subject><subject>Toxicology - methods</subject><issn>1056-8719</issn><issn>1873-488X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtr3DAURkVp6EzS_oQGrUqycKpr-SGtQhjygoEs2kJ3wpavPCpjayJpDPPvq3mELLPSFZzvPg4h34HdAIPq5y9gZZWJGuQVg2vGoCwz-ETmIGqeFUL8_ZzqN2RGzkP4xxjjEoovZAZQlyUXYk76OxrssFkjHTCuXEejo3acMETbNxFpXGH6r2xro_M7isagjoE6Qzu_7VMx0r4J0VtNcdjEnR37xB9ig9uGfZhOdnJfyZlp1gG_nd4L8ufh_vfiKVu-PD4v7paZ5jKPWc5BF0KLtslljnXL2s40bcWwYEYC01hiVRWSc522L2Qj81rU2hghEYDLgl-QH8e-G-9et-kMNdigcb1uRkz7KBBFDTXLE1geQe1dCB6N2ng7NH6ngKm9YXUwrPb6FAN1MKwg5S5PA7btgN176qQ0AbdHANOZk0WvgrY4auysT-5U5-wHI_4D_W2Lsw</recordid><startdate>20010501</startdate><enddate>20010501</enddate><creator>Yeung, Chi-Kong</creator><creator>McCurrie, Janice R.</creator><creator>Wood, Diana</creator><general>Elsevier Inc</general><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20010501</creationdate><title>A simple method to investigate the inhibitory effects of drugs on gastric emptying in the mouse in vivo</title><author>Yeung, Chi-Kong ; McCurrie, Janice R. ; Wood, Diana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-231c48c8ba292e7b0bdfab60e40f910ce5e664933c38849a92787cff89e113943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Administration, Oral</topic><topic>Animal Feed</topic><topic>Animals</topic><topic>Atropine - toxicity</topic><topic>Benzopyrans - toxicity</topic><topic>Carbachol - toxicity</topic><topic>Cromakalim - toxicity</topic><topic>Cyclopentanes - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Gastric emptying</topic><topic>Gastric Emptying - drug effects</topic><topic>Gastric Emptying - physiology</topic><topic>Inhibition of gastric motility</topic><topic>Male</topic><topic>Methods</topic><topic>Metoclopramide - toxicity</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Morphine - toxicity</topic><topic>Mouse</topic><topic>Organ Size - drug effects</topic><topic>Pinacidil - toxicity</topic><topic>Potassium Channel Blockers - administration & dosage</topic><topic>Potassium Channel Blockers - toxicity</topic><topic>Potassium channel openers</topic><topic>Stomach</topic><topic>Stomach - drug effects</topic><topic>Stomach - pathology</topic><topic>Toxicology - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yeung, Chi-Kong</creatorcontrib><creatorcontrib>McCurrie, Janice R.</creatorcontrib><creatorcontrib>Wood, Diana</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of pharmacological and toxicological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yeung, Chi-Kong</au><au>McCurrie, Janice R.</au><au>Wood, Diana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A simple method to investigate the inhibitory effects of drugs on gastric emptying in the mouse in vivo</atitle><jtitle>Journal of pharmacological and toxicological methods</jtitle><addtitle>J Pharmacol Toxicol Methods</addtitle><date>2001-05-01</date><risdate>2001</risdate><volume>45</volume><issue>3</issue><spage>235</spage><epage>240</epage><pages>235-240</pages><issn>1056-8719</issn><eissn>1873-488X</eissn><abstract>Introduction: The aim was to develop a simple method to study modification of gastric motility in the mouse in vivo. Methods: Mice were fed a hydrated diet in which the fluid content of standard laboratory chow was increased by adding water. Gastric emptying was assessed at specified times following a 1-h treatment period with orally administered pharmacological agents. Results: We demonstrated consistent and progressive gastric emptying over a 4-h period, stomach content being decreased from 7.52±0.90 at time zero to 2.80±0.25 mg/g body weight after 4 h. Results demonstrated typical effects of inhibitory agents (atropine and morphine) and showed inhibitory effects of three potassium channel opening agents, pinacidil, cromakalim, and SDZ PCO400: the residue remaining in the stomach was increased by 3.66±0.84, 6.56±1.35, and 5.68±1.33 mg/g body weight respectively 1 h after treatment with 10 mg/kg of these agents, compared to vehicle controls. Discussion: The inhibitory activity observed correlated well with previous studies on the effects of potassium channel opening agents on mouse gastrointestinal motility in vivo and in vitro. The present model may thus be of value in the pharmacological investigation of gastrointestinal motility owing to cost and convenience advantages, together with the possibility of its application to studies using transgenic animals.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11755388</pmid><doi>10.1016/S1056-8719(01)00155-1</doi><tpages>6</tpages></addata></record> |
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subjects | Administration, Oral Animal Feed Animals Atropine - toxicity Benzopyrans - toxicity Carbachol - toxicity Cromakalim - toxicity Cyclopentanes - toxicity Dose-Response Relationship, Drug Gastric emptying Gastric Emptying - drug effects Gastric Emptying - physiology Inhibition of gastric motility Male Methods Metoclopramide - toxicity Mice Mice, Inbred Strains Morphine - toxicity Mouse Organ Size - drug effects Pinacidil - toxicity Potassium Channel Blockers - administration & dosage Potassium Channel Blockers - toxicity Potassium channel openers Stomach Stomach - drug effects Stomach - pathology Toxicology - methods |
title | A simple method to investigate the inhibitory effects of drugs on gastric emptying in the mouse in vivo |
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