Pharmacokinetics of cimetidine in dogs after oral administration of cimetidine tablets
Long-term oral treatment with cimetidine is recommended to reduce vomiting in dogs with chronic gastritis. Despite this, few studies have specifically examined the plasma disposition and pharmacokinetics of cimetidine in dogs, particularly following repeated oral administration. The pharmacokinetics...
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Veröffentlicht in: | Journal of veterinary pharmacology and therapeutics 2009-06, Vol.32 (3), p.213-218 |
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description | Long-term oral treatment with cimetidine is recommended to reduce vomiting in dogs with chronic gastritis. Despite this, few studies have specifically examined the plasma disposition and pharmacokinetics of cimetidine in dogs, particularly following repeated oral administration. The pharmacokinetics of cimetidine following oral administration as tablets was investigated in healthy dogs. Cimetidine was absorbed rapidly post-treatment (tmax = 0.5 h). A mean absolute bioavailability of 75% was calculated following a single oral administration of 5 mg cimetidine/kg body weight. After intravenous administration, a plasma half-life of 1.6 h was calculated. Repeated oral administration at the recommended dose rate and regime (5 mg/kg body weight three times daily) for 30 consecutive days did not lead to any accumulation of cimetidine in plasma. Food intake concomitant with oral administration of cimetidine delayed (tmax = 2.25 h) and decreased the rate and extent of absorption (AUC) by about 40%. Cimetidine was well absorbed in fasted dogs. Administration of food decreased the bioavailability of cimetidine by 40%. Cimetidine does not accumulate over time in plasma when administered long term to dogs. |
doi_str_mv | 10.1111/j.1365-2885.2008.01026.x |
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Despite this, few studies have specifically examined the plasma disposition and pharmacokinetics of cimetidine in dogs, particularly following repeated oral administration. The pharmacokinetics of cimetidine following oral administration as tablets was investigated in healthy dogs. Cimetidine was absorbed rapidly post-treatment (tmax = 0.5 h). A mean absolute bioavailability of 75% was calculated following a single oral administration of 5 mg cimetidine/kg body weight. After intravenous administration, a plasma half-life of 1.6 h was calculated. Repeated oral administration at the recommended dose rate and regime (5 mg/kg body weight three times daily) for 30 consecutive days did not lead to any accumulation of cimetidine in plasma. Food intake concomitant with oral administration of cimetidine delayed (tmax = 2.25 h) and decreased the rate and extent of absorption (AUC) by about 40%. Cimetidine was well absorbed in fasted dogs. Administration of food decreased the bioavailability of cimetidine by 40%. Cimetidine does not accumulate over time in plasma when administered long term to dogs.</description><identifier>ISSN: 0140-7783</identifier><identifier>EISSN: 1365-2885</identifier><identifier>DOI: 10.1111/j.1365-2885.2008.01026.x</identifier><identifier>PMID: 19646084</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Animal Feed ; Animals ; Anti-Ulcer Agents - administration & dosage ; Anti-Ulcer Agents - blood ; Anti-Ulcer Agents - pharmacokinetics ; bioavailability ; Biological Availability ; Chromatography, High Pressure Liquid - veterinary ; cimetidine ; Cimetidine - administration & dosage ; Cimetidine - blood ; Cimetidine - pharmacokinetics ; Cross-Over Studies ; dog diseases ; dogs ; Dogs - blood ; Dogs - metabolism ; dosage ; drug formulations ; Female ; gastritis ; Gastritis - drug therapy ; Gastritis - veterinary ; Injections, Intravenous - veterinary ; intravenous injection ; Male ; oral administration ; pharmacokinetics ; stomach ; Tablets ; vomiting</subject><ispartof>Journal of veterinary pharmacology and therapeutics, 2009-06, Vol.32 (3), p.213-218</ispartof><rights>2008 Intervet/Schering‐Plough Corporation. Journal compilation © 2008 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4306-fb91004ecd15537738b92b7e689100fe92b3944bbec8ad5d88ae6cbd94f9d1123</citedby><cites>FETCH-LOGICAL-c4306-fb91004ecd15537738b92b7e689100fe92b3944bbec8ad5d88ae6cbd94f9d1123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2885.2008.01026.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2885.2008.01026.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19646084$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LE TRAON, G</creatorcontrib><creatorcontrib>BURGAUD, S</creatorcontrib><creatorcontrib>HORSPOOL, L.J.I</creatorcontrib><title>Pharmacokinetics of cimetidine in dogs after oral administration of cimetidine tablets</title><title>Journal of veterinary pharmacology and therapeutics</title><addtitle>J Vet Pharmacol Ther</addtitle><description>Long-term oral treatment with cimetidine is recommended to reduce vomiting in dogs with chronic gastritis. Despite this, few studies have specifically examined the plasma disposition and pharmacokinetics of cimetidine in dogs, particularly following repeated oral administration. The pharmacokinetics of cimetidine following oral administration as tablets was investigated in healthy dogs. Cimetidine was absorbed rapidly post-treatment (tmax = 0.5 h). A mean absolute bioavailability of 75% was calculated following a single oral administration of 5 mg cimetidine/kg body weight. After intravenous administration, a plasma half-life of 1.6 h was calculated. Repeated oral administration at the recommended dose rate and regime (5 mg/kg body weight three times daily) for 30 consecutive days did not lead to any accumulation of cimetidine in plasma. Food intake concomitant with oral administration of cimetidine delayed (tmax = 2.25 h) and decreased the rate and extent of absorption (AUC) by about 40%. Cimetidine was well absorbed in fasted dogs. Administration of food decreased the bioavailability of cimetidine by 40%. Cimetidine does not accumulate over time in plasma when administered long term to dogs.</description><subject>Administration, Oral</subject><subject>Animal Feed</subject><subject>Animals</subject><subject>Anti-Ulcer Agents - administration & dosage</subject><subject>Anti-Ulcer Agents - blood</subject><subject>Anti-Ulcer Agents - pharmacokinetics</subject><subject>bioavailability</subject><subject>Biological Availability</subject><subject>Chromatography, High Pressure Liquid - veterinary</subject><subject>cimetidine</subject><subject>Cimetidine - administration & dosage</subject><subject>Cimetidine - blood</subject><subject>Cimetidine - pharmacokinetics</subject><subject>Cross-Over Studies</subject><subject>dog diseases</subject><subject>dogs</subject><subject>Dogs - blood</subject><subject>Dogs - metabolism</subject><subject>dosage</subject><subject>drug formulations</subject><subject>Female</subject><subject>gastritis</subject><subject>Gastritis - drug therapy</subject><subject>Gastritis - veterinary</subject><subject>Injections, Intravenous - veterinary</subject><subject>intravenous injection</subject><subject>Male</subject><subject>oral administration</subject><subject>pharmacokinetics</subject><subject>stomach</subject><subject>Tablets</subject><subject>vomiting</subject><issn>0140-7783</issn><issn>1365-2885</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1v1DAQhi0EokvhL0BunBI8cWI7Bw5sRT_QClaCluPIsZ3ibRIXOyu2_x6HrIrECV88M37esfQQkgEtIJ13uwIYr_NSyrooKZUFBVry4vCErB4fnpIVhYrmQkh2Ql7EuKOUMgnwnJxAwytOZbUiN9sfKgxK-zs32snpmPku025ItUmTzI2Z8bcxU91kQ-aD6jNlBje6OAU1OT_-w0-q7e0UX5JnneqjfXW8T8n1-cdvZ5f55svF1dmHTa4rRnnetQ1QWlltoK6ZEEy2TdkKy-U872xqWFNVbWu1VKY2UirLdWuaqmsMQMlOydtl733wP_c2Tji4qG3fq9H6fUTBWC3qsmGJlAupg48x2A7vgxtUeECgOEvFHc7ucHaHs1T8IxUPKfr6-Mm-Haz5GzxaTMD7Bfjlevvw34vx0812rlI-X_LJqj085lW4Qy6YqPH75wtcr9fncgMb3Cb-zcJ3yqO6DS7i9deSAqPAGQNg7DexHp6G</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>LE TRAON, G</creator><creator>BURGAUD, S</creator><creator>HORSPOOL, L.J.I</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>BSCLL</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>200906</creationdate><title>Pharmacokinetics of cimetidine in dogs after oral administration of cimetidine tablets</title><author>LE TRAON, G ; BURGAUD, S ; HORSPOOL, L.J.I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4306-fb91004ecd15537738b92b7e689100fe92b3944bbec8ad5d88ae6cbd94f9d1123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Administration, Oral</topic><topic>Animal Feed</topic><topic>Animals</topic><topic>Anti-Ulcer Agents - administration & dosage</topic><topic>Anti-Ulcer Agents - blood</topic><topic>Anti-Ulcer Agents - pharmacokinetics</topic><topic>bioavailability</topic><topic>Biological Availability</topic><topic>Chromatography, High Pressure Liquid - veterinary</topic><topic>cimetidine</topic><topic>Cimetidine - administration & dosage</topic><topic>Cimetidine - blood</topic><topic>Cimetidine - pharmacokinetics</topic><topic>Cross-Over Studies</topic><topic>dog diseases</topic><topic>dogs</topic><topic>Dogs - blood</topic><topic>Dogs - metabolism</topic><topic>dosage</topic><topic>drug formulations</topic><topic>Female</topic><topic>gastritis</topic><topic>Gastritis - drug therapy</topic><topic>Gastritis - veterinary</topic><topic>Injections, Intravenous - veterinary</topic><topic>intravenous injection</topic><topic>Male</topic><topic>oral administration</topic><topic>pharmacokinetics</topic><topic>stomach</topic><topic>Tablets</topic><topic>vomiting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LE TRAON, G</creatorcontrib><creatorcontrib>BURGAUD, S</creatorcontrib><creatorcontrib>HORSPOOL, L.J.I</creatorcontrib><collection>AGRIS</collection><collection>Istex</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 veterinary pharmacology and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LE TRAON, G</au><au>BURGAUD, S</au><au>HORSPOOL, L.J.I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics of cimetidine in dogs after oral administration of cimetidine tablets</atitle><jtitle>Journal of veterinary pharmacology and therapeutics</jtitle><addtitle>J Vet Pharmacol Ther</addtitle><date>2009-06</date><risdate>2009</risdate><volume>32</volume><issue>3</issue><spage>213</spage><epage>218</epage><pages>213-218</pages><issn>0140-7783</issn><eissn>1365-2885</eissn><abstract>Long-term oral treatment with cimetidine is recommended to reduce vomiting in dogs with chronic gastritis. Despite this, few studies have specifically examined the plasma disposition and pharmacokinetics of cimetidine in dogs, particularly following repeated oral administration. The pharmacokinetics of cimetidine following oral administration as tablets was investigated in healthy dogs. Cimetidine was absorbed rapidly post-treatment (tmax = 0.5 h). A mean absolute bioavailability of 75% was calculated following a single oral administration of 5 mg cimetidine/kg body weight. After intravenous administration, a plasma half-life of 1.6 h was calculated. Repeated oral administration at the recommended dose rate and regime (5 mg/kg body weight three times daily) for 30 consecutive days did not lead to any accumulation of cimetidine in plasma. Food intake concomitant with oral administration of cimetidine delayed (tmax = 2.25 h) and decreased the rate and extent of absorption (AUC) by about 40%. Cimetidine was well absorbed in fasted dogs. Administration of food decreased the bioavailability of cimetidine by 40%. Cimetidine does not accumulate over time in plasma when administered long term to dogs.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>19646084</pmid><doi>10.1111/j.1365-2885.2008.01026.x</doi><tpages>6</tpages></addata></record> |
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subjects | Administration, Oral Animal Feed Animals Anti-Ulcer Agents - administration & dosage Anti-Ulcer Agents - blood Anti-Ulcer Agents - pharmacokinetics bioavailability Biological Availability Chromatography, High Pressure Liquid - veterinary cimetidine Cimetidine - administration & dosage Cimetidine - blood Cimetidine - pharmacokinetics Cross-Over Studies dog diseases dogs Dogs - blood Dogs - metabolism dosage drug formulations Female gastritis Gastritis - drug therapy Gastritis - veterinary Injections, Intravenous - veterinary intravenous injection Male oral administration pharmacokinetics stomach Tablets vomiting |
title | Pharmacokinetics of cimetidine in dogs after oral administration of cimetidine tablets |
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