The effect of high-dose pentaerythritol tetranitrate on the development of nitrate tolerance in rabbits
Experimental studies with therapeutic doses of pentaerythritol tetranitrate (PETN) have shown unexpected actions such as a lack of nitrate tolerance and vasoprotective effects in atherosclerosis. We investigated the effect of a 3-week treatment with low- (6 mg kg(-1) day(-1), n=10) and high-dose (10...
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Veröffentlicht in: | Naunyn-Schmiedeberg's archives of pharmacology 2001-09, Vol.364 (3), p.269-275 |
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creator | Müllenheim, J Müller, S Laber, U Thämer, V Meyer, W Bassenge, E Fink, B Kojda, G |
description | Experimental studies with therapeutic doses of pentaerythritol tetranitrate (PETN) have shown unexpected actions such as a lack of nitrate tolerance and vasoprotective effects in atherosclerosis. We investigated the effect of a 3-week treatment with low- (6 mg kg(-1) day(-1), n=10) and high-dose (100 mg kg(-1) day(-1), n=10) oral PETN given twice daily on the development of nitrate tolerance in rabbits. We measured aortic relaxation in response to acetylcholine, S-nitroso-N-acetyl-D,L-penicillamine and PETN, constriction in response to phenylephrine and production of reactive oxygen species (ROS). Mean aortic pressure (AOPmean) and heart rate were measured after a single oral dose of PETN (50 mg kg(-1), n=6) and after increasing doses of pentaerythritol dinitrate (PEDN, n=5) and pentaerythritol mononitrate (PEMN, n=5) in anaesthetized rabbits. Oral PETN, even at high dosage, was not associated with nitrate tolerance. None of the aortic ring studies showed a difference in the responses to the vasodilators, while the vasoconstriction to phenylephrine was slightly reduced in both PETN groups. The production of vascular ROS was also not different. Oral PETN reduced AOPmean transiently (-19.3+/-4.4%, P |
doi_str_mv | 10.1007/s002100100464 |
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We investigated the effect of a 3-week treatment with low- (6 mg kg(-1) day(-1), n=10) and high-dose (100 mg kg(-1) day(-1), n=10) oral PETN given twice daily on the development of nitrate tolerance in rabbits. We measured aortic relaxation in response to acetylcholine, S-nitroso-N-acetyl-D,L-penicillamine and PETN, constriction in response to phenylephrine and production of reactive oxygen species (ROS). Mean aortic pressure (AOPmean) and heart rate were measured after a single oral dose of PETN (50 mg kg(-1), n=6) and after increasing doses of pentaerythritol dinitrate (PEDN, n=5) and pentaerythritol mononitrate (PEMN, n=5) in anaesthetized rabbits. Oral PETN, even at high dosage, was not associated with nitrate tolerance. None of the aortic ring studies showed a difference in the responses to the vasodilators, while the vasoconstriction to phenylephrine was slightly reduced in both PETN groups. The production of vascular ROS was also not different. Oral PETN reduced AOPmean transiently (-19.3+/-4.4%, P<0.01 vs. controls) and i.v. administration of both PEMN and PEDN reduced AOPmean dose dependently (P<0.05, ANOVA). These results suggest that oral PETN elicits minor nitrate tolerance. This unique feature might be due to the slow onset of vasodilator activity of the predominantly active metabolites PEDN and PEMN and might contribute to the vasoprotective activity of PETN in atherosclerosis.</description><identifier>ISSN: 0028-1298</identifier><identifier>EISSN: 1432-1912</identifier><identifier>DOI: 10.1007/s002100100464</identifier><identifier>PMID: 11521170</identifier><language>eng</language><publisher>Germany</publisher><subject>Animals ; Drug Tolerance ; Hemodynamics - drug effects ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - metabolism ; Nitrates - pharmacology ; Pentaerythritol Tetranitrate - pharmacology ; Rabbits ; Reactive Oxygen Species - metabolism ; Vasodilator Agents - pharmacology</subject><ispartof>Naunyn-Schmiedeberg's archives of pharmacology, 2001-09, Vol.364 (3), p.269-275</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c289t-2659ee918bfaafaaaac8e85b466fba64a7a19d3f1d5a4fb88cc81f0a6918b4303</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11521170$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Müllenheim, J</creatorcontrib><creatorcontrib>Müller, S</creatorcontrib><creatorcontrib>Laber, U</creatorcontrib><creatorcontrib>Thämer, V</creatorcontrib><creatorcontrib>Meyer, W</creatorcontrib><creatorcontrib>Bassenge, E</creatorcontrib><creatorcontrib>Fink, B</creatorcontrib><creatorcontrib>Kojda, G</creatorcontrib><title>The effect of high-dose pentaerythritol tetranitrate on the development of nitrate tolerance in rabbits</title><title>Naunyn-Schmiedeberg's archives of pharmacology</title><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><description>Experimental studies with therapeutic doses of pentaerythritol tetranitrate (PETN) have shown unexpected actions such as a lack of nitrate tolerance and vasoprotective effects in atherosclerosis. We investigated the effect of a 3-week treatment with low- (6 mg kg(-1) day(-1), n=10) and high-dose (100 mg kg(-1) day(-1), n=10) oral PETN given twice daily on the development of nitrate tolerance in rabbits. We measured aortic relaxation in response to acetylcholine, S-nitroso-N-acetyl-D,L-penicillamine and PETN, constriction in response to phenylephrine and production of reactive oxygen species (ROS). Mean aortic pressure (AOPmean) and heart rate were measured after a single oral dose of PETN (50 mg kg(-1), n=6) and after increasing doses of pentaerythritol dinitrate (PEDN, n=5) and pentaerythritol mononitrate (PEMN, n=5) in anaesthetized rabbits. Oral PETN, even at high dosage, was not associated with nitrate tolerance. None of the aortic ring studies showed a difference in the responses to the vasodilators, while the vasoconstriction to phenylephrine was slightly reduced in both PETN groups. The production of vascular ROS was also not different. Oral PETN reduced AOPmean transiently (-19.3+/-4.4%, P<0.01 vs. controls) and i.v. administration of both PEMN and PEDN reduced AOPmean dose dependently (P<0.05, ANOVA). These results suggest that oral PETN elicits minor nitrate tolerance. This unique feature might be due to the slow onset of vasodilator activity of the predominantly active metabolites PEDN and PEMN and might contribute to the vasoprotective activity of PETN in atherosclerosis.</description><subject>Animals</subject><subject>Drug Tolerance</subject><subject>Hemodynamics - drug effects</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Nitrates - pharmacology</subject><subject>Pentaerythritol Tetranitrate - pharmacology</subject><subject>Rabbits</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Vasodilator Agents - pharmacology</subject><issn>0028-1298</issn><issn>1432-1912</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkMFLwzAUxoMobk6PXiUnb9W8tE3TowynwsDLPJc0fVkrbVOTTNh_b8YmIjzee_D9vu_wEXIL7AEYKx49Yzw-cTKRnZE5ZClPoAR-TuZRkgnwUs7IlfefjDEBeX5JZgA5ByjYnGw3LVI0BnWg1tC227ZJYz3SCceg0O1D67pgexowODV2cQWkdqQh-hr8xt5OQ0QP5l814hhZjbQbqVN13QV_TS6M6j3enO6CfKyeN8vXZP3-8rZ8WieayzIkXOQlYgmyNkrFUUpLlHmdCWFqJTJVKCib1ECTq8zUUmotwTAlDpYsZemC3B9zJ2e_duhDNXReY9-rEe3OVwUAB85EBJMjqJ313qGpJtcNyu0rYNWh2epfs5G_OwXv6gGbP_pUZfoDaOV1mw</recordid><startdate>20010901</startdate><enddate>20010901</enddate><creator>Müllenheim, J</creator><creator>Müller, S</creator><creator>Laber, U</creator><creator>Thämer, V</creator><creator>Meyer, W</creator><creator>Bassenge, E</creator><creator>Fink, B</creator><creator>Kojda, G</creator><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>20010901</creationdate><title>The effect of high-dose pentaerythritol tetranitrate on the development of nitrate tolerance in rabbits</title><author>Müllenheim, J ; Müller, S ; Laber, U ; Thämer, V ; Meyer, W ; Bassenge, E ; Fink, B ; Kojda, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c289t-2659ee918bfaafaaaac8e85b466fba64a7a19d3f1d5a4fb88cc81f0a6918b4303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Drug Tolerance</topic><topic>Hemodynamics - drug effects</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Nitrates - pharmacology</topic><topic>Pentaerythritol Tetranitrate - pharmacology</topic><topic>Rabbits</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Vasodilator Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Müllenheim, J</creatorcontrib><creatorcontrib>Müller, S</creatorcontrib><creatorcontrib>Laber, U</creatorcontrib><creatorcontrib>Thämer, V</creatorcontrib><creatorcontrib>Meyer, W</creatorcontrib><creatorcontrib>Bassenge, E</creatorcontrib><creatorcontrib>Fink, B</creatorcontrib><creatorcontrib>Kojda, G</creatorcontrib><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>Naunyn-Schmiedeberg's archives of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Müllenheim, J</au><au>Müller, S</au><au>Laber, U</au><au>Thämer, V</au><au>Meyer, W</au><au>Bassenge, E</au><au>Fink, B</au><au>Kojda, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of high-dose pentaerythritol tetranitrate on the development of nitrate tolerance in rabbits</atitle><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><date>2001-09-01</date><risdate>2001</risdate><volume>364</volume><issue>3</issue><spage>269</spage><epage>275</epage><pages>269-275</pages><issn>0028-1298</issn><eissn>1432-1912</eissn><abstract>Experimental studies with therapeutic doses of pentaerythritol tetranitrate (PETN) have shown unexpected actions such as a lack of nitrate tolerance and vasoprotective effects in atherosclerosis. We investigated the effect of a 3-week treatment with low- (6 mg kg(-1) day(-1), n=10) and high-dose (100 mg kg(-1) day(-1), n=10) oral PETN given twice daily on the development of nitrate tolerance in rabbits. We measured aortic relaxation in response to acetylcholine, S-nitroso-N-acetyl-D,L-penicillamine and PETN, constriction in response to phenylephrine and production of reactive oxygen species (ROS). Mean aortic pressure (AOPmean) and heart rate were measured after a single oral dose of PETN (50 mg kg(-1), n=6) and after increasing doses of pentaerythritol dinitrate (PEDN, n=5) and pentaerythritol mononitrate (PEMN, n=5) in anaesthetized rabbits. Oral PETN, even at high dosage, was not associated with nitrate tolerance. None of the aortic ring studies showed a difference in the responses to the vasodilators, while the vasoconstriction to phenylephrine was slightly reduced in both PETN groups. The production of vascular ROS was also not different. Oral PETN reduced AOPmean transiently (-19.3+/-4.4%, P<0.01 vs. controls) and i.v. administration of both PEMN and PEDN reduced AOPmean dose dependently (P<0.05, ANOVA). These results suggest that oral PETN elicits minor nitrate tolerance. This unique feature might be due to the slow onset of vasodilator activity of the predominantly active metabolites PEDN and PEMN and might contribute to the vasoprotective activity of PETN in atherosclerosis.</abstract><cop>Germany</cop><pmid>11521170</pmid><doi>10.1007/s002100100464</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Drug Tolerance Hemodynamics - drug effects Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - metabolism Nitrates - pharmacology Pentaerythritol Tetranitrate - pharmacology Rabbits Reactive Oxygen Species - metabolism Vasodilator Agents - pharmacology |
title | The effect of high-dose pentaerythritol tetranitrate on the development of nitrate tolerance in rabbits |
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