Long-term effects of early administered sildenafil and NO donor on the cardiovascular system of SHR
We evaluated the long-term effect of NO-donor, pentaerythrityl tetranitrate (Petn), and sildenafil citrate (sildenafil) on the cardiovascular system of the spontaneously hypertensive rat (SHR). Petn (100 mg/kg/day) and sildenafil (10 mg/kg/day) were administered to SHR individually or together from...
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Veröffentlicht in: | Journal of physiology and pharmacology : an official journal of the Polish Physiological Society 2007-03, Vol.58 (1), p.33-43 |
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description | We evaluated the long-term effect of NO-donor, pentaerythrityl tetranitrate (Petn), and sildenafil citrate (sildenafil) on the cardiovascular system of the spontaneously hypertensive rat (SHR). Petn (100 mg/kg/day) and sildenafil (10 mg/kg/day) were administered to SHR individually or together from week 4 (pre-hypertensive period) to week 9 of age. Blood pressure (BP) was measured using a plethysmographic method. The animals were perfused with a glutaraldehyde fixative (120 mmHg). Carotid (AC) and coronary artery (RS) were processed according to electron microscopy procedure. Geometry of the arteries was measured on semi-thin sections using light microscopy. Administration of Petn and sildenafil to SHR individually or together did not prevent an increase of BP, but evoked a decrease of cardiac hypertrophy. Petn and sildenafil affected the geometry of RS and AC differently. In the RS, an increase of inner diameter (ID) without an increase of wall thickness (WT) resulted in increased WT/ID and circumferential stress. In the AC, changes in ID were accompanied by changes in WT and, thereby, WT/ID and circumferential stress remained unchanged. The arterial wall mass of both arteries was increased. The data suggest that administration of the NO donor, Petn, and/or sildenafil does not result in a beneficial effect on the myocardium or on the geometry of the carotid and coronary arteries. |
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Petn (100 mg/kg/day) and sildenafil (10 mg/kg/day) were administered to SHR individually or together from week 4 (pre-hypertensive period) to week 9 of age. Blood pressure (BP) was measured using a plethysmographic method. The animals were perfused with a glutaraldehyde fixative (120 mmHg). Carotid (AC) and coronary artery (RS) were processed according to electron microscopy procedure. Geometry of the arteries was measured on semi-thin sections using light microscopy. Administration of Petn and sildenafil to SHR individually or together did not prevent an increase of BP, but evoked a decrease of cardiac hypertrophy. Petn and sildenafil affected the geometry of RS and AC differently. In the RS, an increase of inner diameter (ID) without an increase of wall thickness (WT) resulted in increased WT/ID and circumferential stress. In the AC, changes in ID were accompanied by changes in WT and, thereby, WT/ID and circumferential stress remained unchanged. The arterial wall mass of both arteries was increased. The data suggest that administration of the NO donor, Petn, and/or sildenafil does not result in a beneficial effect on the myocardium or on the geometry of the carotid and coronary arteries.</description><identifier>ISSN: 0867-5910</identifier><identifier>PMID: 17440224</identifier><language>eng</language><publisher>Poland</publisher><subject><![CDATA[Animals ; Antihypertensive Agents - administration & dosage ; Antihypertensive Agents - pharmacology ; Blood Pressure - drug effects ; Cardiomegaly - etiology ; Cardiomegaly - pathology ; Cardiomegaly - physiopathology ; Cardiomegaly - prevention & control ; Cardiovascular System - drug effects ; Carotid Arteries - drug effects ; Carotid Arteries - pathology ; Coronary Vessels - drug effects ; Coronary Vessels - pathology ; Disease Models, Animal ; Disease Progression ; Drug Administration Schedule ; Drug Therapy, Combination ; Hypertension - complications ; Hypertension - drug therapy ; Hypertension - pathology ; Hypertension - physiopathology ; Nitric Oxide Donors - administration & dosage ; Nitric Oxide Donors - pharmacology ; Pentaerythritol Tetranitrate - administration & dosage ; Phosphodiesterase Inhibitors - administration & dosage ; Phosphodiesterase Inhibitors - pharmacology ; Piperazines - administration & dosage ; Piperazines - pharmacology ; Purines - administration & dosage ; Purines - pharmacology ; Rats ; Rats, Inbred SHR ; Rats, Wistar ; Sildenafil Citrate ; Sulfones - administration & dosage ; Sulfones - pharmacology ; Time Factors ; Vasodilator Agents - administration & dosage ; Vasodilator Agents - pharmacology]]></subject><ispartof>Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 2007-03, Vol.58 (1), p.33-43</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17440224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kristek, F</creatorcontrib><creatorcontrib>Koprdová, R</creatorcontrib><creatorcontrib>Cebová, M</creatorcontrib><title>Long-term effects of early administered sildenafil and NO donor on the cardiovascular system of SHR</title><title>Journal of physiology and pharmacology : an official journal of the Polish Physiological Society</title><addtitle>J Physiol Pharmacol</addtitle><description>We evaluated the long-term effect of NO-donor, pentaerythrityl tetranitrate (Petn), and sildenafil citrate (sildenafil) on the cardiovascular system of the spontaneously hypertensive rat (SHR). Petn (100 mg/kg/day) and sildenafil (10 mg/kg/day) were administered to SHR individually or together from week 4 (pre-hypertensive period) to week 9 of age. Blood pressure (BP) was measured using a plethysmographic method. The animals were perfused with a glutaraldehyde fixative (120 mmHg). Carotid (AC) and coronary artery (RS) were processed according to electron microscopy procedure. Geometry of the arteries was measured on semi-thin sections using light microscopy. Administration of Petn and sildenafil to SHR individually or together did not prevent an increase of BP, but evoked a decrease of cardiac hypertrophy. Petn and sildenafil affected the geometry of RS and AC differently. In the RS, an increase of inner diameter (ID) without an increase of wall thickness (WT) resulted in increased WT/ID and circumferential stress. In the AC, changes in ID were accompanied by changes in WT and, thereby, WT/ID and circumferential stress remained unchanged. The arterial wall mass of both arteries was increased. The data suggest that administration of the NO donor, Petn, and/or sildenafil does not result in a beneficial effect on the myocardium or on the geometry of the carotid and coronary arteries.</description><subject>Animals</subject><subject>Antihypertensive Agents - administration & dosage</subject><subject>Antihypertensive Agents - pharmacology</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiomegaly - etiology</subject><subject>Cardiomegaly - pathology</subject><subject>Cardiomegaly - physiopathology</subject><subject>Cardiomegaly - prevention & control</subject><subject>Cardiovascular System - drug effects</subject><subject>Carotid Arteries - drug effects</subject><subject>Carotid Arteries - pathology</subject><subject>Coronary Vessels - drug effects</subject><subject>Coronary Vessels - pathology</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>Drug Administration Schedule</subject><subject>Drug Therapy, Combination</subject><subject>Hypertension - complications</subject><subject>Hypertension - drug therapy</subject><subject>Hypertension - pathology</subject><subject>Hypertension - physiopathology</subject><subject>Nitric Oxide Donors - administration & dosage</subject><subject>Nitric Oxide Donors - pharmacology</subject><subject>Pentaerythritol Tetranitrate - administration & dosage</subject><subject>Phosphodiesterase Inhibitors - administration & dosage</subject><subject>Phosphodiesterase Inhibitors - pharmacology</subject><subject>Piperazines - administration & dosage</subject><subject>Piperazines - pharmacology</subject><subject>Purines - administration & dosage</subject><subject>Purines - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Rats, Wistar</subject><subject>Sildenafil Citrate</subject><subject>Sulfones - administration & dosage</subject><subject>Sulfones - pharmacology</subject><subject>Time Factors</subject><subject>Vasodilator Agents - administration & dosage</subject><subject>Vasodilator Agents - pharmacology</subject><issn>0867-5910</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kEtLAzEcxHNQbK1-BcnJ20Jeu5s9SlErFAs-zkse_2gkm9RkV9hvb4v1NIeZ-cHMGVoS2bRV3VGyQJelfBHCqODNBVrQVgjCmFgis03xoxohDxicAzMWnBwGlcOMlR189OVggsXFBwtROR-wihY_77BNMWWcIh4_ARuVrU8_qpgpqIzLfKgNR9Tr5uUKnTsVClyfdIXeH-7f1ptqu3t8Wt9tqz0j3VjpRsoaNLOgpXTC1lYKzZuGdNQRYJxTJiworhrQXUtMTY4bDOWk0622hK_Q7R93n9P3BGXsB18MhKAipKn0LeGSUSoPwZtTcNID2H6f_aDy3P_fwn8BOKZdqw</recordid><startdate>200703</startdate><enddate>200703</enddate><creator>Kristek, F</creator><creator>Koprdová, R</creator><creator>Cebová, M</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200703</creationdate><title>Long-term effects of early administered sildenafil and NO donor on the cardiovascular system of SHR</title><author>Kristek, F ; Koprdová, R ; Cebová, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p209t-b6885eb2deb88f4d5d84b366091f0e233124dea3a6eb970c504022c1309b7bd03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Antihypertensive Agents - administration & dosage</topic><topic>Antihypertensive Agents - pharmacology</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiomegaly - etiology</topic><topic>Cardiomegaly - pathology</topic><topic>Cardiomegaly - physiopathology</topic><topic>Cardiomegaly - prevention & control</topic><topic>Cardiovascular System - drug effects</topic><topic>Carotid Arteries - drug effects</topic><topic>Carotid Arteries - pathology</topic><topic>Coronary Vessels - drug effects</topic><topic>Coronary Vessels - pathology</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>Drug Administration Schedule</topic><topic>Drug Therapy, Combination</topic><topic>Hypertension - complications</topic><topic>Hypertension - drug therapy</topic><topic>Hypertension - pathology</topic><topic>Hypertension - physiopathology</topic><topic>Nitric Oxide Donors - administration & dosage</topic><topic>Nitric Oxide Donors - pharmacology</topic><topic>Pentaerythritol Tetranitrate - administration & dosage</topic><topic>Phosphodiesterase Inhibitors - administration & dosage</topic><topic>Phosphodiesterase Inhibitors - pharmacology</topic><topic>Piperazines - administration & dosage</topic><topic>Piperazines - pharmacology</topic><topic>Purines - administration & dosage</topic><topic>Purines - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Rats, Wistar</topic><topic>Sildenafil Citrate</topic><topic>Sulfones - administration & dosage</topic><topic>Sulfones - pharmacology</topic><topic>Time Factors</topic><topic>Vasodilator Agents - administration & dosage</topic><topic>Vasodilator Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kristek, F</creatorcontrib><creatorcontrib>Koprdová, R</creatorcontrib><creatorcontrib>Cebová, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of physiology and pharmacology : an official journal of the Polish Physiological Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kristek, F</au><au>Koprdová, R</au><au>Cebová, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term effects of early administered sildenafil and NO donor on the cardiovascular system of SHR</atitle><jtitle>Journal of physiology and pharmacology : an official journal of the Polish Physiological Society</jtitle><addtitle>J Physiol Pharmacol</addtitle><date>2007-03</date><risdate>2007</risdate><volume>58</volume><issue>1</issue><spage>33</spage><epage>43</epage><pages>33-43</pages><issn>0867-5910</issn><abstract>We evaluated the long-term effect of NO-donor, pentaerythrityl tetranitrate (Petn), and sildenafil citrate (sildenafil) on the cardiovascular system of the spontaneously hypertensive rat (SHR). Petn (100 mg/kg/day) and sildenafil (10 mg/kg/day) were administered to SHR individually or together from week 4 (pre-hypertensive period) to week 9 of age. Blood pressure (BP) was measured using a plethysmographic method. The animals were perfused with a glutaraldehyde fixative (120 mmHg). Carotid (AC) and coronary artery (RS) were processed according to electron microscopy procedure. Geometry of the arteries was measured on semi-thin sections using light microscopy. Administration of Petn and sildenafil to SHR individually or together did not prevent an increase of BP, but evoked a decrease of cardiac hypertrophy. Petn and sildenafil affected the geometry of RS and AC differently. In the RS, an increase of inner diameter (ID) without an increase of wall thickness (WT) resulted in increased WT/ID and circumferential stress. In the AC, changes in ID were accompanied by changes in WT and, thereby, WT/ID and circumferential stress remained unchanged. The arterial wall mass of both arteries was increased. The data suggest that administration of the NO donor, Petn, and/or sildenafil does not result in a beneficial effect on the myocardium or on the geometry of the carotid and coronary arteries.</abstract><cop>Poland</cop><pmid>17440224</pmid><tpages>11</tpages></addata></record> |
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subjects | Animals Antihypertensive Agents - administration & dosage Antihypertensive Agents - pharmacology Blood Pressure - drug effects Cardiomegaly - etiology Cardiomegaly - pathology Cardiomegaly - physiopathology Cardiomegaly - prevention & control Cardiovascular System - drug effects Carotid Arteries - drug effects Carotid Arteries - pathology Coronary Vessels - drug effects Coronary Vessels - pathology Disease Models, Animal Disease Progression Drug Administration Schedule Drug Therapy, Combination Hypertension - complications Hypertension - drug therapy Hypertension - pathology Hypertension - physiopathology Nitric Oxide Donors - administration & dosage Nitric Oxide Donors - pharmacology Pentaerythritol Tetranitrate - administration & dosage Phosphodiesterase Inhibitors - administration & dosage Phosphodiesterase Inhibitors - pharmacology Piperazines - administration & dosage Piperazines - pharmacology Purines - administration & dosage Purines - pharmacology Rats Rats, Inbred SHR Rats, Wistar Sildenafil Citrate Sulfones - administration & dosage Sulfones - pharmacology Time Factors Vasodilator Agents - administration & dosage Vasodilator Agents - pharmacology |
title | Long-term effects of early administered sildenafil and NO donor on the cardiovascular system of SHR |
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