Suppression of Angioplasty-Related Inflammation by Pre-Procedural Treatment with Trimetazidine
Percutaneous transluminal coronary angioplasty (PTCA) has been recognized as a reliable treatment procedure for acute reversible ischemia and reperfusion. Ischemic reperfusion cycle in PTCA leads to the systemic inflammation and extensive tissue injury by the production of reactive oxygen species in...
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Veröffentlicht in: | The Tohoku Journal of Experimental Medicine 2006, Vol.208(3), pp.203-212 |
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description | Percutaneous transluminal coronary angioplasty (PTCA) has been recognized as a reliable treatment procedure for acute reversible ischemia and reperfusion. Ischemic reperfusion cycle in PTCA leads to the systemic inflammation and extensive tissue injury by the production of reactive oxygen species including nitric oxide (NO) radicals. In patients with coronary artery disease, undergoing PTCA, the effects of trimetazidine (TMZ), a piperazine-derivative anti-anginal drug, were studied on several indirect markers of systemic inflammatory response: tumor necrosis factor-α (TNF-α), C-reactive protein (CRP) and NO products (nitrite and nitrate). Patients (n = 11 each group) were untreated or pre-treated with TMZ (20 mg per orally three times a day), begun three days prior to PTCA, and marker levels were measured before the start of TMZ therapy (baseline), just before PTCA (0 hr), and 4, 24, and 48 hrs after PTCA. The baseline levels of markers were not significantly different between the untreated and pre-treated patients. In contrast, all parameters were lower in the TMZ-treated group than those in the matched control group in the pre- and post-angioplasty periods. Interestingly, in the TMZ group, CRP and nitrite levels were significantly lower than in the control group at each time point of the pre- and post-angioplasty periods, but the TNF-α levels were significantly decreased only in the post-angioplasty period. Pre-procedural treatment with oral TMZ for three days significantly suppressed the elevation of inflammatory markers before and shortly after PTCA. We suggest the usefulness of TMZ in preventing inflammatory cardiovascular events after PTCA. |
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Ischemic reperfusion cycle in PTCA leads to the systemic inflammation and extensive tissue injury by the production of reactive oxygen species including nitric oxide (NO) radicals. In patients with coronary artery disease, undergoing PTCA, the effects of trimetazidine (TMZ), a piperazine-derivative anti-anginal drug, were studied on several indirect markers of systemic inflammatory response: tumor necrosis factor-α (TNF-α), C-reactive protein (CRP) and NO products (nitrite and nitrate). Patients (n = 11 each group) were untreated or pre-treated with TMZ (20 mg per orally three times a day), begun three days prior to PTCA, and marker levels were measured before the start of TMZ therapy (baseline), just before PTCA (0 hr), and 4, 24, and 48 hrs after PTCA. The baseline levels of markers were not significantly different between the untreated and pre-treated patients. In contrast, all parameters were lower in the TMZ-treated group than those in the matched control group in the pre- and post-angioplasty periods. Interestingly, in the TMZ group, CRP and nitrite levels were significantly lower than in the control group at each time point of the pre- and post-angioplasty periods, but the TNF-α levels were significantly decreased only in the post-angioplasty period. Pre-procedural treatment with oral TMZ for three days significantly suppressed the elevation of inflammatory markers before and shortly after PTCA. We suggest the usefulness of TMZ in preventing inflammatory cardiovascular events after PTCA.</description><identifier>ISSN: 0040-8727</identifier><identifier>EISSN: 1349-3329</identifier><identifier>DOI: 10.1620/tjem.208.203</identifier><identifier>PMID: 16498228</identifier><language>eng</language><publisher>Japan: Tohoku University Medical Press</publisher><subject>Aged ; Angioplasty, Balloon, Coronary ; Biomarkers - analysis ; C-reactive protein ; C-Reactive Protein - analysis ; Coronary Disease - drug therapy ; Coronary Disease - physiopathology ; Female ; Humans ; Inflammation - prevention & control ; Male ; Middle Aged ; Myocardial Infarction - blood ; Myocardial Infarction - drug therapy ; Myocardial Ischemia - drug therapy ; Myocardial Reperfusion Injury - drug therapy ; Nitrates - blood ; nitric oxide ; Nitrites - blood ; percutaneous transluminal coronary angioplasty ; Reactive Oxygen Species - metabolism ; Time Factors ; Treatment Outcome ; trimetazidine ; Trimetazidine - therapeutic use ; Tumor Necrosis Factor-alpha - analysis ; tumor necrosis factor-α ; Vasodilator Agents - therapeutic use</subject><ispartof>The Tohoku Journal of Experimental Medicine, 2006, Vol.208(3), pp.203-212</ispartof><rights>2006 Tohoku University Medical Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-63120edb39fd9874f9ca0cdfdc24984768e93e9a0dced18c23798fb1fa79acd23</citedby><cites>FETCH-LOGICAL-c476t-63120edb39fd9874f9ca0cdfdc24984768e93e9a0dced18c23798fb1fa79acd23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1883,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16498228$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuralay, Filiz</creatorcontrib><creatorcontrib>Altekin, Emel</creatorcontrib><creatorcontrib>Yazlar, Ayten Sayin</creatorcontrib><creatorcontrib>Onvural, Banu</creatorcontrib><creatorcontrib>Goldeli, Ozhan</creatorcontrib><title>Suppression of Angioplasty-Related Inflammation by Pre-Procedural Treatment with Trimetazidine</title><title>The Tohoku Journal of Experimental Medicine</title><addtitle>Tohoku J. Exp. Med.</addtitle><description>Percutaneous transluminal coronary angioplasty (PTCA) has been recognized as a reliable treatment procedure for acute reversible ischemia and reperfusion. Ischemic reperfusion cycle in PTCA leads to the systemic inflammation and extensive tissue injury by the production of reactive oxygen species including nitric oxide (NO) radicals. In patients with coronary artery disease, undergoing PTCA, the effects of trimetazidine (TMZ), a piperazine-derivative anti-anginal drug, were studied on several indirect markers of systemic inflammatory response: tumor necrosis factor-α (TNF-α), C-reactive protein (CRP) and NO products (nitrite and nitrate). Patients (n = 11 each group) were untreated or pre-treated with TMZ (20 mg per orally three times a day), begun three days prior to PTCA, and marker levels were measured before the start of TMZ therapy (baseline), just before PTCA (0 hr), and 4, 24, and 48 hrs after PTCA. The baseline levels of markers were not significantly different between the untreated and pre-treated patients. In contrast, all parameters were lower in the TMZ-treated group than those in the matched control group in the pre- and post-angioplasty periods. Interestingly, in the TMZ group, CRP and nitrite levels were significantly lower than in the control group at each time point of the pre- and post-angioplasty periods, but the TNF-α levels were significantly decreased only in the post-angioplasty period. Pre-procedural treatment with oral TMZ for three days significantly suppressed the elevation of inflammatory markers before and shortly after PTCA. We suggest the usefulness of TMZ in preventing inflammatory cardiovascular events after PTCA.</description><subject>Aged</subject><subject>Angioplasty, Balloon, Coronary</subject><subject>Biomarkers - analysis</subject><subject>C-reactive protein</subject><subject>C-Reactive Protein - analysis</subject><subject>Coronary Disease - drug therapy</subject><subject>Coronary Disease - physiopathology</subject><subject>Female</subject><subject>Humans</subject><subject>Inflammation - prevention & control</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Myocardial Infarction - blood</subject><subject>Myocardial Infarction - drug therapy</subject><subject>Myocardial Ischemia - drug therapy</subject><subject>Myocardial Reperfusion Injury - drug therapy</subject><subject>Nitrates - blood</subject><subject>nitric oxide</subject><subject>Nitrites - blood</subject><subject>percutaneous transluminal coronary angioplasty</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>trimetazidine</subject><subject>Trimetazidine - therapeutic use</subject><subject>Tumor Necrosis Factor-alpha - analysis</subject><subject>tumor necrosis factor-α</subject><subject>Vasodilator Agents - therapeutic use</subject><issn>0040-8727</issn><issn>1349-3329</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMtLw0AQxhdRtFZvniUnT6buIyTZo4qPQsGi9WqY7M62KXm5u0HqX--WlnqYGYb58c3HR8gVoxOWcnrn19hMOM1DiSMyYiKRsRBcHpMRpQmN84xnZ-TcuTWlIqFZekrOWJrInPN8RL4-hr636FzVtVFnovt2WXV9Dc5v4neswaOOpq2poWnAb5lyE80txnPbKdSDhTpaWATfYOujn8qvwlo16OG30lWLF-TEQO3wcj_H5PP5afH4Gs_eXqaP97NYJVnq41QwTlGXQhot8ywxUgFV2mjFg9GA5CgFSqA6PGW54iKTuSmZgUyC0lyMyc1Ot7fd94DOF03lFNY1tNgNrkizVLKEpgG83YHKds5ZNEUf_ILdFIwW2zyLbZ5FyDOUCPj1XncoG9T_8D7AADzsgLXzsMQDANZXqsZ_NXHo4nBUK7AFtuIPoR2LhQ</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Kuralay, Filiz</creator><creator>Altekin, Emel</creator><creator>Yazlar, Ayten Sayin</creator><creator>Onvural, Banu</creator><creator>Goldeli, Ozhan</creator><general>Tohoku University Medical Press</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>7X8</scope></search><sort><creationdate>20060301</creationdate><title>Suppression of Angioplasty-Related Inflammation by Pre-Procedural Treatment with Trimetazidine</title><author>Kuralay, Filiz ; Altekin, Emel ; Yazlar, Ayten Sayin ; Onvural, Banu ; Goldeli, Ozhan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-63120edb39fd9874f9ca0cdfdc24984768e93e9a0dced18c23798fb1fa79acd23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aged</topic><topic>Angioplasty, Balloon, Coronary</topic><topic>Biomarkers - analysis</topic><topic>C-reactive protein</topic><topic>C-Reactive Protein - analysis</topic><topic>Coronary Disease - drug therapy</topic><topic>Coronary Disease - physiopathology</topic><topic>Female</topic><topic>Humans</topic><topic>Inflammation - prevention & control</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Myocardial Infarction - blood</topic><topic>Myocardial Infarction - drug therapy</topic><topic>Myocardial Ischemia - drug therapy</topic><topic>Myocardial Reperfusion Injury - drug therapy</topic><topic>Nitrates - blood</topic><topic>nitric oxide</topic><topic>Nitrites - blood</topic><topic>percutaneous transluminal coronary angioplasty</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>trimetazidine</topic><topic>Trimetazidine - therapeutic use</topic><topic>Tumor Necrosis Factor-alpha - analysis</topic><topic>tumor necrosis factor-α</topic><topic>Vasodilator Agents - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuralay, Filiz</creatorcontrib><creatorcontrib>Altekin, Emel</creatorcontrib><creatorcontrib>Yazlar, Ayten Sayin</creatorcontrib><creatorcontrib>Onvural, Banu</creatorcontrib><creatorcontrib>Goldeli, Ozhan</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>The Tohoku Journal of Experimental Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuralay, Filiz</au><au>Altekin, Emel</au><au>Yazlar, Ayten Sayin</au><au>Onvural, Banu</au><au>Goldeli, Ozhan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suppression of Angioplasty-Related Inflammation by Pre-Procedural Treatment with Trimetazidine</atitle><jtitle>The Tohoku Journal of Experimental Medicine</jtitle><addtitle>Tohoku J. Exp. Med.</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>208</volume><issue>3</issue><spage>203</spage><epage>212</epage><pages>203-212</pages><issn>0040-8727</issn><eissn>1349-3329</eissn><abstract>Percutaneous transluminal coronary angioplasty (PTCA) has been recognized as a reliable treatment procedure for acute reversible ischemia and reperfusion. Ischemic reperfusion cycle in PTCA leads to the systemic inflammation and extensive tissue injury by the production of reactive oxygen species including nitric oxide (NO) radicals. In patients with coronary artery disease, undergoing PTCA, the effects of trimetazidine (TMZ), a piperazine-derivative anti-anginal drug, were studied on several indirect markers of systemic inflammatory response: tumor necrosis factor-α (TNF-α), C-reactive protein (CRP) and NO products (nitrite and nitrate). Patients (n = 11 each group) were untreated or pre-treated with TMZ (20 mg per orally three times a day), begun three days prior to PTCA, and marker levels were measured before the start of TMZ therapy (baseline), just before PTCA (0 hr), and 4, 24, and 48 hrs after PTCA. The baseline levels of markers were not significantly different between the untreated and pre-treated patients. In contrast, all parameters were lower in the TMZ-treated group than those in the matched control group in the pre- and post-angioplasty periods. Interestingly, in the TMZ group, CRP and nitrite levels were significantly lower than in the control group at each time point of the pre- and post-angioplasty periods, but the TNF-α levels were significantly decreased only in the post-angioplasty period. Pre-procedural treatment with oral TMZ for three days significantly suppressed the elevation of inflammatory markers before and shortly after PTCA. 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subjects | Aged Angioplasty, Balloon, Coronary Biomarkers - analysis C-reactive protein C-Reactive Protein - analysis Coronary Disease - drug therapy Coronary Disease - physiopathology Female Humans Inflammation - prevention & control Male Middle Aged Myocardial Infarction - blood Myocardial Infarction - drug therapy Myocardial Ischemia - drug therapy Myocardial Reperfusion Injury - drug therapy Nitrates - blood nitric oxide Nitrites - blood percutaneous transluminal coronary angioplasty Reactive Oxygen Species - metabolism Time Factors Treatment Outcome trimetazidine Trimetazidine - therapeutic use Tumor Necrosis Factor-alpha - analysis tumor necrosis factor-α Vasodilator Agents - therapeutic use |
title | Suppression of Angioplasty-Related Inflammation by Pre-Procedural Treatment with Trimetazidine |
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