The protective cardiac effects of B-myrcene after global cerebral ischemia/reperfusion in C57BL/J6 mouse
dc.authorid | Gul, Burcu/0000-0002-9122-8953 | |
dc.authorid | Ciftci, Osman/0000-0001-5755-3560 | |
dc.authorid | CETIN, Asli/0000-0003-3902-3210 | |
dc.authorwosid | Gul, Burcu/V-9452-2018 | |
dc.contributor.author | Burcu, Gul Baykalir | |
dc.contributor.author | Osman, Ciftci | |
dc.contributor.author | Asl, Cetin | |
dc.contributor.author | Namik, Oztanir Mustafa | |
dc.contributor.author | Nese, Basak Turkmen | |
dc.date.accessioned | 2024-08-04T20:42:33Z | |
dc.date.available | 2024-08-04T20:42:33Z | |
dc.date.issued | 2016 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | PURPOSE: To investigate the protective effect of beta-myrcene (MYR) on oxidative and histological damage in mice heart tissue caused global cerebral ischemia/reperfusion (IR) in C57BL/J6 mice. METHODS: Animals(n=40) were randomly divided into four groups: (1)control, (2)IR, (3)MYR and (4)MYR+IR. The control group was received 0.1% carboxymethyl cellulose as a vehicle following a medial incision without carotid occlusion. In the IR group, the bilateral carotid arteries were clipped for 15min, and treated with the vehicle intraperitoneally(ip) for 10 days. MYR (200mg/kg) was received dissolved in 0.1%CMC for 10 days. In the MYR+IR group, the IR model was applied exactly as in the IR group, and then they were treated with MYR 10 days. RESULTS: The cerebral IR caused oxidative damage (increase TBARS, decrease antioxidant parameters). Treatment of MYR was increased in GSH,GPx,CAT,SOD activity while TBARS level was decreased. In addition, degenerative changes in I/R group heart tissue were ameliorated by MYR administration. CONCLUSION: The administration of beta-myrcene protects oxidative and histological damage in the heart tissue after global ischemia-reperfusion and may be useful safe alternative treatment for cardiac tissue after ischemic stroke. | en_US |
dc.identifier.doi | 10.1590/S0102-865020160070000005 | |
dc.identifier.endpage | 462 | en_US |
dc.identifier.issn | 0102-8650 | |
dc.identifier.issn | 1678-2674 | |
dc.identifier.issue | 7 | en_US |
dc.identifier.pmid | 27487280 | en_US |
dc.identifier.scopus | 2-s2.0-84979771551 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 456 | en_US |
dc.identifier.uri | https://doi.org/10.1590/S0102-865020160070000005 | |
dc.identifier.uri | https://hdl.handle.net/11616/97445 | |
dc.identifier.volume | 31 | en_US |
dc.identifier.wos | WOS:000380801700005 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Acta Cirurgica Brasileira | en_US |
dc.relation.ispartof | Acta Cirurgica Brasileira | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Brain Ischemia | en_US |
dc.subject | Reperfusion | en_US |
dc.subject | Oxidative Stress | en_US |
dc.subject | Mice | en_US |
dc.title | The protective cardiac effects of B-myrcene after global cerebral ischemia/reperfusion in C57BL/J6 mouse | en_US |
dc.type | Article | en_US |