18?-glycyrrhetinic acid attenuates global cerebral ischemia/reperfusion-induced cardiac damage in C57BL/J6 mice
dc.contributor.author | Turkmen, Nese Basak | |
dc.contributor.author | Yuce, Hande | |
dc.contributor.author | Taslidere, Asli | |
dc.contributor.author | Sahin, Yasemin | |
dc.contributor.author | Ayhan, Idris | |
dc.contributor.author | Unuvar, Songuel | |
dc.contributor.author | Ciftci, Osman | |
dc.date.accessioned | 2024-08-04T20:53:22Z | |
dc.date.available | 2024-08-04T20:53:22Z | |
dc.date.issued | 2022 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | The aim of the present study is to investigate the cardioprotective effects of 1813-glycyrrhetinic acid (1813-GA) against oxidative and histological damage caused by global cerebral ischemia/ reperfusion (I/R) in C57BL/J6 mice. All male mice (n:40) were randomly divided into four groups: (1) sham-operated (Sham), (2) I/R, (3) 1813-GA, and (4) 1813-GA+I/R. Ischemia was not applied to the sham and 1813-GA groups. In the I/R group, the bilateral carotid arteries were clipped for 15 min to induce ischemia, and the mice were treated with the vehicle for 10 days. In the 1813-GA group, the mice were given 1813-GA (100 mg/kg) for 10 days following a median incision without carotid occlusion. In the 1813-GA+I/R group, the ischemic procedure performed to the I/R model was applied to the animals and afterwards they were intraperitoneally (i.p.) treated with 1813-GA (100 mg/kg) for 10 days. It was found that global cerebral I/R increased TBARS levels and decreased antioxidant parameters. The 1813-GA treatment decreased the level of TBARS and increased GSH, GPx, CAT, SOD activities. Also, the control group cardiac tissue samples were observed to have a normal histological appearance with the Hematoxylin-Eosin staining method. Histopathological damage was observed in the heart tissue samples belonging to the I/R group. The 1813-GA treatment ameliorates oxidative and histological injury in the heart tissue after global ischemia reperfusion, and may be a beneficial alternative treatment. | en_US |
dc.identifier.doi | 10.1590/s2175-97902022e21219 | |
dc.identifier.issn | 1984-8250 | |
dc.identifier.issn | 2175-9790 | |
dc.identifier.scopus | 2-s2.0-85146521928 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.uri | https://doi.org/10.1590/s2175-97902022e21219 | |
dc.identifier.uri | https://hdl.handle.net/11616/101122 | |
dc.identifier.volume | 58 | en_US |
dc.identifier.wos | WOS:000924004500001 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Univ Sao Paulo, Conjunto Quimicas | en_US |
dc.relation.ispartof | Brazilian Journal of Pharmaceutical Sciences | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Global cerebral I | en_US |
dc.subject | R | en_US |
dc.subject | 1813-glycyrrhetinic acid | en_US |
dc.subject | Oxidative stress | en_US |
dc.subject | Heart injury | en_US |
dc.title | 18?-glycyrrhetinic acid attenuates global cerebral ischemia/reperfusion-induced cardiac damage in C57BL/J6 mice | en_US |
dc.type | Article | en_US |