Timokinon metotreksatın neden olduğu kalp hasarını azaltır: sıçanlarda histopatolojik bir çalışma

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
Ayşegül Burçin YILDIRIM, Emin KAYMAK, Tayfun CEYLAN, Ali AKIN, Nurhan KULOĞLU, Meryem SAYAN, Necla DEĞER, Esra ÖNAL, Derya KARABULUT
{"title":"Timokinon metotreksatın neden olduğu kalp hasarını azaltır: sıçanlarda histopatolojik bir çalışma","authors":"Ayşegül Burçin YILDIRIM, Emin KAYMAK, Tayfun CEYLAN, Ali AKIN, Nurhan KULOĞLU, Meryem SAYAN, Necla DEĞER, Esra ÖNAL, Derya KARABULUT","doi":"10.17826/cumj.1314101","DOIUrl":null,"url":null,"abstract":"Purpose: The study aimed to evaluate the effect of thymoquinone on cardiac tissue in MTX-induced cardiac toxicity in rats with various parameters.
 Materials and Methods: Group I (n:8) was administered intraperitoneal saline for 10 days. Intraperitoneal olive oil was applied to Group II (n:8) for 10 days. Group III (n:8) was administered a single dose of 20 mg/kg Methotrexate (MTX) (500 mg/20 ml) intraperitoneally on the 1st day of the experiment. Since Methotrexate was in liquid form, no solvent was used. Group IV (n:8) received 10 mg/kg Thymoquinone (THQ) intraperitoneally for 10 days. Group V (n:8) (MTX: (20 mg/kg single dose intraperitoneally on the 1st day); THQ: 10mg/kg i.p. administered for 10 days. At the end of the experimental period, the rats were sacrificed for analysis of heart tissue. The structure of heart tissue was evaluated by haematoxylin-eosin staining. Immunohistochemically, connexin-43, HSP90, and HIF-1α antibodies were stained. The results were analysed statistically. 
 Results: According to our results, thymoquinone has a positive effect on the expression of Cx43, one of the proteins providing transmission in the intercalary discs, HSP90, one of the chaperones in the cell, and HIF-1α expression against MTX toxicity and provides a significant improvement by showing a cardioprotective effect histopathologically.
 Conclusion: THQ could be considered a crucial cardioprotective phytochemical against MTX cardiotoxicity.","PeriodicalId":10748,"journal":{"name":"Cukurova Medical Journal","volume":"10 1","pages":"0"},"PeriodicalIF":0.3000,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cukurova Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17826/cumj.1314101","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: The study aimed to evaluate the effect of thymoquinone on cardiac tissue in MTX-induced cardiac toxicity in rats with various parameters. Materials and Methods: Group I (n:8) was administered intraperitoneal saline for 10 days. Intraperitoneal olive oil was applied to Group II (n:8) for 10 days. Group III (n:8) was administered a single dose of 20 mg/kg Methotrexate (MTX) (500 mg/20 ml) intraperitoneally on the 1st day of the experiment. Since Methotrexate was in liquid form, no solvent was used. Group IV (n:8) received 10 mg/kg Thymoquinone (THQ) intraperitoneally for 10 days. Group V (n:8) (MTX: (20 mg/kg single dose intraperitoneally on the 1st day); THQ: 10mg/kg i.p. administered for 10 days. At the end of the experimental period, the rats were sacrificed for analysis of heart tissue. The structure of heart tissue was evaluated by haematoxylin-eosin staining. Immunohistochemically, connexin-43, HSP90, and HIF-1α antibodies were stained. The results were analysed statistically. Results: According to our results, thymoquinone has a positive effect on the expression of Cx43, one of the proteins providing transmission in the intercalary discs, HSP90, one of the chaperones in the cell, and HIF-1α expression against MTX toxicity and provides a significant improvement by showing a cardioprotective effect histopathologically. Conclusion: THQ could be considered a crucial cardioprotective phytochemical against MTX cardiotoxicity.
胸腺醌可减少甲氨蝶呤引起的心脏损伤:大鼠组织病理学研究
目的:探讨百里醌对mtx致大鼠心脏毒性的影响。 材料与方法:第一组(n:8)腹腔注射生理盐水10 d。II组(n:8)腹腔注射橄榄油10天。第三组(n:8)于实验第1天腹腔注射单剂量甲氨蝶呤(MTX) 20 mg/kg (500 mg/20 ml)。由于甲氨蝶呤是液态的,所以没有使用溶剂。IV组(n:8)腹腔注射百里醌(THQ) 10 mg/kg,持续10 d。V组(8例)(甲氨蝶呤:20 mg/kg单次腹腔注射,第1天);THQ:每次10mg/kg,给药10天。实验结束时,处死大鼠进行心脏组织分析。采用苏木精-伊红染色评价心脏组织结构。免疫组织化学染色,connexin-43, HSP90和HIF-1α抗体。结果进行统计学分析。& # x0D;结果:根据我们的研究结果,百里醌对MTX毒性的传导蛋白Cx43、细胞内伴侣蛋白HSP90和HIF-1α的表达有积极的影响,并通过组织病理学显示出心脏保护作用,显著改善了MTX毒性。结论:THQ可能是一种重要的抗MTX心脏毒性的植物化学物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Cukurova Medical Journal
Cukurova Medical Journal MEDICINE, GENERAL & INTERNAL-
自引率
0.00%
发文量
159
审稿时长
12 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信