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

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Cukurova Medical Journal Pub Date : 2023-09-30 DOI:10.17826/cumj.1314101
Ayşegül Burçin YILDIRIM, Emin KAYMAK, Tayfun CEYLAN, Ali AKIN, Nurhan KULOĞLU, Meryem SAYAN, Necla DEĞER, Esra ÖNAL, Derya KARABULUT
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 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}
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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.
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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。
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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
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