评估辅酶Q10对预防多柔比星诱发大鼠急性心脏毒性的影响

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL
Ola Sadeq AL-Shimaysawee, Fadhil A. Rizij, Rafid Mohammed Ali, Hassan Wasfi
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引用次数: 0

摘要

研究目的方法:将24只雌性大鼠按体重分为三组,第一组接受生理盐水治疗,第二组通过IP注射接受累积剂量为15 mg/kg的DOX治疗,第三组在接受DOX治疗前接受辅酶Q10预处理。方法:将 24 只雌性大鼠按体重分为三组,第一组接受生理盐水,第二组通过 IP 注射接受累积剂量为 15 毫克/千克的 DOX,第三组在接受 DOX 前接受 CoQ10 预处理。数据分析采用单因素方差分析,并进行Bonferroni事后检验,以比较不同组的标记物和组织病理学变化。使用 GraphPad Prism 8.1 版进行统计分析:TNFα和ICAM-1水平的增加(P<0.0001)表明多柔比星诱导的心脏毒性具有统计学意义。此外,DOX+CoQ10 组与对照组的 GSH、SOD 和 caspase-3 水平无明显差异。此外,该物质还诱发了病变和组织学改变。与DOX组相比,服用辅酶Q10后,SOD、GSH和TNFα明显增加(P<0.0001),caspase 3明显减少(P<0.0001),表明心脏毒性显著降低。此外,CMYO评分和病变也得到了显著改善:在这项研究中,辅酶Q10对DOX诱导的小鼠心脏损伤具有保护作用。这一现象可能与抑制和保护氧化应激、细胞凋亡途径和炎症反应有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluate The Effect of Coenzyme Q10 on The Prevention of Doxorubicin-Induced Acute Cardiotoxicity in Rats.
Objective: This study will evaluate the potential protective effects of coenzyme Q10 on DOX-induced cardiotoxicity in female rats, manifested by changes in biochemical parameters in tissue and serum samples histopathological differences, and compare their changes. Methods:24 female rats were divided into three groups based on weight. The first group received saline, the second group received a cumulative dose of 15 mg/kg of DOX via IP injection, and the third group was pre-treated with CoQ10 before receiving DOX. The data were analysed using a one-way ANOVA test with a Bonferroni post hoc test to compare the markers and histopathological changes in different groups. The GraphPad Prism version 8.1 was used to do the statistical analysis. Results: As indicated by a statistically significant increase (P<0.0001) in TNFα and ICAM-1 level, doxorubicin-induced cardiotoxicity. Additionally, the level of GSH, SOD, and caspase-3 did not differ significantly between the DOX+CoQ10 group and the control group. Furthermore, lesions and histological alterations were induced by the substance. Significant reductions in cardiotoxicity were observed with the administration of coenzyme Q10, as indicated by notable increases (P<0.0001) in SOD, GSH, and TNFα and significant decreases (P<0.0001) in caspase 3 when compared to the DOX group. Also, the CMYO score and lesions exhibited a substantial improvement. Conclusion: In this investigation, coenzyme Q10 exhibited cardioprotective effects against DOX-induced damage to the mouse heart. This phenomenon potentially pertains to inhibiting and safeguarding against oxidative stress, the pathway of apoptosis, and the inflammatory response.
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来源期刊
Journal of Contemporary Medical Sciences
Journal of Contemporary Medical Sciences MEDICINE, GENERAL & INTERNAL-
自引率
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发文量
65
审稿时长
12 weeks
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