Protective effect of thymoquinone nanoemulsion in reducing the cardiotoxic effect of 5-fluorouracil in rats

IF 3.5 4区 医学 Q2 CHEMISTRY, MEDICINAL
Bardia Karim, Motahare Arabameri, Fatemeh Alimoradi, Razieh Mansoori, Ali A. Moghadamnia, Sohrab Kazemi, Seyed M. Hosseini
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Abstract

5-Fluorouracil (5-FU), which is one of the most widely used chemotherapy drugs, has various side effects on the heart. Thymoquinone (TMQ), the main bioactive component of Nigella sativa, has antioxidant and protective effects against toxicity. In this study, we investigated the protective effect of thymoquinone against cardiotoxicity caused by 5-FU in vitro and in vivo models. H9C2 cells were exposed to 5-FU and TMQ, and cell viability was evaluated in their presence. Also, 25 male Wistar rats were divided into five control groups, 5-FU, 2.5, and 5 mg TMQ in nanoemulsion form (NTMQ) + 5-FU and 5 mg NTMQ. Cardiotoxicity was assessed through electrocardiography, cardiac enzymes, oxidative stress markers, and histopathology. 5-FU induced cytotoxicity in H9c2 cells, which improved dose-dependently with NTMQ cotreatment. 5-FU caused body weight loss, ECG changes (increased ST segment, prolonged QRS, and QTc), increased cardiac enzymes (aspartate aminotransferase [AST], creatine kinase-myocardial band [CK-MB], and lactate dehydrogenase [LDH]), oxidative stress (increased malondialdehyde, myeloperoxidase, nitric acid; decreased glutathione peroxidase enzyme activity), and histological damage such as necrosis, hyperemia, and tissue hyalinization in rats. NTMQ ameliorated these 5-FU-induced effects. Higher NTMQ dose showed greater protective effects. Thus, the results of our study indicate that NTMQ protects against 5-FU cardiotoxicity likely through antioxidant mechanisms. TMQ warrants further research as an adjuvant to alleviate 5-FU chemotherapy side effects.

胸腺醌纳米乳剂对减轻 5-氟尿嘧啶对大鼠心脏毒性的保护作用
5-氟尿嘧啶(5-FU)是最广泛使用的化疗药物之一,对心脏有各种副作用。胸腺醌(TMQ)是黑升麻的主要生物活性成分,具有抗氧化和抗毒保护作用。在这项研究中,我们在体外和体内模型中研究了胸腺醌对 5-FU 引起的心脏毒性的保护作用。将 H9C2 细胞暴露于 5-FU 和 TMQ,并在它们存在的情况下评估细胞活力。此外,25 只雄性 Wistar 大鼠被分为 5 个对照组、5-FU 组、2.5 毫克 TMQ 纳米乳液(NTMQ)+ 5-FU 组和 5 毫克 NTMQ 组。心脏毒性通过心电图、心肌酶、氧化应激标记物和组织病理学进行评估。5-FU 在 H9c2 细胞中诱导细胞毒性,NTMQ 联合治疗可改善细胞毒性,但与剂量无关。5-FU 导致体重下降、心电图变化(ST 段增高、QRS 和 QTc 延长)、心肌酶(天冬氨酸氨基转移酶 [AST]、肌酸激酶-心肌带 [CK-MB] 和乳酸脱氢酶 [LDH])升高、氧化应激(丙二醛、髓过氧化物酶、硝酸、谷胱甘肽过氧化物酶升高)和组织病理学变化;谷胱甘肽过氧化物酶活性降低),以及组织学损伤,如大鼠坏死、充血和组织透明化。NTMQ 可改善 5-FU 诱导的这些效应。NTMQ 剂量越高,保护作用越强。因此,我们的研究结果表明,NTMQ 可通过抗氧化机制防止 5-FU 的心脏毒性。TMQ作为一种减轻5-FU化疗副作用的辅助药物,值得进一步研究。
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来源期刊
CiteScore
6.40
自引率
2.60%
发文量
104
审稿时长
6-12 weeks
期刊介绍: Drug Development Research focuses on research topics related to the discovery and development of new therapeutic entities. The journal publishes original research articles on medicinal chemistry, pharmacology, biotechnology and biopharmaceuticals, toxicology, and drug delivery, formulation, and pharmacokinetics. The journal welcomes manuscripts on new compounds and technologies in all areas focused on human therapeutics, as well as global management, health care policy, and regulatory issues involving the drug discovery and development process. In addition to full-length articles, Drug Development Research publishes Brief Reports on important and timely new research findings, as well as in-depth review articles. The journal also features periodic special thematic issues devoted to specific compound classes, new technologies, and broad aspects of drug discovery and development.
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