Student Research Committee, Babol University of Medical Sciences, Babol, Iran.
Department of Pharmacology, Ayatollah Amoli Branch, Islamic Azad University, Amol, Iran.
Drug Dev Res. 2024 Apr;85(2):e22171. doi: 10.1002/ddr.22171.
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.
5-氟尿嘧啶(5-FU)是最广泛使用的化疗药物之一,对心脏有多种副作用。黑种草子的主要生物活性成分百里醌(TMQ)具有抗氧化和保护作用,可以防止毒性。在这项研究中,我们研究了百里醌对 5-FU 在体外和体内模型引起的心脏毒性的保护作用。将 H9C2 细胞暴露于 5-FU 和 TMQ 中,并在其存在下评估细胞活力。此外,将 25 只雄性 Wistar 大鼠分为五组:对照组、5-FU 组、2.5 和 5mg 纳米乳液形式的 TMQ(NTMQ)+5-FU 组和 5mg NTMQ 组。通过心电图、心脏酶、氧化应激标志物和组织病理学评估心脏毒性。5-FU 诱导 H9c2 细胞的细胞毒性,其与 NTMQ 共同处理呈剂量依赖性改善。5-FU 导致体重减轻、心电图变化(ST 段升高、QRS 延长和 QTc 延长)、心脏酶(天门冬氨酸氨基转移酶[AST]、肌酸激酶同工酶[CK-MB]和乳酸脱氢酶[LDH])升高、氧化应激(增加丙二醛、髓过氧化物酶、硝酸;减少谷胱甘肽过氧化物酶活性)以及坏死、充血和组织玻璃样变性等组织损伤。NTMQ 改善了这些 5-FU 引起的作用。较高的 NTMQ 剂量显示出更大的保护作用。因此,我们的研究结果表明,NTMQ 通过抗氧化机制保护 5-FU 心脏毒性。TMQ 值得进一步研究作为减轻 5-FU 化疗副作用的辅助药物。