Singh Mandeep, Kadhim Mustafa M, Turki Jalil Abduladheem, Oudah Shamam Kareem, Aminov Zafar, Alsaikhan Fahad, Jawhar Zanko Hassan, Ramírez-Coronel Andrés Alexis, Farhood Bagher
Department of Physical Education, University of Jammu, Srinagar, Jammu, India.
Department of Dentistry, Kut University College, Kut, Wasit, 52001, Iraq.
Cancer Cell Int. 2023 May 10;23(1):88. doi: 10.1186/s12935-023-02936-4.
Although doxorubicin chemotherapy is commonly applied for treating different malignant tumors, cardiotoxicity induced by this chemotherapeutic agent restricts its clinical use. The use of silymarin/silibinin may mitigate the doxorubicin-induced cardiac adverse effects. For this aim, the potential cardioprotective effects of silymarin/silibinin against the doxorubicin-induced cardiotoxicity were systematically reviewed.
In this study, we performed a systematic search in accordance with PRISMA guideline for identifying all relevant studies on "the role of silymarin/silibinin against doxorubicin-induced cardiotoxicity" in different electronic databases up to June 2022. Sixty-one articles were obtained and screened based on the predefined inclusion and exclusion criteria. Thirteen eligible papers were finally included in this review.
According to the echocardiographic and electrocardiographic findings, the doxorubicin-treated groups presented a significant reduction in ejection fraction, tissue Doppler peak mitral annulus systolic velocity, and fractional shortening as well as bradycardia, prolongation of QT and QRS interval. However, these echocardiographic abnormalities were obviously improved in the silymarin plus doxorubicin groups. As well, the doxorubicin administration led to induce histopathological and biochemical changes in the cardiac cells/tissue; in contrast, the silymarin/silibinin co-administration could mitigate these induced alterations (for most of the cases).
According to the findings, it was found that the co-administration of silymarin/silibinin alleviates the doxorubicin-induced cardiac adverse effects. Silymarin/silibinin exerts its cardioprotective effects via antioxidant, anti-inflammatory, anti-apoptotic activities, and other mechanisms.
尽管阿霉素化疗常用于治疗不同的恶性肿瘤,但这种化疗药物引起的心脏毒性限制了其临床应用。水飞蓟素/水飞蓟宾的使用可能减轻阿霉素引起的心脏不良反应。为此,系统评价了水飞蓟素/水飞蓟宾对阿霉素诱导的心脏毒性的潜在心脏保护作用。
在本研究中,我们按照PRISMA指南进行了系统检索,以确定截至2022年6月在不同电子数据库中关于“水飞蓟素/水飞蓟宾对阿霉素诱导的心脏毒性的作用”的所有相关研究。根据预定义的纳入和排除标准,获得并筛选了61篇文章。最终,13篇符合条件的论文被纳入本综述。
根据超声心动图和心电图结果,阿霉素治疗组的射血分数、组织多普勒二尖瓣环收缩期峰值速度、缩短分数显著降低,同时出现心动过缓、QT和QRS间期延长。然而,水飞蓟素加阿霉素组的这些超声心动图异常明显改善。此外,阿霉素给药导致心脏细胞/组织发生组织病理学和生化变化;相比之下,水飞蓟素/水飞蓟宾联合给药可以减轻这些诱导的改变(在大多数情况下)。
根据研究结果,发现水飞蓟素/水飞蓟宾联合给药可减轻阿霉素诱导的心脏不良反应。水飞蓟素/水飞蓟宾通过抗氧化、抗炎、抗凋亡活性及其他机制发挥其心脏保护作用。