Zhang Qian, Wu Lei
Department of Pharmacy, The Bozhou Hospital, Anhui Medical University, Bozhou Anhui 236800, Bozhou 236800, Anhui, China.
Pharmacy Department, Hua Tuo Traditional Chinese Medicine Hospital, Bozhou 236800, Anhui, China.
J Oncol. 2022 Feb 21;2022:7277562. doi: 10.1155/2022/7277562. eCollection 2022.
This study aimed to review the potential chemoprotective effects of curcumin against the doxorubicin-induced cardiotoxicity.
According to the PRISMA guideline, a comprehensive systematic search was performed in different electronic databases (Web of Science, PubMed, and Scopus) up to July 2021. One hundred and sixty-four studies were screened in accordance with a predefined set of inclusion and exclusion criteria. Eighteen eligible articles were finally included in the current systematic review.
According to the in vitro and in vivo findings, it was found that doxorubicin administration leads to decreased cell survival, increased mortality, decreased bodyweight, heart weight, and heart to the bodyweight ratio compared to the control groups. However, curcumin cotreatment demonstrated an opposite pattern in comparison with the doxorubicin-treated groups alone. Other findings showed that doxorubicin significantly induces biochemical changes in the cardiac cells/tissue. Furthermore, the histological changes on the cardiac tissue were observed following doxorubicin treatment. Nevertheless, for most of the cases, these biochemical and histological changes mediated by doxorubicin were reversed near to control groups following curcumin coadministration.
It can be mentioned that coadministration of curcumin alleviates the doxorubicin-induced cardiotoxicity. Curcumin exerts these cardioprotective effects through different mechanisms of antioxidant, antiapoptosis, and anti-inflammatory. Since the finding presented in this systematic review are based on in vitro and in vivo studies, suggesting the use of curcumin in cancer patients as a cardioprotector agent against cardiotoxicity mediated by doxorubicin requires further clinical studies.
本研究旨在综述姜黄素对阿霉素诱导的心脏毒性的潜在化学保护作用。
根据PRISMA指南,截至2021年7月在不同电子数据库(科学网、PubMed和Scopus)中进行了全面的系统检索。根据预先设定的纳入和排除标准筛选了164项研究。最终18篇符合条件的文章被纳入本系统评价。
根据体外和体内研究结果,发现与对照组相比,给予阿霉素会导致细胞存活率降低、死亡率增加、体重、心脏重量以及心脏与体重之比降低。然而,与单独使用阿霉素治疗的组相比,姜黄素联合治疗呈现出相反的模式。其他研究结果表明,阿霉素显著诱导心脏细胞/组织的生化变化。此外,在阿霉素治疗后观察到心脏组织的组织学变化。然而,在大多数情况下,在联合使用姜黄素后,由阿霉素介导的这些生化和组织学变化接近对照组水平。
可以提及的是,联合使用姜黄素可减轻阿霉素诱导的心脏毒性。姜黄素通过抗氧化、抗凋亡和抗炎等不同机制发挥这些心脏保护作用。由于本系统评价中的研究结果基于体外和体内研究,因此建议在癌症患者中使用姜黄素作为预防阿霉素介导的心脏毒性的心脏保护剂需要进一步的临床研究。