Department of Cardiology, Shaoxing People's Hospital (Shaoxing Hospital, Zhejiang University School of Medicine), Shaoxing, China.
The First Clinical Medical College, Wenzhou Medical University, Wenzhou, China.
J Cell Mol Med. 2019 Sep;23(9):6034-6047. doi: 10.1111/jcmm.14466. Epub 2019 Jun 21.
Doxorubicin (DOX) is considered as the major culprit in chemotherapy-induced cardiotoxicity. Yellow wine polyphenolic compounds (YWPC), which are full of polyphenols, have beneficial effects on cardiovascular disease. However, their role in DOX-induced cardiotoxicity is poorly understood. Due to their antioxidant property, we have been suggested that YWPC could prevent DOX-induced cardiotoxicity. In this study, we found that YWPC treatment (30 mg/kg/day) significantly improved DOX-induced cardiac hypertrophy and cardiac dysfunction. YWPC alleviated DOX-induced increase in oxidative stress levels, reduction in endogenous antioxidant enzyme activities and inflammatory response. Besides, administration of YWPC could prevent DOX-induced mitochondria-mediated cardiac apoptosis. Mechanistically, we found that YWPC attenuated DOX-induced reactive oxygen species (ROS) and down-regulation of transforming growth factor beta 1 (TGF-β1)/smad3 pathway by promoting nuclear factor (erythroid-derived 2)-like 2 (Nrf2) nucleus translocation in cultured H9C2 cardiomyocytes. Additionally, YWPC against DOX-induced TGF-β1 up-regulation were abolished by Nrf2 knockdown. Further studies revealed that YWPC could inhibit DOX-induced cardiac fibrosis through inhibiting TGF-β/smad3-mediated ECM synthesis. Collectively, our results revealed that YWPC might be effective in mitigating DOX-induced cardiotoxicity by Nrf2-dependent down-regulation of the TGF-β/smad3 pathway.
多柔比星(DOX)被认为是化疗诱导性心脏毒性的主要罪魁祸首。富含多酚的黄酒多酚化合物(YWPC)对心血管疾病有有益作用。然而,它们在 DOX 诱导的心脏毒性中的作用知之甚少。由于其抗氧化特性,我们认为 YWPC 可以预防 DOX 诱导的心脏毒性。在这项研究中,我们发现 YWPC 治疗(30mg/kg/天)可显著改善 DOX 诱导的心脏肥大和心脏功能障碍。YWPC 减轻了 DOX 诱导的氧化应激水平升高、内源性抗氧化酶活性降低和炎症反应。此外,YWPC 给药可预防 DOX 诱导的线粒体介导的心脏细胞凋亡。在机制上,我们发现 YWPC 通过促进培养的 H9C2 心肌细胞中核因子(红细胞衍生 2)样 2(Nrf2)核易位,减轻了 DOX 诱导的活性氧(ROS)和转化生长因子β1(TGF-β1)/smad3 通路下调。此外,通过 Nrf2 敲低,YWPC 对 DOX 诱导的 TGF-β1 上调的抑制作用被消除。进一步的研究表明,YWPC 可通过抑制 TGF-β/smad3 介导的 ECM 合成来抑制 DOX 诱导的心脏纤维化。总之,我们的结果表明,YWPC 通过 Nrf2 依赖性下调 TGF-β/smad3 通路,可能有效减轻 DOX 诱导的心脏毒性。