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黄酒多酚化合物通过激活 Nrf2 信号通路预防阿霉素所致的心脏毒性。

Yellow Wine Polyphenolic Compounds prevents Doxorubicin-induced cardiotoxicity through activation of the Nrf2 signalling pathway.

机构信息

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.

出版信息

J Cell Mol Med. 2019 Sep;23(9):6034-6047. doi: 10.1111/jcmm.14466. Epub 2019 Jun 21.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de4f/6714138/d1e3211dc9af/JCMM-23-6034-g001.jpg

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