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解毒活血汤可减少球囊损伤后涉及TLR4/NF-κB通路的再狭窄。

Detoxification and activating blood circulation decoction reduces restenosis involving the TLR4/NF-κB pathway after balloon injury.

作者信息

Zou Guohui, Zhu Jinhua, Liu Zhongyong, Wu Lu, Xu Ri, Chen Hongtao, Deng Peng, Deng Changqing

机构信息

Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China.

Jiangxi University of Traditional Chinese Medicine, Nanchang, 330004, China.

出版信息

Prostaglandins Other Lipid Mediat. 2019 Feb;140:1-8. doi: 10.1016/j.prostaglandins.2018.11.002. Epub 2018 Nov 16.

Abstract

Restenosis is a major problem after percutaneous coronary intervention (PCI) treatment. Inflammation is one of the major core mechanisms involved in the occurrence of restenosis, and plays an important role in intimal hyperplasia. Detoxification and activating blood circulation decoction (DABCD) is a traditional Chinese medicine that is used in the treatment and prevention of atherosclerotic and inflammatory diseases. Our previous studies demonstrated that DABCD-mediated cardioprotection involves anti-inflammatory mechanisms and could be developed as a novel drug for the treatment of vascular smooth muscle cell (VSMC) proliferation and aortic restenosis. A rat model of postoperative restenosis after PCI was generated by balloon injury to determine the protective effects and potential mechanisms of DABCD. The injured segments of aortae were collected on days 14 and 28 after the operation to observe the morphological changes in the vascular structure and measure the proportion of inflammatory factors in plasma and vascular tissues, as well as test the proliferative activity of VSMCs. The expression of related proteins, namely, Toll-like receptor (TLR) 4 and nuclear factor (NF)-κB, in the mechanistic study was clarified by western blot analysis. We tested the hypothesis that the cardioprotective effects of DABCD on aortic restenosis are associated with the inhibition of aortic intimal hyperplasia in this model. Our results showed that DABCD has protective effect on rat aortic restenosis and the anti-inflammatory mechanism of DABCD on balloon-induced restenosis in rat may be due to its ability to inhibit TLR4-mediated NF-κB signaling pathways. DABCD may be a potential therapeutic agent against restenosis.

摘要

再狭窄是经皮冠状动脉介入治疗(PCI)后的一个主要问题。炎症是再狭窄发生的主要核心机制之一,在内膜增生中起重要作用。解毒活血汤(DABCD)是一种用于治疗和预防动脉粥样硬化及炎症性疾病的中药。我们之前的研究表明,DABCD介导的心脏保护作用涉及抗炎机制,可开发为治疗血管平滑肌细胞(VSMC)增殖和主动脉再狭窄的新型药物。通过球囊损伤建立PCI术后再狭窄大鼠模型,以确定DABCD的保护作用及潜在机制。术后第14天和第28天收集主动脉损伤段,观察血管结构的形态变化,测量血浆和血管组织中炎症因子的比例,并检测VSMCs的增殖活性。通过蛋白质印迹分析阐明机制研究中相关蛋白,即Toll样受体(TLR)4和核因子(NF)-κB的表达。在该模型中,我们验证了DABCD对主动脉再狭窄的心脏保护作用与抑制主动脉内膜增生相关的假设。我们的结果表明,DABCD对大鼠主动脉再狭窄具有保护作用,DABCD对大鼠球囊诱导的再狭窄的抗炎机制可能是由于其抑制TLR4介导的NF-κB信号通路的能力。DABCD可能是一种潜在的抗再狭窄治疗药物。

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