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川芎嗪通过抑制AKT磷酸化诱导增生性瘢痕来源的成纤维细胞凋亡并抑制其增殖。

Tetramethylpyrazine Induces Apoptosis and Inhibits Proliferation of Hypertrophic Scar-Derived Fibroblasts Inhibiting the Phosphorylation of AKT.

作者信息

Wu Xue, Wang Zheng, Wu Gaofeng, Xu Xiaofan, Zhang Jian, Li Yan, Zhang Hong, Guo Shuzhen

机构信息

School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.

Medical Experiment Center, Shaanxi University of Chinese Medicine, Xianyang, China.

出版信息

Front Pharmacol. 2020 May 5;11:602. doi: 10.3389/fphar.2020.00602. eCollection 2020.

Abstract

Hypertrophic scar (HS) is a serious fibrotic skin disease and often considered as a kind of benign skin tumor. Tetramethylpyrazine (TMP), the main chemical composition of the traditional Chinese medicine Chuanxiong Rhizoma, has shown significant clinical benefits in the treatment of fibrosis disease and tumor, while the role in HS and the concrete mechanisms remain elusive. Herein, the protective effects of TMP in the treatment of HS was investigated and the results showed that the protein expression levels of type I collagen (Col I), type III collagen (Col III), and α-smooth muscle actin (α-SMA) were all inhibited remarkably after addition of TMP in HS-derived fibroblasts (HFs). Moreover, TMP also suppressed fibroblast proliferative and induced cell apoptosis. The protein expression levels of Caspase-3 and Bcl-2 were all decreased comparing with the control group while proapoptotic proteins Bax and Cleaved Caspase-3 were increased. In addition, TMP treatment markedly reduced the phosphorylation levels of AKT. Taken together, our investigations demonstrated that TMP could down-regulate the expression of fibrosis-related molecules, inhibit scar fibroblast proliferation and activate cell apoptosis, during which AKT pathway was involved. Thus, this study shed more light on the pharmacological mechanisms of TMP, and provided a novel therapeutic alternative for prevention and treatment of HS.

摘要

肥厚性瘢痕(HS)是一种严重的纤维化皮肤病,常被视为一种良性皮肤肿瘤。川芎嗪(TMP)是中药川芎的主要化学成分,在纤维化疾病和肿瘤治疗中已显示出显著的临床疗效,但其在HS中的作用及具体机制仍不清楚。在此,研究了TMP治疗HS的保护作用,结果显示,在HS来源的成纤维细胞(HFs)中加入TMP后,I型胶原(Col I)、III型胶原(Col III)和α平滑肌肌动蛋白(α-SMA)的蛋白表达水平均显著受到抑制。此外,TMP还抑制成纤维细胞增殖并诱导细胞凋亡。与对照组相比,Caspase-3和Bcl-2的蛋白表达水平均降低,而促凋亡蛋白Bax和裂解的Caspase-3增加。此外,TMP处理显著降低了AKT的磷酸化水平。综上所述,我们的研究表明,TMP可下调纤维化相关分子的表达,抑制瘢痕成纤维细胞增殖并激活细胞凋亡,其中涉及AKT通路。因此,本研究进一步阐明了TMP的药理机制,为HS的防治提供了一种新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c30a/7214921/ca851cdc292e/fphar-11-00602-g001.jpg

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