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中药配方FTZ通过抑制TGF1-Smad2/3信号通路预防心脏纤维化。

The Traditional Chinese Medicine Formula FTZ Protects against Cardiac Fibrosis by Suppressing the TGF1-Smad2/3 Pathway.

作者信息

Zhang Yue, Wang Dongwei, Wu Kaili, Shao Xiaoqi, Diao Hongtao, Wang Zhiying, Sun Mengxian, Huang Xueying, Li Yun, Tang Xinyuan, Yan Meiling, Guo Jiao

机构信息

Center for Drug Research and Development, Guangdong Pharmaceutical University, Guangzhou 510006, China.

Guangdong Metabolic Diseases Research Center of Integrated Chinese and Western Medicine, Guangzhou 510006, China.

出版信息

Evid Based Complement Alternat Med. 2022 Apr 19;2022:5642307. doi: 10.1155/2022/5642307. eCollection 2022.

Abstract

BACKGROUND

Fu fang Zhen Zhu Tiao Zhi (FTZ) is a patented preparation of Chinese herbal medicine that has been used as a natural medicine to treat several chronic diseases including cardiovascular disease. However, its effects on cardiac fibrosis remain unclear. Therefore, this study was designed to investigate the effects and potential mechanisms of FTZ in treating cardiac fibrosis.

METHODS

FTZ was administered to mice by oral gavage daily at a dosage of 1.2 g/kg or 2.4 g/kg of body weight for 7 weeks after a transverse aorta constriction (TAC) surgery. Doppler echocardiography, hematoxylin and eosin staining, and Masson's trichrome staining were used to assess the effect of FTZ on the cardiac structure and function of mice that had undergone TAC. EdU and wound-healing assays were performed to measure the proliferative and migratory abilities of cardiac fibroblasts. Western blotting and qRT-PCR were used to determine the expression of TGF1, Col1A2, Col3, and -SMA proteins and mRNA levels.

RESULTS

FTZ treatment reduced collagen synthesis, attenuated cardiac fibrosis, and improved cardiac function in mice subjected to TAC. Moreover, FTZ treatment prevented the proliferation and migration of cardiac fibroblasts and reduced Ang-II-induced collagen synthesis. Furthermore, FTZ downregulated the expression of TGF1, p-smad2, and p-smad3 and inhibited the TGF1-Smad2/3 pathway in the setting of cardiac fibrosis.

CONCLUSION

FTZ alleviated the proliferation and migration of cardiac fibroblasts and suppressed collagen synthesis via the TGF1-Smad2/3 pathway during the progression of cardiac fibrosis. These findings indicated the therapeutic potential of FTZ in treating cardiac fibrosis.

摘要

背景

复方贞术调脂(FTZ)是一种中药专利制剂,已被用作治疗包括心血管疾病在内的多种慢性疾病的天然药物。然而,其对心脏纤维化的影响尚不清楚。因此,本研究旨在探讨FTZ治疗心脏纤维化的作用及潜在机制。

方法

在横断主动脉缩窄(TAC)手术后,以1.2 g/kg或2.4 g/kg体重的剂量每日经口灌胃给予小鼠FTZ,持续7周。采用多普勒超声心动图、苏木精-伊红染色和Masson三色染色评估FTZ对TAC小鼠心脏结构和功能的影响。进行EdU和伤口愈合试验以测量心脏成纤维细胞的增殖和迁移能力。采用蛋白质印迹法和qRT-PCR检测TGF1、Col1A2、Col3和α-SMA蛋白的表达及mRNA水平。

结果

FTZ治疗可减少胶原蛋白合成,减轻心脏纤维化,并改善TAC小鼠的心脏功能。此外,FTZ治疗可抑制心脏成纤维细胞的增殖和迁移,并减少血管紧张素II诱导的胶原蛋白合成。此外,在心脏纤维化背景下,FTZ下调TGF1、p-smad2和p-smad3的表达,并抑制TGF1-Smad2/3信号通路。

结论

在心脏纤维化进展过程中,FTZ通过TGF1-Smad2/3信号通路减轻心脏成纤维细胞的增殖和迁移,并抑制胶原蛋白合成。这些发现表明FTZ在治疗心脏纤维化方面具有治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d40e/9042631/c58642db148c/ECAM2022-5642307.001.jpg

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