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Fu-Fang-Jin-Qian-Cao herbal granules protect against the calcium oxalate-induced renal EMT by inhibiting the TGF-β/smad pathway.

Authors :
Liu, Wen-Rui
Lu, Hong-Tao
Zhao, Ting-Ting
Ding, Jia-Rong
Si, Ya-Chen
Chen, Wei
Hou, Jie-Bin
Gao, Song-Yan
Dong, Xin
Yu, Bing
Guo, Zhi-Yong
Lu, Jian-Rao
Source :
Pharmaceutical Biology. Dec2020, Vol. 58 Issue 1, p1124-1131. 8p.
Publication Year :
2020

Abstract

Nephrolithiasis is a major public health problem worldwide and Fu-Fang-Jin-Qian-Cao granules (FFJQC) is a traditional Chinese herbal formula that is used to treat nephrolithiasis. The main component of nephrolithiasis is calcium oxalate (CaOx) and the epithelial-mesenchymal transition (EMT) shown to play a crucial role in CaOx-induced kidney injury. However, the mechanism underlying the therapeutic effect of FFJQC on the CaOx-induced renal EMT is unknown. This study explores the therapeutic benefits and mechanism of FFJQC in oxalate-induced kidney injury. 60 male C57BL/6 mice were used in this experiment and divided into 6 groups. A mouse kidney stone model was created by intraperitoneal injection of glyoxylate at a dose of 100 mg/kg for 6 days. The standardized FFJQC was used to treat mouse crystal kidney injury by gavage at 1.35 and 2.7 g/kg, respectively. Western blotting and immunostaining for E-cadherin, cytokeratin 18 (CK18), vimentin, smooth muscle α-actin (α-SMA) and transforming growth factor β (TGF-β)/Smad pathway were conducted on renal tissues. Following CaOx-induced kidney injury, the levels of E-cadherin and CK18 in kidney decreased, while vimentin and α-SMA levels increased. The FFJQC treatment increased the levels of E-cadherin and CK18 and decreased vimentin and α-SMA levels in varying degrees. What's more, the FFJQC reduced the expression of CaOx-induced fibrosis marker collagen II. FFJQC alleviated the CaOx-induced renal EMT and fibrosis by regulating TGF-β/smad pathway. Therefore, the FFJQC is an important traditional Chinese medicine for the treatment of CaOx-induced renal injury and fibrosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13880209
Volume :
58
Issue :
1
Database :
Academic Search Index
Journal :
Pharmaceutical Biology
Publication Type :
Academic Journal
Accession number :
149693527
Full Text :
https://doi.org/10.1080/13880209.2020.1844241