Chaihuang-Yishen Granule Inhibits Diabetic Kidney Disease in Rats through Blocking TGF-β/Smad3 Signaling

被引:67
作者
Zhao, Ting Ting [1 ]
Zhang, Hao Jun [1 ]
Lu, Xiao Guang [1 ]
Huang, Xiao Ru [2 ,3 ,4 ]
Zhang, Wei Ku [1 ]
Wang, Hua [1 ]
Lan, Hui Yao [2 ,3 ,4 ]
Li, Ping [1 ]
机构
[1] China Japan Friendship Hosp, Inst Clin Med Sci, Dept Pharmacol, Beijing, Peoples R China
[2] Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Hong Kong, Hong Kong, Peoples R China
[4] CUHK Shenzhen Res Inst, Shenzhen, Peoples R China
关键词
GROWTH-FACTOR-BETA; TGF-BETA; RENAL FIBROSIS; DIVERSE ROLES; NEPHROPATHY; RECEPTOR; MICRORNA; SMAD3; INFLAMMATION; ACTIVATION;
D O I
10.1371/journal.pone.0090807
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective: Increasing evidence shows that TGF-beta 1 is a key mediator in diabetic nephropathy (DN) and induces renal fibrosis positively by Smad3 but negatively by Smad7. However, treatment of DN by blocking the TGF-beta/Smad pathway remains limited. The present study investigated the anti-fibrotic effect of a traditional Chinese medicine, Chaihuang-Yishen granule (CHYS), on DN. Research Design and Methods: Protective role of CHYS in DN was examined in an accelerated type 1 DN induced by streptozotocin in uninephrectomized Wistar rats. CHYS, at a dose of 0.56 g/kg body weight, was administered by a daily gastric gavage for 20 weeks and the therapeutic effect and potential mechanisms of CHYS on diabetic kidney injury were examined. Results: Treatment with CHYS attenuated diabetic kidney injury by significantly inhibiting 24-h proteinuria and progressive renal fibrosis including glomerulosclerotic index, tubulointerstitial fibrosis index, and upregulation of extracellular matrix (collagen I, IV, and fibronectin), despite the same levels of blood glucose. Further studies revealed that inhibition of renal fibrosis in CHYS-treated diabetic rats was associated with inhibition of TGF-beta 1/Smad3 signaling as demonstrated by upregulation of Smad7 but downregulation of TGF-beta 1, TGF-beta receptors, activation of Smad3, and expression of miRNA-21. Conclusions: CHYS may be a therapeutic agent for DN. CHYS attenuates DN by blocking TGF-beta/Smad3-mediated renal fibrosis.
引用
收藏
页数:10
相关论文
共 38 条
[1]   TGF-β-dependent mechanisms mediate restoration of self-tolerance induced by antibodies to CD3 in overt autoimmune diabetes [J].
Belghith, M ;
Bluestone, JA ;
Barriot, S ;
Mégret, J ;
Bach, JF ;
Chatenoud, L .
NATURE MEDICINE, 2003, 9 (09) :1202-1208
[2]   The Protective Role of Smad7 in Diabetic Kidney Disease: Mechanism and Therapeutic Potential [J].
Chen, Hai Yong ;
Huang, Xiao R. ;
Wang, Wansheng ;
Li, Jin Hua ;
Heuchel, Rainer L. ;
Chung, Arthur C. K. ;
Lan, Hui Yao .
DIABETES, 2011, 60 (02) :590-601
[3]   Stimulation of type I collagen transcription in human skin fibroblasts by TGF-β:: Involvement of Smad 3 [J].
Chen, SJ ;
Yuan, WH ;
Mori, Y ;
Levenson, A ;
Trojanowska, M ;
Varga, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (01) :49-57
[4]   MicroRNA and nephropathy: emerging concepts [J].
Chung, Arthur C. K. ;
Yu, Xueqing ;
Lan, Hui Y. .
INTERNATIONAL JOURNAL OF NEPHROLOGY AND RENOVASCULAR DISEASE, 2013, 6 :169-179
[5]  
Critchley JAJH, 2002, CHINESE MED J-PEKING, V115, P129
[6]   Smad-dependent and Smad-independent pathways in TGF-β family signalling [J].
Derynck, R ;
Zhang, YE .
NATURE, 2003, 425 (6958) :577-584
[7]   Mice lacking Smad3 are protected against streptozotocin-induced diabetic glomerulopathy [J].
Fujimoto, M ;
Maezawa, Y ;
Yokote, K ;
Joh, K ;
Kobayashi, K ;
Kawamura, H ;
Nishimura, M ;
Roberts, AB ;
Saito, Y ;
Mori, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 305 (04) :1002-1007
[8]   The MAD-related protein Smad7 associates with the TGF beta receptor and functions as an antagonist of TGF beta signaling [J].
Hayashi, H ;
Abdollah, S ;
Qiu, YB ;
Cai, JX ;
Xu, YY ;
Grinnell, BW ;
Richardson, MA ;
Topper, JN ;
Gimbrone, MA ;
Wrana, JL ;
Falb, D .
CELL, 1997, 89 (07) :1165-1173
[9]  
Hong SW, 2001, AM J PATHOL, V158, P1653
[10]   Ultrasound-microbubble-mediated gene transfer of inducible Smad7 blocks transforming growth factor-β signaling and fibrosis in rat remnant kidney [J].
Hou, CC ;
Wang, WS ;
Huang, XR ;
Fu, P ;
Chen, TH ;
Sheikh-Hamad, D ;
Lan, HY .
AMERICAN JOURNAL OF PATHOLOGY, 2005, 166 (03) :761-771