Literature DB >> 31399988

New Therapies for the Treatment of Renal Fibrosis.

Feng Liu1, Shougang Zhuang2,3.   

Abstract

Renal fibrosis is the common pathway for progression of chronic kidney disease (CKD) to end stage of renal disease. It is now widely accepted that the degree of renal fibrosis correlates with kidney function and CKD stages. The key cellular basis of renal fibrosis includes activation of myofibroblasts, excessive production of extracellular matrix components, and infiltration of inflammatory cells. Many cellular mechanisms responsible for renal fibrosis have been identified, and some antifibrotic agents show a greater promise in slowing down and even reversing fibrosis in animal models; however, translating basic findings into effective antifibrotic therapies in human has been limited. In this chapter, we will discuss the effects and mechanisms of some novel antifibrotic agents in both preclinical studies and clinical trials.

Entities:  

Keywords:  Anti-fibrosis treatment; Clinical trial; Mechanism; Renal fibrosis

Mesh:

Year:  2019        PMID: 31399988     DOI: 10.1007/978-981-13-8871-2_31

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  8 in total

1.  Pharmacological and Genetic Inhibition of HDAC4 Alleviates Renal Injury and Fibrosis in Mice.

Authors:  Fengchen Shen; Xiying Hou; Tingting Li; Jianjun Yu; Huizhen Chen; Na Liu; Andong Qiu; Shougang Zhuang
Journal:  Front Pharmacol       Date:  2022-06-28       Impact factor: 5.988

2.  Sprr2f protects against renal injury by decreasing the level of reactive oxygen species in female mice.

Authors:  Kieu My Huynh; Anny Chuu-Yun Wong; Bo Wu; Marc Horschman; Hongjuan Zhao; James D Brooks
Journal:  Am J Physiol Renal Physiol       Date:  2020-10-05

3.  Extracellular vesicles produced by bone marrow mesenchymal stem cells attenuate renal fibrosis, in part by inhibiting the RhoA/ROCK pathway, in a UUO rat model.

Authors:  Zhengzhou Shi; Qi Wang; Youbo Zhang; Dapeng Jiang
Journal:  Stem Cell Res Ther       Date:  2020-06-26       Impact factor: 6.832

4.  The Expression of TRIM6 Activates the mTORC1 Pathway by Regulating the Ubiquitination of TSC1-TSC2 to Promote Renal Fibrosis.

Authors:  Weiwei Liu; Yang Yi; Chuanfu Zhang; Baojuan Zhou; Lin Liao; Wenrui Liu; Jing Hu; Qiming Xu; Jie Chen; Jianrao Lu
Journal:  Front Cell Dev Biol       Date:  2021-02-09

5.  Tengdan Capsule Prevents Hypertensive Kidney Damage in SHR by Inhibiting Periostin-Mediated Renal Fibrosis.

Authors:  Xiaoli Du; Qianqian Tao; Hongxia Du; Zhenbang Zhao; Yu Dong; Shuang He; Rui Shao; Yule Wang; Wenrun Han; Xintong Wang; Yan Zhu
Journal:  Front Pharmacol       Date:  2021-05-18       Impact factor: 5.810

6.  Bibliometric Analysis of Renal Fibrosis in Diabetic Kidney Disease From 1985 to 2020.

Authors:  Yuqing Zhang; Yingying Duan; Yuehong Zhang; Liyun Duan; Fengmei Lian; Xiaolin Tong
Journal:  Front Public Health       Date:  2022-02-04

7.  Protective Effects of Nootkatone on Renal Inflammation, Apoptosis, and Fibrosis in a Unilateral Ureteral Obstructive Mouse Model.

Authors:  Chang-Mu Chen; Chen-Yu Lin; Yao-Pang Chung; Chia-Hung Liu; Kuo-Tong Huang; Siao-Syun Guan; Cheng-Tien Wu; Shing-Hwa Liu
Journal:  Nutrients       Date:  2021-11-01       Impact factor: 5.717

8.  (-)-Epigallocatechin-3-gallate (EGCG) attenuates salt-induced hypertension and renal injury in Dahl salt-sensitive rats.

Authors:  Dan Luo; Jianping Xu; Xuejiao Chen; Xu Zhu; Shuang Liu; Jie Li; Xinting Xu; Xiao Ma; Jinhua Zhao; Xu Ji
Journal:  Sci Rep       Date:  2020-03-16       Impact factor: 4.379

  8 in total

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