Literature DB >> 32561685

Renoprotective Effects of a Novel Receptor-interacting Protein Kinase 2 Inhibitor, AS3334034, in Uninephrectomized Adriamycin-induced Chronic Kidney Disease Rats.

Yusuke Wada1, Mitsuhiro Kondo2, Kumi Sakairi2, Akira Nagashima2, Kenichi Tokita2, Hiroaki Tominaga2, Hiroshi Tomiyama3, Tomohisa Ishikawa4.   

Abstract

Renal inflammation is a final common pathway of chronic kidney disease (CKD), and its progression can be used to effectively gauge the degree of renal dysfunction. Inflammatory mechanisms contribute to glomerulosclerosis and tubulointerstitial fibrosis, which are hallmarks of CKD leading to end-stage renal disease. Receptor-interacting protein kinase 2 (RIP2) is largely committed to nucleotide-binding oligomerization domain signaling as a direct effector and transmits nuclear factor-κB (NF-κB)-mediated proinflammatory cytokine production. In the present study, we hypothesized that if inflammation via RIP2 and NF-κB signaling plays an important role in renal failure, then the anti-inflammatory effect of RIP2 inhibitors should be effective in improving CKD. To determine its pharmacologic potency, we investigated the renoprotective properties of the novel RIP2 inhibitor AS3334034 (7-methoxy-6-(2-methylpropane-2-sulfonyl)-N-(4-methyl-1H-pyrazol-3-yl)quinolin-4-amine) in uninephrectomized adriamycin-induced CKD rats. Six weeks' repeated administration of AS3334034 (10 mg/kg, once daily) significantly reduced urinary protein excretion and prevented the development of glomerulosclerosis and tubulointerstitial fibrosis. In addition, AS3334034 showed beneficial effects on renal function, as demonstrated by a decrease in levels of plasma creatinine and blood urea nitrogen and attenuation of a decline in creatinine clearance. Furthermore, AS3334034 significantly attenuated inflammation, renal apoptosis, and glomerular podocyte loss. These results suggest that the RIP2 inhibitor AS3334034 suppresses the progression of chronic renal failure via an anti-inflammatory effect, and is therefore potentially useful in treating patients with CKD. SIGNIFICANCE STATEMENT: The receptor-interacting protein kinase 2 (RIP2) inhibitor AS3334034 suppresses the progression of chronic renal failure via an anti-inflammatory effect, suggesting that the nucleotide-binding oligomerization domain (NOD)-RIP2 axis might play a crucial role in pathogenesis of inflammatory kidney diseases. AS3334034 is expected to be potentially useful in the treatment of patients with chronic kidney disease. The American Society for Pharmacology and Experimental Therapeutics.

Entities:  

Keywords:  NFkappaB; anti-inflammatory drugs; apoptosis; cell death; cell injury; chronic renal failure; drug discovery; epithelial cells; kidney; renal failure

Year:  2020        PMID: 32561685     DOI: 10.1124/jpet.120.265678

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  3 in total

1.  Effect of Fushengong Decoction on PTEN/PI3K/AKT/NF-κB Pathway in Rats With Chronic Renal Failure via Dual-Dimension Network Pharmacology Strategy.

Authors:  Hongyu Luo; Munan Wang; Ke Xu; Qiyao Peng; Bo Zou; Shi Yin; Chao Yu; Lingyan Ren; Ping Li; Li Tang; Yongbo Peng; Xuekuan Huang
Journal:  Front Pharmacol       Date:  2022-03-15       Impact factor: 5.810

2.  Clinical characteristics of catheter-related infection in patients with chronic renal failure End Stage Renal failure undergoing semi-permanent catheter placement during maintenance hemodialysis through tunnelled cuffed hemodialysis catheter.

Authors:  Jun Dou; Xuebing Wu; Hua Ao; Qiuling Zhang; Ming Li
Journal:  Pak J Med Sci       Date:  2022 Jul-Aug       Impact factor: 2.340

3.  Verbena Attenuates Adriamycin-Induced Renal Tubular Injury via Inhibition of ROS-ERK1/2-NLRP3 Signal Pathway.

Authors:  Yicen Zhou; Qijing Wu; Zhenfang Du; Min Huang; Kun Gao; Xiaowei Ma; Hui Zhang; Sheng Qiang; Wei Sun
Journal:  Evid Based Complement Alternat Med       Date:  2022-09-28       Impact factor: 2.650

  3 in total

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