Clinical study, network pharmacology, and molecular docking of Kunxian capsule in treating idiopathic membranous nephropathy

ObjectiveA new Tripterygium wilfordii preparation called Kunxian capsule (KX) has been approved in China. However, it is still unknown whether KX is safe and effective for idiopathic membranous nephropathy (IMN) and its therapeutic mechanism of action is unclear.MethodsWe conducted a retrospective s...

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Main Authors: Jia Lv, Xinyu Gao, Lihua Liu, Libing He, Geng Tian, Xuehong Lu
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-02-01
Series:Frontiers in Medicine
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Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2025.1506972/full
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author Jia Lv
Xinyu Gao
Lihua Liu
Libing He
Geng Tian
Xuehong Lu
author_facet Jia Lv
Xinyu Gao
Lihua Liu
Libing He
Geng Tian
Xuehong Lu
author_sort Jia Lv
collection DOAJ
description ObjectiveA new Tripterygium wilfordii preparation called Kunxian capsule (KX) has been approved in China. However, it is still unknown whether KX is safe and effective for idiopathic membranous nephropathy (IMN) and its therapeutic mechanism of action is unclear.MethodsWe conducted a retrospective study of 39 patients with IMN who received KX to investigate its efficacy and side effects of KX in treating IMN. We also used network pharmacology and molecular docking methods to explore the potential mechanism of action of KX in IMN.ResultsIn patients with IMN receiving KX treatment, 24 h urine protein was markedly decreased, whereas serum albumin levels increased. The overall clinical response rate was 79.49% after 6 months of treatment, and there were no significant adverse events. Quercetin, luteolin and kaempferol were the main bioactive ingredients of KX in treating IMN. AKT1, IL6, and TNF were core targets. The main potential mechanism of KX in treating IMN were pathways involved in cancer, the AGE-RAGE signaling pathway in diabetic complications, lipid and atherosclerosis. Molecular docking results showed that the binding force between the active ingredient and core target was relatively stable.ConclusionKX is a safe and effective treatment option for IMN and can effectively improve serum albumin and 24 h urine protein levels in patients with IMN. This study preliminarily reveals the possible mechanism of KX in the treatment of IMN and provides a theoretical basis for future clinical research.
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spelling doaj-art-f45ddeb89f8f4ffab5594d654d76a15c2025-02-06T07:09:36ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2025-02-011210.3389/fmed.2025.15069721506972Clinical study, network pharmacology, and molecular docking of Kunxian capsule in treating idiopathic membranous nephropathyJia Lv0Xinyu Gao1Lihua Liu2Libing He3Geng Tian4Xuehong Lu5Department of Nephrology, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Gynecology and Obstetrics, The Second Hospital of Jilin University, Changchun, ChinaDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, ChinaObjectiveA new Tripterygium wilfordii preparation called Kunxian capsule (KX) has been approved in China. However, it is still unknown whether KX is safe and effective for idiopathic membranous nephropathy (IMN) and its therapeutic mechanism of action is unclear.MethodsWe conducted a retrospective study of 39 patients with IMN who received KX to investigate its efficacy and side effects of KX in treating IMN. We also used network pharmacology and molecular docking methods to explore the potential mechanism of action of KX in IMN.ResultsIn patients with IMN receiving KX treatment, 24 h urine protein was markedly decreased, whereas serum albumin levels increased. The overall clinical response rate was 79.49% after 6 months of treatment, and there were no significant adverse events. Quercetin, luteolin and kaempferol were the main bioactive ingredients of KX in treating IMN. AKT1, IL6, and TNF were core targets. The main potential mechanism of KX in treating IMN were pathways involved in cancer, the AGE-RAGE signaling pathway in diabetic complications, lipid and atherosclerosis. Molecular docking results showed that the binding force between the active ingredient and core target was relatively stable.ConclusionKX is a safe and effective treatment option for IMN and can effectively improve serum albumin and 24 h urine protein levels in patients with IMN. This study preliminarily reveals the possible mechanism of KX in the treatment of IMN and provides a theoretical basis for future clinical research.https://www.frontiersin.org/articles/10.3389/fmed.2025.1506972/fullKunxian capsuleidiopathic membranous nephropathyclinical studynetwork pharmacologymolecular docking
spellingShingle Jia Lv
Xinyu Gao
Lihua Liu
Libing He
Geng Tian
Xuehong Lu
Clinical study, network pharmacology, and molecular docking of Kunxian capsule in treating idiopathic membranous nephropathy
Frontiers in Medicine
Kunxian capsule
idiopathic membranous nephropathy
clinical study
network pharmacology
molecular docking
title Clinical study, network pharmacology, and molecular docking of Kunxian capsule in treating idiopathic membranous nephropathy
title_full Clinical study, network pharmacology, and molecular docking of Kunxian capsule in treating idiopathic membranous nephropathy
title_fullStr Clinical study, network pharmacology, and molecular docking of Kunxian capsule in treating idiopathic membranous nephropathy
title_full_unstemmed Clinical study, network pharmacology, and molecular docking of Kunxian capsule in treating idiopathic membranous nephropathy
title_short Clinical study, network pharmacology, and molecular docking of Kunxian capsule in treating idiopathic membranous nephropathy
title_sort clinical study network pharmacology and molecular docking of kunxian capsule in treating idiopathic membranous nephropathy
topic Kunxian capsule
idiopathic membranous nephropathy
clinical study
network pharmacology
molecular docking
url https://www.frontiersin.org/articles/10.3389/fmed.2025.1506972/full
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