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首页|期刊导航|中国比较医学杂志|基于Wnt/β-catenin通路探究槲皮素对腹膜透析大鼠腹膜纤维化的影响及机制

基于Wnt/β-catenin通路探究槲皮素对腹膜透析大鼠腹膜纤维化的影响及机制

佀双双 孙源博 王莉莉 李钰 陈博文 李悦

中国比较医学杂志2026,Vol.36Issue(5):51-60,10.
中国比较医学杂志2026,Vol.36Issue(5):51-60,10.DOI:10.3969/j.issn.1671-7856.2026.05.005

基于Wnt/β-catenin通路探究槲皮素对腹膜透析大鼠腹膜纤维化的影响及机制

Effect and mechanism of quercetin on peritoneal fibrosis in peritoneal dialysis rats based on the Wnt/β-catenin pathway

佀双双 1孙源博 1王莉莉 2李钰 1陈博文 2李悦1

作者信息

  • 1. 牡丹江医科大学附属红旗医院 肾脏内科,黑龙江 牡丹江 157011||牡丹江医科大学 第一临床医学院,黑龙江 牡丹江 157011
  • 2. 牡丹江医科大学 护理学院,黑龙江 牡丹江 157011
  • 折叠

摘要

Abstract

Objective To explore the effect and mechanism of quercetin(QCT)on peritoneal fibrosis(PF)in peritoneal dialysis(PD)rats based on the Wnt/β-catenin pathway.Methods PD rat model was constructed,and successfully modeled rats were stochastically classified into LiCl-N(LiCl,0 mg/kg),LiCl-L(LiCl,30 mg/kg)、LiCl-M(LiCl,60 mg/kg),LiCl-H(LiCl,90 mg/kg),PD,QCT-L(QCT,17.5 mg/kg),QCT-H(QCT,35 mg/kg),and QCT-H+LiCl-M(QCT,35 mg/kg+LiCl,60 mg/kg)groups.Another 12 rats served as the Ctrl group.Rats in the Ctrl and PD groups were given an equal amount of 0.9%sodium chloride solution at the same time and location by gavage once a day for 4 weeks.Peritoneal function was assessed using the peritoneal balance test.Changes in peritoneal tissue were observed by hematoxylin-eosin staining and peritoneal tissue fibrosis was detected by Masson staining.Levels of the inflammatory factors tumor necrosis factor(TNF)-α,interleukin(IL)-1β,and IL-6 were detected by enzyme-linked immunosorbent assay.α-smooth muscle actin(SMA),collagen type 1(CoL-1),and E-cadherin protein levels were detected by immunohistochemistry,and Wnt3a,low-density lipoprotein receptor-related protein 5(LRP5),lymphoid enhancer-binding factor 1(LEF-1),glycogen synthase kinase-(GSK)-3β,and β-catenin proteins were measured by Western blot.Results Compared with the LiCl-N group,rats in the LiCl-L groups showed no effects on serum creatinine(Scr)and blood urea nitrogen(BUN)levels,mass transfer of glucose(MTG),ultrafiltration volume(UF),Wnt3a,and β-catenin protein(P>0.05),Rats in the LiCl-M groups showed same effects,while Wnt3a,β-catenin prote were increased(P<0.05).Rats in the LiCl-H groups showed more Scr and BUN levels,mass transfer of glucose(MTG),and Wnt3a and β-catenin protein(P<0.05),while UF were decreased(P<0.05).Thus,60 mg/kg was selected as the LiCl concentration.Rats in the PD group shed peritoneal mesothelial cells compared with the Ctrl group's number of inflammatory cells,relative area of collagen fiber deposition,peritoneal thickness,Scr and BUN levels,MTG,peritoneal tissue TNF-α,IL-1β,IL-6,α-SMA,CoL-1,Wnt3a,LRP5,LEF-1,and β-catenin were all increased(P<0.05),while UF,E-cadherin,and GSK-3β proteins decreased(P<0.05).Compared with the PD group,rats in the QCT-L and QCT-H groups showed less mesothelial cell shedding,number of inflammatory cells,relative area of collagen fiber deposition,peritoneal thickness,SCr,BUN,MTG,peritoneal tissue TNF-α,IL-1β,and IL-6 levels,and α-SMA,CoL-1,Wnt3a,LRP5,LEF-1,and β-catenin proteins were decreased(P<0.05),while UF,E-cadherin,and GSK-3β were increased(P<0.05).Compared with the QCT-H group,rats in the QCT-H+LiCl-M group showed increased peritoneal tissue damage,increased number of inflammatory cells,relative area of collagen fiber deposition,peritoneal thickness,Scr and BUN levels,MTG,peritoneal tissue TNF-α,IL-1β,and IL-6 levels,and α-SMA,CoL-1,Wnt3a,LRP5,LEF-1,β-catenin proteins(P<0.05),and decreased UF,E-cadherin,and GSK-3β(P<0.05).Conclusions QCT alleviates PF in PD rats by inhibiting the inflammatory response and peritoneal mesothelial cell mesenchymal transition process,possibly acting via inhibition of the Wnt/β-catenin signaling pathway.

关键词

槲皮素/Wnt/β-连环蛋白/腹膜透析/腹膜纤维化

Key words

quercetin/Wnt/β-catenin/peritoneal dialysis/peritoneal fibrosis

分类

医药卫生

引用本文复制引用

佀双双,孙源博,王莉莉,李钰,陈博文,李悦..基于Wnt/β-catenin通路探究槲皮素对腹膜透析大鼠腹膜纤维化的影响及机制[J].中国比较医学杂志,2026,36(5):51-60,10.

基金项目

黑龙江省省属高等学校基本科研业务费科研项目(2023-KYYWF-0920) (2023-KYYWF-0920)

牡丹江医学院护理学院强基科研计划项目(HLQJ-202412). (HLQJ-202412)

中国比较医学杂志

1671-7856

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