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作 者:张乃群 袁飘漂 曹琳茸 应娜 杨涛涛 ZHANG Naiqun;YUAN Piaopiao;CAO Linrong;YING Na;YANG Taotao(The No.4 People's Hospital of Yuyao,Yuyao 315470,China;Ningbo Medical Center Lihuili Hospital,Ningbo 315000,China)
机构地区:[1]余姚市第四人民医院,余姚315470 [2]宁波市医疗中心李惠利医院,宁波315000
出 处:《实验动物与比较医学》2024年第5期543-549,共7页Laboratory Animal and Comparative Medicine
基 金:余姚市卫生健康科技计划项目“基于U-PNR检测探究缬沙坦和卡托普利对DKD蛋白尿一级预防作用研究”(2022YYB13);浙江省药学会医院药学专项科研资助项目“基于尿PNR检测的DN早期诊断及缬沙坦的干预作用研究”(2017ZYY24)。
摘 要:目的通过监测肾小球足细胞相关分子podocin和nephrin的mRNA比值(podocin mRNA:nephrin mRNA ratio,PNR)在大鼠糖尿病肾脏疾病(diabetic kidney disease,DKD)早期模型中的变化,并将其与尿白蛋白-肌酐比值(urinary albumin to creatinine ratio,U-ACR)对比,评价PNR作为DKD早期诊断指标的可行性;并比较缬沙坦和福辛普利钠对DKD的早期干预作用。方法采用尾静脉注射链脲霉素(streptozotocin,STZ)(60 mg/kg)建立DKD大鼠模型,监测对比PNR与U-ACR的早期变化,适时给予缬沙坦和福辛普利钠干预;采用苏木精-伊红(hematoxylin and eosin staining,HE)染色观察肾小球结构形态,透射电子显微镜观察肾小球足细胞超微结构。结果造模后PNR在第9天达临界值(≥1),较U-ACR在第15天达临界值(≥30 mg/g)更早;造模后第9天给予缬沙坦和福辛普利钠干预,发现其对U-ACR均有显著降低作用(P<0.05),且缬沙坦低剂量优于高剂量(P>0.05),而福辛普利钠高剂量优于低剂量(P>0.05);低剂量的缬沙坦和福辛普利钠均对PNR有明显降低作用(P<0.05),高剂量未见明显影响;缬沙坦和福辛普利钠干预对肾小球结构及足细胞排布均具有一定的改善和维持作用。结论PNR较U-ACR更早变化,对大鼠DKD早期诊断具有一定的提示作用,缬沙坦和福辛普利钠早期干预对大鼠DKD有一定的治疗作用。Objective This study aims to monitor the mRNA ratio of podocin to nephrin(PNR)in glomerular podocytes of early diabetic kidney disease(DKD)rat models.The feasibility of using PNR as an early diagnostic indicator for DKD was evaluated by comparing it with the urinary albumin-to-creatinine ratio(U-ACR).Additionally,the early intervention effects of valsartan and fosinopril sodium on DKD were compared.Methods The DKD rat model was established by caudal intravenous injection of streptozotocin(STZ)at a dosage of 60 mg/kg.The early changes in PNR and U-ACR were monitored and compared,followed by timely intervention with valsartan and fosinopril sodium.Hematoxylin and eosin staining(HE)was used to observe glomerular structure,while transmission electron microscopy examined the ultrastructure of glomerular podocytes.Results PNR reached the critical value(≥1)on day 9 after modeling,earlier than U-ACR,which reached the critical value(≥30 mg/g)on day 15.Intervention with valsartan and fosinopril sodium on day 9 after modeling significantly reduced U-ACR(P<0.05),with lowdose valsartan showing better results than high-dose(P>0.05),while high-dose fosinopril sodium outperformed low-dose(P>0.05).Both low doses of valsartan and fosinopril sodium significantly reduced PNR(P<0.05),with no significant effect observed for high doses.The interventions with valsartan and fosinopril sodium improved and maintained glomerular structure and podocyte arrangement.Conclusion PNR changes earlier than U-ACR,indicating its potential as an early diagnostic marker for DKD in rats.Early intervention with valsartan and fosinopril sodium demonstrates a therapeutic effect on DKD in rats.
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