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首页|期刊导航|中国中药杂志|参芪地黄汤加味方抑制铁死亡改善糖尿病肾脏疾病中肾脏衰老和肾小管/间质纤维化的作用和机制

参芪地黄汤加味方抑制铁死亡改善糖尿病肾脏疾病中肾脏衰老和肾小管/间质纤维化的作用和机制

李雅静 涂玥 CHONG Fee-lan 曹东维 吴薇 万毅刚 沈昊雯 何其函 桑天庆 刘莹露 房其军

中国中药杂志2026,Vol.51Issue(18):5131-5145,15.
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中国中药杂志2026,Vol.51Issue(18):5131-5145,15.DOI:10.19540/j.cnki.cjcmm.20260317.701

参芪地黄汤加味方抑制铁死亡改善糖尿病肾脏疾病中肾脏衰老和肾小管/间质纤维化的作用和机制

Effects and mechanisms of Supplemented Shenqi Dihuang Decoction Formula improving renal aging and tubulointerstitial fibrosis in diabetic kidney disease by inhibiting ferroptosis

李雅静 1涂玥 2CHONG Fee-lan 3曹东维 4吴薇 5万毅刚 5沈昊雯 1何其函 6桑天庆 7刘莹露 8房其军8

作者信息

  • 1. 南京中医药大学 鼓楼临床医学院 中医科,江苏 南京 210008
  • 2. 南京中医药大学 针灸推拿学院·养生康复学院,江苏 南京 210023
  • 3. the School of Pharmacy,Management and Science University,Shah Alam 40100,Malaysia
  • 4. 复旦大学 附属浦东医院 全科医学科,上海 201399
  • 5. 南京中医药大学 鼓楼临床医学院 中医科,江苏 南京 210008||南京大学 医学院 附属鼓楼医院 中医科,江苏 南京 210008||南京大学 中医研究院,江苏 南京 210008
  • 6. 南京中医药大学 鼓楼临床医学院 中医科,江苏 南京 210008||南京大学 医学院 附属鼓楼医院 中医科,江苏 南京 210008
  • 7. 南京大学 医学院 附属鼓楼医院 中医科,江苏 南京 210008||南京大学 中医研究院,江苏 南京 210008
  • 8. 南京大学 医学院 附属鼓楼医院 中医科,江苏 南京 210008
  • 折叠

摘要

Abstract

This study aimed to explore the effects and mechanisms of Supplemented Shenqi Dihuang Decoction Formula(SSDDF)in ameliorating renal aging(RA)and tubulointerstitial fibrosis(TIF)in diabetic kidney disease(DKD)by inhibiting ferroptosis,in comparison with empagliflozin(EMPA),a novel hypoglycemic agent.For the in vivo experiment,a type 2 DKD rat model with histopathological characteristics of RA and TIF was established.After successful modeling,the model rats were divided into the low-dose SSDDF(SSDDF-L)group,high-dose SSDDF(SSDDF-H)group,EMPA group and normal saline control group,and were administrated by gavage for six consecutive weeks for intervention.For the in vitro experiment,a senescent model of renal tubular epithelial cells was constructed by treating NRK-52E cells with high glucose(HG),which was then intervened with SSDDF-L containing serum,SSDDF-H containing serum,EMPA,as well as ferroptosis and iron metabolism inhibitors.In both in vivo and in vitro studies,aging phenotypes and related physiological indicators including body weight(BW)and blood glucose(BG),renal injury indicators including serum creatinine(Scr),blood urea nitrogen(BUN)and urinary N-acetyl-β-D-glucosaminidase(UNAG),aging characteristics of renal tissues and cells including senescence-associated β-galactosidase(SA-β-gal)staining and protein expression of klotho and p16,TIF pathological features and cellular fibrotic injury,senescence-associated secretory phenotype(SASP),and ferroptosis characteristics(lipid peroxidation-dependent ferroptosis detected by FerroOrange fluorescent probe and mitochondrial transmission electron microscopy)were examined and compared.Meanwhile,an"SSDDF-component-target"network was constructed via network pharmacology,and Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)pathway enrichment analyses were combined to screen the core signaling pathways.Non-targeted metabolomics was adopted to analyze the characteristics of renal tissues,screen potential biomarkers and enrich related metabolic pathways.The results indicated that the effect of SSDDF in ameliorating RA and TIF in DKD rats might be associated with the regulation of ferroptosis signaling pathways.In the in vivo experiment,SSDDF ameliorated the aging phenotypes,BW,BG,UNAG levels,as well as RA and TIF in DKD model rats,with SSDDF-H exerting a superior effect to SSDDF-L;notably,SSDDF-H showed a better effect than EMPA in improving Scr and BUN levels.SSDDF also ameliorated renal lipid peroxidation-dependent ferroptosis in DKD rats,where SSDDF-H had a better effect than SSDDF-L and an equivalent effect to EMPA.In the in vitro experiment,SSDDF-H containing serum multi-targetedly improved HG-induced senescence,fibrotic injury,SASP expression,ferroptosis marker levels and mitochondrial ultrastructural damage in renal tubular epithelial cells,with its effect comparable to that of ferroptosis or iron metabolism inhibitors.In conclusion,both SSDDF and EMPA can multi-targetedly ameliorate RA and TIF in DKD model rats with similar anti-aging and anti-fibrotic effects,and their core mechanism is the inhibition of renal lipid peroxidation-dependent ferroptosis.Based on this,the clinical establishment of a combined therapy regimen of SSDDF plus EMPA featured by"coordination of traditional Chinese and Western medicine"for elderly patients with DKD is expected to exert a dual synergistic effect in anti-aging and anti-fibrosis.

关键词

参芪地黄汤加味方/糖尿病肾脏疾病/肾脏衰老/肾小管/间质纤维化/铁死亡

Key words

Supplemented Shenqi Dihuang Decoction Formula/diabetic kidney disease/renal aging/tubulointerstitial fibrosis/fer-roptosis

引用本文复制引用

李雅静,涂玥,CHONG Fee-lan,曹东维,吴薇,万毅刚,沈昊雯,何其函,桑天庆,刘莹露,房其军..参芪地黄汤加味方抑制铁死亡改善糖尿病肾脏疾病中肾脏衰老和肾小管/间质纤维化的作用和机制[J].中国中药杂志,2026,51(18):5131-5145,15.

基金项目

国家自然科学基金面上项目(82374364,82174472) (82374364,82174472)

国家自然科学基金青年科学基金项目(82505305) (82505305)

国家中医药管理局重大疑难疾病中西医临床协作项目(国中医药综结合发[2024-3号]-92) (国中医药综结合发[2024-3号]-92)

江苏省自然科学基金面上项目(BK20231123) (BK20231123)

江苏省自然科学基金青年项目(BK20250243) (BK20250243)

江苏省中医药领军人才培养项目(SLJ0301) (SLJ0301)

南京市医学科技发展项目(ZKX24015,YKK24077) (ZKX24015,YKK24077)

南京鼓楼医院临床研究专项(2024-LCYJ-ZXY-01) (2024-LCYJ-ZXY-01)

上海市卫生健康委员会临床研究专项面上项目(202340138) (202340138)

复旦大学附属浦东医院扶持学科建设项目(Yjfcxk2025-07) (Yjfcxk2025-07)

复旦大学附属浦东医院引进人才科研启动项目(YJYJRC202502) (YJYJRC202502)

中国中药杂志

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