JiangyaTongluo decoction ameliorates tubulointerstitial fibrosis via regulating the SIRT1/PGC-1α/mitophagy axis in hypertensive nephropathy DOI Creative Commons
Yun Zhao, Jia Qi, Gaimei Hao

et al.

Frontiers in Pharmacology, Journal Year: 2024, Volume and Issue: 15

Published: Dec. 12, 2024

Introduction With the increasing prevalence of hypertension, incidence kidney diseases is also increasing, resulting in a serious public burden. Jiangya Tongluo decoction (JYTL), recognized prescription traditional Chinese medicine (TCM), commonly used to calm an overactive liver and reduce excess yang, while promoting blood flow alleviate obstructions meridians. Previous research has indicated that JYTL may help mitigate damage caused by hypertension; however, underlying mechanisms have not been thoroughly assessed. Methods First, amalgamation UPLC-QE/MS network pharmacology techniques was employed pinpoint potential active components, primary targets, crucial action treating hypertensive nephropathy (HN). Then, we spontaneous rats (SHRs) Wistar-Kyoto (WKYs) evaluate efficacy on HN with valsartan as positive reference. We conducted DCFH-DA fluorescence staining rat renal tissues detect level ROS. Western blotting immunohistochemistry were performed investigate further effect key targets signaling pathways. Results Through analysis, 189 ingredients 5 hub identified from JYTL. GSEA MitoCarta3.0 database PPI analysis revealed predominantly engages Sirt1-mitophagy pathway. Tanshinone iia, quercetin, adenosine are main for HN. In vivo validation showed could improve function, ameliorate tubulointerstitial fibrosis (TIF), mitochondrial function inhibiting ROS production regulating dynamics SHRs. treatment increase expression SIRT1, PGC-1α, Nrf1, TFAM, activate PINK1/Parkin-mediated mitophagy. Conclusion exert protective anti-fibrosis effects ameliorating SIRT1/PGC-1α-mitophagy

Language: Английский

Research dynamics and drug treatment of renal fibrosis from a mitochondrial perspective: a historical text data analysis based on bibliometrics DOI

Xu Li,

Lan Hu,

Qin Hu

et al.

Naunyn-Schmiedeberg s Archives of Pharmacology, Journal Year: 2025, Volume and Issue: unknown

Published: April 14, 2025

Language: Английский

Citations

0

Spatially resolved multi-omics reveals the renal cortex-metabolic reprogramming of Shenhua Tablet for intervention on IgA nephropathy DOI Creative Commons

Fengting Yin,

Ping Li, Chang Liu

et al.

Phytomedicine, Journal Year: 2025, Volume and Issue: 141, P. 156742 - 156742

Published: April 14, 2025

Language: Английский

Citations

0

The dual role of NSD2 in mitochondrial function: Insights into interstitial fibrosis and renal cancer DOI Creative Commons
Chien‐Wei Huang, Chen‐Yueh Wen, Po-Hung Chen

et al.

Pharmacological Research, Journal Year: 2024, Volume and Issue: 207, P. 107320 - 107320

Published: July 18, 2024

Language: Английский

Citations

1

Energy insufficiency induced by high purine diet: catalysts for renal impairment in hyperuricemia nephropathy rat model DOI Creative Commons
Zhenxiong Zhao, Zhikun Li,

Yu-Bin Xu

et al.

Current Research in Food Science, Journal Year: 2024, Volume and Issue: 9, P. 100864 - 100864

Published: Jan. 1, 2024

Language: Английский

Citations

1

JiangyaTongluo decoction ameliorates tubulointerstitial fibrosis via regulating the SIRT1/PGC-1α/mitophagy axis in hypertensive nephropathy DOI Creative Commons
Yun Zhao, Jia Qi, Gaimei Hao

et al.

Frontiers in Pharmacology, Journal Year: 2024, Volume and Issue: 15

Published: Dec. 12, 2024

Introduction With the increasing prevalence of hypertension, incidence kidney diseases is also increasing, resulting in a serious public burden. Jiangya Tongluo decoction (JYTL), recognized prescription traditional Chinese medicine (TCM), commonly used to calm an overactive liver and reduce excess yang, while promoting blood flow alleviate obstructions meridians. Previous research has indicated that JYTL may help mitigate damage caused by hypertension; however, underlying mechanisms have not been thoroughly assessed. Methods First, amalgamation UPLC-QE/MS network pharmacology techniques was employed pinpoint potential active components, primary targets, crucial action treating hypertensive nephropathy (HN). Then, we spontaneous rats (SHRs) Wistar-Kyoto (WKYs) evaluate efficacy on HN with valsartan as positive reference. We conducted DCFH-DA fluorescence staining rat renal tissues detect level ROS. Western blotting immunohistochemistry were performed investigate further effect key targets signaling pathways. Results Through analysis, 189 ingredients 5 hub identified from JYTL. GSEA MitoCarta3.0 database PPI analysis revealed predominantly engages Sirt1-mitophagy pathway. Tanshinone iia, quercetin, adenosine are main for HN. In vivo validation showed could improve function, ameliorate tubulointerstitial fibrosis (TIF), mitochondrial function inhibiting ROS production regulating dynamics SHRs. treatment increase expression SIRT1, PGC-1α, Nrf1, TFAM, activate PINK1/Parkin-mediated mitophagy. Conclusion exert protective anti-fibrosis effects ameliorating SIRT1/PGC-1α-mitophagy

Language: Английский

Citations

1