Evidence map›Paper›PMID 41843713›Full record

ArticleKidney & blood pressure research2026

Nobiletin from Xiaoyu Xiezhuo Decoction: Restoring Mitochondrial Dynamics and Alleviating Renal Ischemia-Reperfusion Injury via M1 Macrophage Modulation.

Yuan Yuan, Jing Huang, Yinchao Zhou, Zhibo Weng, Yiru Weng, Zhouzhou Dong

Abstract read
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Article in Kidney & blood pressure research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yuan YuanDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital, Ningbo University, Ningbo, China.
Jing HuangDepartment of Hepatopancreatobiliary Surgery, Ningbo Medical Center Lihuili Hospital, Ningbo University, Ningbo, China.
Yinchao ZhouDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital, Ningbo University, Ningbo, China.
Zhibo WengDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital, Ningbo University, Ningbo, China.
Yiru WengDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital, Ningbo University, Ningbo, China.
Zhouzhou DongDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital, Ningbo University, Ningbo, China, dongzhouzhou_dzz@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThere have been reports that the traditional Chinese medicine formula Xiaoyu Xiezhuo Decoction (XYXZD) protects against kidney injury. Its possible mechanisms in renal ischemia-reperfusion injury (IRI) remain unclear, though. Investigating XYXZD's function and possible therapeutic effects on renal IRI is the goal of this investigation.

methodsLiquid chromatography-mass spectrometry and network pharmacology were applied to identify key target genes associated with XYXZD and renal IRI. Molecular docking was employed to forecast the binding affinity of bioactive compounds to these targets. The effects of nobiletin (NOB) on macrophage polarization, inflammatory cytokine production, mitochondrial function, and oxidative stress were evaluated. The impact of NOB on HK-2 mitochondrial dynamics through M1 macrophage polarization was evaluated via the cell counting kit-8 assay, enzyme-linked immunosorbent assay, Western blotting, and transmission electron microscopy.

resultsNetwork pharmacology analysis identified matrix metalloproteinase-9 (MMP9) and poly(ADP-ribose) polymerase 1 (PARP1) as key regulatory factors linking macrophage polarization and mitochondrial function. Molecular docking revealed a strong binding affinity between NOB and MMP9. NOB reduced M1 macrophage polarization, along with the downregulation of pro-inflammatory cytokines interleukin-1 beta and interleukin-6. In HK-2 cells, NOB mitigated mitochondrial dysfunction by modulating M1 macrophage polarization, reducing reactive oxygen species production, and restoring mitochondrial dynamics.

conclusionBy preventing M1 macrophage polarization, lowering inflammation, and reestablishing mitochondrial homeostasis in renal tubular epithelial cells, this study showed that NOB has renoprotective benefits. These results provided fresh perspectives on NOB's potential as a treatment for renal IRI.

Indexed as

Drugs, Chinese HerbalFlavonesKidneyMacrophagesMitochondrial DynamicsReperfusion InjuryAnimalsCell LineHumansMolecular Docking SimulationDrugs, Chinese HerbalFlavonesnobiletinM1 macrophageMatrix metalloproteinase-9Mitochondrial dynamicsNobiletinRenal ischemia-reperfusion injury

Identifiers

PMID41843713
PMCPMC13197149

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.