Evidence map›Paper›PMID 40728098›Full record

ArticleImmunity, inflammation and disease2025

Alleviative Effects of Ciprofol on Hepatic Ischemia/Reperfusion Injury Through Inhibiting Macrophage Polarization.

Hanjian Chen, Heng Wen, Dongdong Tian, Huina Su, Ru Zhang, Lijia Zhang

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Article in Immunity, inflammation and disease, 2025. 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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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hanjian ChenDepartment of Anesthesiology, The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Heng WenDepartment of Anesthesiology, The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.ORCID 0000-0001-8925-7643
Dongdong TianDepartment of Anesthesiology, The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Huina SuDepartment of Anesthesiology, The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Ru ZhangDepartment of Anesthesiology, School of Medicine, Yan'an University, Yan'an, China.
Lijia ZhangDepartment of Surgical Anesthesiology, The First Hospital of Yulin, Yulin, China.ORCID 0009-0007-1668-5883

Funding

This study was supported by the Zhejiang Provincial Natural Science Foundation (LQ22H010003).
6 · The paper itself

Abstract

backgroundPrevious studies have demonstrated the protective role of ciprofol against ischemia/reperfusion (I/R) injury, with the present investigation focusing on elucidating its effects on hepatic I/R injury.

methodsA hepatic I/R injury animal model was established, and macrophages were polarized using lipopolysaccharide (LPS) induction. Hepatic tissue damage and apoptosis were assessed through hematoxylin-eosin and TUNEL staining. Liver function parameters, including aspartate aminotransferase (AST) and alanine aminotransferase (ALT), as well as pro-inflammatory cytokine levels, were quantified using commercial assay kits. Macrophage polarization was evaluated via quantitative real-time PCR, immunofluorescence, and immunoblotting, with flow cytometry additionally employed to assess cellular polarization. Pro-inflammatory cytokine concentrations were also measured.

resultsIn the I/R model mice, ciprofol, comparable to the positive control propofol, and the macrophage eliminator gadolinium chloride (GdCl

conclusionThese findings suggest that ciprofol exerts hepatoprotective effects against I/R injury by modulating macrophage polarization.

Indexed as

LiverMacrophagesReperfusion InjuryAnimalsApoptosisCell PolarityCyclopropanesCytokinesDisease Models, AnimalLipopolysaccharidesMacrophage ActivationMaleMiceMice, Inbred C57BL(2-(1R)-1-cyclopropyl)ethyl-6-isopropyl-phenolCyclopropanesCytokinesLipopolysaccharidesciprofolhepatic ischemia/reperfusion injuryhypothesismacrophage polarizationtherapeutic

Identifiers

PMID40728098
PMCPMC12305461

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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 Socratic graph.