Evidence map›Paper›PMID 38741132›Full record

ArticleJournal of translational medicine2024

Neuroprotective effects of apigenin on retinal ganglion cells in ischemia/reperfusion: modulating mitochondrial dynamics in in vivo and in vitro models.

Jiawen Wu, Daowei Zhang, Hongli Liu, Jufeng Li, Ting Li, Jihong Wu, Shenghai Zhang

Abstract read
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Apigenin Prevents Ovarian Aging by Regulating CaAntioxidants (Basel, Switzerland) · 2026
    Article
  4. Food science & nutrition · 2026
    Review
  5. Phytochemical and Anti-Ischemic Stroke Properties from theDrug design, development and therapy · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Retinal Ischemia: Therapeutic Effects and Mechanisms of Paeoniflorin.International journal of molecular sciences · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Jiawen WuEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Daowei ZhangEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Hongli LiuEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Jufeng LiEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Ting LiEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Jihong WuEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China. Jihongwu@fudan.edu.cn.
Shenghai ZhangEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China. zsheent@163.com.ORCID 0000-0001-9771-8024

Funding

National Natural Science Foundation of China 82171055National Natural Science Foundation of China 82171085
6 · The paper itself

Abstract

backgroundRetinal ischemia/reperfusion (RIR) is implicated in various forms of optic neuropathies, yet effective treatments are lacking. RIR leads to the death of retinal ganglion cells (RGCs) and subsequent vision loss, posing detrimental effects on both physical and mental health. Apigenin (API), derived from a wide range of sources, has been reported to exert protective effects against ischemia/reperfusion injuries in various organs, such as the brain, kidney, myocardium, and liver. In this study, we investigated the protective effect of API and its underlying mechanisms on RGC degeneration induced by retinal ischemia/reperfusion (RIR).

methodsAn in vivo model was induced by anterior chamber perfusion following intravitreal injection of API one day prior to the procedure. Meanwhile, an in vitro model was established through 1% oxygen and glucose deprivation. The neuroprotective effects of API were evaluated using H&E staining, spectral-domain optical coherence tomography (SD-OCT), Fluoro-Gold retrograde labeling, and Photopic negative response (PhNR). Furthermore, transmission electron microscopy (TEM) was employed to observe mitochondrial crista morphology and integrity. To elucidate the underlying mechanisms of API, the terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay, flow cytometry assay, western blot, cell counting kit-8 (CCK-8) assay, lactate dehydrogenase (LDH) assay, JC-1 kit assay, dichlorofluorescein-diacetate (DCFH-DA) assay, as well as TMRE and Mito-tracker staining were conducted.

resultsAPI treatment protected retinal inner plexiform layer (IPL) and ganglion cell complex (GCC), and improved the function of retinal ganglion cells (RGCs). Additionally, API reduced RGC apoptosis and decreased lactate dehydrogenase (LDH) release by upregulating Bcl-2 and Bcl-xL expression, while downregulating Bax and cleaved caspase-3 expression. Furthermore, API increased mitochondrial membrane potential (MMP) and decreased extracellular reactive oxygen species (ROS) production. These effects were achieved by enhancing mitochondrial function, restoring mitochondrial cristae morphology and integrity, and regulating the expression of OPA1, MFN2, and DRP1, thereby regulating mitochondrial dynamics involving fusion and fission.

conclusionAPI protects RGCs against RIR injury by modulating mitochondrial dynamics, promoting mitochondrial fusion and fission.

Indexed as

ApigeninMitochondrial DynamicsNeuroprotective AgentsReperfusion InjuryRetinal Ganglion CellsAnimalsApoptosisMaleMice, Inbred C57BLMitochondriaModels, BiologicalReactive Oxygen SpeciesApigeninNeuroprotective AgentsReactive Oxygen SpeciesApigeninMitochondrial dynamicsNeuroprotectionRetina ischemia/reperfusionRetinal ganglion cells

Identifiers

PMID38741132
PMCPMC11089678

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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.