Evidence map›Paper›PMID 40447676›Full record

ArticleScientific reports2025

Chlorogenic acid attenuates oxidative damage in rat lacrimal gland epithelial cells via PI3K/AKT/FoxO3 signaling: network pharmacology and experimental evidence.

Yu Tang, Yuan Zhong, Jian Shi, Lihao Chen, Huimei Chen, Qinghua Peng, Xiaolei Yao

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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.

Yu TangThe First Clinical College of Chinese Medicine, Hunan University of Chinese Medicine, Changsha, 410007, China.
Yuan ZhongThe First Clinical College of Chinese Medicine, Hunan University of Chinese Medicine, Changsha, 410007, China.
Jian ShiHunan Provincial Key Laboratory for Prevention and Treatment of Ophthalmology and Otolaryngology Diseases with Chinese Medicine, Changsha, 410208, China.
Lihao ChenHunan Provincial Key Laboratory for Prevention and Treatment of Ophthalmology and Otolaryngology Diseases with Chinese Medicine, Changsha, 410208, China.
Huimei ChenThe First Clinical College of Chinese Medicine, Hunan University of Chinese Medicine, Changsha, 410007, China.
Qinghua PengThe First Clinical College of Chinese Medicine, Hunan University of Chinese Medicine, Changsha, 410007, China. pengqinghua@hnucm.edu.cn.
Xiaolei YaoThe First Clinical College of Chinese Medicine, Hunan University of Chinese Medicine, Changsha, 410007, China. yxlshh@126.com.

Funding

Key Program of Administration of Chinese Medicine of Hunan Province of China 2021023Key Project of Educational Commission of Hunan Province of China 20A370National Natural Science Foundation of China 82174443Natural Science Foundation of Hunan Province of China 2021JJ30527Open Fund Project of Hunan Provincial Engineering Technology Research Center for the Prevention and Treatment of Ophthalmology and Otolaryngology Diseases and Visual Function Protection with Chinese Medicine 2018YZD02
6 · The paper itself

Abstract

Oxidative stress and inflammation are crucial in dry eye pathogenesis. The antioxidant and anti-inflammatory activities of chlorogenic acid (CGA) have been studied in various fields, including ophthalmology. However, its therapeutic effects on dry eye remain unclear. This study aims to predict and validate the mechanisms of CGA in treating dry eye through data mining and in vitro experiments. Data mining integrated multiple online databases to predict potential therapeutic targets of CGA for dry eye and performed target enrichment analysis. In vitro experiments involved dividing rat lacrimal gland epithelial cells (LGECs) into seven groups: (1) control, (2) H2O2 model (200µM), (3) H2O2 + AKT inhibitor (MK-2206, 2.5µM), (4) H2O2 + AKT activator (SC79, 10ng/ml), (5) H2O2 + CGA (500nM), (6) H2O2 + AKT inhibitor + CGA, (7) H2O2 + AKT activator + CGA. We measured cell viability, mitochondrial ROS, PI3K/AKT/FoxO3 pathway proteins, and key indicators like Caspase3, TRAIL, Bcl-2, and SOD2. Results showed that CGA treatment and AKT activation could activate the PI3K/AKT/FoxO3 pathway, reduce ROS in LGECs, increase SOD2 production, and inhibit apoptosis. These findings suggest CGA as a promising candidate for further research in dry eye prevention and treatment.

Indexed as

Chlorogenic AcidEpithelial CellsForkhead Box Protein O3Lacrimal ApparatusOxidative StressPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionAnimalsAntioxidantsApoptosisCell SurvivalHydrogen PeroxideNetwork PharmacologyRatsReactive Oxygen SpeciesAntioxidantsChlorogenic AcidForkhead Box Protein O3FOXO3 protein, ratHydrogen PeroxidePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReactive Oxygen SpeciesAntioxidantChlorogenic acidDry eyeOxidative stressPI3K/AKT signaling pathway

Identifiers

PMID40447676
PMCPMC12125342

What Socratic holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.