Evidence map›Paper›PMID 41857627›Full record

ArticleBMC complementary medicine and therapies2026

Arabica coffee oil extract enhances neuronal resilience under hypoxic stress through HIF-1α and EGFR signaling modulation.

Piyanee Ratanachamnong, Bhasirie Thuamsang, Pajaree Sonsungsan, Natta Wiriyakun, Prae Charoenwoodhipong, Yamaratee Jaisin, Nattinee Jantaratnotai, Poommaree Namchaiw

Abstract read
In one paragraph

Article in BMC complementary medicine and therapies, 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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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Piyanee RatanachamnongDepartment of Pharmacology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Bhasirie ThuamsangBiological Engineering Program, Faculty of Engineering, King Mongkut's University of Technology Thonburi, Bangkok, Thailand.
Pajaree SonsungsanMathematics and Statistics, School of Science, Walailak University, Nakhon Si Thammarat, Thailand.
Natta WiriyakunNSTDA Characterization and Testing Service Center (NCTC), National Science and Technology Development Agency (NSTDA), Pathum Thani, Thailand.
Prae CharoenwoodhipongDepartment of Home Economics, Faculty of Agriculture, Kasetsart University, Bangkok, Thailand.
Yamaratee JaisinDepartment of Pharmacology, Faculty of Medicine, Srinakharinwirot University, Bangkok, Thailand.
Nattinee JantaratnotaiDepartment of Pharmacology, Faculty of Science, Mahidol University, Bangkok, Thailand. nattinee.jan@mahidol.ac.th.
Poommaree NamchaiwBiological Engineering Program, Faculty of Engineering, King Mongkut's University of Technology Thonburi, Bangkok, Thailand. poommaree.anm@mail.kmutt.ac.th.

Funding

King Mongkut's University of Technology Thonburi Research Strengthening Project of the Faculty of EngineeringMahidol University and the Office of National Higher Education Science Research and Innovation Policy Council through Program Management Unit for Competitiveness C10F630097
6 · The paper itself

Abstract

backgroundHypoxia is a critical factor contributing to neuronal injury, primarily through dysregulation of hypoxia-inducible factor-1 alpha (HIF-1α). This study aimed to investigate the neuroprotective effects of Arabica coffee oil extract under hypoxic conditions in neuronal cells and to elucidate the underlying molecular mechanisms.

methodsHuman SH-SY5Y neuron-like cells were exposed to cobalt chloride (CoCl₂) to induce chemical hypoxia. Hypoxic conditions were validated by quantitative PCR analysis of gene expression and by observation of neuronal morphology. Proteomic profiling using LC-MS/MS was then performed to identify differentially expressed proteins (DEPs) and enriched biological pathways, in order to elucidate the molecular mechanisms underlying Arabica oil extract–mediated modulation.

resultsHypoxic stress significantly altered the expression of genes and proteins associated with vesicular trafficking, protein folding, and transcriptional regulation, along with morphological changes indicative of synaptic loss. One-hour pretreatment with Arabica oil extract markedly mitigated these effects, restoring 841 DEPs to expression patterns resembling normoxic conditions. Enrichment analyses revealed that Arabica pretreatment supported mitochondrial function, calcium signaling, and synaptic organization, while maintaining proteostasis through regulation of HIF-1–dependent and EGFR-associated pathways.

conclusionArabica coffee oil extract confers neuroprotection under hypoxic stress by restoring protein homeostasis, preserving synaptic integrity, and modulating key stress-response and translational pathways. These findings provide novel insight into the molecular mechanisms by which Arabica oil extract enhances neuronal resilience to hypoxic injury.

Indexed as

CoffeaCoffeeHypoxia-Inducible Factor 1, alpha SubunitNeuronsNeuroprotective AgentsPlant ExtractsPlant OilsCell HypoxiaCell Line, TumorErbB ReceptorsHumansSignal TransductionCoffeeEGFR protein, humanErbB ReceptorsHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitNeuroprotective AgentsPlant ExtractsPlant OilsArabicaCoffee oil extractHIF-1αHypoxia

Identifiers

PMID41857627
PMCPMC13122917

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.