Evidence map›Paper›PMID 38334198›Full record

ArticleJournal of cellular and molecular medicine2024

Ginkgetin effectively mitigates collagen and AA-induced platelet activation via PLCγ2 but not cyclic nucleotide-dependent pathway in human.

Chih-Wei Hsia, Lan-Hsin Shu, Ai-Wei Lee, Oanh-Thi Tran, Chih-Hao Yang, Ting-Lin Yen, Wei-Chieh Huang, Chih-Hsuan Hsia, Thanasekaran Jayakumar, Kuan-Rau Chiou and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.6field-weighted citation impact, top 9% of its field
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

7 citing papers in PubMed, 5 citations in OpenAlex.

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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

11 authors at 6 institutions in 3 countries.

Chih-Wei HsiaGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0002-4508-6181
Lan-Hsin ShuGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Ai-Wei LeeDepartment of Anatomy and Cell Biology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Oanh-Thi TranInternational Master/Ph.D. Program in Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Chih-Hao YangGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Ting-Lin YenDepartment of Medical Research, Cathay General Hospital, Taipei, Taiwan.
Wei-Chieh HuangGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Chih-Hsuan HsiaTranslational Medicine Center, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
Thanasekaran JayakumarDepartment of Ecology and Environmental Sciences, Pondicherry University, Puducherry, India.
Kuan-Rau ChiouDivision of Cardiology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Joen-Rong SheuGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.ORCID 0000-0001-8265-3678
Taipei Medical University · TWTaipei Medical University Hospital · TWCathay General Hospital · TWNational Taiwan University · TWPondicherry University · INTaipei Medical University-Shuang Ho Hospital · TW

Funding

Collaborative Research Project of College of Medicine, Taipei Medical UniversityNational Science and Technology Council MOST 107-2320-B-038-035-MY2National Science and Technology Council MOST 108-2320-B-038-031-MY3National Science and Technology Council NSTC 112-2320-B-038-037-MY3Taipei Medical University DP2-TMU-112-N-11Taipei Medical University-Shuang Ho Hospital 109TMU-SHH-05
6 · The paper itself

Abstract

Platelets assume a pivotal role in the cardiovascular diseases (CVDs). Thus, targeting platelet activation is imperative for mitigating CVDs. Ginkgetin (GK), from Ginkgo biloba L, renowned for its anticancer and neuroprotective properties, remains unexplored concerning its impact on platelet activation, particularly in humans. In this investigation, we delved into the intricate mechanisms through which GK influences human platelets. At low concentrations (0.5-1 μM), GK exhibited robust inhibition of collagen and arachidonic acid (AA)-induced platelet aggregation. Intriguingly, thrombin and U46619 remained impervious to GK's influence. GK's modulatory effect extended to ATP release, P-selectin expression, intracellular calcium ([Ca

Indexed as

BiflavonoidsNucleotides, CyclicPhospholipasesAnimalsArachidonic AcidBlood PlateletsCollagenHumansMicePhosphatidylinositol 3-KinasesPhospholipase C gammaPhosphorylationPlatelet ActivationPlatelet AggregationPlatelet Aggregation InhibitorsProtein Kinase CArachidonic AcidBiflavonoidsCollagenginkgetinNucleotides, CyclicPhosphatidylinositol 3-KinasesPhospholipase C gammaPhospholipasesPlatelet Aggregation InhibitorsProtein Kinase Cginkgetinhuman plateletsMAPKPI3K/AktPLCγ2vascular thrombosis

Identifiers

PMID38334198
PMCPMC10853947
OpenAlexW4391682399

What OpenQuestion holds

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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 OpenQuestion graph.