Evidence map›Paper›PMID 24117220›Full record

ArticleBritish journal of pharmacology2014

Platelet P2Y₁₂ receptors are involved in the haemostatic effect of notoginsenoside Ft1, a saponin isolated from Panax notoginseng.

B Gao, L Huang, H Liu, H Wu, E Zhang, L Yang, X Wu, Z Wang

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
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  11. Phytochemical constituents ofFood science & nutrition · 2022
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  14. Sex Difference of Effect ofEvidence-based complementary and alternative medicine : eCAM · 2022
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  15. Article
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  17. Interactions between clopidogrel and traditional Chinese medicine.Journal of thrombosis and thrombolysis · 2019
    Review
  18. Biosynthesis of rare 20(Journal of ginseng research · 2019
    Article
  19. Article
  20. 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

8 authors at 3 institutions in 1 country.

B GaoShanghai Key laboratory of Complex Prescriptions, The Ministry of Education Key Laboratory for Standardization of Chinese Medicines, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai, China; Department of Pharmacognosy, China Pharmaceutical University, Nanjing, China.
L Huang
H Liu
H Wu
E Zhang
L Yang
X Wu
Z Wang
Shanghai University of Traditional Chinese Medicine · CNChina Pharmaceutical University · CNShanghai University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeSaponins isolated from Panax notoginseng (Burk.) F.H. Chen have been shown to relieve thrombogenesis and facilitate haemostasis. However, it is not known which saponin accounts for this haemostatic effect. Hence, in the present study we aimed to identify which saponins contribute to its haemostatic activity and to elucidate the possible underlying mechanisms. EXPERIMENTAL APPROACH: Platelet aggregation was analysed using a platelet aggregometer. Prothrombin time, activated partial thromboplastin time and thrombin time were measured using a blood coagulation analyser, which was further corroborated with bleeding time and thrombotic assays. The interaction of notoginsenoside Ft1 with the platelet P2Y₁₂ receptor was determined by molecular docking analysis, cytosolic Ca(2+) and cAMP measurements, and phosphorylation of PI3K and Akt assays. KEY

resultsAmong the saponins examined, Ft1 was the most potent procoagulant and induced dose-dependent platelet aggregation. Ft1 reduced plasma coagulation indexes, decreased tail bleeding time and increased thrombogenesis. Moreover, it potentiated ADP-induced platelet aggregation and increased cytosolic Ca(2+) accumulation, effects that were attenuated by clopidogrel. Molecular docking analysis suggested that Ft1 binds to platelet P2Y₁₂ receptors. The increase in intracellular Ca(2+) evoked by Ft1 in HEK293 cells overexpressing P2Y₁₂ receptors could be blocked by ticagrelor. Ft1 also affected the production of cAMP and increased phosphorylation of PI3K and Akt downstream of P2Y₁₂ signalling pathways. CONCLUSION AND IMPLICATIONS: Ft1 enhanced platelet aggregation by activating a signalling network mediated through P2Y₁₂ receptors. These novel findings may contribute to the effective utilization of this compound in the therapy of haematological disorders.

Indexed as

Panax notoginsengAnimalsBinding SitesBlood PlateletsCalciumCyclic AMPDose-Response Relationship, DrugHEK293 CellsHemostasisHumansMolecular Docking SimulationPartial Thromboplastin TimePhosphatidylinositol 3-KinasesPhosphorylationPhytotherapyPlant ExtractsCalciumCyclic AMPnotoginsenoside Ft1P2ry12 protein, ratPhosphatidylinositol 3-KinasesPlant ExtractsPlatelet Aggregation InhibitorsProto-Oncogene Proteins c-aktPurinergic P2Y Receptor AntagonistsReceptors, Purinergic P2Receptors, Purinergic P2Y12Saponinshaemostasisnotoginsenoside Ft1P2Y12 receptorPanax notoginsengsaponin

Identifiers

PMID24117220
PMCPMC3874708
OpenAlexW1946134662

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.