Evidence map›Paper›PMID 27377432›Full record

ArticleInternational journal of experimental pathology2016

New approaches in tail-bleeding assay in mice: improving an important method for designing new anti-thrombotic agents.

Max Seidy Saito, André Luiz Lourenço, Hye Chung Kang, Carlos Rangel Rodrigues, Lucio Mendes Cabral, Helena Carla Castro, Plínio Cunha Satlher

Abstract read
In one paragraph

Article in International journal of experimental pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Frontiers in pharmacology · 2022
    Article
  6. Article
  7. Article
  8. GPR56/ADGRG1 is a platelet collagen-responsive GPCR and hemostatic sensor of shear force.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. Microvascular thrombosis: experimental and clinical implications.Translational research : the journal of laboratory and clinical medicine · 2020
    Review
  10. The Role of RIPK1 and RIPK3 in Cardiovascular Disease.International journal of molecular sciences · 2020
    Review
  11. Review
  12. Article
  13. Article
  14. Synthesis, characterization and anticoagulant activity of chitosan derivatives.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2020
    Article
  15. Assessing Blood Clotting and Coagulation Factors in Mice.Current protocols in mouse biology · 2019
    Article
  16. Article
  17. 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.

Max Seidy SaitoLaboratório de Antibióticos Bioquímica Ensino e Modelagem Molecular (LABiEMol) - Instituto de Biologia, Universidade Federal Fluminense, Niterói, RJ, Brazil.
André Luiz LourençoLaboratório de Antibióticos Bioquímica Ensino e Modelagem Molecular (LABiEMol) - Instituto de Biologia, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Hye Chung KangPrograma de Pós-Graduação em Patologia (PPG-UFF) - Hospital Universitário Antônio Pedro, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Carlos Rangel RodriguesLaboratório de Modelagem Molecular e QSAR (ModMolQSAR) - Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Lucio Mendes CabralLaboratório de Tecnologia Industrial Farmacêutica (LabTIF) - Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Helena Carla CastroLaboratório de Antibióticos Bioquímica Ensino e Modelagem Molecular (LABiEMol) - Instituto de Biologia, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Plínio Cunha SatlherLaboratório de Antibióticos Bioquímica Ensino e Modelagem Molecular (LABiEMol) - Instituto de Biologia, Universidade Federal Fluminense, Niterói, RJ, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This report describes a modified, simple, low-cost and more sensitive method to determine bleeding patterns and haemoglobin concentration in a tail-bleeding assay using BALB/c mice and tail tip amputation. The cut tail was immersed in Drabkin's reagent to promote erythrocyte lysis and haemoglobin release, which was monitored over 30 min. The operator was blinded to individual conditions of the mice, which were treated with either saline (NaCl 0.15m), DMSO (0.5%) or clinical anti-thrombotic drugs. Our experimental protocols showed good reproducibility and repeatability of results when using Drabkin's reagent than water. Thus, the use of Drabkin's reagent offered a simple and low-cost method to observe and quantify the bleeding and rebleeding episodes. We also observed the bleeding pattern and total haemoglobin loss using untreated animals or those under anti-coagulant therapy in order to validate the new Drabkin method and thus confirm that it is a useful protocol to quantify haemoglobin concentrations in tail-bleeding assay. This modified method provided a more accurate results for bleeding patterns in mice and for identifying new anti-thrombotic drugs.

Indexed as

AnimalsDisease Models, AnimalFemaleFibrinolytic AgentsGPI-Linked ProteinsHemochromatosis ProteinHemorrhageMaleMembrane ProteinsMice, Inbred BALB CReproducibility of ResultsTailFibrinolytic AgentsGPI-Linked ProteinsHemochromatosis ProteinHJV protein, mouseMembrane Proteinsanti-thrombotic agentsbleeding timetail-bleeding assay

Identifiers

PMID27377432
PMCPMC4960579

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.