Evidence map›Paper›PMID 33921462›Full record

ReviewMolecules (Basel, Switzerland)2021

Snake Venom Components: Tools and Cures to Target Cardiovascular Diseases.

Jacinthe Frangieh, Mohamad Rima, Ziad Fajloun, Daniel Henrion, Jean-Marc Sabatier, Christian Legros, César Mattei

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
9.2field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Phospholipases ABiomolecules · 2025
    Review
  8. Therapeutic Promise and Biotechnological Prospects ofInternational journal of molecular sciences · 2025
    Review
  9. Molecular mechanism of human αCommunications biology · 2025
    Article
  10. Review
  11. Article
  12. Review
  13. Peptide Fraction fromAntioxidants (Basel, Switzerland) · 2025
    Article
  14. Article
  15. Molecular interaction assaysThe journal of venomous animals and toxins including tropical diseases · 2025
    Article
  16. Article
  17. Review
  18. Article
  19. Review
  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

7 authors at 3 institutions in 2 countries.

Jacinthe FrangiehLaboratory of Applied Biotechnology (LBA3B), Azm Center for Research in Biotechnology and Its Applications, EDST, Lebanese University, Tripoli 1300, Lebanon.ORCID 0000-0002-3413-8732
Mohamad RimaInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM, CNRS, Université de Strasbourg, 67400 Illkirch, France.ORCID 0000-0002-0335-9882
Ziad FajlounLaboratory of Applied Biotechnology (LBA3B), Azm Center for Research in Biotechnology and Its Applications, EDST, Lebanese University, Tripoli 1300, Lebanon.ORCID 0000-0002-6502-3110
Daniel HenrionUniversity Angers, INSERM U1083, CNRS UMR6015, MITOVASC, Team 2 CarMe, SFR ICAT, 49000 Angers, France.ORCID 0000-0003-1094-0285
Jean-Marc SabatierFaculté de Médecine Secteur Nord, 51, Institut de Neuro-Physiopathologie, Université Aix-Marseille, UMR 7051, Boulevard Pierre Dramard-CS80011, CEDEX 15, 13344 Marseille, France.ORCID 0000-0002-9040-5647
Christian LegrosUniversity Angers, INSERM U1083, CNRS UMR6015, MITOVASC, Team 2 CarMe, SFR ICAT, 49000 Angers, France.
César MatteiUniversity Angers, INSERM U1083, CNRS UMR6015, MITOVASC, Team 2 CarMe, SFR ICAT, 49000 Angers, France.ORCID 0000-0002-2214-2611
Centre National de la Recherche Scientifique · FRInstitut de Neurophysiopathologie · FRLebanese University · LB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular diseases (CVDs) are considered as a major cause of death worldwide. Therefore, identifying and developing therapeutic strategies to treat and reduce the prevalence of CVDs is a major medical challenge. Several drugs used for the treatment of CVDs, such as captopril, emerged from natural products, namely snake venoms. These venoms are complex mixtures of bioactive molecules, which, among other physiological networks, target the cardiovascular system, leading to them being considered in the development and design of new drugs. In this review, we describe some snake venom molecules targeting the cardiovascular system such as phospholipase A2 (PLA2), natriuretic peptides (NPs), bradykinin-potentiating peptides (BPPs), cysteine-rich secretory proteins (CRISPs), disintegrins, fibrinolytic enzymes, and three-finger toxins (3FTXs). In addition, their molecular targets, and mechanisms of action-vasorelaxation, inhibition of platelet aggregation, cardioprotective activities-are discussed. The dissection of their biological effects at the molecular scale give insights for the development of future snake venom-derived drugs.

Indexed as

AnimalsCardiovascular AgentsCardiovascular DiseasesCardiovascular SystemHumansModels, BiologicalSnake VenomsCardiovascular AgentsSnake Venomsanti-platelet agentcardiovascular diseasesdrugs discoveryhypotensive agentsnake venomvasorelaxant effect

Identifiers

PMID33921462
PMCPMC8070158
OpenAlexW3155178216

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.