Evidence map›Paper›PMID 39992594›Full record

ArticlePurinergic signalling2025

First evidence of Tityus confluens Borelli, 1899 (Buthidae) venom altering purine metabolism in rat blood cells.

Romário da Silva Portilho, Igor Leal Brito, Andreza Negreli Santos, Bruna Pache Moreschi, Malson Neilson de Lucena, Jeandre Augusto Otsubo Jaques

Abstract read
In one paragraph

Article in Purinergic signalling, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Romário da Silva PortilhoBiochemistry Sector, Institute of Biosciences, Federal University of Mato Grosso Do Sul (UFMS), Campo Grande, Mato Grosso Do Sul, 79070-900, Brazil.ORCID 0009-0002-8193-865X
Igor Leal BritoBiochemistry Sector, Institute of Biosciences, Federal University of Mato Grosso Do Sul (UFMS), Campo Grande, Mato Grosso Do Sul, 79070-900, Brazil.ORCID 0000-0003-0660-8861
Andreza Negreli SantosBiochemistry Sector, Institute of Biosciences, Federal University of Mato Grosso Do Sul (UFMS), Campo Grande, Mato Grosso Do Sul, 79070-900, Brazil.ORCID 0000-0003-1339-3889
Bruna Pache MoreschiBiochemistry Sector, Institute of Biosciences, Federal University of Mato Grosso Do Sul (UFMS), Campo Grande, Mato Grosso Do Sul, 79070-900, Brazil.ORCID 0000-0001-5352-4893
Malson Neilson de LucenaBiochemistry Sector, Institute of Biosciences, Federal University of Mato Grosso Do Sul (UFMS), Campo Grande, Mato Grosso Do Sul, 79070-900, Brazil.ORCID 0000-0003-2566-5642
Jeandre Augusto Otsubo JaquesBiochemistry Sector, Institute of Biosciences, Federal University of Mato Grosso Do Sul (UFMS), Campo Grande, Mato Grosso Do Sul, 79070-900, Brazil. jeandre.jaques@ufms.br.ORCID 0000-0002-2498-1013

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purinergic signaling pathways play crucial roles in regulating hemostatic and inflammatory responses, both of which are impacted by scorpion envenomation. Scorpion venoms are complex mixtures of various toxins, such as peptides, enzymes, and nucleotides. Previous research showed that the action of scorpion toxins on the purinergic system stems from their effects on purinergic receptors. Additionally, a study identified a putative ectonucleotidase in scorpion venom. This study aimed to investigate the ability of Tityus confluens venom (10, 50, and 100 µg/mL) to metabolize adenine nucleotides and its potential effects on purinergic enzyme activity in rat platelets and lymphocytes. The effects of T. confluens venom on E-NTPDase (ATP and ADP hydrolysis), E-5'-NT (AMP hydrolysis), and E-ADA (ADO hydrolysis) activities were analyzed. The results revealed that crude venom from T. confluens exhibited ATP hydrolysis activity at all tested concentrations. In lymphocytes, ADP hydrolysis was inhibited by 100 µg/mL crude venom, whereas ADO hydrolysis was increased by all venom concentrations. In platelets, ATP hydrolysis was inhibited by 50 and 100 µg/mL crude venom, whereas AMP and ADO hydrolysis were inhibited by all concentrations. When considered collectively, the data suggested an elevation in extracellular ATP levels and a reduction in extracellular ADO. These findings are in alignment with clinical manifestations of scorpion envenomation characterized by a pro-inflammatory milieu. Furthermore, this study demonstrated the intrinsic ATPase activity of T. confluens venom and its ability to modulate E-NTPDase, E-5'-NT, and E-ADA activities in rat blood cells.

Indexed as

Blood CellsBlood PlateletsLymphocytesPurinesScorpion VenomsAdenosine TriphosphateAnimalsMaleRatsRats, WistarAdenosine TriphosphatePurinesScorpion VenomsAdenine nucleotidesAdenosine deaminaseEctonucleotidasesScorpionVenom

Identifiers

PMID39992594
PMCPMC12595173

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Registered trials

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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.