Evidence map›Paper›PMID 40002483›Full record

ArticleBrain sciences2025

Vinpocetine, a Phosphodiesterase Type 1 Inhibitor, Mitigates Locomotor Hyperactivity in Female Mice Exposed to Lead During Development.

Ulisses C Araujo, Fernanda Nunes, Bruno S Gonçalves, Regina A A Gomes, Maria de Fátima R Moreira, Andre Nunes-Freitas, Thomas E Krahe, Yael de Abreu-Villaça, Alex C Manhães, Cláudio C Filgueiras

Abstract read
In one paragraph

Article in Brain sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

10 authors.

Ulisses C AraujoDepartamento de Ciências Fisiológicas, Universidade do Estado do Rio de Janeiro, Av. Prof. Manoel de Abreu 444, 5 andar, Vila Isabel, Rio de Janeiro 20550-170, RJ, Brazil.
Fernanda NunesDepartamento de Ciências Fisiológicas, Universidade do Estado do Rio de Janeiro, Av. Prof. Manoel de Abreu 444, 5 andar, Vila Isabel, Rio de Janeiro 20550-170, RJ, Brazil.ORCID 0009-0000-1384-6820
Bruno S GonçalvesDepartamento de Ciências Fisiológicas, Universidade do Estado do Rio de Janeiro, Av. Prof. Manoel de Abreu 444, 5 andar, Vila Isabel, Rio de Janeiro 20550-170, RJ, Brazil.
Regina A A GomesCentro de Estudos da Saúde do Trabalhador e Ecologia Humana (CESTEH), Escola Nacional de Saúde Pública, Rua Leopoldo Bulhões 1480, Manguinhos, Rio de Janeiro 21040-210, RJ, Brazil.
Maria de Fátima R MoreiraCentro de Estudos da Saúde do Trabalhador e Ecologia Humana (CESTEH), Escola Nacional de Saúde Pública, Rua Leopoldo Bulhões 1480, Manguinhos, Rio de Janeiro 21040-210, RJ, Brazil.ORCID 0000-0002-4521-1050
Andre Nunes-FreitasDepartamento de Ciências Fisiológicas, Universidade do Estado do Rio de Janeiro, Av. Prof. Manoel de Abreu 444, 5 andar, Vila Isabel, Rio de Janeiro 20550-170, RJ, Brazil.
Thomas E KraheDepartamento de Psicologia, Pontifícia Universidade Católica do Rio de Janeiro, Rio de Janeiro 22451-000, RJ, Brazil.ORCID 0000-0002-4686-9284
Yael de Abreu-VillaçaDepartamento de Ciências Fisiológicas, Universidade do Estado do Rio de Janeiro, Av. Prof. Manoel de Abreu 444, 5 andar, Vila Isabel, Rio de Janeiro 20550-170, RJ, Brazil.ORCID 0000-0002-9801-6179
Alex C ManhãesDepartamento de Ciências Fisiológicas, Universidade do Estado do Rio de Janeiro, Av. Prof. Manoel de Abreu 444, 5 andar, Vila Isabel, Rio de Janeiro 20550-170, RJ, Brazil.ORCID 0000-0003-4629-8343
Cláudio C FilgueirasDepartamento de Ciências Fisiológicas, Universidade do Estado do Rio de Janeiro, Av. Prof. Manoel de Abreu 444, 5 andar, Vila Isabel, Rio de Janeiro 20550-170, RJ, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq-BRAZIL) 313500/2021-5Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro - FAPERJ E-26/204.246/2024
6 · The paper itself

Abstract

Background/Objectives Studies in rodents indicate that disruptions in both cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) signaling pathways are involved in the development of hyperactive behavior. We examined whether vinpocetine, a phosphodiesterase type 1 inhibitor that enhances brain cAMP and cGMP levels, could mitigate locomotor hyperactivity in mice exposed to lead during early development. Methods Swiss mice were exposed to 90 ppm of lead in their drinking water throughout gestation and the first ten postnatal days. At postnatal day 10 (PN10), blood lead levels (BLLs) were about 30 µg/dL. At PN30, animals either received vinpocetine (20 mg/kg, i.p.) or a vehicle 4 h before the evaluation of locomotor activity in the open field. Results Lead-exposed males did not display differences in locomotor activity compared to controls, while lead-exposed females showed a significant increase in locomotion. Vinpocetine treatment significantly reversed the lead-induced hyperactivity in females. Conclusions These findings suggest that the cAMP and cGMP signaling pathways play a role in the hyperactivity induced by lead exposure.

Indexed as

cyclic nucleotidesheavy metallocomotor hyperactivitytype 1 phosphodiesterase

Identifiers

PMID40002483
PMCPMC11852739

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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.