Evidence map›Paper›PMID 26939579›Full record

ArticlePurinergic signalling2016

Variations of ATP and its metabolites in the hippocampus of rats subjected to pilocarpine-induced temporal lobe epilepsy.

Flávia Doná, Isaltino Marcelo Conceição, Henning Ulrich, Eliane Beraldi Ribeiro, Thalma Ariani Freitas, Ana Leonor Abrahao Nencioni, Maria José da Silva Fernandes

Open access · greenAbstract read
In one paragraph

Article in Purinergic signalling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Modern Analytical Techniques in Epilepsy Research.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. The P2X7 Receptor as a Mechanistic Biomarker for Epilepsy.International journal of molecular sciences · 2023
    Review
  10. Article
  11. The role of NaCNS neuroscience & therapeutics · 2022
    Review
  12. Adenosine AScientific reports · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Role of Adenosine in Epilepsy and Seizures.Journal of caffeine and adenosine research · 2020
    Review
  18. Article
  19. Article
  20. 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

7 authors at 4 institutions in 1 country.

Flávia DonáDepartamento de Neurologia e Neurocirurgia, Disciplina de Neurociências, Universidade Federal de São Paulo, UNIFESP, Rua Pedro de Toledo, 669 - 2° andar, CEP 04039-032, São Paulo, Brazil.ORCID 0000-0002-9138-4438
Isaltino Marcelo ConceiçãoLaboratório de Farmacologia, Instituto Butantan, São Paulo, Brazil.
Henning UlrichDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, Brazil.
Eliane Beraldi RibeiroDepartamento Fisiologia, Disciplina de Neurofisiologia e Fisiologia Endócrina, UNIFESP, São Paulo, Brazil.
Thalma Ariani FreitasLaboratório de Farmacologia, Instituto Butantan, São Paulo, Brazil.
Ana Leonor Abrahao NencioniLaboratório de Farmacologia, Instituto Butantan, São Paulo, Brazil.
Maria José da Silva FernandesDepartamento de Neurologia e Neurocirurgia, Disciplina de Neurociências, Universidade Federal de São Paulo, UNIFESP, Rua Pedro de Toledo, 669 - 2° andar, CEP 04039-032, São Paulo, Brazil. fernandesepm@gmail.com.
Instituto Butantan · BRUniversidade Federal de São Paulo · BRAnhanguera-Uniderp University · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although purinergic receptor activity has lately been associated with epilepsy, little is known about the exact role of purines in epileptogenesis. We have used a rat model of temporal lobe epilepsy induced by pilocarpine to study the dynamics of purine metabolism in the hippocampus during different times of status epilepticus (SE) and the chronic phase. Concentrations of adenosine 5'-triphosphate (ATP), adenosine diphosphate (ADP), adenosine monophosphate (AMP), and adenosine in normal and epileptic rat hippocampus were determined by microdialysis in combination with high-performance liquid chromatography (HPLC). Extracellular ATP concentrations did not vary along 4 h of SE onset. However, AMP concentration was elevated during the second hour, whereas ADP and adenosine concentrations augmented during the third and fourth hour following SE. During chronic phase, extracellular ATP, ADP, AMP, and adenosine concentrations decreased, although these levels again increased significantly during spontaneous seizures. These results suggest that the increased turnover of ATP during the acute period is a compensatory mechanism able to reduce the excitatory role of ATP. Increased adenosine levels following 4 h of SE may contribute to block seizures. On the other hand, the reduction of purine levels in the hippocampus of chronic epileptic rats may result from metabolic changes and be part of the mechanisms involved in the onset of spontaneous seizures. This work provides further insights into purinergic signaling during establishment and chronic phase of epilepsy.

Indexed as

Adenosine TriphosphateAnimalsChromatography, High Pressure LiquidConvulsantsDisease Models, AnimalEpilepsy, Temporal LobeHippocampusMaleMicrodialysisPilocarpineRatsRats, WistarAdenosine TriphosphateConvulsantsPilocarpineAdenosineATP metabolismHPLCMicrodialysisTemporal lobe epilepsy

Identifiers

PMID26939579
PMCPMC4854830
OpenAlexW2292615460

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.