Evidence map›Paper›PMID 26695181›Full record

ArticlePurinergic signalling2016

Intranasal guanosine administration presents a wide therapeutic time window to reduce brain damage induced by permanent ischemia in rats.

Denise Barbosa Ramos, Gabriel Cardozo Muller, Guilherme Botter Maio Rocha, Gustavo Hirata Dellavia, Roberto Farina Almeida, Leticia Ferreira Pettenuzzo, Samanta Oliveira Loureiro, Gisele Hansel, Ângelo Cássio Magalhães Horn, Diogo Onofre Souza and 1 more

Abstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Glutathione-Mediated Neuroprotective Effect of Purine Derivatives.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Purinergic Signalling: Therapeutic Developments.Frontiers in pharmacology · 2017
    Review
  15. Article
  16. 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

11 authors at 2 institutions in 1 country.

Denise Barbosa RamosDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. denibaramos@yahoo.com.br.
Gabriel Cardozo MullerDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. mullergabriel94@gmail.com.
Guilherme Botter Maio RochaDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. guilhermebmrocha@gmail.com.
Gustavo Hirata DellaviaDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. hirata.dellavia@ufrgs.br.
Roberto Farina AlmeidaDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. almeida_rf@yahoo.com.br.
Leticia Ferreira PettenuzzoDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. leticiapettenuzzo@gmail.com.
Samanta Oliveira LoureiroDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. dasamanta@yahoo.com.br.
Gisele HanselDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. gihansel@gmail.com.
Ângelo Cássio Magalhães HornInstituto Federal de Educação, Ciência e Tecnologia do Rio Grande do Sul, IFRS, Campus Porto Alegre, Rua Ramiro Barcelos, 2777, Santana, 90035-007, Porto Alegre, RS, Brazil. angelo.horn@poa.ifrs.edu.br.
Diogo Onofre SouzaDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. diogo@ufrgs.br.
Marcelo GanzellaDepartamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600 - anexo, Santana, 90035-003, Porto Alegre, RS, Brazil. ganzellam@gmail.com.
Universidade Federal do Rio Grande do Sul · BRInstituto Federal de Educação, Ciência e Tecnologia do Rio Grande do Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In addition to its intracellular roles, the nucleoside guanosine (GUO) also has extracellular effects that identify it as a putative neuromodulator signaling molecule in the central nervous system. Indeed, GUO can modulate glutamatergic neurotransmission, and it can promote neuroprotective effects in animal models involving glutamate neurotoxicity, which is the case in brain ischemia. In the present study, we aimed to investigate a new in vivo GUO administration route (intranasal, IN) to determine putative improvement of GUO neuroprotective effects against an experimental model of permanent focal cerebral ischemia. Initially, we demonstrated that IN [(3)H] GUO administration reached the brain in a dose-dependent and saturable pattern in as few as 5 min, presenting a higher cerebrospinal GUO level compared with systemic administration. IN GUO treatment started immediately or even 3 h after ischemia onset prevented behavior impairment. The behavior recovery was not correlated to decreased brain infarct volume, but it was correlated to reduced mitochondrial dysfunction in the penumbra area. Therefore, we showed that the IN route is an efficient way to promptly deliver GUO to the CNS and that IN GUO treatment prevented behavioral and brain impairment caused by ischemia in a therapeutically wide time window.

Indexed as

Administration, IntranasalAnimalsBehavior, AnimalBrain IschemiaCerebral InfarctionDose-Response Relationship, DrugExploratory BehaviorGuanosineMaleMitochondriaNeuroprotective AgentsRatsRats, WistarStrokeGuanosineNeuroprotective AgentsGuanosineIntranasalIschemiaNeuroprotectionPurines

Identifiers

PMID26695181
PMCPMC4749534
OpenAlexW2292028295

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.