Evidence map›Paper›PMID 36695923›Full record

ArticleLasers in medical science2023

Bothrops atrox mice experimental envenoming treatment using light-emitting diode (led) as an adjunct therapy to conventional serum therapy.

Alex Augusto Ferreira E Ferreira, Valdison Pereira Dos Reis, Hallison Mota Santana, Neriane Monteiro Nery, Jaína Rodrigues Evangelista, Suzanne Nery Serrath, Ricardo Segundo da Silva Dutra, Cristina Matiele Alves Rego, Maria Naiara Macedo Tavares, Milena Daniela Souza Silva and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Lasers in medical science, 2023. 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
2.8field-weighted citation impact, top 9% 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

1 citing paper in PubMed, 9 citations in OpenAlex.

  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

14 authors at 2 institutions in 1 country.

Alex Augusto Ferreira E FerreiraLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Valdison Pereira Dos ReisLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Hallison Mota SantanaLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Neriane Monteiro NeryLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Jaína Rodrigues EvangelistaLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Suzanne Nery SerrathLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Ricardo Segundo da Silva DutraLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Cristina Matiele Alves RegoLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Maria Naiara Macedo TavaresLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Milena Daniela Souza SilvaLaboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil.
Andreimar Martins SoaresLaboratório de Biotecnologia de Proteínas E Compostos Bioativos da Amazônia Ocidental, Centro de Estudos de Biomoléculas Aplicadas À Saúde (CEBio), - Fundação Oswaldo Cruz, FIOCRUZ Rondônia, Porto Velho, Rondônia, Brazil.
Moreno Magalhães S RodriguesLaboratório de Análise e Visualização de Dados - Fundação Oswaldo Cruz, FIOCRUZ Rondônia, Porto Velho, Rondônia, Brazil.
Stella Regina Zamuner *Universidade Nove de Julho (UNINOVE), São Paulo-SP, Brazil. stellazamuner@hotmail.com.
Juliana Pavan Zuliani *Laboratório de Imunologia Celular Aplicada À Saúde, FIOCRUZ Rondônia, Rua da Beira, 7671 BR364, Km 3,5 - CEP 76812-245 - Porto Velho, Rondônia, Brazil. juliana.zuliani@fiocruz.br.ORCID http://orcid.org/0000-0001-9221-7749
Universidade Federal de Rondônia · BRUniversidade Nove de Julho · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of anti-venom is one of the main control measures for snakebite envenoming when applied immediately after the snakebite. Systemic effects of the envenoming are usually reversed; however, neutralization of local effects is hardly achieved. The need for adjuvant therapies associated with serum therapy can improve the treatment for local effects of envenoming, with greater effectiveness in preventing or delaying the progression of damage, reducing the clinical signs and symptoms of victims of snakebites. The purpose of the study was to evaluate the photobiomodulation therapy using LED and/or dexamethasone associated with conventional serum therapy for the treatment of local damage caused by Bothrops atrox envenomation in a murine model. For this, experimental envenoming was carried out in the gastrocnemius muscle of male Swiss mice weighing 18 to 22 g divided into 8 groups of animals, distributed in groups non-treat, treated with anti-bothropic serum, dexamethasone, and LED, or the associated treatments, by intramuscular inoculation of 50 µg of venom or sterile PBS (control). After 30 min, the proposed treatments were administered alone or in combination. After 3 h, blood and muscle samples were collected for myotoxicity, cytotoxicity, histological analysis, and IL-1β assays. The evaluation of the treatment alone showed that serum therapy is not effective for the treatment of local damage and photobiomodulation demonstrated to be an effective therapy to reduce leukocyte infiltration, hemorrhage, and myotoxicity in experimental envenoming; dexamethasone proved to be a good resource for the treatment of the inflammatory process reducing the leukocyte infiltration. The association of serum therapy, LED, and dexamethasone was the best treatment to reduce the local effects caused by Bothrops atrox venom. All in all, the association of photobiomodulation therapy using LED with conventional serum therapy and the anti-inflammatory drug is the best treatment for reducing the undesirable local effects caused by snakebite accidents involving B. atrox species.

Indexed as

BothropsCrotalid VenomsSnake BitesAnimalsDexamethasoneMaleMiceMuscle, SkeletalMyotoxicityCrotalid VenomsDexamethasoneBothrops atroxDexamethasoneEnvenomationLEDPhotobiomodulation

Identifiers

PMID36695923
OpenAlexW4317889648

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.