Evidence map›Paper›PMID 42687980›Full record

ArticleFrontiers in veterinary science2026

Comparative analysis of anesthetic protocols in spontaneously hypertensive rats with sepsis-induced hemodynamic instability.

Maria Alcione Silva Gomes, Aline Aparecida Macedo Marques, Gabriela Pereira da Silva, Luana Ale Bertoncello Pael, Maria Medina de Azevedo, Maria Luiza Fidelis da Silva, Joyner David Anaya Miranda, Bianca Viana Silva, Telma Lélia Gonçalves Schultz de Carvalho, Isabela Marafon Souza Féliz and 5 more

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Maria Alcione Silva GomesLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Aline Aparecida Macedo MarquesLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Gabriela Pereira da SilvaLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Luana Ale Bertoncello PaelLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Maria Medina de AzevedoLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Maria Luiza Fidelis da SilvaLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Joyner David Anaya MirandaLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Bianca Viana SilvaLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Telma Lélia Gonçalves Schultz de CarvalhoLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.
Isabela Marafon Souza FélizUniversity Center of Grande Dourados (UNIGRAN), Dourados, Mato Grosso do Sul, Brazil.
Sílvia Beatriz Bürger TinelliGraduate Program in Biotechnology Applied to Agriculture, Paranaense University, Umuarama, Paraná, Brazil.
Juliana CappellariGraduate Program in Medicinal Plants and Phytotherapy in Primary Health Care, Paranaense University, Umuarama, Paraná, Brazil.
Salviano Tramontin BellettiniGraduate Program in Animal Science with Emphasis on Bioactive Products, Paranaense University, Umuarama, Paraná, Brazil.
Emerson Luiz Botelho LourençoGraduate Program in Medicinal Plants and Phytotherapy in Primary Health Care, Paranaense University, Umuarama, Paraná, Brazil.
Arquimedes Gasparotto JuniorLaboratory of Cardiovascular Pharmacology (LaFaC), Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, Mato Grosso do Sul, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Sepsis remains a significant clinical challenge characterized by complex inflammatory responses and hemodynamic instability, often modeled via cecal ligation and puncture (CLP). This study investigated the cardiovascular impacts of various anesthetic protocols in spontaneously hypertensive rats (SHR) subjected to abdominal sepsis. Methods: Septic SHR were allocated into five anesthetic groups: ketamine-xylazine, fentanyl-diazepam, fentanyl-dexmedetomidine, ketamine-dexmedetomidine, and inhaled isoflurane (2-3%), alongside an unanesthetized septic control. Evaluations included electrocardiography, arterial blood pressure monitoring, blood gas analysis, biochemical profiling, mesenteric vascular reactivity, and histopathology of the heart, kidney, and aorta. Results: Injectable combinations (ketamine-xylazine, fentanyl-diazepam, fentanyl-dexmedetomidine, and ketamine-dexmedetomidine) induced significant electrocardiographic alterations, hypotension, tissue hypoxia, increased oxidative stress, and elevated serum creatinine. Conversely, isoflurane-anesthetized rats maintained hemodynamic and biochemical stability, showing no significant deviations from the septic control group. Conclusion: Isoflurane demonstrated superior cardiovascular safety in hypertensive rats during sepsis-induced instability. These findings suggest that while isoflurane is the preferred anesthetic for this specific model, protocol selection must be tailored to the experimental context.

Indexed as

dexmedetomidinediazepamfentanylisofluraneketaminexylazine

Identifiers

PMID42687980
PMCPMC13533722

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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.