Evidence map›Paper›PMID 34981315›Full record

ArticleInflammation2022

Autonomic Disbalance During Systemic Inflammation is Associated with Oxidative Stress Changes in Sepsis Survivor Rats.

Mateus R Amorim, Aline A de Jesus, Nilton N Santos-Junior, Maria J A Rocha, Jonatas E Nogueira, Marcelo E Batalhão, Evelin C Cárnio, Luiz G S Branco

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Carotid body denervation improves hyperglycemia in obese mice.Journal of applied physiology (Bethesda, Md. : 1985) · 2024
    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

8 authors at 3 institutions in 2 countries.

Mateus R AmorimDental School of Ribeirão Preto, University of São Paulo, Avenida Do Café s/n, São Paulo, 14040-904, Ribeirão Preto, Brazil. amorimmr@hotmail.com.
Aline A de JesusMedical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Nilton N Santos-JuniorMedical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Maria J A RochaDental School of Ribeirão Preto, University of São Paulo, Avenida Do Café s/n, São Paulo, 14040-904, Ribeirão Preto, Brazil.
Jonatas E NogueiraSchool of Physical Education and Sports of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Marcelo E BatalhãoNursing School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, 14040-902, Brazil.
Evelin C CárnioNursing School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, 14040-902, Brazil.
Luiz G S BrancoDental School of Ribeirão Preto, University of São Paulo, Avenida Do Café s/n, São Paulo, 14040-904, Ribeirão Preto, Brazil. branco@forp.usp.br.ORCID http://orcid.org/0000-0003-0292-4947
Universidade de São Paulo · BRJohns Hopkins University · USUniversidade de Ribeirão Preto · BR

Funding

fapesp #2016/17681-9fapesp #2017/09878-0
6 · The paper itself

Abstract

Sepsis affects 31.5 million people worldwide. It is characterized by an intense drop in blood pressure driving to cardiovascular morbidity and mortality. Modern supportive care has increased survival in patients; however, after experiencing sepsis, several complications are observed, which may be potentiated by new inflammatory events. Nevertheless, the interplay between sepsis survivors and a new immune challenge in cardiovascular regulation has not been previously defined. We hypothesized that cecal ligation and puncture (CLP) cause persistent cardiovascular dysfunctions in rats as well as changes in autonomic-induced cardiovascular responses to lipopolysaccharide (LPS). Male Wistar rats had mean arterial pressure (MAP) and heart rate (HR) recorded before and after LPS or saline administration to control or CLP survivor rats. CLP survivor rats had similar baseline MAP and HR when compared to control. LPS caused a drop in MAP accompanied by tachycardia in control, while CLP survivor rats had a noteworthy enhanced MAP and a blunted tachycardia. LPS-induced hemodynamic changes were related to an autonomic disbalance to the heart and resistance vessels that were expressed as an increased low- and high-frequency power of pulse interval in CLP survivors after saline and enhancement in the low-frequency power of systolic arterial pressure in control rats after LPS. LPS-induced plasma interferon γ, but not interleukin-10 surges, was blunted in CLP survivor rats. To further access whether or not LPS-induced autonomic disbalance in CLP survivor rats was associated with oxidative stress dysregulation, superoxide dismutase (SOD) activity and thiobarbituric acid reactive substances (TBARS) plasma levels changes were measured. LPS-induced oxidative stress was higher in CLP survivor rats. These findings indicate that key changes in hemodynamic regulation of CLP survivors rats take place in response to LPS that are associated with oxidative stress changes, i.e., reduced SOD activity and increased TBARS levels.

Indexed as

LipopolysaccharidesSepsisAnimalsCecumDisease Models, AnimalInflammationMaleOxidative StressRatsRats, WistarSuperoxide DismutaseThiobarbituric Acid Reactive SubstancesLipopolysaccharidesSuperoxide DismutaseThiobarbituric Acid Reactive Substancesblood pressurececal ligation and punctureendotoxin.septic shock

Identifiers

PMID34981315
OpenAlexW4205093458

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.