Evidence map›Paper›PMID 30792425›Full record

ArticleScientific reports2019

Cholinergic Stimulation by Pyridostigmine Bromide Before Myocardial Infarction Prevent Cardiac and Autonomic Dysfunction.

C A Barboza, A R Fukushima, N Carrozzi, J F Machi, P M M Dourado, C T Mostarda, M C Irigoyen, L Nathanson, M Morris, E C Caperuto and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Pharmacodynamics, Safety, and Tolerability of Pyridostigmine Bromide in Heart Failure.Current therapeutic research, clinical and experimental · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
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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 5 institutions in 2 countries.

C A BarbozaSchool of Physical Education, University of Campinas - UNICAMP, Campinas, SP, Brazil.ORCID 0000-0002-1096-8432
A R FukushimaDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo - USP, São Paulo, SP, Brazil.
N CarrozziHuman Movement Laboratory, São Judas Tadeu University - USJT, São Paulo, SP, Brazil.
J F MachiInstitute of Neuro-Immune Medicine, Nova Southeastern University, Miami, FL, USA.
P M M DouradoHypertension Unit, Heart Institute (InCor), Medical School of University of São Paulo, São Paulo, SP, Brazil.
C T MostardaDepartment of Physical Education, Federal University of Maranhão - UFMA, São Luís, MA, Brazil.
M C IrigoyenHypertension Unit, Heart Institute (InCor), Medical School of University of São Paulo, São Paulo, SP, Brazil.
L NathansonInstitute of Neuro-Immune Medicine, Nova Southeastern University, Miami, FL, USA.
M MorrisInstitute of Neuro-Immune Medicine, Nova Southeastern University, Miami, FL, USA.
E C CaperutoHuman Movement Laboratory, São Judas Tadeu University - USJT, São Paulo, SP, Brazil.
B RodriguesSchool of Physical Education, University of Campinas - UNICAMP, Campinas, SP, Brazil. prof.brodrigues@gmail.com.
Nova Southeastern University · USUniversidade de São Paulo · BRUniversidade Estadual de Campinas (UNICAMP) · BRUniversidade São Judas Tadeu · BRUniversidade Federal do Maranhão · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory processes and cardiovascular autonomic imbalance are very relevant characteristic of the enormous dynamic process that is a myocardial infarction (MI). In this sense, some studies are investigating pharmacological therapies using acetylcholinesterase inhibitors, such as pyridostigmine bromide (PYR), aiming to increase parasympathetic tone after MI. Here we hypothesized that the use of PYR before the MI might bring an additional positive effect to the autonomic function, and consequently, in the inflammatory response and cardiac function. The present study aimed to evaluate left ventricular function, baroreflex sensitivity, autonomic modulation, and inflammatory profile in PYR-treated rats previously to MI.

methodsMale Wistar rats (250-300 g) were treated for 60 days with PYR. After treatment, they were submitted to the MI. After the MI, the autonomic and ventricular function were evaluated, as well as the systemic, left ventricle, and adipose tissue inflammatory profile.

resultsPYR, performed before MI, prevented HR increase, systolic function impairment, baroreflex sensitivity drop, as well as pulse interval variance, RMSSD, blood pressure and parasympathetic modulation reduction in treated rats compared to untreated rats. Also, this positive functional changes may have been a result of the reduced inflammatory parameters in the left ventricle (IFN-γ, IL-6, and IL-1β), as well as increased IL-10 expression and IL-10/TNF-α ratio in treated animals before MI.

conclusionPrior treatment with PYR prevents impairment of the autonomic nervous system after MI, which may be associated with the attenuated expression of inflammatory factors and heart dysfunction.

Indexed as

AnimalsAutonomic Nervous SystemBlood PressureCholinesterase InhibitorsDisease Models, AnimalGene Expression RegulationInterferon-gammaInterleukin-10Interleukin-1betaInterleukin-6MaleMyocardial InfarctionPyridostigmine BromideRatsRats, WistarVentricular Function, LeftCholinesterase InhibitorsIL1B protein, ratIl6 protein, ratInterferon-gammaInterleukin-10Interleukin-1betaInterleukin-6Pyridostigmine Bromide

Identifiers

PMID30792425
PMCPMC6385301
OpenAlexW2915294120

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.