Evidence map›Paper›PMID 39396923›Full record

ArticlePhysiological reports2024

Fructose-1,6-bisphosphate reverses hypotensive effect caused by L-kynurenine in Wistar male rats.

Anderson Velasque Catarina, Gisele Branchini, Rafael Andrade Caceres, Renata Streck Fernandes, Bruna Pasqualotto Costa, Kleiton Lima De Godoy Machado, Tiago Becker, Luis Fernando Ferreira, Katya Rigatto, Jarbas Rodrigues de Oliveira and 1 more

Abstract read
In one paragraph

Article in Physiological reports, 2024. 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
–field-weighted citation impact
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.

  1. 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.

Anderson Velasque CatarinaGraduate Program in Pathology-Laboratory of Computational, Molecular, and Cellular Biophysics-Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.
Gisele BranchiniGraduate Program in Pathology-Laboratory of Computational, Molecular, and Cellular Biophysics-Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.
Rafael Andrade CaceresDepartment of Pharmacosciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.
Renata Streck FernandesGraduate Program in Health Sciences-Laboratory of Translational Physiology-Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.
Bruna Pasqualotto CostaLaboratory of Inflammation and Cellular Biophysics-Pontifícia Universidade Católica Do Rio Grande Do Sul (PUCRS), Porto Alegre, Brazil.
Kleiton Lima De Godoy MachadoDepartment of Plant Biology, Universidade Federal de Viçosa (UFV), Viçosa, Brazil.
Tiago BeckerDepartment of Mechanical Engineering, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Luis Fernando FerreiraSchool of Electronics, Electrical Engineering and Computer Sciences, Queen's University of Belfast, Belfast, UK.ORCID 0000-0002-9496-4884
Katya RigattoGraduate Program in Health Sciences-Laboratory of Translational Physiology-Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.
Jarbas Rodrigues de OliveiraLaboratory of Inflammation and Cellular Biophysics-Pontifícia Universidade Católica Do Rio Grande Do Sul (PUCRS), Porto Alegre, Brazil.
Fernanda Bordignon NunesGraduate Program in Pathology-Laboratory of Computational, Molecular, and Cellular Biophysics-Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypotension is one of the main characteristics of the systemic inflammation, basically caused by endothelial dysfunction. Studies have shown that the amino acid L-kynurenine (KYN) causes vasodilation in mammals, leading to hypotensive shock. In hypotensive shock, when activated by the KYN, the voltage-gated potassium channel encoded by the family KCNQ (Kv7) gene can cause vasodilation. Fructose-1,6-bisphosphate (FBP) it is being considered in studies an anti-inflammatory, antioxidant, immunomodulator, and a modulator of some ion channels (Ca2+, Na+, and K+). We analyzed the effects of KYN and FBP on mean blood pressure (MBP), systolic and diastolic (DBP) blood pressure, and heart rate variability (HRV) in Wistar rats. Results demonstrated that the administration of KYN significant decreased MBP, DBP, and increased HRV. Importantly, the FBP treatment reversed the KYN effects on MBP, DBP, and HRV. Molecular Docking Simulations suggested that KYN and FBP present a very close estimated free energy of binding and the same position into structure of KCNQ4. Our results did demonstrate that FBP blunted the decrease in BP, provoked by KYN. Results raise new hypotheses for future and studies in the treatment of hypotension resulting from inflammation.

Indexed as

Blood PressureFructosediphosphatesHeart RateHypotensionKynurenineRats, WistarAnimalsMaleMolecular Docking SimulationRatsfructose-1,6-diphosphateFructosediphosphatesKynureninefructose‐1,6‐bisphosphatehypotensioninflammationL‐kynureninepotassium‐voltage‐gated channels

Identifiers

PMID39396923
PMCPMC11471349

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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.