Evidence map›Paper›PMID 32382155›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2020

Antihypertensive activity of a new c-Jun N-terminal kinase inhibitor in spontaneously hypertensive rats.

Mark B Plotnikov, Oleg I Aliev, Aleksandr Y Shamanaev, Anastasia V Sidekhmenova, Anna M Anishchenko, Tatiana I Fomina, Victoria S Rydchenko, Andrei I Khlebnikov, Yana J Anfinogenova, Igor A Schepetkin and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Chemistry and Biological Activity of 11Molecules (Basel, Switzerland) · 2026
    Review
  2. Article
  3. Novel Tryptanthrin Derivatives with Selectivity asMolecules (Basel, Switzerland) · 2023
    Article
  4. Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11Molecules (Basel, Switzerland) · 2021
    Article
  5. Review
  6. Review
  7. 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

11 authors at 6 institutions in 2 countries.

Mark B PlotnikovGoldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, 3 Lenin Av., Tomsk, 634028, Russia. mbp2001@mail.ru.
Oleg I AlievGoldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, 3 Lenin Av., Tomsk, 634028, Russia.
Aleksandr Y ShamanaevGoldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, 3 Lenin Av., Tomsk, 634028, Russia.
Anastasia V SidekhmenovaGoldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, 3 Lenin Av., Tomsk, 634028, Russia.
Anna M AnishchenkoGoldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, 3 Lenin Av., Tomsk, 634028, Russia.
Tatiana I FominaGoldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, 3 Lenin Av., Tomsk, 634028, Russia.
Victoria S RydchenkoDepartment of Biophysics, Siberian State Medical University, 2 Moskovsky Trakt, Tomsk, 634050, Russia.
Andrei I KhlebnikovKizhner Research Center, Tomsk Polytechnic University, Tomsk, 634050, Russia.
Yana J AnfinogenovaKizhner Research Center, Tomsk Polytechnic University, Tomsk, 634050, Russia.
Igor A SchepetkinKizhner Research Center, Tomsk Polytechnic University, Tomsk, 634050, Russia.
Dmitriy N AtochinKizhner Research Center, Tomsk Polytechnic University, Tomsk, 634050, Russia.
Research Institute of Pharmacology and Regenerative Medicine named ED Goldberg · RUTomsk National Research Medical Center · RUSiberian State Medical University · RUAltai State University · RUNational Research Tomsk State University · RUTomsk Polytechnic University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

c-Jun N-terminal kinases (JNKs) are involved in the myocardial and aortic remodeling, increased arterial tone, and arterial blood pressure elevation associated with hypertension. The aim of the present study was to investigate the antihypertensive effect of a new JNK inhibitor, 1H-indeno[1,2-b]quinoxalin-11-one oxime sodium salt (IQ-1S), on spontaneously hypertensive rats (SHRs). Experiments were performed using normotensive Wistar-Kyoto (WKY) rats and SHRs. Experimental groups of SHRs received IQ-1S intragastrically for 6 weeks in daily doses of 5 and 50 mg/kg; experimental groups of WKY rats received 50 mg/kg IQ-1S according to the same regimen. The IQ-1S administration regimen induced decreases in systolic blood pressure, mean arterial blood pressure, total peripheral resistance, blood viscosity, hematocrit, myocardial cell cross-sectional area, and aortic wall thickness in SHRs vs untreated SHRs. There were no significant differences in systolic blood pressure values between the control and experimental groups of WKY rats during the treatment period. A concentration-dependent decrease in the tone of carotid arterial rings isolated from SHRs was observed after JNK inhibitor application in vitro. Application of the JNK inhibitor diminished endothelin-1 secretion by human umbilical vein endothelial cells in vitro. The main mechanisms of the antihypertensive effect of IQ-1S included the attenuation of blood viscosity due to decreased hematocrit, a vasodilatory effect on arterial smooth muscle cells, and a decrease in endothelin-1 production by endothelial cells.

Indexed as

AnimalsAorta, ThoracicBlood ViscosityDrug Evaluation, PreclinicalHeartHematocritHemodynamicsHumansHuman Umbilical Vein Endothelial CellsHypertensionJNK Mitogen-Activated Protein KinasesMaleOximesQuinoxalinesRats, Inbred SHRRats, Inbred WKY11H-indeno(1,2-b)quinoxalin-11-one oximeJNK Mitogen-Activated Protein KinasesOximesQuinoxalines1H-indeno[1,2-b]quinoxalin-11-one oxime sodium saltAntihypertensive activityEndothelin-1 production by endothelial cellsInhibition of myocardial and aorta remodelingJNK inhibitor

Identifiers

PMID32382155
OpenAlexW3021339469

What Socratic 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 Socratic graph.