Evidence map›Paper›PMID 29110282›Full record

ArticleJournal of endocrinological investigation2018

Metabolic benefits of 1-(3-(4-(o-tolyl)piperazin-1-yl)propyl)pyrrolidin-2-one: a non-selective α-adrenoceptor antagonist.

Magdalena Kotańska, Katarzyna Kulig, Monika Marcinkowska, Marek Bednarski, Katarzyna Malawska, Paula Zaręba

Open access · hybridAbstract read
In one paragraph

Article in Journal of endocrinological investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Evaluation of Some Safety Parameters of Dual Histamine HInternational journal of molecular sciences · 2023
    Article
  3. Article
  4. Are the Hydantoin-1,3,5-triazine 5-HTMolecules (Basel, Switzerland) · 2019
    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

6 authors at 1 institution in 1 country.

Magdalena KotańskaDepartment of Pharmacodynamics, Jagiellonian University Medical College, 9 Medyczna Street, 30-688, Kraków, Poland. magda.dudek@uj.edu.pl.
Katarzyna KuligChair of Pharmaceutical Chemistry, Department of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9, 30-688, Kraków, Poland.
Monika MarcinkowskaChair of Pharmaceutical Chemistry, Department of Medicinal Chemistry, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9, 30-688, Kraków, Poland.
Marek BednarskiDepartment of Pharmacological Screening, Jagiellonian University Medical College, 9 Medyczna Street, 30-688, Kraków, Poland.
Katarzyna MalawskaChair of Pharmaceutical Chemistry, Department of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9, 30-688, Kraków, Poland.
Paula ZarębaChair of Pharmaceutical Chemistry, Department of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9, 30-688, Kraków, Poland.
Jagiellonian University · PL

Funding

National Science Center in Poland DEC-2011/03/B/NZ7/00635
6 · The paper itself

Abstract

purposePrevious studies have shown that several components of the metabolic syndrome, such as hypertension, obesity or imbalanced lipid and carbohydrate homeostasis, are associated with the sympathetic nervous system overactivity. Therefore, the inhibition of the adrenergic nervous system seems to be a reasonable and appropriate therapeutic approach for the treatment of metabolic disturbances. It has been suggested that non-selective adrenoceptor antagonists could be particularly beneficial, since α

methodsThe α

resultsThe intrinistic activity studies revealed that the tested compound is a potent, non-selective antagonist of α

conclusionNon-selective α-adrenoceptor antagonist seems to carry potential benefits in the improvement of the reduction of elevated glucose and triglyceride level. The lack of influence on blood pressure suggests that compounds with such a pharmacological profile may be particulary beneficial for the patients with disturbed lipid and carbohydrate profile, who do not suffer from hypertension. These results are particulary valuable, since currently there are no safe α

Indexed as

Adrenergic alpha-1 Receptor AntagonistsAnimalsBlood PressureBody TemperatureBody WeightDiet, High-FatLocomotionMaleObesityPiperazinePiperazinesPyrrolidinesRadioligand AssayRatsRats, WistarReceptors, Adrenergic, alpha-11-(3-(4-(o-tolyl)piperazin-1-yl)propyl)pyrrolidin-2-oneAdrenergic alpha-1 Receptor AntagonistsPiperazinePiperazinesPyrrolidinesReceptors, Adrenergic, alpha-1HyperglycemiaMetabolic disordersPyrrolidin-2-one derivativeα-Adrenoceptor antagonist

Identifiers

PMID29110282
PMCPMC5902538
OpenAlexW2767500216

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.