Evidence map›Paper›PMID 29339795›Full record

ArticleNutrition & diabetes2018

Lipidized prolactin-releasing peptide improved glucose tolerance in metabolic syndrome: Koletsky and spontaneously hypertensive rat study.

Barbora Mikulášková, Martina Holubová, Veronika Pražienková, Jana Zemenová, Lucie Hrubá, Martin Haluzík, Blanka Železná, Jaroslav Kuneš, Lenka Maletínská

Open access · goldAbstract read
In one paragraph

Article in Nutrition & diabetes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Prolactin-Releasing Peptide: Physiological and Pharmacological Properties.International journal of molecular sciences · 2019
    Review
  9. 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

9 authors at 3 institutions in 1 country.

Barbora MikuláškováInstitute of Organic Chemistry and Biochemistry AS CR, Prague, Czech Republic.
Martina HolubováInstitute of Organic Chemistry and Biochemistry AS CR, Prague, Czech Republic.
Veronika PražienkováInstitute of Organic Chemistry and Biochemistry AS CR, Prague, Czech Republic.
Jana ZemenováInstitute of Organic Chemistry and Biochemistry AS CR, Prague, Czech Republic.
Lucie HrubáInstitute of Organic Chemistry and Biochemistry AS CR, Prague, Czech Republic.
Martin HaluzíkCentre for Experimental Medicine and Diabetes Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Blanka ŽeleznáInstitute of Organic Chemistry and Biochemistry AS CR, Prague, Czech Republic.
Jaroslav KunešInstitute of Organic Chemistry and Biochemistry AS CR, Prague, Czech Republic.
Lenka MaletínskáInstitute of Organic Chemistry and Biochemistry AS CR, Prague, Czech Republic. maletin@uochb.cas.cz.
Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry · CZCharles University · CZCzech Academy of Sciences, Institute of Physiology · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesProlactin-releasing peptide (PrRP) has a potential to decrease food intake and ameliorate obesity, but is ineffective after peripheral administration. We have previously shown that our novel lipidized analogs PrRP enhances its stability in the circulation and enables its central effect after peripheral application. The purpose of this study was to explore if sub-chronic administration of novel PrRP analog palmitoylated in position 11 (palm SUBJECTS/

methodsThe SHROB rats (n = 16) were used for this study and age-matched hypertensive lean SHR littermates (n = 16) served as controls. Palm

resultsAt the end of the experiment, vehicle-treated SHROB rats showed typical metabolic syndrome parameters, including obesity, glucose intolerance, dyslipidemia, and hypertension. Peripheral treatment with palm

conclusionsWe demonstrated that our new lipidized PrRP analog is capable of improving glucose tolerance in obese SHROB rats after peripheral application, suggesting that its effect on glucose metabolism is independent of leptin signaling and body weight lowering. These data suggest that this analog has the potential to be a compound with both anti-obesity and glucose-lowering properties.

Indexed as

Glucose IntoleranceMetabolic SyndromeObesityAdipose TissueAnimalsBlood GlucoseBlood PressureBody WeightBrainGlucagonGlucose Tolerance TestHypertensionInsulinInsulin Receptor Substrate ProteinsInsulin ResistanceLipidsBlood GlucoseGlucagonInsulinInsulin Receptor Substrate ProteinsLipidsProlactin-Releasing Hormone

Identifiers

PMID29339795
PMCPMC5851428
OpenAlexW2784036837

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.