Evidence map›Paper›PMID 35456900›Full record

ArticleInternational journal of molecular sciences2022

Pep19 Has a Positive Effect on Insulin Sensitivity and Ameliorates Both Hepatic and Adipose Tissue Phenotype of Diet-Induced Obese Mice.

Renata Silvério, Robson Barth, Andrea S Heimann, Patrícia Reckziegel, Gustavo J Dos Santos, Silvana Y Romero-Zerbo, Francisco J Bermúdez-Silva, Alex Rafacho, Emer S Ferro

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06359327 (Effect of Consumption of Pep19 on Quality of Life), which is not on this map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 32% 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.

NCT06359327 nacompletednot on this mapstarted 2024, after this paper: background citation

Effect of Consumption of Pep19 on Quality of Life

TypeinterventionalSponsorProteimax Biotechnology Israel LTDRan2024 to 2024Enrolled24ConditionsQuality of Life, Obesity, Sleep QualityArmsPlacebo, Pep19 2 mg, Pep19 5 mg
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Neurolysin Knockout Mice in a Diet-Induced Obesity Model.International journal of molecular sciences · 2023
    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 2 countries.

Renata SilvérioGraduate Program in Pharmacology, Federal University of Santa Catarina (UFSC), Florianópolis 88040-900, Brazil.ORCID 0000-0001-7765-6727
Robson BarthLaboratory of Investigation in Chronic Diseases, Department of Physiological Sciences, Federal University of Santa Catarina (UFSC), Florianópolis 88040-900, Brazil.
Andrea S HeimannProteimax BioTechnology Israel LTD, 4 Duvdevan Street, Pardes Hana, Haifa 3708973, Israel.
Patrícia ReckziegelDepartment of Pharmacology, Biomedical Science Institute, University of São Paulo (USP), São Paulo 05508-000, Brazil.
Gustavo J Dos SantosLaboratory of Investigation in Chronic Diseases, Department of Physiological Sciences, Federal University of Santa Catarina (UFSC), Florianópolis 88040-900, Brazil.ORCID 0000-0001-9135-7184
Silvana Y Romero-ZerboInstituto de Investigación Biomédica de Málaga-IBIMA, UGC Endocrinología y Nutrición Hospital Regional Universitario de Málaga, Universidad de Málaga, 29009 Málaga, Spain.
Francisco J Bermúdez-SilvaInstituto de Investigación Biomédica de Málaga-IBIMA, UGC Endocrinología y Nutrición Hospital Regional Universitario de Málaga, Universidad de Málaga, 29009 Málaga, Spain.ORCID 0000-0003-3133-9691
Alex RafachoGraduate Program in Pharmacology, Federal University of Santa Catarina (UFSC), Florianópolis 88040-900, Brazil.ORCID 0000-0002-8637-6097
Emer S FerroDepartment of Pharmacology, Biomedical Science Institute, University of São Paulo (USP), São Paulo 05508-000, Brazil.ORCID 0000-0003-1651-9192
Universidade Federal de Santa Catarina · BRCentro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas · ESUniversidade de São Paulo · BR

Funding

National Council for Scientific and Technological Development 302809/2016-3National Council for Scientific and Technological Development 304388/2020-3São Paulo Research Foundation 2016/04000-3São Paulo Research Foundation 2019/25943-1São Paulo Research Foundation 2021/02953-1
6 · The paper itself

Abstract

Peptide DIIADDEPLT (Pep19) has been previously suggested to improve metabolic parameters, without adverse central nervous system effects, in a murine model of diet-induced obesity. Here, we aimed to further evaluate whether Pep19 oral administration has anti-obesogenic effects, in a well-established high-fat diet-induced obesity model. Male Swiss mice, fed either a standard diet (SD) or high-fat diet (HFD), were orally administrated for 30 consecutive days, once a day, with saline vehicle or Pep19 (1 mg/kg). Next, several metabolic, morphological, and behavioral parameters were evaluated. Oral administration of Pep19 attenuated HFD body-weight gain, reduced in approximately 40% the absolute mass of the endocrine pancreas, and improved the relationship between circulating insulin and peripheral insulin sensitivity. Pep19 treatment of HFD-fed mice attenuated liver inflammation, hepatic fat distribution and accumulation, and lowered plasma alanine aminotransferase activity. The inguinal fat depot from the SD group treated with Pep19 showed multilocular brown-fat-like cells and increased mRNA expression of uncoupling protein 1 (UCP1), suggesting browning on inguinal white adipose cells. Morphological analysis of brown adipose tissue (BAT) from HFD mice showed the presence of larger white-like unilocular cells, compared to BAT from SD, Pep19-treated SD or HFD mice. Pep19 treatment produced no alterations in mice behavior. Oral administration of Pep19 ameliorates some metabolic traits altered by diet-induced obesity in a Swiss mice model.

Indexed as

Insulin ResistanceAdipose TissueAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsDiet, High-FatLiverMaleMiceMice, Inbred C57BLMice, ObeseNerve Tissue ProteinsObesityPhenotypeNerve Tissue ProteinsPcp4 protein, mousebioactive peptidesintracellular peptidesmetabolismobesityorally active peptidesoverweight

Identifiers

PMID35456900
PMCPMC9030859
OpenAlexW4224229636

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.