Evidence map›Paper›PMID 24162089›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2014

Oral administration of angiotensin-(1-7) ameliorates type 2 diabetes in rats.

Sérgio H S Santos, Jorge F Giani, Valeria Burghi, Johanna G Miquet, Fatimunnisa Qadri, Janaina F Braga, Mihail Todiras, Katarina Kotnik, Natalia Alenina, Fernando P Dominici and 2 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 86 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. VASCULAR AND RENAL MECHANISMS OF PREECLAMPSIA.Current opinion in physiology · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

12 authors at 4 institutions in 3 countries.

Sérgio H S SantosNational Institute in Science and Technology NanoBioFar (INCT NanoBioFar) and Laboratory of Hypertension and Department of Physiology and Biophysics, Department of Pharmacology, Biological Sciences Institute (ICB), Federal University of Minas Gerais (UFMG), Av Antonio Carlos 6627-ICB, 31270-901, Belo Horizonte, MG, Brazil.
Jorge F Giani
Valeria Burghi
Johanna G Miquet
Fatimunnisa Qadri
Janaina F Braga
Mihail Todiras
Katarina Kotnik
Natalia Alenina
Fernando P Dominici
Robson A S Santos
Michael Bader
Max Delbrück Center · DEUniversidade Federal de Minas Gerais · BRInstituto de Química y Fisicoquímica Biológicas · ARUniversity of Buenos Aires · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledDiabetes mellitus type 2 (DM2) is a disease with increasing importance in modern societies and insufficient treatment options. Pharmacological stimulation of insulin signaling, which is blunted in DM2, is a promising approach to treat this disease. It has been shown that activation of the angiotensin (Ang)-(1-7)/Mas axis of the renin-angiotensin system leads to an improved glucose uptake. In this study, we intended to evaluate, whether this effect could be exploited therapeutically. We first confirmed that Ang-(1-7) improves insulin signaling and glucose uptake in vitro in cultured cardiomyocytes. We then evaluated the therapeutic effect of a newly developed hydro-xypropyl-β-cyclodextrin-based Ang-(1-7) nano-formulation in a novel transgenic rat model of inducible insulin resistance and DM2. The chronic administration of this compound prevented the marked elevation in blood glucose levels in these rats at a dose of 30 μg/kg, reversed the established hyperglycemic state at a dose of 100 μg/kg, and resulted in improved insulin sensitivity, reduced plasma insulin and decreased diabetic nephropathy. In conclusion, an oral Ang-(1-7) formulation reverses hyperglycemia and its consequences in an animal model of DM2 and represents a novel therapeutic option for the treatment of DM2 and other cardio-metabolic diseases. KEY MESSAGE: A novel rat model with inducible diabetes can be used to evaluate new therapies. Angiotensin-(1-7) is effective in an oral formulation packaged in cyclodextrine. Angiotensin-(1-7) is a promising antidiabetic drug.

Indexed as

Administration, OralAngiotensin IAnimalsAnimals, NewbornDeoxyglucoseDiabetes Mellitus, Type 2HyperglycemiaHypoglycemic AgentsInsulinMaleMyocytes, CardiacPeptide FragmentsPhosphorylationProto-Oncogene Proteins c-aktRatsRats, Sprague-DawleyAngiotensin Iangiotensin I (1-7)DeoxyglucoseHypoglycemic AgentsInsulinPeptide FragmentsProto-Oncogene Proteins c-akt

Identifiers

PMID24162089
OpenAlexW2029152760

What OpenQuestion 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 OpenQuestion graph.