Evidence map›Paper›PMID 29085013›Full record

ArticleScientific reports2017

Angiotensin II-derived constrained peptides with antiplasmodial activity and suppressed vasoconstriction.

Adriana Farias Silva, Marcelo Der Torossian Torres, Leandro Souza Silva, Flavio Lopes Alves, Ana Acácia de Sá Pinheiro, Antonio Miranda, Margareth Lara Capurro, Cesar de la Fuente-Nunez, Vani Xavier Oliveira

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
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  8. Review
  9. Advances in pathogenesis and treatment of essential hypertension.Frontiers in cardiovascular medicine · 2022
    Review
  10. Review
  11. Article
  12. Role of Nitric Oxide in the Cardiovascular and Renal Systems.International journal of molecular sciences · 2018
    Review
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 5 institutions in 2 countries.

Adriana Farias SilvaCentro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André, SP, Brazil.
Marcelo Der Torossian TorresCentro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André, SP, Brazil.
Leandro Souza SilvaInstituto de Biofísica Carlos Chagas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Flavio Lopes AlvesDepartamento de Biofísica, Universidade Federal de São Paulo, São Paulo, Brazil.
Ana Acácia de Sá PinheiroInstituto de Biofísica Carlos Chagas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Antonio MirandaDepartamento de Biofísica, Universidade Federal de São Paulo, São Paulo, Brazil.
Margareth Lara CapurroDepartamento de Parasitologia, Instituto de Ciências Biomédicas II, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID 0000-0002-7480-2116
Cesar de la Fuente-NunezSynthetic Biology Group, MIT Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA. cfuente@mit.edu.
Vani Xavier OliveiraCentro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André, SP, Brazil. vani.junior@ufabc.edu.br.ORCID 0000-0002-9420-0956
Broad Institute · USUniversidade Federal de São Paulo · BRUniversidade Federal do ABC · BRUniversidade Federal do Rio de Janeiro · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiotensin II (Ang II) is a natural mammalian hormone that has been described to exhibit antiplasmodial activity therefore constituting a promising alternative for the treatment of malaria. Despite its promise, the development of Ang II as an antimalarial is limited by its potent induction of vasoconstriction and its rapid degradation within minutes. Here, we used peptide design to perform targeted chemical modifications to Ang II to generate conformationally restricted (disulfide-crosslinked) peptide derivatives with suppressed vasoconstrictor activity and increased stability. Designed constrained peptides were synthesized chemically and then tested for antiplasmodial activity. Two lead constrained peptides were identified (i.e., peptides 1 and 2), each composed of 10 amino acid residues. These peptides exhibited very promising activity in both our Plasmodium gallinaceum (>80%) and Plasmodium falciparum (>40%) models, an activity that was equivalent to that of Ang II, and led to complete suppression of vasoconstriction. In addition, peptide 5 exhibited selective activity towards the pre-erythrocytic stage (98% of activity against P. gallinaceum), thus suggesting that it may be possible to design peptides that target specific stages of the malaria life cycle. The Ang II derived stable scaffolds presented here may provide the basis for development of a new generation of peptide-based drugs for the treatment of malaria.

Indexed as

Angiotensin IIAnimalsAntimalarialsChemical EngineeringDrug DesignErythrocytesHumansLife Cycle StagesMalaria, FalciparumPeptidesPlasmodium falciparumPlasmodium gallinaceumVasoconstrictionVasodilator AgentsAngiotensin IIAntimalarialsPeptidesVasodilator Agents

Identifiers

PMID29085013
PMCPMC5662717
OpenAlexW2765415873

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.