Evidence map›Paper›PMID 25275456›Full record

ArticlePLoS neglected tropical diseases2014

Ruthenium complex with benznidazole and nitric oxide as a new candidate for the treatment of chagas disease.

Renata Sesti-Costa, Zumira A Carneiro, Maria C Silva, Maíta Santos, Grace K Silva, Cristiane Milanezi, Roberto S da Silva, João S Silva

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 37 citations in OpenAlex.

  1. Potential Role of Antioxidants as Adjunctive Therapy in Chagas Disease.Oxidative medicine and cellular longevity · 2020
    Review
  2. Review
  3. Article
  4. Article
  5. Targeting the mitochondrial VDAC in hepatocellular carcinoma using a polyclonal antibody-conjugated to a nitrosyl ruthenium complex.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2018
    Article
  6. Review
  7. Developments in the management of Chagas cardiomyopathy.Expert review of cardiovascular therapy · 2015
    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

8 authors at 2 institutions in 1 country.

Renata Sesti-CostaDepartment of Biochemistry and Immunology, Medical School of Ribeirão Preto, São Paulo, Brazil.
Zumira A CarneiroSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Maria C SilvaDepartment of Biochemistry and Immunology, Medical School of Ribeirão Preto, São Paulo, Brazil.
Maíta SantosSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Grace K SilvaDepartment of Biochemistry and Immunology, Medical School of Ribeirão Preto, São Paulo, Brazil.
Cristiane MilaneziDepartment of Biochemistry and Immunology, Medical School of Ribeirão Preto, São Paulo, Brazil.
Roberto S da SilvaSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
João S SilvaDepartment of Biochemistry and Immunology, Medical School of Ribeirão Preto, São Paulo, Brazil.
Clinics Hospital of Ribeirão Preto · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChagas disease remains a serious medical and social problem in Latin America and is an emerging concern in nonendemic countries as a result of population movement, transfusion of infected blood or organs and congenital transmission. The current treatment of infected patients is unsatisfactory due to strain-specific drug resistance and the side effects of the current medications. For this reason, the discovery of safer and more effective chemotherapy is mandatory for the successful treatment and future eradication of Chagas disease. METHODS AND

findingsWe investigated the effect of a ruthenium complex with benznidazole and nitric oxide (RuBzNO2) against Trypanosoma cruzi both in vitro and in vivo. Our results demonstrated that RuBzNO2 was more effective than the same concentrations of benznidazole (Bz) in eliminating both the extracellular trypomastigote and the intracellular amastigote forms of the parasite, with no cytotoxic effect in mouse cells. In vivo treatment with the compound improved the survival of infected mice, inhibiting heart damage more efficiently than Bz alone. Accordingly, tissue inflammation and parasitism was significantly diminished after treatment with RuBzNO2 in a more effective manner than that with the same concentrations of Bz.

conclusionsThe complexation of Bz with ruthenium and nitric oxide (RuBzNO2) increases its effectiveness against T. cruzi and enables treatment with lower concentrations of the compound, which may reduce the side effects of Bz. Our findings provide a new potential candidate for the treatment of Chagas disease.

Indexed as

AnimalsChagas DiseaseDrug ResistanceDrug Therapy, CombinationFemaleHeartHumansInflammationMiceNitric OxideNitroimidazolesParasitemiaRutheniumTrypanocidal AgentsTrypanosoma cruzibenzonidazoleNitric OxideNitroimidazolesRutheniumTrypanocidal Agents

Identifiers

PMID25275456
PMCPMC4183476
OpenAlexW1985093668

What OpenQuestion holds

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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.