Evidence map›Paper›PMID 19958044›Full record

ArticleThe Journal of parasitology2010

Anti-trypanosomatid activity of ceragenins.

Diana Lara, Yanshu Feng, Julia Bader, Paul B Savage, Rosa A Maldonado

Open access · greenAbstract read
In one paragraph

Article in The Journal of parasitology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Ligand-lytic peptides for specific targeting ofFrontiers in cellular and infection microbiology · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Turkish journal of pharmaceutical sciences · 2020
    Article
  8. Antibacterial and Antibiofilm Activities of Ceragenins againstTurkish journal of pharmaceutical sciences · 2019
    Article
  9. Article
  10. Article
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  12. Article
  13. Article
  14. Metal-drug synergy: new ruthenium(II) complexes of ketoconazole are highly active against Leishmania major and Trypanosoma cruzi and nontoxic to human or murine normal cells.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2013
    Article
  15. Article
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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

5 authors at 1 institution in 1 country.

Diana LaraDepartment of Biological Sciences, The Border Biomedical Research Center, The University of Texas at El Paso, 500 W University Avenue, El Paso, Texas 79968, USA.
Yanshu Feng
Julia Bader
Paul B Savage
Rosa A Maldonado
The University of Texas at El Paso · US

Funding

TOXICOLOGY PROJECTG12RR008124 · NCRR · UNIVERSITY OF TEXAS EL PASO · PI WALSH, ELIZABETH J · 1992 to 2011
$20.8M
UTEP SCORE InstrumentationS06GM008012 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI GARZA, KRISTINE M · 1989 to 2010
$15.8M
NCRR NIH HHS 5G12RR008124NCRR NIH HHS G12 RR008124NIGMS NIH HHS 2S06GM00812-37NIGMS NIH HHS S06 GM008012
6 · The paper itself

Abstract

Cationic steroid antibiotics (CSAs), or ceragenins, are amphiphilic compounds consisting of a cholic acid backbone that is attached to several cationic amines. In this study, we tested the hypothesis that CSAs possess antiparasitic activities with minimal to no effects on mammalian cells, and thus could be used as potential therapeutic agents against pathogenic trypanosomatids. To investigate this notion, we synthesized CSAs and determined their trypanocidal and leishmanicidal activities in vitro. The 3 ceragenins assayed, i.e., CSA-8, CSA-13, and CSA-54, showed several degrees of parasiticidal activity. CSA-13 was the most effective compound against Leishmania major promastigotes and Trypanosoma cruzi trypomastigotes, at LD(50) 4.9 and 9 microM, respectively. The trypanocidal activities of these ceragenins were also assessed by infectivity experiments. We found CSA-8 was more effective on T. cruzi intracellular amastigotes when the infected host cells were treated for 24 hr (LD(50), 6.7 microM). Macrophages and LLC-MK(2) (treated for 72 hr) showed relative low susceptibility to these compounds. Our results suggest that ceragenins are indeed promising chemotherapeutic agents against trypanosomatids, but they require further investigation.

Indexed as

Analysis of VarianceAnimalsCell LineCells, CulturedLeishmania majorLethal Dose 50Macaca mulattaMacrophagesMiceSteroidsTrypanocidal AgentsTrypanosoma cruziceragenin CSA-13ceragenin CSA-8SteroidsTrypanocidal Agents

Identifiers

PMID19958044
PMCPMC2891312
OpenAlexW2035295596

What OpenQuestion holds

Textmetadata
LicenceTDM
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.