Evidence map›Paper›PMID 27230017›Full record

ArticleParasitology research2016

Derivatives of biarylalkyl carboxylic acid induce pleiotropic phenotypes in adult Schistosoma mansoni in vitro.

Ariane S Blohm, Patrick Mäder, Thomas Quack, Zhigang Lu, Steffen Hahnel, Martin Schlitzer, Christoph G Grevelding

Abstract read
PubMed Publisher
In one paragraph

Article in Parasitology research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

7 authors.

Ariane S BlohmBFS, Institut for Parasitology, Justus-Liebig-University Gießen, Gießen, 35392, Germany.
Patrick MäderInstitute for Pharmaceutic Chemistry, Philipps-University Marburg, Marburg, 35032, Germany.
Thomas QuackBFS, Institut for Parasitology, Justus-Liebig-University Gießen, Gießen, 35392, Germany.
Zhigang LuBFS, Institut for Parasitology, Justus-Liebig-University Gießen, Gießen, 35392, Germany.
Steffen HahnelBFS, Institut for Parasitology, Justus-Liebig-University Gießen, Gießen, 35392, Germany.
Martin SchlitzerInstitute for Pharmaceutic Chemistry, Philipps-University Marburg, Marburg, 35032, Germany.
Christoph G GreveldingBFS, Institut for Parasitology, Justus-Liebig-University Gießen, Gießen, 35392, Germany. christoph.grevelding@vetmed.uni-giessen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schistosomes and other parasitic platyhelminths cause infectious diseases of worldwide significance for humans and animals. Despite their medical and economic importance, vaccines are not available and the number of drugs is alarmingly limited. For most platyhelminths including schistosomes, Praziquantel (PZQ) is the commonly used drug. With respect to its regular application in mass treatment programs, however, there is increasing concern about resistance development.Previous studies demonstrated that inhibitors used to treat non-parasitic human diseases may be useful to be tested for their effects on parasites. To this end, we focused on biarylalkyl carboxylic acids (BACAs) as basis, which had been shown before to be interesting candidates in the context of finding alternative approaches to treat diabetes mellitus. We tested 32 chemically modified derivatives of these substances (biarylalkyl carboxylic acid derivatives (BACADs)) for their effects on adult Schistosoma mansoni in vitro. Treatment with 18 BACADs resulted in egg production-associated phenotypes and reduced pairing stability. In addition, 12 of these derivatives affected vitality and/or caused severe tegument damage, gut dilatation, or other forms of tissue disintegration which led to the death of worms. In most cases (10/12), one derivative caused more than one phenotype at a time. In vitro experiments in the presence of serum albumin (SA) and alpha-acidic glycoprotein (AGP) indicated a varying influence of these blood components on the effects of two selected derivatives. The variety of observed phenotypes suggested that different targets were hit. The results demonstrated that BACADs are interesting substances with respect to their anti-schistosomal effects.

Indexed as

AnimalsCarboxylic AcidsFemaleHumansMaleMolecular StructurePhenotypePraziquantelSchistosoma mansoniSchistosomiasis mansoniCarboxylic AcidsPraziquantelBiarylalkyl carboxylic acidDrug developmentIn vitro culturePlatyhelminthsSchistosoma mansoniSerum component

Identifiers

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.