Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/136293
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dc.creatorGouveia, M
dc.creatorBrindley, P
dc.creatorRinaldi, G
dc.creatorGärtner, F
dc.creatorCosta, J
dc.creatorVale, N
dc.date.accessioned2021-09-20T10:52:46Z-
dc.date.available2021-09-20T10:52:46Z-
dc.date.issued2019
dc.identifier.issn2218-273X
dc.identifier.urihttps://hdl.handle.net/10216/136293-
dc.description.abstractSchistosomiasis is a major neglected tropical disease. Treatment for schistosomiasis with praziquantel (PZQ), which is effective against the parasite, by itself is not capable to counteract infection-associated disease lesions including hepatic fibrosis. There is a pressing need for novel therapies. Due to their biological properties, antioxidant biomolecules might be useful in treating and reverting associated pathological sequelae. Here, we investigated a novel therapy approach based on a combination of anthelmintic drugs with antioxidant biomolecules. We used a host-parasite model involving Bioamphalaria glabrata and newly transformed schistosomula (NTS) of Schistosoma mansoni. For in vitro drug screening assays, was selected several antioxidants and evaluated not only antischistosomal activity but also ability to enhance activity of the anthelmintic drugs praziquantel (PZQ) and artesunate (AS). The morphological alterations induced by compounds alone/combined were assessed on daily basis using an inverted and automated microscope to quantify NTS viability by a fluorometric-based method. The findings indicated that not only do some antioxidants improve antischistosomal activity of the two anthelmintics, but they exhibit activity per se, leading to high mortality of NTS post-exposure. The combination index (CI) of PZQ + Mel (CI = 0.80), PZQ + Resv (CI = 0.74), AS + Resv (CI = 0.34), AS + NAC (CI = 0.89), VDT + Flav (CI = 1.03) and VDT + Resv (CI = 1.06) reveal that they display moderate to strong synergism. The combination of compounds with discrete mechanisms of action might provide a valuable adjunct to contribution for treatment of schistosomiasis-associated disease.
dc.description.sponsorshipThis work was financed by FEDER - Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020 - Operational Programme for Competitiveness and Internationalisation (POCI), Portugal 2020, and by Portuguese funds through FCT - Fundação para a Ciência e a Tecnologia, in the framework of the projects "Institute for Research and Innovation in Health Sciences" (POCI-01-0145-FEDER-007274). NV also acknowledges support from FCT and FEDER (European Union), award number IF/00092/2014/CP1255/CT0004. Acknowledgments: We express our deepest appreciation to Mrs. Maria Lurdes Delgado for expert maintenance of the schistosome life cycle and her technical support. NV thanks FCT by IF position, Fundação Manuel António da Mota (FMAM, Portugal) and Pfizer Portugal by support Nuno Vale Lab. JMCC thanks FCT for Pest-OE/AGR/UI0211/2011 and Strategic Project UI211. PJB acknowledges support from award CA164719 from the National Cancer Institute (NCI), National Institutes of Health (NIH), USA. The contents of this report are solely the responsibility of the authors and do not necessarily represent the official views of the FCT, FMAM, Pfizer Portugal or the NIH.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofBiomolecules, vol.9(2):54
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectAnthelmintic drug
dc.subjectAnticancer drug
dc.subjectAntioxidant biomolecules
dc.subjectCombination therapy
dc.subjectDrug repurposing
dc.subjectNewly transformed schistosomula
dc.subjectSchistosoma mansoni
dc.subject.meshAnimals
dc.subject.meshAntineoplastic Agents
dc.subject.meshAntioxidants
dc.subject.meshAntiprotozoal Agents
dc.subject.meshCell Survival
dc.subject.meshSchistosoma mansoni
dc.titleCombination anthelmintic/antioxidant activity against schistosoma mansoni
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3390/biom9020054
dc.relation.publisherversionhttps://creativecommons.org/licenses/by/4.0/
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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