Oxidative-nitrosative stress and dengue disease: a systematic review of in vivo/in vitro studies

Raimundo Castro Orozco, Hernando Samuel Pinzón-Redondo, Nelson Rafael Alvis-Guzmán

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Objective: In this systematic review the aim was to summarise the in vivo/in vitro evidence on the role of oxidative-nitrosative stress in pathogenesis of dengue.
Methods: We searched electronic databases (PubMed, EMBASE, The COCHRANE library, ScienceDirect, Scopus, SciELO, LILACS via Virtual Health Library, Google Scholar) using the term: dengue, dengue virus, severe dengue, oxidative stress, nitrosative stress, antioxidants, oxidants, free radicals, oxidized lipid products, lipid peroxides, nitric oxide, and nitric oxide synthase. Articles were selected for review by title and abstract excluding letter, review, epidemiological studies, and duplicates studies. Selected articles were reviewed for used animal model or cell cultures, original purposes, strain of virus or type of antibody, main outcomes, methods, and oxidative-nitrosative stress markers values.
Results: In total, 4330 non-duplicates articles were identified from computerized searches of reference databases, of which 32 were eligible for full text searching. The results of in vivo studies were obtained from monkey and knockout and/or wild-type mice. Human peripheral blood mononuclear cells were cell cultures most commonly used in identified in vitro studies, following by human endothelial cells cultures. DENV-2 strains were most used.
Conclusions: In conclusion, a large body of in vivo and in vitro evidences showed that oxidative/nitrosative stress can be related to production of pathogenesis-related protein, increased susceptibility of mice to DENV infection, hemorrhage development in mice, proinflammatory cytokines and transcriptional factor expression, and DENV replication in various cell cultures.

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Copyright (c) 2015 Raimundo Castro Orozco, Hernando Samuel Pinzón-Redondo, Nelson Rafael Alvis-Guzmán

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Esta obra está bajo una licencia de Creative Commons Reconocimiento-NoComercial 4.0 Internacional.