Literature DB >> 22367598

Fructose-1,6-bisphosphate reduces the mortality in Candida albicans bloodstream infection and prevents the septic-induced platelet decrease.

Roberto Christ Vianna Santos1, Rafael Noal Moresco, Miguel Angel Peña Rico, Antonio R García Susperregui, Jose Luis Rosa, Ramon Bartrons, Francesc Ventura, Débora Nunes Mário, Sydney Hartz Alves, Etiane Tatsch, Helena Kober, Ricardo Obalski de Mello, Patrícia Scherer, Henrique Bregolin Dias, Jarbas Rodrigues de Oliveira.   

Abstract

Due to the fact that an increased number of patients have experienced bloodstream infections caused by Candida species and the high mortality of this infection, there is a need for a strategy to reduce this scenery. One possible strategy is the use of new drugs, such as fructose-1,6-bisphosphate (FBP), which is a high-energy glycolytic metabolite and has shown to have therapeutic effects in several pathological conditions such as ischemia, shock, toxic injuries, and bacterial sepsis. The aim of this manuscript was to determine the role of FBP in experimental Candida albicans bloodstream infection. We used mice that were divided into three experimental groups: sham (not induced), bloodstream infection (induced with intratracheal instillation of C. albicans) and FBP (bloodstream infection plus FBP 500 mg/kg i.p.). Blood was taken for assessment of complete hematological profile and cytokine assay (IL-6 and MCP-1). Results of the study demonstrated that mortality decreased significantly in groups that received FBP. All cytokine and hematological indexes of FBP group were similar to bloodstream infection group with exception of platelets count. FBP significantly prevented the decrease in platelets. Taken together, our results demonstrate that FBP prevented the mortality in C. albicans bloodstream infection.

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Year:  2012        PMID: 22367598     DOI: 10.1007/s10753-012-9436-7

Source DB:  PubMed          Journal:  Inflammation        ISSN: 0360-3997            Impact factor:   4.092


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  3 in total

1.  Fructose-1,6-bisphosphate and N-acetylcysteine attenuate the formation of advanced oxidation protein products, a new class of inflammatory mediators, in vitro.

Authors:  Guilherme Vargas Bochi; Vanessa Dorneles Torbitz; Lara Peruzzolo Cargnin; Manuela Borges Sangoi; Roberto Christ Vianna Santos; Patrícia Gomes; Rafael Noal Moresco
Journal:  Inflammation       Date:  2012-12       Impact factor: 4.092

2.  An alternative pathway through the Fenton reaction for the formation of advanced oxidation protein products, a new class of inflammatory mediators.

Authors:  Guilherme Vargas Bochi; Vanessa Dorneles Torbitz; Lara Peruzzolo Cargnin; José Antonio Mainardi de Carvalho; Patrícia Gomes; Rafael Noal Moresco
Journal:  Inflammation       Date:  2014-04       Impact factor: 4.092

3.  Fructose-1,6-bisphosphate prevents pulmonary fibrosis by regulating extracellular matrix deposition and inducing phenotype reversal of lung myofibroblasts.

Authors:  Henrique Bregolin Dias; Jarbas Rodrigues de Oliveira; Márcio Vinícius Fagundes Donadio; Shioko Kimura
Journal:  PLoS One       Date:  2019-09-11       Impact factor: 3.240

  3 in total

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