4.7 Article

Cytotoxic effect of xyloglucan and oxovanadium (IV/V) xyloglucan complex in HepG2 cells

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DOI: 10.1016/j.ijbiomac.2021.06.089

Keywords

Xyloglucan; HepG2 cells; Vanadium

Funding

  1. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior [CAPES-PROEX 1640/2018 (23030.012136/201878)]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico - CNPq [309159/20180, 307244/20180]

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The study investigated the cytotoxic effect of xyloglucan complexed with oxovanadium on hepatocellular carcinoma cells, showing that the complex could intensify its effects on the respiratory chain and reduce mitochondrial membrane potential. Moreover, ATP levels were elevated under complexation, possibly due to enhanced glycolytic flux.
It is well known that the chemical structure of polysaccharides is important to their final biological effect. In this study we investigated the cytotoxic effect of xyloglucan from Copaifera langsdorffii seeds (XGC) and its complex with oxovanadium (XGC:VO) on hepatocellular carcinoma cells (HepG2). After 72 h of incubation, XGC and XGC:VO (200 mu g/mL) reduced cell viability in -20% and -40%, respectively. At same conditions, only XGC:VO increased in -20% the LDH enzyme release. In permeabilized cells, incubated with XGC and XGC:VO (200 mu g/ mL) for 72 h, NADH oxidase activity was reduced by -45% with XGC and XGC:VO. The succinate oxidase activity was reduced by -35% with XGC and -65% with XGC:VO, evidencing that polysaccharide complexation with vanadium could intensify its effects on the respiratory chain. According to this result, the mitochondrial membrane potential was also reduced by -9% for XGC and -30% for XGC:VO, when compared to the control group. Interestingly, ATP levels were more elevated for XGC:VO in respect to XGC, probably due the enhance in glycolytic flux evidenced by increased levels of lactate. These results show that the xyloglucan complexation with oxovanadium (IV/V) potentiates the cytotoxic effect of the native polysaccharide, possibly by impairment of oxidative phosphorylation.

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