4.7 Article

Polygonatum sibiricum polysaccharide extract relieves FB1-induced neurotoxicity by reducing oxidative stress and mitochondrial damage in Caenorhabditis elegans

期刊

FOOD BIOSCIENCE
卷 49, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.fbio.2022.101939

关键词

Polygonatum sibiricum polysaccharide Extract; Fumonisin B1; Caenorhabditis elegans; Neurotoxicity; Oxidative stress; Mitochondria

资金

  1. National Natural Science Foundation of China [32125031]
  2. China Postdoctoral Science Foundation [2021TQ0128]
  3. National first-class discipline program of Food Science and Technology [JUFSTR20180303]
  4. Collaborative Innovation Center for Food Safety and Quality Control, Science and technology project of Chongzuo City [FA2020014]
  5. NIH Office of Research Infrastructure Programs [P40 OD010440]
  6. Research of Polygonatum sibiricum on Efficacy Determination and Intestinal Metabolism [190790]

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The study showed that Polygonatum sibiricum polysaccharide extract (PSPE) significantly improved the neurotoxicity induced by FB1, exhibiting a protective effect in C. elegans, possibly through reducing oxidative stress and regulating mitochondrial function.
Fumonisin B1 (FB1) is a mycotoxin that is harmful to the nervous system; however, there is currently a lack of studies on plant compounds that alleviate the neurotoxicity of FB1. Polygonatum sibiricum polysaccharides exhibit neuroprotective effects, but it is unclear whether they protect against FB1-induced neurotoxicity. Here, Caeno-rhabditis elegans (C. elegans) was used to study the alleviation effects of P. sibiricum polysaccharide extract (PSPE) preprotection on FB1-induced neurotoxicity. PSPE pretreatment improved the behavioral deficits and neuronal damage in FB1-induced C. elegans. In addition, 20-200 mu g/mL PSPE alleviated the oxidative damage in FB1-induced C. elegans by regulating the levels of reactive oxygen species, antioxidant enzyme activities and gene expression. Further studies have shown that PSPE pretreatment induced mitochondrial expression, increased ATP levels and mitochondrial membrane potential, and regulated mitochondrial oxidative phosphorylation and dy-namics. Together, the protective effects of PSPE against FB1-induced neurotoxicity might be closely related with the reduction of oxidative stress and the regulation of mitochondria.

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