A Novel Selenium Polysaccharide Alleviates the Manganese (Mn)-Induced Toxicity in Hep G2 Cells and Caenorhabditis elegans .
Tao ChenXiaoju WangXinchen YanYali DaiTao LiangLijun ZhouShiling FengMing YuanHongyu YangChunbang DingPublished in: International journal of molecular sciences (2022)
Manganese (Mn) is now known to have a variety of toxicities, particularly when exposed to it in the workplace. However, there are still ineffective methods for reducing Mn's hazardous effects. In this study, a new selenium polysaccharide (Se-PCS) was developed from the shell of Camellia oleifera to reduce Mn toxicity in vitro and in vivo. The results revealed that Se-PCS may boost cell survival in Hep G2 cells exposed to Mn and activate antioxidant enzyme activity, lowering ROS and cell apoptosis. Furthermore, after being treated with Se-PCS, Caenorhabditis elegans survived longer under Mn stress. daf-16 , a tolerant critical gene, was turned on. Moreover, the antioxidant system was enhanced as the increase in strong antioxidant enzyme activity and high expression of the sod-3 , ctl-2 , and gst-1 genes. A variety of mutations were also used to confirm that Se-PCS downregulated the insulin signaling pathway. These findings showed that Se-PCS protected Hep G2 cells and C. elegans via the insulin/IGF-1 signaling pathway and that it could be developed into a promising medication to treat Mn toxicity.
Keyphrases
- induced apoptosis
- oxidative stress
- signaling pathway
- cell cycle arrest
- room temperature
- pi k akt
- transition metal
- type diabetes
- metal organic framework
- endoplasmic reticulum stress
- healthcare
- cell death
- dna damage
- diabetic rats
- emergency department
- cell proliferation
- genome wide
- gene expression
- binding protein
- transcription factor
- insulin resistance
- dna methylation
- high glucose
- ionic liquid
- adverse drug