Effect of GSH and niacin combination on protein oxidation, ER stress, glycation and aggregation in HLE cells under high glucose condition
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Supported by the Directorate General of Higher Education(DGHE), National Education Ministry, Republic of Indonesia(No.338.177/UN10.C10/PN/2018)

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    Abstract:

    AIM:To evaluate the effects of reduced glutathione(GSH)and niacin combination on protein oxidative stress, endoplasmic reticulum(ER)stress, glycation, and aggregation of the αβ crystalline in human lens epithelial(HLE)cells treated with high glucose levels.

    METHODS:HLE cells were cultured and exposed to 25 mmol/L glucose to promote high glucose conditions. Groups of cells were co-treated with three different combinations of dosages: 10 μmol/L GSH+2 μmol/L niacin, 30 μmol/L GSH+25 μmol/L niacin, and 100 μmol/L GSH+25 μmol/L niacin. After 72h incubation, protein carbonyl content(PCC)and glucose reactive protein(GRP78)content were assessed using ELISA examinations. After two-week incubation, advanced glycation end products(AGEs)were also assessed and the expression of αβ crystalline was measured using Western Blot examination. The SPSS 18.0 statistical package was used for all data analyses.

    RESULTS:PCC and GRP78 levels in the co-treated groups were not significantly reduced compared to control(P>0.05). In contrast, there was a significant decrease of the AGEs levels in all groups co-treated with GSH and niacin when compared with the control group(P<0.05). In addition, the αβ crystalline expression increased after high dose glucose administration, but decreased in all groups co-treated with GSH and combinations of GSH and niacin.

    CONCLUSION:The results suggest that combinations of GSH and niacin inhibit the aggregation of proteins and prevent glycation in hyperglycemic human lens epithelial cells. This study shows that this combination may play an active role in preventing diabetic cataract mainly from the AGEs pathway.

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Handayani N, Permatasari N, Sujuti H, Rudijanto A.谷胱甘肽和烟酸对高糖状态下人晶状体上皮细胞的影响.国际眼科杂志 2020;20(1):4-8,10.3980/j. issn.1672-5123.2020.1.02

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Publication History
  • Received:January 02,2019
  • Revised:September 30,2019
  • Adopted:
  • Online: December 20,2019
  • Published: