Abstract

Objective To investigate the effect of high concentration of glucose on reactive oxygen species (ROS) production in rabbit corneal epithelial cells (RECEs) and explore whether the increased ROS initiates the apoptosis process of RECEs through oxidative stress and endoplasmic reticulum (ER) stress pathway. Methods RECEs were treated by different concentrations of glucose for a while, and then the production of ROS was detected by flow cytometry. The expressions of PERK, p-PERK, Akt, p-Akt, and CHOP were determined by western blot, and the cell viability was measured by Cell Counting Kit-8 (CCK-8). Flow cytometry was used to detect the early apoptosis rate. Meanwhile, the effects of N-acetyl-L-cysteine (NAC), an active oxygen inhibitor, on the experimental results were observed. Results Compared with the normal glucose concentration group, the fluorescence intensity of ROS in the high concentration (1 mM glucose) of glucose group was significantly increased (P < 0.05). NAC-inhibited ROS production was induced by high concentration of glucose (P < 0.05).Western blot demonstrated that the expressions of the p-PERK and CHOP increased significantly (P < 0.05), the p-Akt expression decreased (P < 0.05), and the PERK and Akt expressions did not change significantly in the high concentration of glucose group compared to the normal concentration group. CCK-8 results revealed that compared with the normal concentration of glucose group, the cell activity of the high concentration of glucose group decreased. For the cells in the high concentration of glucose group, the cell survival rate of NAC-treated cells was higher than that of untreated (P < 0.05). The flow cytometry results indicated that the early apoptosis rate of the cells in the high concentration of glucose group increased in contrast with that in the normal concentration of glucose group (P < 0.05). Treating the cells in the high concentration of glucose group with NAC could reduce the cell apoptosis resulted from high glucose (P < 0.05). Conclusions High concentration of glucose may induce the formation of ROS which leads to oxidative stress and ER stress in RECEs and even leads to cell apoptosis. The reactive oxygen inhibitor, NAC, can play a protective character in the high concentration of glucose environment. These results might provide theoretical basis for the study of the diabetes-related dry eye.

Highlights

  • Diabetes is a group of metabolic diseases characterized by an increase in chronic blood glucose level caused by defects in insulin secretion and function

  • The tear film rupture time and tear secretion are measured in diabetic patients, and it is found that the tear film breakage time and Schirmer value in diabetic patients are significantly lower than those in the control group; the longer the duration of diabetes, the more significant the difference is. ese results uncover that the duration and the stability of the tear film in diabetic patients is poor, and the dry eye is serious [13]

  • We found that the expression of p-protein kinase-like ER kinase (PERK) and CHOP increased in the HCG group

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Summary

Introduction

Diabetes is a group of metabolic diseases characterized by an increase in chronic blood glucose level caused by defects in insulin secretion and function. Diabetes has become one of the most common chronic diseases in developed countries such as Europe and the United States, and China is confronted with the same problem. There are about 109 million adult diabetic patients in China, accounting for 10.9% of the total population [1]. Several abnormalities induced by diabetes, such as decrease of tear secretion, tear composition changes, decreased corneal sensitivity, and delayed corneal epithelial regeneration, would cause ocular surface damage. Experiments uncovered that the concentration of the tear glucose in diabetic patients was 5 times higher than that in normal people, and the concentration of glucose in tears was significantly correlated with blood glucose [3].

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