N-acetyl cysteine attenuates oxidative stress and glutathione-dependent redox imbalance caused by high glucose/high palmitic acid treatment in pancreatic Rin-5F cells

• Published in: PloS one 2019-12, Vol.14 (12), p.e0226696
• Main Authors: Alnahdi, Arwa, John, Annie, Raza, Haider
• Format: Article
• Language: English
• Subjects: Acetylcysteine; Acetylcysteine - pharmacology; Alcohol; Amino acids; Animals; Antioxidants; Antioxidants (Nutrients); Antioxidants - pharmacology; Apoptosis; Beta cells; Biochemistry; Biology and Life Sciences; Catalase - metabolism; Cell culture; Cell Line, Tumor; Cell survival; Cell Survival - drug effects; Cysteine; Cystine; Cytokines - metabolism; Cytotoxicity; Diabetes mellitus; EDTA; Environmental factors; Ethanol; Fatty acids; Flow cytometry; Genetic aspects; Glucose; Glucose - pharmacology; Glutathione; Glutathione - metabolism; Health sciences; Homeostasis; Hydrogen peroxide; Hyperglycemia; Hyperlipidemia; Inflammation; Insulin; Insulin-Secreting Cells - metabolism; Medicine and Health Sciences; Metabolic disorders; Metabolism; Methods; Mitochondria; Molecular modelling; NF-kappa B - metabolism; Nitric Oxide - metabolism; Obesity; Oxidation; Oxidation-Reduction; Oxidative stress; Oxidative Stress - drug effects; Palmitic acid; Palmitic Acid - pharmacology; Pancreas; Pathogenesis; Physical Sciences; Physiological aspects; Rats; Reactive Oxygen Species - metabolism; Saturated fatty acids; Signal Transduction - drug effects; Superoxide Dismutase - metabolism; Toxicity; Tumor necrosis factor-TNF
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0226696

Elevated levels of glucose and fatty acids are the main characteristics of diabetes, obesity and other metabolic disorders, associated with increased oxidative stress, mitochondrial dysfunction and inflammation. Once the primary pathogenesis of diabetes is established, which is potentially linked to both genetic and environmental factors, hyperglycemia and hyperlipidemia exert further destructive and/or toxic effects on β-cells. The concept of glucolipotoxicity has arisen from the combination of deleterious effects of chronic elevation of glucose and fatty acid levels on pancreatic β- cell function and/or survival. Though numerous studies have been conducted in this field, the exact molecular mechanisms and causative factors still need to be established. The aim of the present work was to elucidate the molecular mechanisms of oxidative stress, and inflammatory/antioxidant responses in the presence of high concentrations of glucose/fatty acids in a cell-culture system using an insulin-secreting pancreatic β-cell line (Rin-5F) and to study the effects of the antioxidant, N-acetyl cysteine (NAC) on β-cell toxicity. In our study, we investigated the molecular mechanism of cytotoxicity in the presence of high glucose (up to 25 mM) and high palmitic acid (up to 0.3 mM) on Rin-5F cells. Our results suggest that the cellular and molecular mechanisms underlying β-cell toxicity are mediated by increased oxidative stress, imbalance of redox homeostasis, glutathione (GSH) metabolism and alterations in inflammatory responses. Pre-treatment with NAC attenuated oxidative stress and alterations in GSH metabolism associated with β-cells cytotoxicity.