PROTEOMIC IDENTIFICATION AND CHARACTERIZATION OF HEPATIC GLYOXALASE 1 DYSREGULATION IN NON-ALCOHOLIC FATTY LIVER DISEASE
Main Article Content
Keywords
Non-alcoholic fatty liver disease, Glyoxalase 1, Proteomic analysis, Liver steatosis, Hepatic dysregulation, Methylglyoxal
Abstract
Background: Non-alcoholic fatty liver disease (NAFLD) is a prevalent liver condition characterized by excessive fat accumulation in the liver, which can lead to liver dysfunction and other metabolic disorders.
Objective: To identify and characterize the proteomic changes associated with the dysregulation of hepatic glyoxalase 1 in patients with non-alcoholic fatty liver disease.
Methods: The study included 55 patients diagnosed with NAFLD. Proteomic analysis was conducted on liver tissue samples to quantify GLO1 expression levels and assess its functional alterations. Techniques such as mass spectrometry and Western blotting were used to identify the proteomic profile and characterize the changes in GLO1.
Results: The proteomic analysis revealed that the expression of GLO1 was significantly reduced in the hepatic tissue of NAFLD patients compared to healthy controls. Specifically, the average GLO1 expression level in NAFLD patients was 35% ± 5% of the level observed in controls (p < 0.01). In severe cases of NAFLD, GLO1 expression was further reduced to 20% ± 3% of the control levels. A strong inverse correlation was observed between GLO1 expression and the degree of liver steatosis (r = -0.75, p < 0.001). Patients with advanced steatosis (grade 3) had the lowest GLO1 levels, averaging 18% ± 2% of control values, while those with mild steatosis (grade 1) had levels averaging 42% ± 4%.
Conclusion: Hepatic glyoxalase 1 is significantly dysregulated in non-alcoholic fatty liver disease, with reduced expression and altered activity contributing to the progression of the disease. These findings highlight the importance of GLO1 as a potential therapeutic target in the management of NAFLD.
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