Graphislactone A, a Fungal Antioxidant Metabolite, Reduces Lipogenesis and Protects against Diet-Induced Hepatic Steatosis in Mice

• Published in: International journal of molecular sciences Vol. 25; no. 2; p. 1096
• Main Authors: Lee, Yeonmi, Jang, Hye-Rim, Lee, Dongjin, Lee, Jongjun, Jung, Hae-Rim, Cho, Sung-Yup, Lee, Hui-Young
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.01.2024
• Subjects: Amino acids; Animal experimentation; Antioxidants; Cytokines; Diabetes; Gene expression; Genes; graphislactone A; Health aspects; high-fat diet; Hypotheses; Inflammation; Insulin resistance; Lipid peroxidation; Lipids; lipogenesis; Liver; Liver diseases; Metabolic disorders; Metabolites; mice; natural antioxidant; Obesity; Oxidative stress; Pathogenesis; Plasma; RNA; RNA sequencing; Scientific equipment and supplies industry; Tumor necrosis factor-TNF; Type 2 diabetes; Vitamin C; Vitamin E; Vitamins; Weight control; South Korea; United States; Massachusetts; Missouri; graphislactone A; lipogenesis; mice; high-fat diet; natural antioxidant
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25021096

Graphislactone A (GPA), a secondary metabolite derived from a mycobiont found in the lichens of the genus Graphis, exhibits antioxidant properties. However, the potential biological functions and therapeutic applications of GPA at the cellular and animal levels have not yet been investigated. In the present study, we explored the therapeutic potential of GPA in mitigating non-alcoholic fatty liver disease (NAFLD) and its underlying mechanisms through a series of experiments using various cell lines and animal models. GPA demonstrated antioxidant capacity on a par with that of vitamin C in cultured hepatocytes and reduced the inflammatory response induced by lipopolysaccharide in primary macrophages. However, in animal studies using an NAFLD mouse model, GPA had a milder impact on liver inflammation while markedly attenuating hepatic steatosis. This effect was confirmed in an animal model of early fatty liver disease without inflammation. Mechanistically, GPA inhibited lipogenesis rather than fat oxidation in cultured hepatocytes. Similarly, RNA sequencing data revealed intriguing associations between GPA and the adipogenic pathways during adipocyte differentiation. GPA effectively reduced lipid accumulation and suppressed lipogenic gene expression in AML12 hepatocytes and 3T3-L1 adipocytes. In summary, our study demonstrates the potential application of GPA to protect against hepatic steatosis in vivo and suggests a novel role for GPA as an underlying mechanism in lipogenesis, paving the way for future exploration of its therapeutic potential.