ArticleViewAbstractPharmacognosy Journal,2025,17,1,77-83.DOI:10.5530/pj.2025.17.10Published:January 2025Type:Research ArticleEffects of Citrus aurantifolia Root Ethanolic Extract on Lipogenesis in Palmitate-Induced Lipid Accumulation in HepG2 CellsUrarat Nanna, Jarinyaporn Naowaboot, Linda Chularojmontri, Rawiwun Kaewamatawong, Sudarat Homhual, Suvara Wattanapitayakul, and Wanwisa Suwannaloet Urarat Nanna1, Jarinyaporn Naowaboot1, Linda Chularojmontri1, Rawiwun Kaewamatawong2, Sudarat Homhual2, Suvara Wattanapitayakul3, Wanwisa Suwannaloet4* 1Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathum Thani 12120, THAILAND. 2Faculty of Pharmaceutical Sciences, Ubon Ratchathani University, Ubon Ratchathani, 34190, THAILAND. 3Department of Pharmacology, Faculty of Medicine, Srinakharinwirot University, Bangkok 10110, THAILAND. 4College of Medicine and Public Health, Ubon Ratchathani University, Ubon Ratchathani, 34190, THAILAND. Abstract:Introduction: Citrus aurantifolia (lime) is mostly found in tropical and subtropical region. The lime peel and lime juice extracts have antioxidant, antidiabetic and anti-inflammatory effects. However, the pharmacological effects of the lime root remain widely unknown. Thus, the current study investigated the effects of Citrus aurantifolia root ethanolic extract (CA) on lipogenesis induced by palmitic acid (PA) in HepG2 cells. Methods: The PA-induced lipogenesis in HepG2 cells was used for measuring lipogenic gene expression and lipid accumulation of CA. Phytochemical content was also determined in CA. Results: In PA-treated group showed the state of hepatic lipid accumulation with increased lipogenic gene, acetyl-CoA carboxylase (ACC), fatty acid synthase (FAS) and sterol regulatory element binding protein1c (SREBP1c) as compared to the control group. Interestingly, administration of CA (5-10 μg/mL) effectively reduced lipid storage and significantly decreased the expression of these lipogenic gene in PA-treated cells. Notably, CA treatment increased the gene expression of fatty acid oxidation, carnitine palmitoyl transferase 1A (CPT1A) and peroxisome proliferator-activated receptor α (PPARα). Furthermore, this study found that the major bioactive component from CA was nordentatin (coumarin group). Conclusions: The results indicated that the CA treatment might be a useful agent for improving abnormal lipid metabolism in obesity-related nonalcoholic fatty liver disease. Keywords:Citrus aurantifolia, Lipid metabolism, Lipogenesis, Nonalcoholic fatty liver disease, ObesityView:PDF (558.49 KB) PDF Images Effects of CA on cell viability and lipid accumulation in PA-induced HepG2 cells. (A) Viability of HepG2 cells was performed by MTT assay. (B) Lipid accumulation was extracted by isopropanol and quantitative content was measured at 500 nm. (C) Oil Red O-stained image of HepG2 cells observed under a microscope (×400). Data are expressed as mean ± SEM (n=6). *p < 0.05 vs. the control group (non-treated cells). #p < 0.05 vs. the PA-treated group. ‹ Medicinal Application of the Iceland Poppy (Papaver nudicaule L.) in Traditional Mongolian Medicine up The Mechanism of Nanocurcumin in Inhibiting Parasitemia in Plasmodium berghei ANKA (PbA) Model Mice ›