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Lingonberry Improves Hepatic Lipid Metabolism by Targeting Notch1 Signaling
Susara Madduma Hewage1,2, Kathy K W Au-Yeung1,3, Suvira Prashar1,4
1Canadian Centre for Agri-Food Research in Health and Medicine, St. Boniface Hospital Research Centre, Winnipeg, MB R2H 2A6, Canada.
Lingonberry supplementation improved non-alcoholic fatty liver disease by inhibiting Notch1 signaling and enhancing hepatic lipid metabolism. This natural compound offers a potential therapeutic strategy for fatty liver conditions.
Area of Science:
- Hepatology and Nutritional Science
- Molecular Biology
- Metabolic Disease Research
Background:
- Non-alcoholic fatty liver disease (NAFLD) is characterized by impaired hepatic lipid metabolism and lacks effective treatments.
- Notch signaling pathway plays a crucial role in regulating hepatic lipid metabolism.
- Lingonberry (Vaccinium vitis-idaea L.), rich in anthocyanins, exhibits notable lipid-lowering effects.
Purpose of the Study:
- To investigate the impact of lingonberry on Notch signaling and hepatic lipid metabolism in a mouse model of NAFLD.
- To elucidate the molecular mechanisms underlying lingonberry's potential hepatoprotective effects.
Main Methods:
- Establishment of a high-fat diet (HFD)-induced NAFLD mouse model.
- Administration of lingonberry supplementation to HFD-fed mice.
- Analysis of hepatic gene expression related to lipid metabolism and Notch signaling.
- Validation using a palmitic acid-induced cellular model (HepG2 cells).
Main Results:
- HFD induced fatty liver and activated hepatic Notch1 signaling in mice.
- Lingonberry supplementation inhibited Notch1 signaling and improved lipid profiles.
- Lingonberry extract and cyanidin-3-glucoside reduced intracellular triglyceride accumulation in HepG2 cells.
- Lingonberry modulated genes involved in lipogenesis (SREBP-1c) and fatty acid oxidation (CPT1α, ACOX1).
Conclusions:
- Lingonberry exerts hepatoprotective effects in NAFLD, partly by inhibiting Notch1 signaling.
- This inhibition improves hepatic lipid metabolism, offering a potential therapeutic avenue for NAFLD.
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