Mak-Soon Lee, Bohyeon Kim, Jumi Lee, Yejie Cho, In-Hwan Kim, Yangha Kim
{"title":"Stearidonic Acid-Enriched Buglossoides arvensis Oil Alleviates High-Fat Diet-Induced Hepatic Lipid Accumulation and Inflammation via AMPK/SIRT1 Activation in Rats.","authors":"Mak-Soon Lee, Bohyeon Kim, Jumi Lee, Yejie Cho, In-Hwan Kim, Yangha Kim","doi":"10.1016/j.tjnut.2025.08.005","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Buglossoides arvensis oil (BO) is rich in plant-based omega-3 polyunsaturated fatty acids (n-3 PUFAs), including stearidonic acid (SDA). Dietary oils enriched with n-3 PUFAs have been shown to exert beneficial effects on inflammation and lipid metabolism; however, the effects of SDA-enriched BO (SBO) remain unclear.</p><p><strong>Objectives: </strong>This study aimed to evaluate the effects of SBO (n-3 PUFA: 67.1%, SDA: 38.5%) included in a high-fat (HF; 45% kcal from fat) diet on hepatic lipid accumulation and inflammation.</p><p><strong>Methods: </strong>Four-week-old male Sprague-Dawley rats were randomly divided into 3 groups (n = 6/group) and fed different diets for 9 wk: HF, HF with 10% BO (HF + BO), and HF with 10% SBO (HF + SBO) diet groups. At the end of the experiment, we analyzed lipid profiles in the serum and liver; assessed the expression of genes involved in lipid metabolism and inflammation by reverse transcription-quantitative polymerase chain reaction; measured inflammatory cytokines protein concentrations; and evaluated the activity of adenosine monophosphate-activated protein kinase (AMPK), sirtuin 1 (SIRT1), and nuclear factor kappa B (NF-κB).</p><p><strong>Results: </strong>HF + SBO group significantly reduced bodyweight and hepatic lipid accumulation compared with HF diet feeding (P < 0.05). Serum and hepatic lipid concentrations were significantly lower, whereas fecal lipid excretion was significantly higher in the HF + SBO group compared with the HF group (P < 0.05). The expression of lipid metabolism-related genes was significantly downregulated in the HF + SBO group, and AMPK and SIRT1 activity were increased 1.53- and 2.28-fold, respectively, compared with the HF group (P < 0.05). BO and SBO intake inhibited NF-κB activation by 27.5% and 41.8%, respectively, and reduced the mRNA and protein expression levels of inflammatory cytokines compared with HF diet feeding (P < 0.05). Moreover, SBO was more effective than BO in this regard.</p><p><strong>Conclusions: </strong>These findings suggest that SBO more effectively mitigates hepatic lipid accumulation and inflammation in rats fed HF diet, a phenomenon partly related to the increased activation of AMPK and SIRT1. This indicates that SBO may provide greater benefits than BO in improving lipid metabolism and inflammatory responses.</p>","PeriodicalId":16620,"journal":{"name":"Journal of Nutrition","volume":" ","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Nutrition","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.tjnut.2025.08.005","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NUTRITION & DIETETICS","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Buglossoides arvensis oil (BO) is rich in plant-based omega-3 polyunsaturated fatty acids (n-3 PUFAs), including stearidonic acid (SDA). Dietary oils enriched with n-3 PUFAs have been shown to exert beneficial effects on inflammation and lipid metabolism; however, the effects of SDA-enriched BO (SBO) remain unclear.
Objectives: This study aimed to evaluate the effects of SBO (n-3 PUFA: 67.1%, SDA: 38.5%) included in a high-fat (HF; 45% kcal from fat) diet on hepatic lipid accumulation and inflammation.
Methods: Four-week-old male Sprague-Dawley rats were randomly divided into 3 groups (n = 6/group) and fed different diets for 9 wk: HF, HF with 10% BO (HF + BO), and HF with 10% SBO (HF + SBO) diet groups. At the end of the experiment, we analyzed lipid profiles in the serum and liver; assessed the expression of genes involved in lipid metabolism and inflammation by reverse transcription-quantitative polymerase chain reaction; measured inflammatory cytokines protein concentrations; and evaluated the activity of adenosine monophosphate-activated protein kinase (AMPK), sirtuin 1 (SIRT1), and nuclear factor kappa B (NF-κB).
Results: HF + SBO group significantly reduced bodyweight and hepatic lipid accumulation compared with HF diet feeding (P < 0.05). Serum and hepatic lipid concentrations were significantly lower, whereas fecal lipid excretion was significantly higher in the HF + SBO group compared with the HF group (P < 0.05). The expression of lipid metabolism-related genes was significantly downregulated in the HF + SBO group, and AMPK and SIRT1 activity were increased 1.53- and 2.28-fold, respectively, compared with the HF group (P < 0.05). BO and SBO intake inhibited NF-κB activation by 27.5% and 41.8%, respectively, and reduced the mRNA and protein expression levels of inflammatory cytokines compared with HF diet feeding (P < 0.05). Moreover, SBO was more effective than BO in this regard.
Conclusions: These findings suggest that SBO more effectively mitigates hepatic lipid accumulation and inflammation in rats fed HF diet, a phenomenon partly related to the increased activation of AMPK and SIRT1. This indicates that SBO may provide greater benefits than BO in improving lipid metabolism and inflammatory responses.
期刊介绍:
The Journal of Nutrition (JN/J Nutr) publishes peer-reviewed original research papers covering all aspects of experimental nutrition in humans and other animal species; special articles such as reviews and biographies of prominent nutrition scientists; and issues, opinions, and commentaries on controversial issues in nutrition. Supplements are frequently published to provide extended discussion of topics of special interest.