Ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivo

Background: Despite the large number of studies on ginseng, pharmacological activities of ginseng seed oil (GSO) have not been established. GSO is rich in unsaturated fatty acids, mostly oleic and linoleic acids. Unsaturated fatty acids are known to exert a therapeutic effect in nonalcoholic fatty l...

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Main Authors: Go Woon Kim, Hee Kyung Jo, Sung Hyun Chung
Format: Article
Language:English
Published: Elsevier 2018-10-01
Series:Journal of Ginseng Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1226845316303335
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author Go Woon Kim
Hee Kyung Jo
Sung Hyun Chung
author_facet Go Woon Kim
Hee Kyung Jo
Sung Hyun Chung
author_sort Go Woon Kim
collection DOAJ
description Background: Despite the large number of studies on ginseng, pharmacological activities of ginseng seed oil (GSO) have not been established. GSO is rich in unsaturated fatty acids, mostly oleic and linoleic acids. Unsaturated fatty acids are known to exert a therapeutic effect in nonalcoholic fatty liver disease (NAFLD). In this study, we investigated the protective effect and underlying mechanisms of GSO against NAFLD using in vitro and in vivo models. Methods: In vitro lipid accumulation was induced by free fatty acid mixture in HepG2 cells and by 3 wk of high fat diet (HFD)-feeding in Sprague–Dawley rats prior to hepatocyte isolation. The effects of GSO against diet-induced hepatic steatosis were further examined in C57BL/6J mice fed a HFD for 12 wk. Results: Oil Red O staining and intracellular triglyceride levels showed marked accumulation of lipid droplets in both HepG2 cells and rat hepatocytes, and these were attenuated by GSO treatment. In HFD-fed mice, GSO improved HFD-induced dyslipidemia and hepatic insulin resistance. Increased hepatic lipid contents were observed in HFD-fed mice and it was lowered in GSO (500 mg/kg)-treated mice by 26.4% which was evident in histological analysis. Pathway analysis of hepatic global gene expression indicated that GSO increased the expression of genes associated with β-oxidation (Ppara, Ppargc1a, Sirt1, and Cpt1a) and decreased the expression of lipogenic genes (Srebf1 and Mlxipl), and these were confirmed with reverse transcription and quantitative polymerase-chain reaction. Conclusion: These findings suggest that GSO has a beneficial effect on NAFLD through the suppression of lipogenesis and stimulation of fatty acid degradation pathway. Keywords: dyslipidemia, ginseng seed oil, global gene expression analysis, nonalcoholic fatty liver, triglyceride
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spelling doaj.art-c166ef38ae58436b9bf1e36fe1ba2a472022-12-22T00:04:04ZengElsevierJournal of Ginseng Research1226-84532018-10-01424419428Ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivoGo Woon Kim0Hee Kyung Jo1Sung Hyun Chung2Department of Pharmacology, College of Pharmacy, Kyung Hee University, Seoul, Republic of Korea; Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, Republic of KoreaDepartment of Pharmacology, College of Pharmacy, Kyung Hee University, Seoul, Republic of KoreaDepartment of Pharmacology, College of Pharmacy, Kyung Hee University, Seoul, Republic of Korea; Corresponding author. College of Pharmacy, Kyung Hee University, Kyungheedae-ro 26, Dongdaemun-gu, Seoul 02447, Republic of Korea.Background: Despite the large number of studies on ginseng, pharmacological activities of ginseng seed oil (GSO) have not been established. GSO is rich in unsaturated fatty acids, mostly oleic and linoleic acids. Unsaturated fatty acids are known to exert a therapeutic effect in nonalcoholic fatty liver disease (NAFLD). In this study, we investigated the protective effect and underlying mechanisms of GSO against NAFLD using in vitro and in vivo models. Methods: In vitro lipid accumulation was induced by free fatty acid mixture in HepG2 cells and by 3 wk of high fat diet (HFD)-feeding in Sprague–Dawley rats prior to hepatocyte isolation. The effects of GSO against diet-induced hepatic steatosis were further examined in C57BL/6J mice fed a HFD for 12 wk. Results: Oil Red O staining and intracellular triglyceride levels showed marked accumulation of lipid droplets in both HepG2 cells and rat hepatocytes, and these were attenuated by GSO treatment. In HFD-fed mice, GSO improved HFD-induced dyslipidemia and hepatic insulin resistance. Increased hepatic lipid contents were observed in HFD-fed mice and it was lowered in GSO (500 mg/kg)-treated mice by 26.4% which was evident in histological analysis. Pathway analysis of hepatic global gene expression indicated that GSO increased the expression of genes associated with β-oxidation (Ppara, Ppargc1a, Sirt1, and Cpt1a) and decreased the expression of lipogenic genes (Srebf1 and Mlxipl), and these were confirmed with reverse transcription and quantitative polymerase-chain reaction. Conclusion: These findings suggest that GSO has a beneficial effect on NAFLD through the suppression of lipogenesis and stimulation of fatty acid degradation pathway. Keywords: dyslipidemia, ginseng seed oil, global gene expression analysis, nonalcoholic fatty liver, triglyceridehttp://www.sciencedirect.com/science/article/pii/S1226845316303335
spellingShingle Go Woon Kim
Hee Kyung Jo
Sung Hyun Chung
Ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivo
Journal of Ginseng Research
title Ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivo
title_full Ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivo
title_fullStr Ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivo
title_full_unstemmed Ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivo
title_short Ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivo
title_sort ginseng seed oil ameliorates hepatic lipid accumulation in vitro and in vivo
url http://www.sciencedirect.com/science/article/pii/S1226845316303335
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AT heekyungjo ginsengseedoilameliorateshepaticlipidaccumulationinvitroandinvivo
AT sunghyunchung ginsengseedoilameliorateshepaticlipidaccumulationinvitroandinvivo