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Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue

The Platycodon grandiflorus root, a Korean medicinal food, is well known to have beneficial effects on obesity and diabetes. In this study, we demonstrated the metabolic effects of P. grandiflorus root ethanol extract (PGE), which is rich in platycodins, on diet-induced obesity. C57BL/6J mice (four-...

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Autores principales: Kim, Ye Jin, Choi, Ji-Young, Ryu, Ri, Lee, Jeonghyeon, Cho, Su-Jung, Kwon, Eun-Young, Lee, Mi-Kyung, Liu, Kwang-Hyeon, Rina, Yu, Sung, Mi-Kyung, Choi, Myung-Sook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037519/
https://www.ncbi.nlm.nih.gov/pubmed/27589792
http://dx.doi.org/10.3390/nu8090532
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author Kim, Ye Jin
Choi, Ji-Young
Ryu, Ri
Lee, Jeonghyeon
Cho, Su-Jung
Kwon, Eun-Young
Lee, Mi-Kyung
Liu, Kwang-Hyeon
Rina, Yu
Sung, Mi-Kyung
Choi, Myung-Sook
author_facet Kim, Ye Jin
Choi, Ji-Young
Ryu, Ri
Lee, Jeonghyeon
Cho, Su-Jung
Kwon, Eun-Young
Lee, Mi-Kyung
Liu, Kwang-Hyeon
Rina, Yu
Sung, Mi-Kyung
Choi, Myung-Sook
author_sort Kim, Ye Jin
collection PubMed
description The Platycodon grandiflorus root, a Korean medicinal food, is well known to have beneficial effects on obesity and diabetes. In this study, we demonstrated the metabolic effects of P. grandiflorus root ethanol extract (PGE), which is rich in platycodins, on diet-induced obesity. C57BL/6J mice (four-week-old males) were fed a normal diet (16.58% of kilocalories from fat), high-fat diet (HFD, 60% of kilocalories from fat), and HFD supplemented with 5% (w/w) PGE. In the HFD-fed mice, PGE markedly suppressed the body weight gain and white fat mass to normal control level, with simultaneous increase in the expression of thermogenic genes (such as SIRT1, PPARα, PGC1α, and UCP1), that accompanied changes in fatty acid oxidation (FAO) and energy expenditure. In addition, PGE improved insulin sensitivity through activation of the PPARγ expression, which upregulates adiponectin while decreasing leptin gene expression in adipocytes. Furthermore, PGE improved hepatic steatosis by suppressing hepatic lipogenesis while increasing expression of FAO-associated genes such as PGC1α. PGE normalized body fat and body weight, which is likely associated with the increased energy expenditure and thermogenic gene expression. PGE can protect from HFD-induced insulin resistance, and hepatic steatosis by controlling lipid and glucose metabolism.
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spelling pubmed-50375192016-10-15 Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue Kim, Ye Jin Choi, Ji-Young Ryu, Ri Lee, Jeonghyeon Cho, Su-Jung Kwon, Eun-Young Lee, Mi-Kyung Liu, Kwang-Hyeon Rina, Yu Sung, Mi-Kyung Choi, Myung-Sook Nutrients Article The Platycodon grandiflorus root, a Korean medicinal food, is well known to have beneficial effects on obesity and diabetes. In this study, we demonstrated the metabolic effects of P. grandiflorus root ethanol extract (PGE), which is rich in platycodins, on diet-induced obesity. C57BL/6J mice (four-week-old males) were fed a normal diet (16.58% of kilocalories from fat), high-fat diet (HFD, 60% of kilocalories from fat), and HFD supplemented with 5% (w/w) PGE. In the HFD-fed mice, PGE markedly suppressed the body weight gain and white fat mass to normal control level, with simultaneous increase in the expression of thermogenic genes (such as SIRT1, PPARα, PGC1α, and UCP1), that accompanied changes in fatty acid oxidation (FAO) and energy expenditure. In addition, PGE improved insulin sensitivity through activation of the PPARγ expression, which upregulates adiponectin while decreasing leptin gene expression in adipocytes. Furthermore, PGE improved hepatic steatosis by suppressing hepatic lipogenesis while increasing expression of FAO-associated genes such as PGC1α. PGE normalized body fat and body weight, which is likely associated with the increased energy expenditure and thermogenic gene expression. PGE can protect from HFD-induced insulin resistance, and hepatic steatosis by controlling lipid and glucose metabolism. MDPI 2016-08-30 /pmc/articles/PMC5037519/ /pubmed/27589792 http://dx.doi.org/10.3390/nu8090532 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Ye Jin
Choi, Ji-Young
Ryu, Ri
Lee, Jeonghyeon
Cho, Su-Jung
Kwon, Eun-Young
Lee, Mi-Kyung
Liu, Kwang-Hyeon
Rina, Yu
Sung, Mi-Kyung
Choi, Myung-Sook
Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue
title Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue
title_full Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue
title_fullStr Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue
title_full_unstemmed Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue
title_short Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue
title_sort platycodon grandiflorus root extract attenuates body fat mass, hepatic steatosis and insulin resistance through the interplay between the liver and adipose tissue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037519/
https://www.ncbi.nlm.nih.gov/pubmed/27589792
http://dx.doi.org/10.3390/nu8090532
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