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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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Published in:Nutrients 2016-09, Vol.8 (9), p.532
Main Authors: 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
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creator 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
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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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. 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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.</description><subject>Adipokines - blood</subject><subject>Adipose Tissue, Brown - drug effects</subject><subject>Adipose Tissue, Brown - metabolism</subject><subject>Adipose Tissue, Brown - physiopathology</subject><subject>Adipose Tissue, White - drug effects</subject><subject>Adipose Tissue, White - metabolism</subject><subject>Adipose Tissue, White - physiopathology</subject><subject>Adiposity - drug effects</subject><subject>Adiposity - genetics</subject><subject>Animals</subject><subject>Anti-Obesity Agents - isolation &amp; purification</subject><subject>Anti-Obesity Agents - pharmacology</subject><subject>Body fat</subject><subject>Diabetes</subject><subject>Diet</subject><subject>Diet, High-Fat</subject><subject>Disease Models, Animal</subject><subject>energy expenditure</subject><subject>Energy Metabolism - drug effects</subject><subject>Ethanol</subject><subject>Fatty acids</subject><subject>Food science</subject><subject>free fatty acid oxidation</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Genomics</subject><subject>Glucose</subject><subject>Hyperlipidemia</subject><subject>Hypoglycemic Agents - isolation &amp; purification</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Insulin resistance</subject><subject>Insulin Resistance - genetics</subject><subject>Lipids</subject><subject>Lipids - blood</subject><subject>Lipogenesis - drug effects</subject><subject>Liver</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Liver - physiopathology</subject><subject>Male</subject><subject>Metabolism</subject><subject>Mice, Inbred C57BL</subject><subject>Non-alcoholic Fatty Liver Disease - blood</subject><subject>Non-alcoholic Fatty Liver Disease - genetics</subject><subject>Non-alcoholic Fatty Liver Disease - physiopathology</subject><subject>Non-alcoholic Fatty Liver Disease - prevention &amp; control</subject><subject>Nutrition research</subject><subject>Obesity</subject><subject>Obesity - blood</subject><subject>Obesity - genetics</subject><subject>Obesity - physiopathology</subject><subject>Obesity - prevention &amp; control</subject><subject>Oxidation</subject><subject>Phytotherapy</subject><subject>Plant Extracts - isolation &amp; purification</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Roots - chemistry</subject><subject>Plants, Medicinal</subject><subject>Platycodon - chemistry</subject><subject>Platycodon grandiflorus root</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>thermogenesis</subject><subject>Time Factors</subject><subject>Tuberculosis</subject><subject>Weight Gain - drug effects</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdks1uEzEQgFcIRKvSAy-ALHEBiYB_du31BSlULY0UBCrlvPLPbOJoYwfbW8jr8KQ4SYlafBlr5vOn8Wiq6iXB7xmT-IMfWyxxw-iT6pRiQSec1-zpg_tJdZ7SCu-OwIKz59UJFU0rhaSn1Z9vg8pbE2zwaBGVt64fQhwTugkho8vfOSqT0TRn8KPKkNCnYLfoSmX0RaX0Dl3DRmVn0PcMKofkEioONPNpHJxHN1AyWXkDKC9jGBfLEqGUM8TNoLZIQ_4F4PfZubuDuH8-tW4TEqBbl9IIL6pnvRoSnN_Hs-rH1eXtxfVk_vXz7GI6n5iGyTwhtW1lqynVxJBet1pjKikXXBLdyh6r3taNMlZowQThTPSWGCqsqDnVVGB2Vs0OXhvUqttEt1Zx2wXlun0ixEWnYvnrAB1VYBTlsq-ZqRnFuq6x1LalPQbdclVcHw-uzajXYA34MsjhkfRxxbtltwh3XYOZaIgsgjf3ghh-jpByt3bJwDAoD2FMHWmJaDjhpCno6__QVRijL6PaUZJQjumOenugTAwpReiPzRDc7RapOy5SYV897P5I_lsb9hcJPcWm</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Kim, Ye Jin</creator><creator>Choi, Ji-Young</creator><creator>Ryu, Ri</creator><creator>Lee, Jeonghyeon</creator><creator>Cho, Su-Jung</creator><creator>Kwon, Eun-Young</creator><creator>Lee, Mi-Kyung</creator><creator>Liu, Kwang-Hyeon</creator><creator>Rina, Yu</creator><creator>Sung, Mi-Kyung</creator><creator>Choi, Myung-Sook</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3285-5594</orcidid></search><sort><creationdate>20160901</creationdate><title>Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-14d898b22b1c1fb8bb029267691b89f0afd45acd7b7371637fd1c27d7462b2703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adipokines - blood</topic><topic>Adipose Tissue, Brown - drug effects</topic><topic>Adipose Tissue, Brown - metabolism</topic><topic>Adipose Tissue, Brown - physiopathology</topic><topic>Adipose Tissue, White - drug effects</topic><topic>Adipose Tissue, White - metabolism</topic><topic>Adipose Tissue, White - physiopathology</topic><topic>Adiposity - drug effects</topic><topic>Adiposity - genetics</topic><topic>Animals</topic><topic>Anti-Obesity Agents - isolation &amp; purification</topic><topic>Anti-Obesity Agents - pharmacology</topic><topic>Body fat</topic><topic>Diabetes</topic><topic>Diet</topic><topic>Diet, High-Fat</topic><topic>Disease Models, Animal</topic><topic>energy expenditure</topic><topic>Energy Metabolism - drug effects</topic><topic>Ethanol</topic><topic>Fatty acids</topic><topic>Food science</topic><topic>free fatty acid oxidation</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Genomics</topic><topic>Glucose</topic><topic>Hyperlipidemia</topic><topic>Hypoglycemic Agents - isolation &amp; 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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.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>27589792</pmid><doi>10.3390/nu8090532</doi><orcidid>https://orcid.org/0000-0002-3285-5594</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adipokines - blood
Adipose Tissue, Brown - drug effects
Adipose Tissue, Brown - metabolism
Adipose Tissue, Brown - physiopathology
Adipose Tissue, White - drug effects
Adipose Tissue, White - metabolism
Adipose Tissue, White - physiopathology
Adiposity - drug effects
Adiposity - genetics
Animals
Anti-Obesity Agents - isolation & purification
Anti-Obesity Agents - pharmacology
Body fat
Diabetes
Diet
Diet, High-Fat
Disease Models, Animal
energy expenditure
Energy Metabolism - drug effects
Ethanol
Fatty acids
Food science
free fatty acid oxidation
Gene expression
Gene Expression Regulation
Genomics
Glucose
Hyperlipidemia
Hypoglycemic Agents - isolation & purification
Hypoglycemic Agents - pharmacology
Insulin resistance
Insulin Resistance - genetics
Lipids
Lipids - blood
Lipogenesis - drug effects
Liver
Liver - drug effects
Liver - metabolism
Liver - physiopathology
Male
Metabolism
Mice, Inbred C57BL
Non-alcoholic Fatty Liver Disease - blood
Non-alcoholic Fatty Liver Disease - genetics
Non-alcoholic Fatty Liver Disease - physiopathology
Non-alcoholic Fatty Liver Disease - prevention & control
Nutrition research
Obesity
Obesity - blood
Obesity - genetics
Obesity - physiopathology
Obesity - prevention & control
Oxidation
Phytotherapy
Plant Extracts - isolation & purification
Plant Extracts - pharmacology
Plant Roots - chemistry
Plants, Medicinal
Platycodon - chemistry
Platycodon grandiflorus root
RNA, Messenger - genetics
RNA, Messenger - metabolism
thermogenesis
Time Factors
Tuberculosis
Weight Gain - drug effects
title Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue
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