Ethanolic extract of seabuckthorn ( Hippophae rhamnoides L ) prevents high-fat diet–induced obesity in mice through down-regulation of adipogenic and lipogenic gene expression

Abstract Phenolic compounds and flavonoids ameliorate bodyweight, blood glucose, and serum lipid profile. Since seabuckthorn ( Hippophae rhamnoides L. ) is known as a rich source of isoflavones and flavonoids, we hypothesized that ethanolic extract of seabuckthorn leaves (SL) may have anti-obesity a...

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Veröffentlicht in:Nutrition research (New York, N.Y.) N.Y.), 2012-11, Vol.32 (11), p.856-864
Hauptverfasser: Pichiah, P.B. Tirupathi, Moon, Hye-Jung, Park, Jeong-Eun, Moon, Yeon-Jeong, Cha, Youn-Soo
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container_title Nutrition research (New York, N.Y.)
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creator Pichiah, P.B. Tirupathi
Moon, Hye-Jung
Park, Jeong-Eun
Moon, Yeon-Jeong
Cha, Youn-Soo
description Abstract Phenolic compounds and flavonoids ameliorate bodyweight, blood glucose, and serum lipid profile. Since seabuckthorn ( Hippophae rhamnoides L. ) is known as a rich source of isoflavones and flavonoids, we hypothesized that ethanolic extract of seabuckthorn leaves (SL) may have anti-obesity and hypoglycemic effects. To investigate the effect of ethanolic extract of SL, 32 C57BL/6J mice were randomly divided into 4 dietary groups, containing 8 mice in each group: normal diet group; high-fat diet (HD) control group; high-fat diet with SL extract, 500 mg/kg body weight (BW) (SL1) group; and high-fat diet with SL extract, 1000 mg/kg BW (SL2) group. After 13 weeks, it was observed that oral administration of SL extract significantly reduced the energy intake; BW gain; epididymal fat pad weight; hepatic triglyceride, hepatic, and serum total cholesterol levels; and serum leptin levels in the SL groups compared to the HD group. However, differences in serum triglyceride and insulin levels in the SL groups were not significant in comparison to the HD group. The hepatic mRNA expression of peroxisome proliferator-activated receptor (PPAR) α and carnitine palmitoyltransferase 1 along with PPAR- γ were significantly increased in SL groups, whereas the level of acetyl-CoA carboxylase was significantly reduced in SL groups compared to HD group. Our results indicated that SL is effective in preventing BW gain and fat accumulation in the liver; it also reduced adipose tissue mass, hepatic lipid profile, and serum leptin level in the mouse. Together, these observations suggest that SL is a potential agent to study in the management of obesity and related disorders.
doi_str_mv 10.1016/j.nutres.2012.09.015
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Tirupathi ; Moon, Hye-Jung ; Park, Jeong-Eun ; Moon, Yeon-Jeong ; Cha, Youn-Soo</creator><creatorcontrib>Pichiah, P.B. Tirupathi ; Moon, Hye-Jung ; Park, Jeong-Eun ; Moon, Yeon-Jeong ; Cha, Youn-Soo</creatorcontrib><description>Abstract Phenolic compounds and flavonoids ameliorate bodyweight, blood glucose, and serum lipid profile. Since seabuckthorn ( Hippophae rhamnoides L. ) is known as a rich source of isoflavones and flavonoids, we hypothesized that ethanolic extract of seabuckthorn leaves (SL) may have anti-obesity and hypoglycemic effects. To investigate the effect of ethanolic extract of SL, 32 C57BL/6J mice were randomly divided into 4 dietary groups, containing 8 mice in each group: normal diet group; high-fat diet (HD) control group; high-fat diet with SL extract, 500 mg/kg body weight (BW) (SL1) group; and high-fat diet with SL extract, 1000 mg/kg BW (SL2) group. After 13 weeks, it was observed that oral administration of SL extract significantly reduced the energy intake; BW gain; epididymal fat pad weight; hepatic triglyceride, hepatic, and serum total cholesterol levels; and serum leptin levels in the SL groups compared to the HD group. However, differences in serum triglyceride and insulin levels in the SL groups were not significant in comparison to the HD group. The hepatic mRNA expression of peroxisome proliferator-activated receptor (PPAR) α and carnitine palmitoyltransferase 1 along with PPAR- γ were significantly increased in SL groups, whereas the level of acetyl-CoA carboxylase was significantly reduced in SL groups compared to HD group. Our results indicated that SL is effective in preventing BW gain and fat accumulation in the liver; it also reduced adipose tissue mass, hepatic lipid profile, and serum leptin level in the mouse. 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Psychology ; Gastroenterology and Hepatology ; Hippophae - chemistry ; Hippophae rhamnoides ; Hippophae rhamnoides L ; Insulin - blood ; Leptin ; Leptin - blood ; Lipid metabolism ; Lipogenesis - drug effects ; Lipogenesis - genetics ; Liver - drug effects ; Liver - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Obesity ; Obesity - etiology ; Obesity - prevention &amp; control ; Phytotherapy ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; PPAR alpha - genetics ; PPAR alpha - metabolism ; PPAR gamma - genetics ; PPAR gamma - metabolism ; Random Allocation ; RNA, Messenger - metabolism ; Seabuckthorn ; Triglycerides - metabolism ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Weight Gain - drug effects</subject><ispartof>Nutrition research (New York, N.Y.), 2012-11, Vol.32 (11), p.856-864</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Inc. 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Tirupathi</creatorcontrib><creatorcontrib>Moon, Hye-Jung</creatorcontrib><creatorcontrib>Park, Jeong-Eun</creatorcontrib><creatorcontrib>Moon, Yeon-Jeong</creatorcontrib><creatorcontrib>Cha, Youn-Soo</creatorcontrib><title>Ethanolic extract of seabuckthorn ( Hippophae rhamnoides L ) prevents high-fat diet–induced obesity in mice through down-regulation of adipogenic and lipogenic gene expression</title><title>Nutrition research (New York, N.Y.)</title><addtitle>Nutr Res</addtitle><description>Abstract Phenolic compounds and flavonoids ameliorate bodyweight, blood glucose, and serum lipid profile. Since seabuckthorn ( Hippophae rhamnoides L. ) is known as a rich source of isoflavones and flavonoids, we hypothesized that ethanolic extract of seabuckthorn leaves (SL) may have anti-obesity and hypoglycemic effects. To investigate the effect of ethanolic extract of SL, 32 C57BL/6J mice were randomly divided into 4 dietary groups, containing 8 mice in each group: normal diet group; high-fat diet (HD) control group; high-fat diet with SL extract, 500 mg/kg body weight (BW) (SL1) group; and high-fat diet with SL extract, 1000 mg/kg BW (SL2) group. After 13 weeks, it was observed that oral administration of SL extract significantly reduced the energy intake; BW gain; epididymal fat pad weight; hepatic triglyceride, hepatic, and serum total cholesterol levels; and serum leptin levels in the SL groups compared to the HD group. However, differences in serum triglyceride and insulin levels in the SL groups were not significant in comparison to the HD group. The hepatic mRNA expression of peroxisome proliferator-activated receptor (PPAR) α and carnitine palmitoyltransferase 1 along with PPAR- γ were significantly increased in SL groups, whereas the level of acetyl-CoA carboxylase was significantly reduced in SL groups compared to HD group. Our results indicated that SL is effective in preventing BW gain and fat accumulation in the liver; it also reduced adipose tissue mass, hepatic lipid profile, and serum leptin level in the mouse. Together, these observations suggest that SL is a potential agent to study in the management of obesity and related disorders.</description><subject>Acetyl-CoA Carboxylase - metabolism</subject><subject>Adipogenesis - drug effects</subject><subject>Adipogenesis - genetics</subject><subject>Adipose Tissue - drug effects</subject><subject>Adipose Tissue - metabolism</subject><subject>Administration, Oral</subject><subject>Animals</subject><subject>Anti-Obesity Agents - pharmacology</subject><subject>Anti-Obesity Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Carnitine O-Palmitoyltransferase - genetics</subject><subject>Carnitine O-Palmitoyltransferase - metabolism</subject><subject>Cholesterol - metabolism</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Down-Regulation</subject><subject>Energy Intake - drug effects</subject><subject>Fatty liver</subject><subject>Feeding. 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Tirupathi ; Moon, Hye-Jung ; Park, Jeong-Eun ; Moon, Yeon-Jeong ; Cha, Youn-Soo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-fe3ff16853ed4fc8832a7c8da6176244f853559e75d00d737cdf737512b8e5f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Acetyl-CoA Carboxylase - metabolism</topic><topic>Adipogenesis - drug effects</topic><topic>Adipogenesis - genetics</topic><topic>Adipose Tissue - drug effects</topic><topic>Adipose Tissue - metabolism</topic><topic>Administration, Oral</topic><topic>Animals</topic><topic>Anti-Obesity Agents - pharmacology</topic><topic>Anti-Obesity Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Carnitine O-Palmitoyltransferase - genetics</topic><topic>Carnitine O-Palmitoyltransferase - metabolism</topic><topic>Cholesterol - metabolism</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Down-Regulation</topic><topic>Energy Intake - drug effects</topic><topic>Fatty liver</topic><topic>Feeding. Feeding behavior</topic><topic>Flavonoids - pharmacology</topic><topic>Flavonoids - therapeutic use</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology and Hepatology</topic><topic>Hippophae - chemistry</topic><topic>Hippophae rhamnoides</topic><topic>Hippophae rhamnoides L</topic><topic>Insulin - blood</topic><topic>Leptin</topic><topic>Leptin - blood</topic><topic>Lipid metabolism</topic><topic>Lipogenesis - drug effects</topic><topic>Lipogenesis - genetics</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Obesity</topic><topic>Obesity - etiology</topic><topic>Obesity - prevention &amp; control</topic><topic>Phytotherapy</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>PPAR alpha - genetics</topic><topic>PPAR alpha - metabolism</topic><topic>PPAR gamma - genetics</topic><topic>PPAR gamma - metabolism</topic><topic>Random Allocation</topic><topic>RNA, Messenger - metabolism</topic><topic>Seabuckthorn</topic><topic>Triglycerides - metabolism</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Weight Gain - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pichiah, P.B. Tirupathi</creatorcontrib><creatorcontrib>Moon, Hye-Jung</creatorcontrib><creatorcontrib>Park, Jeong-Eun</creatorcontrib><creatorcontrib>Moon, Yeon-Jeong</creatorcontrib><creatorcontrib>Cha, Youn-Soo</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Nutrition research (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pichiah, P.B. Tirupathi</au><au>Moon, Hye-Jung</au><au>Park, Jeong-Eun</au><au>Moon, Yeon-Jeong</au><au>Cha, Youn-Soo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ethanolic extract of seabuckthorn ( Hippophae rhamnoides L ) prevents high-fat diet–induced obesity in mice through down-regulation of adipogenic and lipogenic gene expression</atitle><jtitle>Nutrition research (New York, N.Y.)</jtitle><addtitle>Nutr Res</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>32</volume><issue>11</issue><spage>856</spage><epage>864</epage><pages>856-864</pages><issn>0271-5317</issn><eissn>1879-0739</eissn><coden>NTRSDC</coden><abstract>Abstract Phenolic compounds and flavonoids ameliorate bodyweight, blood glucose, and serum lipid profile. Since seabuckthorn ( Hippophae rhamnoides L. ) is known as a rich source of isoflavones and flavonoids, we hypothesized that ethanolic extract of seabuckthorn leaves (SL) may have anti-obesity and hypoglycemic effects. To investigate the effect of ethanolic extract of SL, 32 C57BL/6J mice were randomly divided into 4 dietary groups, containing 8 mice in each group: normal diet group; high-fat diet (HD) control group; high-fat diet with SL extract, 500 mg/kg body weight (BW) (SL1) group; and high-fat diet with SL extract, 1000 mg/kg BW (SL2) group. After 13 weeks, it was observed that oral administration of SL extract significantly reduced the energy intake; BW gain; epididymal fat pad weight; hepatic triglyceride, hepatic, and serum total cholesterol levels; and serum leptin levels in the SL groups compared to the HD group. However, differences in serum triglyceride and insulin levels in the SL groups were not significant in comparison to the HD group. The hepatic mRNA expression of peroxisome proliferator-activated receptor (PPAR) α and carnitine palmitoyltransferase 1 along with PPAR- γ were significantly increased in SL groups, whereas the level of acetyl-CoA carboxylase was significantly reduced in SL groups compared to HD group. Our results indicated that SL is effective in preventing BW gain and fat accumulation in the liver; it also reduced adipose tissue mass, hepatic lipid profile, and serum leptin level in the mouse. Together, these observations suggest that SL is a potential agent to study in the management of obesity and related disorders.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>23176796</pmid><doi>10.1016/j.nutres.2012.09.015</doi><tpages>9</tpages></addata></record>
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ispartof Nutrition research (New York, N.Y.), 2012-11, Vol.32 (11), p.856-864
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subjects Acetyl-CoA Carboxylase - metabolism
Adipogenesis - drug effects
Adipogenesis - genetics
Adipose Tissue - drug effects
Adipose Tissue - metabolism
Administration, Oral
Animals
Anti-Obesity Agents - pharmacology
Anti-Obesity Agents - therapeutic use
Biological and medical sciences
Carnitine O-Palmitoyltransferase - genetics
Carnitine O-Palmitoyltransferase - metabolism
Cholesterol - metabolism
Diet, High-Fat - adverse effects
Down-Regulation
Energy Intake - drug effects
Fatty liver
Feeding. Feeding behavior
Flavonoids - pharmacology
Flavonoids - therapeutic use
Fundamental and applied biological sciences. Psychology
Gastroenterology and Hepatology
Hippophae - chemistry
Hippophae rhamnoides
Hippophae rhamnoides L
Insulin - blood
Leptin
Leptin - blood
Lipid metabolism
Lipogenesis - drug effects
Lipogenesis - genetics
Liver - drug effects
Liver - metabolism
Male
Mice
Mice, Inbred C57BL
Obesity
Obesity - etiology
Obesity - prevention & control
Phytotherapy
Plant Extracts - pharmacology
Plant Extracts - therapeutic use
PPAR alpha - genetics
PPAR alpha - metabolism
PPAR gamma - genetics
PPAR gamma - metabolism
Random Allocation
RNA, Messenger - metabolism
Seabuckthorn
Triglycerides - metabolism
Vertebrates: anatomy and physiology, studies on body, several organs or systems
Weight Gain - drug effects
title Ethanolic extract of seabuckthorn ( Hippophae rhamnoides L ) prevents high-fat diet–induced obesity in mice through down-regulation of adipogenic and lipogenic gene expression
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