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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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. Together, these observations suggest that SL is a potential agent to study in the management of obesity and related disorders.</description><identifier>ISSN: 0271-5317</identifier><identifier>EISSN: 1879-0739</identifier><identifier>DOI: 10.1016/j.nutres.2012.09.015</identifier><identifier>PMID: 23176796</identifier><identifier>CODEN: NTRSDC</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>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</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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c546t-fe3ff16853ed4fc8832a7c8da6176244f853559e75d00d737cdf737512b8e5f73</citedby><cites>FETCH-LOGICAL-c546t-fe3ff16853ed4fc8832a7c8da6176244f853559e75d00d737cdf737512b8e5f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.nutres.2012.09.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26711677$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23176796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><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. Feeding behavior</subject><subject>Flavonoids - pharmacology</subject><subject>Flavonoids - therapeutic use</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology and Hepatology</subject><subject>Hippophae - chemistry</subject><subject>Hippophae rhamnoides</subject><subject>Hippophae rhamnoides L</subject><subject>Insulin - blood</subject><subject>Leptin</subject><subject>Leptin - blood</subject><subject>Lipid metabolism</subject><subject>Lipogenesis - drug effects</subject><subject>Lipogenesis - genetics</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Obesity</subject><subject>Obesity - etiology</subject><subject>Obesity - prevention & control</subject><subject>Phytotherapy</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>PPAR alpha - genetics</subject><subject>PPAR alpha - metabolism</subject><subject>PPAR gamma - genetics</subject><subject>PPAR gamma - metabolism</subject><subject>Random Allocation</subject><subject>RNA, Messenger - metabolism</subject><subject>Seabuckthorn</subject><subject>Triglycerides - metabolism</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Weight Gain - drug effects</subject><issn>0271-5317</issn><issn>1879-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkstu1DAUhiMEokPhDRDyBqksEnyJ42SDhKpCkUZiAawtj30y8TRjB9spzI534El4JZ4ERzMUiU03x7fv3PyfonhOcEUwaV7vKjenALGimNAKdxUm_EGxIq3oSixY97BYYSpIyRkRZ8WTGHcYE0EYe1yc0XzXiK5ZFb-u0qCcH61G8D0FpRPyPYqgNrO-SYMPDl2gaztNfhoUoDCovfPWQERr9ApNAW7BpYgGux3KXiVkLKTfP35aZ2YNBvkNRJsOyDq0txpQGoKftwMy_psrA2znUSXr3ZJTGTv5LbhciXIGjXenbCEXl3PFmNmnxaNejRGendbz4su7q8-X1-X64_sPl2_XpeZ1k8oeWN-TpuUMTN3rtmVUCd0a1eTWaV33-YXzDgQ3GBvBhDZ9tpzQTQs8b8-Li2PcKfivM8Qk9zZqGEflwM9REsFbWmPK2f0opZg1ouV1RusjqoOPMUAvp2D3KhwkwXLRVe7kUVe56CpxJ7Ou2e3FKcO82YO5c_orZAZengAVtRr7oJy28R_XCEIasXT15shB_rpbC0FGbcFlrWwAnaTx9r5K_g-gR5tlUuMNHCDu_BxclkUSGbOP_LTM4DKChGJMcYPZH23Q28Y</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Pichiah, P.B. Tirupathi</creator><creator>Moon, Hye-Jung</creator><creator>Park, Jeong-Eun</creator><creator>Moon, Yeon-Jeong</creator><creator>Cha, Youn-Soo</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20121101</creationdate><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><author>Pichiah, P.B. 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 & 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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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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