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Octreotide promotes weight loss via suppression of intestinal MTP and apoB48 expression in diet-induced obesity rats
Abstract Objective The goal of this study was to investigate the effect of octreotide on the expression of intestinal fat absorption-associated apolipoproteinB48 (apoB48), microsomal triglyceride transfer protein (MTP) and apolipoproteinAIV (apoAIV) in a high-fat diet-induced obesity rat model. Meth...
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Published in: | Nutrition (Burbank, Los Angeles County, Calif.) Los Angeles County, Calif.), 2013-10, Vol.29 (10), p.1259-1265 |
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creator | Huang, Wei, M.D Liu, Rui, Ph.D Ou, Yan, M.D Li, Xian, B.S Qiang, Ou, B.S Yu, Tao, M.D Tang, Cheng-Wei, M.D., Ph.D |
description | Abstract Objective The goal of this study was to investigate the effect of octreotide on the expression of intestinal fat absorption-associated apolipoproteinB48 (apoB48), microsomal triglyceride transfer protein (MTP) and apolipoproteinAIV (apoAIV) in a high-fat diet-induced obesity rat model. Methods Sprague–Dawley rats were placed into a control or high-fat diet group. Obese rats from the high-fat diet group were further divided into an obese group and an octreotide-treated group. Rats in the octreotide-treated group were subcutaneously injected with octreotide (40 μg/kg body weight) twice daily for 8 d. Body weight, fasting plasma glucose (FPG), fasting serum insulin, triglyceride (TG), total cholesterol (TC), and high density lipoprotein-cholesterol (HDL-C) were measured. Intestinal MTP, apoB48, and apoAIV expression levels were determined by real-time polymerase chain reaction, Western blot, or enzyme-linked immunosorbent assay analysis. Results We found high-fat diet-induced obesity rats express more apoB, MTP, and apoAIV mRNA as well as apoB48 and MTP protein in the intestine than normal chow-fed rats. This observation occurred along with increased body weight, FPG, TG, TC, fasting serum insulin, and Homeostatic Model Assessment value. Octreotide intervention significantly decreased body weight and blood parameters, and down-regulated expression of apoB mRNA and apoB48 protein, as well as MTP mRNA and proteins. However, apoAIV mRNA was not significantly different between obese and octreotide-treated rats although it was decreased by 47%. Conclusion High-fat diet-induced obesity is associated with increased expression of apoB48, MTP, and apoAIV in the intestine. Octreotide intervention inhibited the overexpression of apoB48 and MTP, and consequently brought about reduced fat absorption and weight loss. |
doi_str_mv | 10.1016/j.nut.2013.01.013 |
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Methods Sprague–Dawley rats were placed into a control or high-fat diet group. Obese rats from the high-fat diet group were further divided into an obese group and an octreotide-treated group. Rats in the octreotide-treated group were subcutaneously injected with octreotide (40 μg/kg body weight) twice daily for 8 d. Body weight, fasting plasma glucose (FPG), fasting serum insulin, triglyceride (TG), total cholesterol (TC), and high density lipoprotein-cholesterol (HDL-C) were measured. Intestinal MTP, apoB48, and apoAIV expression levels were determined by real-time polymerase chain reaction, Western blot, or enzyme-linked immunosorbent assay analysis. Results We found high-fat diet-induced obesity rats express more apoB, MTP, and apoAIV mRNA as well as apoB48 and MTP protein in the intestine than normal chow-fed rats. This observation occurred along with increased body weight, FPG, TG, TC, fasting serum insulin, and Homeostatic Model Assessment value. Octreotide intervention significantly decreased body weight and blood parameters, and down-regulated expression of apoB mRNA and apoB48 protein, as well as MTP mRNA and proteins. However, apoAIV mRNA was not significantly different between obese and octreotide-treated rats although it was decreased by 47%. Conclusion High-fat diet-induced obesity is associated with increased expression of apoB48, MTP, and apoAIV in the intestine. Octreotide intervention inhibited the overexpression of apoB48 and MTP, and consequently brought about reduced fat absorption and weight loss.</description><identifier>ISSN: 0899-9007</identifier><identifier>EISSN: 1873-1244</identifier><identifier>DOI: 10.1016/j.nut.2013.01.013</identifier><identifier>PMID: 23911221</identifier><identifier>CODEN: NUTRER</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Absorption ; Alimentary obesity ; animal models ; Animals ; Apolipoprotein B-48 - genetics ; Apolipoprotein B-48 - metabolism ; ApolipoproteinAIV ; ApolipoproteinB48 ; Apolipoproteins A - genetics ; Apolipoproteins A - metabolism ; Biological and medical sciences ; blood glucose ; Blood Glucose - metabolism ; Body weight ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; Cholesterol ; Cholesterol - blood ; Diet ; Diet, High-Fat - adverse effects ; Down-Regulation ; Enzyme-Linked Immunosorbent Assay ; Fasting ; Feeding. Feeding behavior ; Fundamental and applied biological sciences. Psychology ; Gastroenterology and Hepatology ; gene expression regulation ; high fat diet ; Insulin ; Insulin - blood ; Intestinal Absorption - drug effects ; Intestines - drug effects ; Intestines - metabolism ; Male ; Medical sciences ; messenger RNA ; Metabolic diseases ; Microsomal triglyceride transfer protein ; Obesity ; Obesity - etiology ; Octreotide ; Octreotide - pharmacology ; proteins ; quantitative polymerase chain reaction ; Rats ; Rats, Sprague-Dawley ; Rodents ; Triglycerides - blood ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Weight control ; weight loss ; Weight Loss - drug effects ; Western blotting</subject><ispartof>Nutrition (Burbank, Los Angeles County, Calif.), 2013-10, Vol.29 (10), p.1259-1265</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Oct 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c556t-14b9f8c72e0efe30a504c858fa8ce00452e029768febf1790acb5bf40f8b2c873</citedby><cites>FETCH-LOGICAL-c556t-14b9f8c72e0efe30a504c858fa8ce00452e029768febf1790acb5bf40f8b2c873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27739465$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23911221$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Wei, M.D</creatorcontrib><creatorcontrib>Liu, Rui, Ph.D</creatorcontrib><creatorcontrib>Ou, Yan, M.D</creatorcontrib><creatorcontrib>Li, Xian, B.S</creatorcontrib><creatorcontrib>Qiang, Ou, B.S</creatorcontrib><creatorcontrib>Yu, Tao, M.D</creatorcontrib><creatorcontrib>Tang, Cheng-Wei, M.D., Ph.D</creatorcontrib><title>Octreotide promotes weight loss via suppression of intestinal MTP and apoB48 expression in diet-induced obesity rats</title><title>Nutrition (Burbank, Los Angeles County, Calif.)</title><addtitle>Nutrition</addtitle><description>Abstract Objective The goal of this study was to investigate the effect of octreotide on the expression of intestinal fat absorption-associated apolipoproteinB48 (apoB48), microsomal triglyceride transfer protein (MTP) and apolipoproteinAIV (apoAIV) in a high-fat diet-induced obesity rat model. Methods Sprague–Dawley rats were placed into a control or high-fat diet group. Obese rats from the high-fat diet group were further divided into an obese group and an octreotide-treated group. Rats in the octreotide-treated group were subcutaneously injected with octreotide (40 μg/kg body weight) twice daily for 8 d. Body weight, fasting plasma glucose (FPG), fasting serum insulin, triglyceride (TG), total cholesterol (TC), and high density lipoprotein-cholesterol (HDL-C) were measured. Intestinal MTP, apoB48, and apoAIV expression levels were determined by real-time polymerase chain reaction, Western blot, or enzyme-linked immunosorbent assay analysis. Results We found high-fat diet-induced obesity rats express more apoB, MTP, and apoAIV mRNA as well as apoB48 and MTP protein in the intestine than normal chow-fed rats. This observation occurred along with increased body weight, FPG, TG, TC, fasting serum insulin, and Homeostatic Model Assessment value. Octreotide intervention significantly decreased body weight and blood parameters, and down-regulated expression of apoB mRNA and apoB48 protein, as well as MTP mRNA and proteins. However, apoAIV mRNA was not significantly different between obese and octreotide-treated rats although it was decreased by 47%. Conclusion High-fat diet-induced obesity is associated with increased expression of apoB48, MTP, and apoAIV in the intestine. Octreotide intervention inhibited the overexpression of apoB48 and MTP, and consequently brought about reduced fat absorption and weight loss.</description><subject>Absorption</subject><subject>Alimentary obesity</subject><subject>animal models</subject><subject>Animals</subject><subject>Apolipoprotein B-48 - genetics</subject><subject>Apolipoprotein B-48 - metabolism</subject><subject>ApolipoproteinAIV</subject><subject>ApolipoproteinB48</subject><subject>Apolipoproteins A - genetics</subject><subject>Apolipoproteins A - metabolism</subject><subject>Biological and medical sciences</subject><subject>blood glucose</subject><subject>Blood Glucose - metabolism</subject><subject>Body weight</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>Cholesterol</subject><subject>Cholesterol - blood</subject><subject>Diet</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Down-Regulation</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Fasting</subject><subject>Feeding. Feeding behavior</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology and Hepatology</subject><subject>gene expression regulation</subject><subject>high fat diet</subject><subject>Insulin</subject><subject>Insulin - blood</subject><subject>Intestinal Absorption - drug effects</subject><subject>Intestines - drug effects</subject><subject>Intestines - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>messenger RNA</subject><subject>Metabolic diseases</subject><subject>Microsomal triglyceride transfer protein</subject><subject>Obesity</subject><subject>Obesity - etiology</subject><subject>Octreotide</subject><subject>Octreotide - pharmacology</subject><subject>proteins</subject><subject>quantitative polymerase chain reaction</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rodents</subject><subject>Triglycerides - blood</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Weight control</subject><subject>weight loss</subject><subject>Weight Loss - drug effects</subject><subject>Western blotting</subject><issn>0899-9007</issn><issn>1873-1244</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkl9rFDEUxQdR7Fr9AL5oQARfZr1JJjsJBUGL_6BSoe1zyGRuatbZyZpkqvvtzXbXFvqgQiAP-d2bc8-5VfWUwpwCXbxezscpzxlQPgdaDr9XzahseU1Z09yvZiCVqhVAe1A9SmkJAFQt1MPqgHFFKWN0VuVTmyOG7Hsk6xhWIWMiP9FffstkCCmRK29ImtbriCn5MJLgiB8LlP1oBvLl_CsxY0_MOrxrJMFfN5wfSe8x137sJ4s9CR0mnzckmpweVw-cGRI-2d-H1cWH9-fHn-qT04-fj9-e1FaIRa5p0yknbcsQ0CEHI6CxUkhnpEWARpQHptqFdNg52iowthOda8DJjtniw2H1ate3TPZjKpr1yieLw2BGDFPSVPKWM04X4t9oI6TgXCr-HyinTDUSWEFf3EGXYYrFuGsKmOALCYWiO8rG4nhEp9fRr0zcaAp6G7Re6hK03gatgZazFfFs33nqVtjfVPxJtgAv94BJ1gwumtH6dMu1LVfN9eDPd5wzQZvLWJiLs_JTU7alhWJiIY52BJaorjxGnazHsYTqI9qs--D_KvTNnWo7-NEXSd9xg-nWD52YBn223dntylJeBAgh-G8fvOMj</recordid><startdate>20131001</startdate><enddate>20131001</enddate><creator>Huang, Wei, M.D</creator><creator>Liu, Rui, Ph.D</creator><creator>Ou, Yan, M.D</creator><creator>Li, Xian, B.S</creator><creator>Qiang, Ou, B.S</creator><creator>Yu, Tao, M.D</creator><creator>Tang, Cheng-Wei, M.D., Ph.D</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Limited</general><scope>FBQ</scope><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>3V.</scope><scope>7RQ</scope><scope>7RV</scope><scope>7TS</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20131001</creationdate><title>Octreotide promotes weight loss via suppression of intestinal MTP and apoB48 expression in diet-induced obesity rats</title><author>Huang, Wei, M.D ; Liu, Rui, Ph.D ; Ou, Yan, M.D ; Li, Xian, B.S ; Qiang, Ou, B.S ; Yu, Tao, M.D ; Tang, Cheng-Wei, M.D., Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c556t-14b9f8c72e0efe30a504c858fa8ce00452e029768febf1790acb5bf40f8b2c873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Absorption</topic><topic>Alimentary obesity</topic><topic>animal models</topic><topic>Animals</topic><topic>Apolipoprotein B-48 - genetics</topic><topic>Apolipoprotein B-48 - metabolism</topic><topic>ApolipoproteinAIV</topic><topic>ApolipoproteinB48</topic><topic>Apolipoproteins A - genetics</topic><topic>Apolipoproteins A - metabolism</topic><topic>Biological and medical sciences</topic><topic>blood glucose</topic><topic>Blood Glucose - metabolism</topic><topic>Body weight</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - metabolism</topic><topic>Cholesterol</topic><topic>Cholesterol - blood</topic><topic>Diet</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Down-Regulation</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Fasting</topic><topic>Feeding. Feeding behavior</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology and Hepatology</topic><topic>gene expression regulation</topic><topic>high fat diet</topic><topic>Insulin</topic><topic>Insulin - blood</topic><topic>Intestinal Absorption - drug effects</topic><topic>Intestines - drug effects</topic><topic>Intestines - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>messenger RNA</topic><topic>Metabolic diseases</topic><topic>Microsomal triglyceride transfer protein</topic><topic>Obesity</topic><topic>Obesity - etiology</topic><topic>Octreotide</topic><topic>Octreotide - pharmacology</topic><topic>proteins</topic><topic>quantitative polymerase chain reaction</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rodents</topic><topic>Triglycerides - blood</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Weight control</topic><topic>weight loss</topic><topic>Weight Loss - drug effects</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Wei, M.D</creatorcontrib><creatorcontrib>Liu, Rui, Ph.D</creatorcontrib><creatorcontrib>Ou, Yan, M.D</creatorcontrib><creatorcontrib>Li, Xian, B.S</creatorcontrib><creatorcontrib>Qiang, Ou, B.S</creatorcontrib><creatorcontrib>Yu, Tao, M.D</creatorcontrib><creatorcontrib>Tang, Cheng-Wei, M.D., Ph.D</creatorcontrib><collection>AGRIS</collection><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>ProQuest Central (Corporate)</collection><collection>Career & Technical Education Database</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest research library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Nutrition (Burbank, Los Angeles County, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Wei, M.D</au><au>Liu, Rui, Ph.D</au><au>Ou, Yan, M.D</au><au>Li, Xian, B.S</au><au>Qiang, Ou, B.S</au><au>Yu, Tao, M.D</au><au>Tang, Cheng-Wei, M.D., Ph.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Octreotide promotes weight loss via suppression of intestinal MTP and apoB48 expression in diet-induced obesity rats</atitle><jtitle>Nutrition (Burbank, Los Angeles County, Calif.)</jtitle><addtitle>Nutrition</addtitle><date>2013-10-01</date><risdate>2013</risdate><volume>29</volume><issue>10</issue><spage>1259</spage><epage>1265</epage><pages>1259-1265</pages><issn>0899-9007</issn><eissn>1873-1244</eissn><coden>NUTRER</coden><abstract>Abstract Objective The goal of this study was to investigate the effect of octreotide on the expression of intestinal fat absorption-associated apolipoproteinB48 (apoB48), microsomal triglyceride transfer protein (MTP) and apolipoproteinAIV (apoAIV) in a high-fat diet-induced obesity rat model. Methods Sprague–Dawley rats were placed into a control or high-fat diet group. Obese rats from the high-fat diet group were further divided into an obese group and an octreotide-treated group. Rats in the octreotide-treated group were subcutaneously injected with octreotide (40 μg/kg body weight) twice daily for 8 d. Body weight, fasting plasma glucose (FPG), fasting serum insulin, triglyceride (TG), total cholesterol (TC), and high density lipoprotein-cholesterol (HDL-C) were measured. Intestinal MTP, apoB48, and apoAIV expression levels were determined by real-time polymerase chain reaction, Western blot, or enzyme-linked immunosorbent assay analysis. Results We found high-fat diet-induced obesity rats express more apoB, MTP, and apoAIV mRNA as well as apoB48 and MTP protein in the intestine than normal chow-fed rats. This observation occurred along with increased body weight, FPG, TG, TC, fasting serum insulin, and Homeostatic Model Assessment value. Octreotide intervention significantly decreased body weight and blood parameters, and down-regulated expression of apoB mRNA and apoB48 protein, as well as MTP mRNA and proteins. However, apoAIV mRNA was not significantly different between obese and octreotide-treated rats although it was decreased by 47%. Conclusion High-fat diet-induced obesity is associated with increased expression of apoB48, MTP, and apoAIV in the intestine. Octreotide intervention inhibited the overexpression of apoB48 and MTP, and consequently brought about reduced fat absorption and weight loss.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>23911221</pmid><doi>10.1016/j.nut.2013.01.013</doi><tpages>7</tpages></addata></record> |
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subjects | Absorption Alimentary obesity animal models Animals Apolipoprotein B-48 - genetics Apolipoprotein B-48 - metabolism ApolipoproteinAIV ApolipoproteinB48 Apolipoproteins A - genetics Apolipoproteins A - metabolism Biological and medical sciences blood glucose Blood Glucose - metabolism Body weight Carrier Proteins - genetics Carrier Proteins - metabolism Cholesterol Cholesterol - blood Diet Diet, High-Fat - adverse effects Down-Regulation Enzyme-Linked Immunosorbent Assay Fasting Feeding. Feeding behavior Fundamental and applied biological sciences. Psychology Gastroenterology and Hepatology gene expression regulation high fat diet Insulin Insulin - blood Intestinal Absorption - drug effects Intestines - drug effects Intestines - metabolism Male Medical sciences messenger RNA Metabolic diseases Microsomal triglyceride transfer protein Obesity Obesity - etiology Octreotide Octreotide - pharmacology proteins quantitative polymerase chain reaction Rats Rats, Sprague-Dawley Rodents Triglycerides - blood Vertebrates: anatomy and physiology, studies on body, several organs or systems Weight control weight loss Weight Loss - drug effects Western blotting |
title | Octreotide promotes weight loss via suppression of intestinal MTP and apoB48 expression in diet-induced obesity rats |
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