Detrimental metabolic effects of combining long-term cigarette smoke exposure and high-fat diet in mice

1 Department of Pharmacology, School of Medical Sciences, University of New South Wales, New South Wales; 2 Department of Pharmacology; 3 Cooperative Research Centre for Chronic Inflammatory Diseases; and 4 Department of Medicine, Royal Melbourne Hospital, The University of Melbourne, Melbourne, Vic...

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Veröffentlicht in:American journal of physiology: endocrinology and metabolism 2007-12, Vol.293 (6), p.E1564-E1571
Hauptverfasser: Chen, Hui, Hansen, Michelle J, Jones, Jessica E, Vlahos, Ross, Anderson, Gary P, Morris, Margaret J
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container_end_page E1571
container_issue 6
container_start_page E1564
container_title American journal of physiology: endocrinology and metabolism
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creator Chen, Hui
Hansen, Michelle J
Jones, Jessica E
Vlahos, Ross
Anderson, Gary P
Morris, Margaret J
description 1 Department of Pharmacology, School of Medical Sciences, University of New South Wales, New South Wales; 2 Department of Pharmacology; 3 Cooperative Research Centre for Chronic Inflammatory Diseases; and 4 Department of Medicine, Royal Melbourne Hospital, The University of Melbourne, Melbourne, Victoria, Australia Submitted 8 July 2007 ; accepted in final form 14 October 2007 Obesity and cigarette smoking are both important risk factors for insulin resistance, cardiovascular disease, and cancer. Smoking reduces appetite, which makes many people reluctant to quit. Few studies have documented the metabolic impact of combined smoke exposure (se) and high-fat-diet (HFD). Neuropeptide Y (NPY) is a powerful hypothalamic feeding stimulator that promotes obesity. We investigated how chronic se affects caloric intake, adiposity, plasma hormones, inflammatory mediators, and hypothalamic NPY peptide in animals fed a palatable HFD. Balb/c mice (5 wk old, male) were exposed to smoke (2 cigarettes, twice/day, 6 days/wk, for 7 wk) with or without HFD. Sham-exposed mice were handled similarly without se. Plasma leptin, hypothalamic NPY, and adipose triglyceride lipase (ATGL) mRNA were measured. HFD induced a 2.3-fold increase in caloric intake, increased adiposity, and glucose in both sham and se cohorts. Smoke exposure decreased caloric intake by 23%, with reduced body weight in both dietary groups. Fat mass and glucose were reduced only by se in the chow-fed animals. ATGL mRNA was reduced by HFD in se animals. Total hypothalamic NPY was reduced by HFD, but only in sham-exposed animals; se increased arcuate NPY. We conclude that although se ameliorated hyperphagia and reversed the weight gain associated with HFD, it failed to reverse fat accumulation and hyperglycemia. The reduced ATGL mRNA expression induced by combined HFD and se may contribute to fat retention. Our data support a powerful health message that smoking in the presence of an unhealthy Western diet increases metabolic disorders and fat accumulation. adipose triglyceride lipase; appetite; leptin; neuropeptide Y; tumor necrosis factor- Address for reprint requests and other correspondence: M. J. Morris, Dept. of Pharmacology, Univ. of New South Wales, NSW 2052, Australia (e-mail: m.morris{at}unsw.edu.au )
doi_str_mv 10.1152/ajpendo.00442.2007
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Smoking reduces appetite, which makes many people reluctant to quit. Few studies have documented the metabolic impact of combined smoke exposure (se) and high-fat-diet (HFD). Neuropeptide Y (NPY) is a powerful hypothalamic feeding stimulator that promotes obesity. We investigated how chronic se affects caloric intake, adiposity, plasma hormones, inflammatory mediators, and hypothalamic NPY peptide in animals fed a palatable HFD. Balb/c mice (5 wk old, male) were exposed to smoke (2 cigarettes, twice/day, 6 days/wk, for 7 wk) with or without HFD. Sham-exposed mice were handled similarly without se. Plasma leptin, hypothalamic NPY, and adipose triglyceride lipase (ATGL) mRNA were measured. HFD induced a 2.3-fold increase in caloric intake, increased adiposity, and glucose in both sham and se cohorts. Smoke exposure decreased caloric intake by 23%, with reduced body weight in both dietary groups. Fat mass and glucose were reduced only by se in the chow-fed animals. ATGL mRNA was reduced by HFD in se animals. Total hypothalamic NPY was reduced by HFD, but only in sham-exposed animals; se increased arcuate NPY. We conclude that although se ameliorated hyperphagia and reversed the weight gain associated with HFD, it failed to reverse fat accumulation and hyperglycemia. The reduced ATGL mRNA expression induced by combined HFD and se may contribute to fat retention. Our data support a powerful health message that smoking in the presence of an unhealthy Western diet increases metabolic disorders and fat accumulation. adipose triglyceride lipase; appetite; leptin; neuropeptide Y; tumor necrosis factor- Address for reprint requests and other correspondence: M. J. 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Smoking reduces appetite, which makes many people reluctant to quit. Few studies have documented the metabolic impact of combined smoke exposure (se) and high-fat-diet (HFD). Neuropeptide Y (NPY) is a powerful hypothalamic feeding stimulator that promotes obesity. We investigated how chronic se affects caloric intake, adiposity, plasma hormones, inflammatory mediators, and hypothalamic NPY peptide in animals fed a palatable HFD. Balb/c mice (5 wk old, male) were exposed to smoke (2 cigarettes, twice/day, 6 days/wk, for 7 wk) with or without HFD. Sham-exposed mice were handled similarly without se. Plasma leptin, hypothalamic NPY, and adipose triglyceride lipase (ATGL) mRNA were measured. HFD induced a 2.3-fold increase in caloric intake, increased adiposity, and glucose in both sham and se cohorts. Smoke exposure decreased caloric intake by 23%, with reduced body weight in both dietary groups. Fat mass and glucose were reduced only by se in the chow-fed animals. ATGL mRNA was reduced by HFD in se animals. Total hypothalamic NPY was reduced by HFD, but only in sham-exposed animals; se increased arcuate NPY. We conclude that although se ameliorated hyperphagia and reversed the weight gain associated with HFD, it failed to reverse fat accumulation and hyperglycemia. The reduced ATGL mRNA expression induced by combined HFD and se may contribute to fat retention. Our data support a powerful health message that smoking in the presence of an unhealthy Western diet increases metabolic disorders and fat accumulation. adipose triglyceride lipase; appetite; leptin; neuropeptide Y; tumor necrosis factor- Address for reprint requests and other correspondence: M. J. Morris, Dept. of Pharmacology, Univ. of New South Wales, NSW 2052, Australia (e-mail: m.morris{at}unsw.edu.au )</description><subject>Adipose Tissue - drug effects</subject><subject>Adipose Tissue - metabolism</subject><subject>Animals</subject><subject>Blood Glucose - metabolism</subject><subject>Body Weight - drug effects</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Carboxyhemoglobin - metabolism</subject><subject>Carboxylic Ester Hydrolases - genetics</subject><subject>Corticosterone - blood</subject><subject>Cytokines - genetics</subject><subject>Dietary Fats - administration &amp; dosage</subject><subject>Dietary Fats - pharmacology</subject><subject>Energy Intake - drug effects</subject><subject>Gene Expression - drug effects</subject><subject>Insulin - blood</subject><subject>Ion Channels - genetics</subject><subject>Leptin - blood</subject><subject>Lipase</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Metabolic disorders</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mitochondrial Proteins - genetics</subject><subject>Neuropeptide Y - blood</subject><subject>Neuropeptide Y - metabolism</subject><subject>Obesity</subject><subject>Oils &amp; fats</subject><subject>Peptides</subject><subject>Risk factors</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Rodents</subject><subject>Smoking</subject><subject>Tobacco Smoke Pollution - adverse effects</subject><subject>Triglycerides - blood</subject><subject>Uncoupling Protein 1</subject><issn>0193-1849</issn><issn>1522-1555</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtv1DAYRS0EokPLH2CBLBbsMvWzSdih0gJSJTbt2rKTLxkPjh1sR-38-3o6w0NIXXnhc67sexF6R8maUsnO9XYG34c1IUKwNSOkfoFW5YJVVEr5Eq0IbXlFG9GeoDcpbUkhpGCv0QmtW0EYFSs0foEc7QQ-a4cnyNoEZzsMwwBdTjgMuAuTsd76EbvgxypDnHBnRx0hZ8BpCj8Bw8Mc0hIBa9_jjR031aAz7i1kbD2ebAdn6NWgXYK3x_MU3V1f3V5-q25-fP1--fmm6iSVuWo5tNxIQg2npuZiGDhooXUHvOmhYYYSYQwQ3nND68YQAbouHzRN3_O6lfwUfTzkzjH8WiBlNdnUgXPaQ1iSYkTUjDdNAT_8B27DEn15m2KccSqkqAvEDlAXQ0oRBjWXsnTcKUrUfgN13EA9baD2GxTp_TF5MRP0f5Vj6QVYH4B9U_c2gpo3u2SDC-PuTyBrubpQV1Re7IVPzwvXi3O38JB_m_-Iau4H_ggXdKo9</recordid><startdate>20071201</startdate><enddate>20071201</enddate><creator>Chen, Hui</creator><creator>Hansen, Michelle J</creator><creator>Jones, Jessica E</creator><creator>Vlahos, Ross</creator><creator>Anderson, Gary P</creator><creator>Morris, Margaret J</creator><general>American Physiological Society</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>7QP</scope><scope>7TS</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20071201</creationdate><title>Detrimental metabolic effects of combining long-term cigarette smoke exposure and high-fat diet in mice</title><author>Chen, Hui ; 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fats</topic><topic>Peptides</topic><topic>Risk factors</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Rodents</topic><topic>Smoking</topic><topic>Tobacco Smoke Pollution - adverse effects</topic><topic>Triglycerides - blood</topic><topic>Uncoupling Protein 1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Hui</creatorcontrib><creatorcontrib>Hansen, Michelle J</creatorcontrib><creatorcontrib>Jones, Jessica E</creatorcontrib><creatorcontrib>Vlahos, Ross</creatorcontrib><creatorcontrib>Anderson, Gary P</creatorcontrib><creatorcontrib>Morris, Margaret J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>American journal of physiology: endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Hui</au><au>Hansen, Michelle J</au><au>Jones, Jessica E</au><au>Vlahos, Ross</au><au>Anderson, Gary P</au><au>Morris, Margaret J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detrimental metabolic effects of combining long-term cigarette smoke exposure and high-fat diet in mice</atitle><jtitle>American journal of physiology: endocrinology and metabolism</jtitle><addtitle>Am J Physiol Endocrinol Metab</addtitle><date>2007-12-01</date><risdate>2007</risdate><volume>293</volume><issue>6</issue><spage>E1564</spage><epage>E1571</epage><pages>E1564-E1571</pages><issn>0193-1849</issn><eissn>1522-1555</eissn><coden>AJPMD9</coden><abstract>1 Department of Pharmacology, School of Medical Sciences, University of New South Wales, New South Wales; 2 Department of Pharmacology; 3 Cooperative Research Centre for Chronic Inflammatory Diseases; and 4 Department of Medicine, Royal Melbourne Hospital, The University of Melbourne, Melbourne, Victoria, Australia Submitted 8 July 2007 ; accepted in final form 14 October 2007 Obesity and cigarette smoking are both important risk factors for insulin resistance, cardiovascular disease, and cancer. Smoking reduces appetite, which makes many people reluctant to quit. Few studies have documented the metabolic impact of combined smoke exposure (se) and high-fat-diet (HFD). Neuropeptide Y (NPY) is a powerful hypothalamic feeding stimulator that promotes obesity. We investigated how chronic se affects caloric intake, adiposity, plasma hormones, inflammatory mediators, and hypothalamic NPY peptide in animals fed a palatable HFD. Balb/c mice (5 wk old, male) were exposed to smoke (2 cigarettes, twice/day, 6 days/wk, for 7 wk) with or without HFD. Sham-exposed mice were handled similarly without se. Plasma leptin, hypothalamic NPY, and adipose triglyceride lipase (ATGL) mRNA were measured. HFD induced a 2.3-fold increase in caloric intake, increased adiposity, and glucose in both sham and se cohorts. Smoke exposure decreased caloric intake by 23%, with reduced body weight in both dietary groups. Fat mass and glucose were reduced only by se in the chow-fed animals. ATGL mRNA was reduced by HFD in se animals. Total hypothalamic NPY was reduced by HFD, but only in sham-exposed animals; se increased arcuate NPY. We conclude that although se ameliorated hyperphagia and reversed the weight gain associated with HFD, it failed to reverse fat accumulation and hyperglycemia. The reduced ATGL mRNA expression induced by combined HFD and se may contribute to fat retention. Our data support a powerful health message that smoking in the presence of an unhealthy Western diet increases metabolic disorders and fat accumulation. adipose triglyceride lipase; appetite; leptin; neuropeptide Y; tumor necrosis factor- Address for reprint requests and other correspondence: M. J. Morris, Dept. of Pharmacology, Univ. of New South Wales, NSW 2052, Australia (e-mail: m.morris{at}unsw.edu.au )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>17940214</pmid><doi>10.1152/ajpendo.00442.2007</doi></addata></record>
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source MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adipose Tissue - drug effects
Adipose Tissue - metabolism
Animals
Blood Glucose - metabolism
Body Weight - drug effects
Brain - drug effects
Brain - metabolism
Carboxyhemoglobin - metabolism
Carboxylic Ester Hydrolases - genetics
Corticosterone - blood
Cytokines - genetics
Dietary Fats - administration & dosage
Dietary Fats - pharmacology
Energy Intake - drug effects
Gene Expression - drug effects
Insulin - blood
Ion Channels - genetics
Leptin - blood
Lipase
Liver - drug effects
Liver - metabolism
Male
Metabolic disorders
Mice
Mice, Inbred BALB C
Mitochondrial Proteins - genetics
Neuropeptide Y - blood
Neuropeptide Y - metabolism
Obesity
Oils & fats
Peptides
Risk factors
RNA, Messenger - genetics
RNA, Messenger - metabolism
Rodents
Smoking
Tobacco Smoke Pollution - adverse effects
Triglycerides - blood
Uncoupling Protein 1
title Detrimental metabolic effects of combining long-term cigarette smoke exposure and high-fat diet in mice
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