Changed preference for sweet taste in adulthood induced by perinatal exposure to bisphenol A—A probable link to overweight and obesity

Abstract Background The preference of obesity has risen dramatically worldwide over the past decades. Some latest reports showed significant increase of obesity in men compared to women. Implication of environmental endocrine disruptors has been focused more and more. Numerous studies in vitro and v...

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Veröffentlicht in:Neurotoxicology and teratology 2011-07, Vol.33 (4), p.458-463
Hauptverfasser: Xu, Xiaobin, Tan, Luei, Himi, Toshiyuki, Sadamatsu, Miyuki, Tsutsumi, Shunsuke, Akaike, Masashi, Kato, Nobumasa
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container_end_page 463
container_issue 4
container_start_page 458
container_title Neurotoxicology and teratology
container_volume 33
creator Xu, Xiaobin
Tan, Luei
Himi, Toshiyuki
Sadamatsu, Miyuki
Tsutsumi, Shunsuke
Akaike, Masashi
Kato, Nobumasa
description Abstract Background The preference of obesity has risen dramatically worldwide over the past decades. Some latest reports showed significant increase of obesity in men compared to women. Implication of environmental endocrine disruptors has been focused more and more. Numerous studies in vitro and vivo implied metabolic actions of bisphenol A (BPA), however much less consideration is given to the possibility of BPA exposure-induced change in gender-specific behaviors which result in obesity and overweight. Objectives To examine whether perinatal exposure to BPA at relative dose to environmental levels can influence sweet preference of male and female rats and consequently lead to alteration in bodyweight. Methods Rats perinatally exposed to BPA at doses of 0.01, 0.1 and 1.0 mg/L were tested sweet preference for 0.25%, 0.5% saccharin and 15% sucrose by two-bottle choice (water vs. saccharin/sucrose). The food intake, liquid consumption and bodyweight of each rat were monitored daily. At the end of the test, the fat percentage and tail blood pressure were measured. Results Significant sex difference of preference for 0.25% and 0.5% saccharin was shown in control and all BPA-treated groups (p < 0.001, female vs. male). 0.1 and 1.0 mg/L BPA treatment induced the increase of preference for 0.25% saccharin solution in males, but not in females. 0.1 mg/L BPA treatment increased sucrose preference in males at postnatal day (PND) 70 and 140 (p < 0.05 and p < 0.001, compared to control respectively) but decreased sucrose preference in females at PND 140 (p < 0.05, compared to control). The males treated by BPA showed overweight (p < 0.001), high fat percentage (p < 0.001) and tail blood pressure (p < 0.05) than control at PND 140. Conclusion Perinatal exposure to a low dose of BPA could increase sweet preference of male rats. Calorie intake may be programmed during early life, leading to changes of body weight depending on the gender. Although further researches concerning the mechanism are required, the results of the present study are particularly important with regards to the more significant increasing prevalence of obesity in men and the environmental endocrine disruptors.
doi_str_mv 10.1016/j.ntt.2011.06.002
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Some latest reports showed significant increase of obesity in men compared to women. Implication of environmental endocrine disruptors has been focused more and more. Numerous studies in vitro and vivo implied metabolic actions of bisphenol A (BPA), however much less consideration is given to the possibility of BPA exposure-induced change in gender-specific behaviors which result in obesity and overweight. Objectives To examine whether perinatal exposure to BPA at relative dose to environmental levels can influence sweet preference of male and female rats and consequently lead to alteration in bodyweight. Methods Rats perinatally exposed to BPA at doses of 0.01, 0.1 and 1.0 mg/L were tested sweet preference for 0.25%, 0.5% saccharin and 15% sucrose by two-bottle choice (water vs. saccharin/sucrose). The food intake, liquid consumption and bodyweight of each rat were monitored daily. At the end of the test, the fat percentage and tail blood pressure were measured. Results Significant sex difference of preference for 0.25% and 0.5% saccharin was shown in control and all BPA-treated groups (p < 0.001, female vs. male). 0.1 and 1.0 mg/L BPA treatment induced the increase of preference for 0.25% saccharin solution in males, but not in females. 0.1 mg/L BPA treatment increased sucrose preference in males at postnatal day (PND) 70 and 140 (p < 0.05 and p < 0.001, compared to control respectively) but decreased sucrose preference in females at PND 140 (p < 0.05, compared to control). The males treated by BPA showed overweight (p < 0.001), high fat percentage (p < 0.001) and tail blood pressure (p < 0.05) than control at PND 140. Conclusion Perinatal exposure to a low dose of BPA could increase sweet preference of male rats. Calorie intake may be programmed during early life, leading to changes of body weight depending on the gender. Although further researches concerning the mechanism are required, the results of the present study are particularly important with regards to the more significant increasing prevalence of obesity in men and the environmental endocrine disruptors.]]></description><identifier>ISSN: 0892-0362</identifier><identifier>EISSN: 1872-9738</identifier><identifier>DOI: 10.1016/j.ntt.2011.06.002</identifier><identifier>PMID: 21704699</identifier><identifier>CODEN: NETEEC</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adipose Tissue - drug effects ; Animals ; Benzhydryl Compounds ; Biological and medical sciences ; Bisphenol A ; Blood pressure ; Blood Pressure - drug effects ; Body weight ; Body Weight - drug effects ; Calories ; Dietary Sucrose - administration &amp; dosage ; Dose-Response Relationship, Drug ; Eating - drug effects ; Emergency ; Endocrine disruptors ; Endocrine Disruptors - toxicity ; Environmental disruptors ; Female ; Food intake ; Food Preferences - drug effects ; Gender ; Male ; Medical Education ; Medical sciences ; Metabolic diseases ; Obesity ; Obesity - etiology ; Obesity - physiopathology ; Overweight - etiology ; Overweight - physiopathology ; Perinatal exposure ; Phenols - toxicity ; Pregnancy ; Prenatal Exposure Delayed Effects - chemically induced ; Prenatal Exposure Delayed Effects - physiopathology ; Rats ; Rats, Sprague-Dawley ; Saccharin ; Sex differences ; Sex Factors ; Sexual dimorphism ; Sucrose ; Sweet preference ; Sweet taste ; Tails ; Taste ; Toxicology</subject><ispartof>Neurotoxicology and teratology, 2011-07, Vol.33 (4), p.458-463</ispartof><rights>Elsevier Inc.</rights><rights>2011 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c535t-4e278064d75eabde0ba4cba958fc0c4738fbf43aad20d50697222404fb6e86f93</citedby><cites>FETCH-LOGICAL-c535t-4e278064d75eabde0ba4cba958fc0c4738fbf43aad20d50697222404fb6e86f93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0892036211000742$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24414530$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21704699$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Xiaobin</creatorcontrib><creatorcontrib>Tan, Luei</creatorcontrib><creatorcontrib>Himi, Toshiyuki</creatorcontrib><creatorcontrib>Sadamatsu, Miyuki</creatorcontrib><creatorcontrib>Tsutsumi, Shunsuke</creatorcontrib><creatorcontrib>Akaike, Masashi</creatorcontrib><creatorcontrib>Kato, Nobumasa</creatorcontrib><title>Changed preference for sweet taste in adulthood induced by perinatal exposure to bisphenol A—A probable link to overweight and obesity</title><title>Neurotoxicology and teratology</title><addtitle>Neurotoxicol Teratol</addtitle><description><![CDATA[Abstract Background The preference of obesity has risen dramatically worldwide over the past decades. Some latest reports showed significant increase of obesity in men compared to women. Implication of environmental endocrine disruptors has been focused more and more. Numerous studies in vitro and vivo implied metabolic actions of bisphenol A (BPA), however much less consideration is given to the possibility of BPA exposure-induced change in gender-specific behaviors which result in obesity and overweight. Objectives To examine whether perinatal exposure to BPA at relative dose to environmental levels can influence sweet preference of male and female rats and consequently lead to alteration in bodyweight. Methods Rats perinatally exposed to BPA at doses of 0.01, 0.1 and 1.0 mg/L were tested sweet preference for 0.25%, 0.5% saccharin and 15% sucrose by two-bottle choice (water vs. saccharin/sucrose). The food intake, liquid consumption and bodyweight of each rat were monitored daily. At the end of the test, the fat percentage and tail blood pressure were measured. Results Significant sex difference of preference for 0.25% and 0.5% saccharin was shown in control and all BPA-treated groups (p < 0.001, female vs. male). 0.1 and 1.0 mg/L BPA treatment induced the increase of preference for 0.25% saccharin solution in males, but not in females. 0.1 mg/L BPA treatment increased sucrose preference in males at postnatal day (PND) 70 and 140 (p < 0.05 and p < 0.001, compared to control respectively) but decreased sucrose preference in females at PND 140 (p < 0.05, compared to control). The males treated by BPA showed overweight (p < 0.001), high fat percentage (p < 0.001) and tail blood pressure (p < 0.05) than control at PND 140. Conclusion Perinatal exposure to a low dose of BPA could increase sweet preference of male rats. Calorie intake may be programmed during early life, leading to changes of body weight depending on the gender. Although further researches concerning the mechanism are required, the results of the present study are particularly important with regards to the more significant increasing prevalence of obesity in men and the environmental endocrine disruptors.]]></description><subject>Adipose Tissue - drug effects</subject><subject>Animals</subject><subject>Benzhydryl Compounds</subject><subject>Biological and medical sciences</subject><subject>Bisphenol A</subject><subject>Blood pressure</subject><subject>Blood Pressure - drug effects</subject><subject>Body weight</subject><subject>Body Weight - drug effects</subject><subject>Calories</subject><subject>Dietary Sucrose - administration &amp; dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Eating - drug effects</subject><subject>Emergency</subject><subject>Endocrine disruptors</subject><subject>Endocrine Disruptors - toxicity</subject><subject>Environmental disruptors</subject><subject>Female</subject><subject>Food intake</subject><subject>Food Preferences - drug effects</subject><subject>Gender</subject><subject>Male</subject><subject>Medical Education</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Obesity</subject><subject>Obesity - etiology</subject><subject>Obesity - physiopathology</subject><subject>Overweight - etiology</subject><subject>Overweight - physiopathology</subject><subject>Perinatal exposure</subject><subject>Phenols - toxicity</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects - chemically induced</subject><subject>Prenatal Exposure Delayed Effects - physiopathology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Saccharin</subject><subject>Sex differences</subject><subject>Sex Factors</subject><subject>Sexual dimorphism</subject><subject>Sucrose</subject><subject>Sweet preference</subject><subject>Sweet taste</subject><subject>Tails</subject><subject>Taste</subject><subject>Toxicology</subject><issn>0892-0362</issn><issn>1872-9738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksuKFDEUQAtRnHb0A9xINuKqy5tU6oUgNI2jwoALdR3yuDWdnuqkTVIz9s7lfIBf6JeYolsFF7oKgXOf5xbFUwolBdq83JYupZIBpSU0JQC7Vyxo17Jl31bd_WIBXc-WUDXsrHgU4xYA2obCw-KM0RZ40_eL4m69ke4KDdkHHDCg00gGH0i8RUwkyZiQWEekmca08d7kj5l05tWB7DFYJ5McCX7d-zgFJMkTZeN-g86PZPXj2_dVTuyVVCOS0brrGfA3GG7RXm0Skc4QrzDadHhcPBjkGPHJ6T0vPl-8-bR-t7z88Pb9enW51HVVpyVH1nbQcNPWKJVBUJJrJfu6GzRonuce1MArKQ0DU0PTt4wxDnxQDXbN0FfnxYtj3tzXlwljEjsbNY6jdOinKLquAsaAw__JtudtX_E6k_RI6uBjzIsU-2B3MhwEBTGbEluRTYnZlIBGZFM55tkp-6R2aH5H_FKTgecnQEYtxyFIp238w3FOc-m5zVdHDvPWbiwGEbWdPRobUCdhvP1nG6__itbZk80Fr_GAceun4LIOQUVkAsTH-aTmi6J0vibOqp919cif</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Xu, Xiaobin</creator><creator>Tan, Luei</creator><creator>Himi, Toshiyuki</creator><creator>Sadamatsu, Miyuki</creator><creator>Tsutsumi, Shunsuke</creator><creator>Akaike, Masashi</creator><creator>Kato, Nobumasa</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>7QR</scope><scope>7ST</scope><scope>7T2</scope><scope>7TK</scope><scope>7TS</scope><scope>7U2</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope></search><sort><creationdate>20110701</creationdate><title>Changed preference for sweet taste in adulthood induced by perinatal exposure to bisphenol A—A probable link to overweight and obesity</title><author>Xu, Xiaobin ; Tan, Luei ; Himi, Toshiyuki ; Sadamatsu, Miyuki ; Tsutsumi, Shunsuke ; Akaike, Masashi ; Kato, Nobumasa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c535t-4e278064d75eabde0ba4cba958fc0c4738fbf43aad20d50697222404fb6e86f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adipose Tissue - drug effects</topic><topic>Animals</topic><topic>Benzhydryl Compounds</topic><topic>Biological and medical sciences</topic><topic>Bisphenol A</topic><topic>Blood pressure</topic><topic>Blood Pressure - drug effects</topic><topic>Body weight</topic><topic>Body Weight - drug effects</topic><topic>Calories</topic><topic>Dietary Sucrose - administration &amp; dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Eating - drug effects</topic><topic>Emergency</topic><topic>Endocrine disruptors</topic><topic>Endocrine Disruptors - toxicity</topic><topic>Environmental disruptors</topic><topic>Female</topic><topic>Food intake</topic><topic>Food Preferences - drug effects</topic><topic>Gender</topic><topic>Male</topic><topic>Medical Education</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Obesity</topic><topic>Obesity - etiology</topic><topic>Obesity - physiopathology</topic><topic>Overweight - etiology</topic><topic>Overweight - physiopathology</topic><topic>Perinatal exposure</topic><topic>Phenols - toxicity</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects - chemically induced</topic><topic>Prenatal Exposure Delayed Effects - physiopathology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Saccharin</topic><topic>Sex differences</topic><topic>Sex Factors</topic><topic>Sexual dimorphism</topic><topic>Sucrose</topic><topic>Sweet preference</topic><topic>Sweet taste</topic><topic>Tails</topic><topic>Taste</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Xiaobin</creatorcontrib><creatorcontrib>Tan, Luei</creatorcontrib><creatorcontrib>Himi, Toshiyuki</creatorcontrib><creatorcontrib>Sadamatsu, Miyuki</creatorcontrib><creatorcontrib>Tsutsumi, Shunsuke</creatorcontrib><creatorcontrib>Akaike, Masashi</creatorcontrib><creatorcontrib>Kato, Nobumasa</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>Chemoreception Abstracts</collection><collection>Environment Abstracts</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Neurotoxicology and teratology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Xiaobin</au><au>Tan, Luei</au><au>Himi, Toshiyuki</au><au>Sadamatsu, Miyuki</au><au>Tsutsumi, Shunsuke</au><au>Akaike, Masashi</au><au>Kato, Nobumasa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changed preference for sweet taste in adulthood induced by perinatal exposure to bisphenol A—A probable link to overweight and obesity</atitle><jtitle>Neurotoxicology and teratology</jtitle><addtitle>Neurotoxicol Teratol</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>33</volume><issue>4</issue><spage>458</spage><epage>463</epage><pages>458-463</pages><issn>0892-0362</issn><eissn>1872-9738</eissn><coden>NETEEC</coden><abstract><![CDATA[Abstract Background The preference of obesity has risen dramatically worldwide over the past decades. Some latest reports showed significant increase of obesity in men compared to women. Implication of environmental endocrine disruptors has been focused more and more. Numerous studies in vitro and vivo implied metabolic actions of bisphenol A (BPA), however much less consideration is given to the possibility of BPA exposure-induced change in gender-specific behaviors which result in obesity and overweight. Objectives To examine whether perinatal exposure to BPA at relative dose to environmental levels can influence sweet preference of male and female rats and consequently lead to alteration in bodyweight. Methods Rats perinatally exposed to BPA at doses of 0.01, 0.1 and 1.0 mg/L were tested sweet preference for 0.25%, 0.5% saccharin and 15% sucrose by two-bottle choice (water vs. saccharin/sucrose). The food intake, liquid consumption and bodyweight of each rat were monitored daily. At the end of the test, the fat percentage and tail blood pressure were measured. Results Significant sex difference of preference for 0.25% and 0.5% saccharin was shown in control and all BPA-treated groups (p < 0.001, female vs. male). 0.1 and 1.0 mg/L BPA treatment induced the increase of preference for 0.25% saccharin solution in males, but not in females. 0.1 mg/L BPA treatment increased sucrose preference in males at postnatal day (PND) 70 and 140 (p < 0.05 and p < 0.001, compared to control respectively) but decreased sucrose preference in females at PND 140 (p < 0.05, compared to control). The males treated by BPA showed overweight (p < 0.001), high fat percentage (p < 0.001) and tail blood pressure (p < 0.05) than control at PND 140. Conclusion Perinatal exposure to a low dose of BPA could increase sweet preference of male rats. Calorie intake may be programmed during early life, leading to changes of body weight depending on the gender. Although further researches concerning the mechanism are required, the results of the present study are particularly important with regards to the more significant increasing prevalence of obesity in men and the environmental endocrine disruptors.]]></abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>21704699</pmid><doi>10.1016/j.ntt.2011.06.002</doi><tpages>6</tpages></addata></record>
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subjects Adipose Tissue - drug effects
Animals
Benzhydryl Compounds
Biological and medical sciences
Bisphenol A
Blood pressure
Blood Pressure - drug effects
Body weight
Body Weight - drug effects
Calories
Dietary Sucrose - administration & dosage
Dose-Response Relationship, Drug
Eating - drug effects
Emergency
Endocrine disruptors
Endocrine Disruptors - toxicity
Environmental disruptors
Female
Food intake
Food Preferences - drug effects
Gender
Male
Medical Education
Medical sciences
Metabolic diseases
Obesity
Obesity - etiology
Obesity - physiopathology
Overweight - etiology
Overweight - physiopathology
Perinatal exposure
Phenols - toxicity
Pregnancy
Prenatal Exposure Delayed Effects - chemically induced
Prenatal Exposure Delayed Effects - physiopathology
Rats
Rats, Sprague-Dawley
Saccharin
Sex differences
Sex Factors
Sexual dimorphism
Sucrose
Sweet preference
Sweet taste
Tails
Taste
Toxicology
title Changed preference for sweet taste in adulthood induced by perinatal exposure to bisphenol A—A probable link to overweight and obesity
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