Identification of Drosophila-based endpoints for the assessment and understanding of xenobiotic-mediated male reproductive adversities
Men are at risk of becoming completely infertile due to innumerable environmental chemicals and pollutants. These xenobiotics, hence, should be tested for their potential adverse effects on male fertility. However, the testing load, a monumental challenge for employing conventional animal models, co...
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Veröffentlicht in: | Toxicological sciences 2014-09, Vol.141 (1), p.278-291 |
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creator | Misra, Snigdha Singh, Anshuman C H, Ratnasekhar Sharma, Vandana Reddy Mudiam, Mohana Krishna Ram, Kristipati Ravi |
description | Men are at risk of becoming completely infertile due to innumerable environmental chemicals and pollutants. These xenobiotics, hence, should be tested for their potential adverse effects on male fertility. However, the testing load, a monumental challenge for employing conventional animal models, compels the pursuit of alternative models. Towards this direction, we show here that Drosophila melanogaster, an invertebrate, with its well characterized/conserved male reproductive processes/proteome, recapitulates male reproductive toxicity phenotypes observed in mammals when exposed to a known reproductive toxicant, dibutyl phthalate (DBP). Analogous to mammals, exposure to DBP reduced fertility, sperm counts, seminal proteins, increased oxidative modification/damage in reproductive tract proteins and altered the activity of a hormone receptor (estrogen related receptor) in Drosophila males. In addition, we show here that DBP is metabolized to monobutyl phthalate (MBP) in exposed Drosophila males and that MBP is more toxic than DBP, as observed in higher organisms. These findings suggest Drosophila as a potential alternative to traditional animal models for the prescreening of chemicals for their reproductive adversities and also to gain mechanistic insights into chemical-mediated endocrine disruption and male infertility. |
doi_str_mv | 10.1093/toxsci/kfu125 |
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These xenobiotics, hence, should be tested for their potential adverse effects on male fertility. However, the testing load, a monumental challenge for employing conventional animal models, compels the pursuit of alternative models. Towards this direction, we show here that Drosophila melanogaster, an invertebrate, with its well characterized/conserved male reproductive processes/proteome, recapitulates male reproductive toxicity phenotypes observed in mammals when exposed to a known reproductive toxicant, dibutyl phthalate (DBP). Analogous to mammals, exposure to DBP reduced fertility, sperm counts, seminal proteins, increased oxidative modification/damage in reproductive tract proteins and altered the activity of a hormone receptor (estrogen related receptor) in Drosophila males. In addition, we show here that DBP is metabolized to monobutyl phthalate (MBP) in exposed Drosophila males and that MBP is more toxic than DBP, as observed in higher organisms. These findings suggest Drosophila as a potential alternative to traditional animal models for the prescreening of chemicals for their reproductive adversities and also to gain mechanistic insights into chemical-mediated endocrine disruption and male infertility.</description><identifier>ISSN: 1096-6080</identifier><identifier>EISSN: 1096-0929</identifier><identifier>DOI: 10.1093/toxsci/kfu125</identifier><identifier>PMID: 24973093</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animals ; Dibutyl Phthalate - pharmacokinetics ; Dibutyl Phthalate - toxicity ; Drosophila melanogaster - drug effects ; Drosophila melanogaster - growth & development ; Drosophila melanogaster - metabolism ; Environmental Pollutants - pharmacokinetics ; Environmental Pollutants - toxicity ; Fertility - drug effects ; Fertility - genetics ; Infertility, Male - chemically induced ; Infertility, Male - genetics ; Infertility, Male - pathology ; Male ; Microscopy, Confocal ; Modeling Male Reproductive Toxicity in Flies ; Phthalic Acids - pharmacokinetics ; Phthalic Acids - toxicity ; Reproduction - drug effects ; Reproduction - genetics ; Sperm Count ; Spermatozoa - drug effects ; Spermatozoa - metabolism ; Spermatozoa - pathology ; Transcriptome - drug effects ; Xenobiotics - pharmacokinetics ; Xenobiotics - toxicity</subject><ispartof>Toxicological sciences, 2014-09, Vol.141 (1), p.278-291</ispartof><rights>The Author 2014. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><rights>The Author 2014. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please email: 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-9335bf5a1a983b358fec27f9b8661572778a3d04332b7fbf0a474a48311634d53</citedby><cites>FETCH-LOGICAL-c387t-9335bf5a1a983b358fec27f9b8661572778a3d04332b7fbf0a474a48311634d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,778,782,883,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24973093$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Misra, Snigdha</creatorcontrib><creatorcontrib>Singh, Anshuman</creatorcontrib><creatorcontrib>C H, Ratnasekhar</creatorcontrib><creatorcontrib>Sharma, Vandana</creatorcontrib><creatorcontrib>Reddy Mudiam, Mohana Krishna</creatorcontrib><creatorcontrib>Ram, Kristipati Ravi</creatorcontrib><title>Identification of Drosophila-based endpoints for the assessment and understanding of xenobiotic-mediated male reproductive adversities</title><title>Toxicological sciences</title><addtitle>Toxicol Sci</addtitle><description>Men are at risk of becoming completely infertile due to innumerable environmental chemicals and pollutants. These xenobiotics, hence, should be tested for their potential adverse effects on male fertility. However, the testing load, a monumental challenge for employing conventional animal models, compels the pursuit of alternative models. Towards this direction, we show here that Drosophila melanogaster, an invertebrate, with its well characterized/conserved male reproductive processes/proteome, recapitulates male reproductive toxicity phenotypes observed in mammals when exposed to a known reproductive toxicant, dibutyl phthalate (DBP). Analogous to mammals, exposure to DBP reduced fertility, sperm counts, seminal proteins, increased oxidative modification/damage in reproductive tract proteins and altered the activity of a hormone receptor (estrogen related receptor) in Drosophila males. In addition, we show here that DBP is metabolized to monobutyl phthalate (MBP) in exposed Drosophila males and that MBP is more toxic than DBP, as observed in higher organisms. These findings suggest Drosophila as a potential alternative to traditional animal models for the prescreening of chemicals for their reproductive adversities and also to gain mechanistic insights into chemical-mediated endocrine disruption and male infertility.</description><subject>Animals</subject><subject>Dibutyl Phthalate - pharmacokinetics</subject><subject>Dibutyl Phthalate - toxicity</subject><subject>Drosophila melanogaster - drug effects</subject><subject>Drosophila melanogaster - growth & development</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Environmental Pollutants - pharmacokinetics</subject><subject>Environmental Pollutants - toxicity</subject><subject>Fertility - drug effects</subject><subject>Fertility - genetics</subject><subject>Infertility, Male - chemically induced</subject><subject>Infertility, Male - genetics</subject><subject>Infertility, Male - pathology</subject><subject>Male</subject><subject>Microscopy, Confocal</subject><subject>Modeling Male Reproductive Toxicity in Flies</subject><subject>Phthalic Acids - pharmacokinetics</subject><subject>Phthalic Acids - toxicity</subject><subject>Reproduction - drug effects</subject><subject>Reproduction - genetics</subject><subject>Sperm Count</subject><subject>Spermatozoa - drug effects</subject><subject>Spermatozoa - metabolism</subject><subject>Spermatozoa - pathology</subject><subject>Transcriptome - drug effects</subject><subject>Xenobiotics - pharmacokinetics</subject><subject>Xenobiotics - toxicity</subject><issn>1096-6080</issn><issn>1096-0929</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkctOwzAQRS0EoqWwZIv8A6F2nOcGCZVXpUpsYB352RoSO7KdqvwA342rlApWHnnuPfbMBeAao1uMajIPdue5nn-qAaf5CZjGyyJBdVqfHuoCVWgCLrz_QAjjAtXnYJJmdUmiewq-l0KaoJXmNGhroFXwwVlv-41uacKolwJKI3qrTfBQWQfDRkLqvfS-i05IjYCDEdL5EEtt1nvEThrLtA2aJ50UmoZI6WgroZO9s2LgQW8jRWyjTQct_SU4U7T18upwzsD70-Pb4iVZvT4vF_erhJOqDElNSM5UTjGtK8JIXinJ01LVrCoKnJdpWVaUCJQRkrJSMYVoVmY0q0gcnGQiJzNwN3L7gcWf8TiBo23TO91R99VYqpv_HaM3zdpum8iIEBwByQjgcUveSXX0YtTsA2nGQJoxkKi_-fvgUf2bAPkB7XmOWA</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Misra, Snigdha</creator><creator>Singh, Anshuman</creator><creator>C H, Ratnasekhar</creator><creator>Sharma, Vandana</creator><creator>Reddy Mudiam, Mohana Krishna</creator><creator>Ram, Kristipati Ravi</creator><general>Oxford University Press</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>5PM</scope></search><sort><creationdate>20140901</creationdate><title>Identification of Drosophila-based endpoints for the assessment and understanding of xenobiotic-mediated male reproductive adversities</title><author>Misra, Snigdha ; Singh, Anshuman ; C H, Ratnasekhar ; Sharma, Vandana ; Reddy Mudiam, Mohana Krishna ; Ram, Kristipati Ravi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-9335bf5a1a983b358fec27f9b8661572778a3d04332b7fbf0a474a48311634d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Dibutyl Phthalate - pharmacokinetics</topic><topic>Dibutyl Phthalate - toxicity</topic><topic>Drosophila melanogaster - drug effects</topic><topic>Drosophila melanogaster - growth & development</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Environmental Pollutants - pharmacokinetics</topic><topic>Environmental Pollutants - toxicity</topic><topic>Fertility - drug effects</topic><topic>Fertility - genetics</topic><topic>Infertility, Male - chemically induced</topic><topic>Infertility, Male - genetics</topic><topic>Infertility, Male - pathology</topic><topic>Male</topic><topic>Microscopy, Confocal</topic><topic>Modeling Male Reproductive Toxicity in Flies</topic><topic>Phthalic Acids - pharmacokinetics</topic><topic>Phthalic Acids - toxicity</topic><topic>Reproduction - drug effects</topic><topic>Reproduction - genetics</topic><topic>Sperm Count</topic><topic>Spermatozoa - drug effects</topic><topic>Spermatozoa - metabolism</topic><topic>Spermatozoa - pathology</topic><topic>Transcriptome - drug effects</topic><topic>Xenobiotics - pharmacokinetics</topic><topic>Xenobiotics - toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Misra, Snigdha</creatorcontrib><creatorcontrib>Singh, Anshuman</creatorcontrib><creatorcontrib>C H, Ratnasekhar</creatorcontrib><creatorcontrib>Sharma, Vandana</creatorcontrib><creatorcontrib>Reddy Mudiam, Mohana Krishna</creatorcontrib><creatorcontrib>Ram, Kristipati Ravi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Toxicological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Misra, Snigdha</au><au>Singh, Anshuman</au><au>C H, Ratnasekhar</au><au>Sharma, Vandana</au><au>Reddy Mudiam, Mohana Krishna</au><au>Ram, Kristipati Ravi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of Drosophila-based endpoints for the assessment and understanding of xenobiotic-mediated male reproductive adversities</atitle><jtitle>Toxicological sciences</jtitle><addtitle>Toxicol Sci</addtitle><date>2014-09-01</date><risdate>2014</risdate><volume>141</volume><issue>1</issue><spage>278</spage><epage>291</epage><pages>278-291</pages><issn>1096-6080</issn><eissn>1096-0929</eissn><abstract>Men are at risk of becoming completely infertile due to innumerable environmental chemicals and pollutants. These xenobiotics, hence, should be tested for their potential adverse effects on male fertility. However, the testing load, a monumental challenge for employing conventional animal models, compels the pursuit of alternative models. Towards this direction, we show here that Drosophila melanogaster, an invertebrate, with its well characterized/conserved male reproductive processes/proteome, recapitulates male reproductive toxicity phenotypes observed in mammals when exposed to a known reproductive toxicant, dibutyl phthalate (DBP). Analogous to mammals, exposure to DBP reduced fertility, sperm counts, seminal proteins, increased oxidative modification/damage in reproductive tract proteins and altered the activity of a hormone receptor (estrogen related receptor) in Drosophila males. In addition, we show here that DBP is metabolized to monobutyl phthalate (MBP) in exposed Drosophila males and that MBP is more toxic than DBP, as observed in higher organisms. These findings suggest Drosophila as a potential alternative to traditional animal models for the prescreening of chemicals for their reproductive adversities and also to gain mechanistic insights into chemical-mediated endocrine disruption and male infertility.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>24973093</pmid><doi>10.1093/toxsci/kfu125</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Dibutyl Phthalate - pharmacokinetics Dibutyl Phthalate - toxicity Drosophila melanogaster - drug effects Drosophila melanogaster - growth & development Drosophila melanogaster - metabolism Environmental Pollutants - pharmacokinetics Environmental Pollutants - toxicity Fertility - drug effects Fertility - genetics Infertility, Male - chemically induced Infertility, Male - genetics Infertility, Male - pathology Male Microscopy, Confocal Modeling Male Reproductive Toxicity in Flies Phthalic Acids - pharmacokinetics Phthalic Acids - toxicity Reproduction - drug effects Reproduction - genetics Sperm Count Spermatozoa - drug effects Spermatozoa - metabolism Spermatozoa - pathology Transcriptome - drug effects Xenobiotics - pharmacokinetics Xenobiotics - toxicity |
title | Identification of Drosophila-based endpoints for the assessment and understanding of xenobiotic-mediated male reproductive adversities |
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