Ameliorative effect of vitamin E to mouse dams and their pups following exposure of mothers to chlorpyrifos during gestation and lactation periods
Pesticides are omnipresent in environment, water, fruits, and vegetables and are considered as risk factors for human health. Consumers are mainly exposed to pesticides through diet, and the main question to be answered concerns the impact of such exposure on health. In this study, we developed a mo...
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Veröffentlicht in: | Toxicology and industrial health 2016-07, Vol.32 (7), p.1179-1196 |
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description | Pesticides are omnipresent in environment, water, fruits, and vegetables and are considered as risk factors for human health. Consumers are mainly exposed to pesticides through diet, and the main question to be answered concerns the impact of such exposure on health. In this study, we developed a mouse model to mimic consumer exposure. During gestation and lactation periods, the experimental mouse dams (M) received one of the following treatments: (a) diet-free of pesticides; (b) diet enriched with chlorpyrifos (CPF; 44.0 μg kg−1); c) diet + oral vitamin E (vit. E; α-tocopherol; 200 mg/kg/mouse); and (d) diet enriched with CPF (44.0 μg/kg + oral vit. E (200 mg/kg/mouse). At weaning, pups (P) and dams were killed, and organs as well as blood samples were collected. Compared with control results, CPF induced alteration of measured parameters (e.g. organ weight, alkaline phosphatase, urea, malondialdehyde, superoxide dismutase, and cholinesterase) either in mouse dams or in their offspring. Also, CPF induced histological impairment in kidney, liver, and ovary. Administration of vit. E in conjunction with CPF clearly alleviated deviation of these parameters than those of control ones. In conclusion, a dietary exposure of mice during gestation and lactation to low dose of CPF led to significant changes in the mother but also in the weaned animals that have not been directly exposed to this pesticide. These biological and histological modifications could be reversed by an oral supplementation of vit. E. |
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Consumers are mainly exposed to pesticides through diet, and the main question to be answered concerns the impact of such exposure on health. In this study, we developed a mouse model to mimic consumer exposure. During gestation and lactation periods, the experimental mouse dams (M) received one of the following treatments: (a) diet-free of pesticides; (b) diet enriched with chlorpyrifos (CPF; 44.0 μg kg−1); c) diet + oral vitamin E (vit. E; α-tocopherol; 200 mg/kg/mouse); and (d) diet enriched with CPF (44.0 μg/kg + oral vit. E (200 mg/kg/mouse). At weaning, pups (P) and dams were killed, and organs as well as blood samples were collected. Compared with control results, CPF induced alteration of measured parameters (e.g. organ weight, alkaline phosphatase, urea, malondialdehyde, superoxide dismutase, and cholinesterase) either in mouse dams or in their offspring. Also, CPF induced histological impairment in kidney, liver, and ovary. Administration of vit. E in conjunction with CPF clearly alleviated deviation of these parameters than those of control ones. In conclusion, a dietary exposure of mice during gestation and lactation to low dose of CPF led to significant changes in the mother but also in the weaned animals that have not been directly exposed to this pesticide. These biological and histological modifications could be reversed by an oral supplementation of vit. E.</description><identifier>ISSN: 0748-2337</identifier><identifier>EISSN: 1477-0393</identifier><identifier>DOI: 10.1177/0748233714548207</identifier><identifier>PMID: 25234640</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Alkaline Phosphatase - blood ; alpha-Tocopherol - pharmacology ; Animals ; Chlorpyrifos ; Chlorpyrifos - toxicity ; Cholinesterase Inhibitors - toxicity ; Cholinesterases - blood ; Dams ; Diet ; Diets ; Dose-Response Relationship, Drug ; Enrichment ; Exposure ; Female ; Gestation ; Health ; Insecticides - toxicity ; Kidney - drug effects ; Kidney - metabolism ; Lactation ; Life Sciences ; Liver - drug effects ; Liver - metabolism ; Male ; Malondialdehyde - blood ; Maternal Exposure ; Mice ; Mice, Inbred C57BL ; No-Observed-Adverse-Effect Level ; Organ Size - drug effects ; Ovary - drug effects ; Ovary - metabolism ; Pesticides ; Superoxide Dismutase - blood ; Urea - blood ; Weaning ; Xenobiotics - toxicity</subject><ispartof>Toxicology and industrial health, 2016-07, Vol.32 (7), p.1179-1196</ispartof><rights>The Author(s) 2014</rights><rights>The Author(s) 2014.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-d56d63e37cd6e5a05b7d4d98e408a01ad80c3b3b005f301854bb8d3377627a843</citedby><cites>FETCH-LOGICAL-c437t-d56d63e37cd6e5a05b7d4d98e408a01ad80c3b3b005f301854bb8d3377627a843</cites><orcidid>0000-0003-1681-8491</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0748233714548207$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0748233714548207$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,776,780,881,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25234640$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02630364$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Mansour, Sameeh Abdel-Kader</creatorcontrib><creatorcontrib>Gamet-Payrastre, Laurence</creatorcontrib><title>Ameliorative effect of vitamin E to mouse dams and their pups following exposure of mothers to chlorpyrifos during gestation and lactation periods</title><title>Toxicology and industrial health</title><addtitle>Toxicol Ind Health</addtitle><description>Pesticides are omnipresent in environment, water, fruits, and vegetables and are considered as risk factors for human health. Consumers are mainly exposed to pesticides through diet, and the main question to be answered concerns the impact of such exposure on health. In this study, we developed a mouse model to mimic consumer exposure. During gestation and lactation periods, the experimental mouse dams (M) received one of the following treatments: (a) diet-free of pesticides; (b) diet enriched with chlorpyrifos (CPF; 44.0 μg kg−1); c) diet + oral vitamin E (vit. E; α-tocopherol; 200 mg/kg/mouse); and (d) diet enriched with CPF (44.0 μg/kg + oral vit. E (200 mg/kg/mouse). At weaning, pups (P) and dams were killed, and organs as well as blood samples were collected. Compared with control results, CPF induced alteration of measured parameters (e.g. organ weight, alkaline phosphatase, urea, malondialdehyde, superoxide dismutase, and cholinesterase) either in mouse dams or in their offspring. Also, CPF induced histological impairment in kidney, liver, and ovary. Administration of vit. E in conjunction with CPF clearly alleviated deviation of these parameters than those of control ones. In conclusion, a dietary exposure of mice during gestation and lactation to low dose of CPF led to significant changes in the mother but also in the weaned animals that have not been directly exposed to this pesticide. These biological and histological modifications could be reversed by an oral supplementation of vit. E.</description><subject>Alkaline Phosphatase - blood</subject><subject>alpha-Tocopherol - pharmacology</subject><subject>Animals</subject><subject>Chlorpyrifos</subject><subject>Chlorpyrifos - toxicity</subject><subject>Cholinesterase Inhibitors - toxicity</subject><subject>Cholinesterases - blood</subject><subject>Dams</subject><subject>Diet</subject><subject>Diets</subject><subject>Dose-Response Relationship, Drug</subject><subject>Enrichment</subject><subject>Exposure</subject><subject>Female</subject><subject>Gestation</subject><subject>Health</subject><subject>Insecticides - toxicity</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Lactation</subject><subject>Life Sciences</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Malondialdehyde - blood</subject><subject>Maternal Exposure</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>No-Observed-Adverse-Effect Level</subject><subject>Organ Size - drug effects</subject><subject>Ovary - drug effects</subject><subject>Ovary - metabolism</subject><subject>Pesticides</subject><subject>Superoxide Dismutase - blood</subject><subject>Urea - blood</subject><subject>Weaning</subject><subject>Xenobiotics - toxicity</subject><issn>0748-2337</issn><issn>1477-0393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhi0Eokvhzgn5CIfAOP7scVUVirQSFzhbTjzZdZXEwU6W9m_wi3HYpQckJE7-mOd9Z_QOIa8ZvGdM6w-ghak510zIcgH9hGyY0LoCfsWfks1artb6BXmR8x0AKCXr5-SiljUXSsCG_NwO2IeY3ByOSLHrsJ1p7OgxzG4II72hc6RDXDJS74ZM3ejpfMCQ6LRMmXax7-OPMO4p3k8xLwlX8RALkvIqbQ99TNNDCl3M1C9pRfeY59Ivjr_deteeXxOmEH1-SZ51rs_46nxekm8fb75e31a7L58-X293VSu4nisvlVccuW69QulANtoLf2VQgHHAnDfQ8oY3ALLjwIwUTWN8CUOrWjsj-CV5d_I9uN5OKQwuPdjogr3d7uz6B7XiwJU4ssK-PbFTit-XMr8dQm6x792IJRzLTC0lFwbUf6BglFidCwontE0x54Td4xgM7Lpg-_eCi-TN2X1pBvSPgj8bLUB1ArLbo72LSxpLiP82_AUBoq5S</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Mansour, Sameeh Abdel-Kader</creator><creator>Gamet-Payrastre, Laurence</creator><general>SAGE Publications</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>7T2</scope><scope>7U2</scope><scope>7U7</scope><scope>C1K</scope><scope>7TA</scope><scope>7TB</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-1681-8491</orcidid></search><sort><creationdate>20160701</creationdate><title>Ameliorative effect of vitamin E to mouse dams and their pups following exposure of mothers to chlorpyrifos during gestation and lactation periods</title><author>Mansour, Sameeh Abdel-Kader ; Gamet-Payrastre, Laurence</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-d56d63e37cd6e5a05b7d4d98e408a01ad80c3b3b005f301854bb8d3377627a843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Alkaline Phosphatase - blood</topic><topic>alpha-Tocopherol - pharmacology</topic><topic>Animals</topic><topic>Chlorpyrifos</topic><topic>Chlorpyrifos - toxicity</topic><topic>Cholinesterase Inhibitors - toxicity</topic><topic>Cholinesterases - blood</topic><topic>Dams</topic><topic>Diet</topic><topic>Diets</topic><topic>Dose-Response Relationship, Drug</topic><topic>Enrichment</topic><topic>Exposure</topic><topic>Female</topic><topic>Gestation</topic><topic>Health</topic><topic>Insecticides - toxicity</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Lactation</topic><topic>Life Sciences</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Malondialdehyde - blood</topic><topic>Maternal Exposure</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>No-Observed-Adverse-Effect Level</topic><topic>Organ Size - drug effects</topic><topic>Ovary - drug effects</topic><topic>Ovary - metabolism</topic><topic>Pesticides</topic><topic>Superoxide Dismutase - blood</topic><topic>Urea - blood</topic><topic>Weaning</topic><topic>Xenobiotics - toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mansour, Sameeh Abdel-Kader</creatorcontrib><creatorcontrib>Gamet-Payrastre, Laurence</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Toxicology and industrial health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mansour, Sameeh Abdel-Kader</au><au>Gamet-Payrastre, Laurence</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ameliorative effect of vitamin E to mouse dams and their pups following exposure of mothers to chlorpyrifos during gestation and lactation periods</atitle><jtitle>Toxicology and industrial health</jtitle><addtitle>Toxicol Ind Health</addtitle><date>2016-07-01</date><risdate>2016</risdate><volume>32</volume><issue>7</issue><spage>1179</spage><epage>1196</epage><pages>1179-1196</pages><issn>0748-2337</issn><eissn>1477-0393</eissn><abstract>Pesticides are omnipresent in environment, water, fruits, and vegetables and are considered as risk factors for human health. Consumers are mainly exposed to pesticides through diet, and the main question to be answered concerns the impact of such exposure on health. In this study, we developed a mouse model to mimic consumer exposure. During gestation and lactation periods, the experimental mouse dams (M) received one of the following treatments: (a) diet-free of pesticides; (b) diet enriched with chlorpyrifos (CPF; 44.0 μg kg−1); c) diet + oral vitamin E (vit. E; α-tocopherol; 200 mg/kg/mouse); and (d) diet enriched with CPF (44.0 μg/kg + oral vit. E (200 mg/kg/mouse). At weaning, pups (P) and dams were killed, and organs as well as blood samples were collected. Compared with control results, CPF induced alteration of measured parameters (e.g. organ weight, alkaline phosphatase, urea, malondialdehyde, superoxide dismutase, and cholinesterase) either in mouse dams or in their offspring. Also, CPF induced histological impairment in kidney, liver, and ovary. Administration of vit. E in conjunction with CPF clearly alleviated deviation of these parameters than those of control ones. In conclusion, a dietary exposure of mice during gestation and lactation to low dose of CPF led to significant changes in the mother but also in the weaned animals that have not been directly exposed to this pesticide. These biological and histological modifications could be reversed by an oral supplementation of vit. E.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>25234640</pmid><doi>10.1177/0748233714548207</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-1681-8491</orcidid></addata></record> |
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subjects | Alkaline Phosphatase - blood alpha-Tocopherol - pharmacology Animals Chlorpyrifos Chlorpyrifos - toxicity Cholinesterase Inhibitors - toxicity Cholinesterases - blood Dams Diet Diets Dose-Response Relationship, Drug Enrichment Exposure Female Gestation Health Insecticides - toxicity Kidney - drug effects Kidney - metabolism Lactation Life Sciences Liver - drug effects Liver - metabolism Male Malondialdehyde - blood Maternal Exposure Mice Mice, Inbred C57BL No-Observed-Adverse-Effect Level Organ Size - drug effects Ovary - drug effects Ovary - metabolism Pesticides Superoxide Dismutase - blood Urea - blood Weaning Xenobiotics - toxicity |
title | Ameliorative effect of vitamin E to mouse dams and their pups following exposure of mothers to chlorpyrifos during gestation and lactation periods |
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