Low-Dose Effects of Ammonium Perchlorate on the Hypothalamic-Pituitary-Thyroid Axis of Adult Male Rats Pretreated with PCB126
The objective of this research was to characterize the disturbances in the hypothalamic-pituitary-thyroid (HPT) axis resulting from exposure to a binary mixture, 3,3′,4,4′,5-pentachlorobiphenyl (PCB126) and perchlorate (ClO4−), known to cause hypothyroidism by different modes of action. Two studies...
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creator | McLanahan, Eva D. Campbell, Jerry L. Ferguson, Duncan C. Harmon, Barry Hedge, Joan M. Crofton, Kevin M. Mattie, David R. Braverman, Lewis Keys, Deborah A. Mumtaz, Moiz Fisher, Jeffrey W. |
description | The objective of this research was to characterize the disturbances in the hypothalamic-pituitary-thyroid (HPT) axis resulting from exposure to a binary mixture, 3,3′,4,4′,5-pentachlorobiphenyl (PCB126) and perchlorate (ClO4−), known to cause hypothyroidism by different modes of action. Two studies were conducted to determine the HPT axis effects of ClO4− on adult male Sprague-Dawley rats pretreated with PCB126. In dosing study I, rats were administered a single oral dose of PCB126 (0, 7.5, or 75 μg/kg) on day 0 and 9 days later ClO4− (0, 0.01, 0.1, or 1 mg/kg day) was added to the drinking water until euthanasia on day 22. Significant dose-dependent trends were found for all thyroid function indices measured following ClO4− in drinking water for 14 days. Seventy-five micrograms PCB126/kg resulted in a significant increase in hepatic T4-glucuronide formation, causing a decline in serum thyroxine and fT4, and resulting in increased serum thyroid-stimulating hormone (TSH). Serum TSH was also increased in animals that received 7.5 μg PCB126/kg; no other HPT axis alterations were found in these animals. When pretreated with PCB126, the ClO4− dose trends disappeared, suggesting a less than additive effect on the HPT axis. In dosing study II, animals were given lower doses of PCB126 (0, 0.075, 0.75, or 7.5 μg/kg) on day 0, and followed with ClO4− (0 or 0.01 mg/kg day) in drinking water beginning on day 1 and continuing for several days to explore transient HPT axis effects. No statistical effects were seen for PCB126 or ClO4− alone, and no perturbations were found when administered sequentially in dosing study II. In conclusion, these studies demonstrate that HPT axis disturbances following exposure to ClO4− are less than additive when pretreated with relatively high doses of PCB126. At relatively low doses, at or near the no-observed-effect-level for PCB126 and ClO4−, no interactions between the chemicals occur. |
doi_str_mv | 10.1093/toxsci/kfm063 |
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Two studies were conducted to determine the HPT axis effects of ClO4− on adult male Sprague-Dawley rats pretreated with PCB126. In dosing study I, rats were administered a single oral dose of PCB126 (0, 7.5, or 75 μg/kg) on day 0 and 9 days later ClO4− (0, 0.01, 0.1, or 1 mg/kg day) was added to the drinking water until euthanasia on day 22. Significant dose-dependent trends were found for all thyroid function indices measured following ClO4− in drinking water for 14 days. Seventy-five micrograms PCB126/kg resulted in a significant increase in hepatic T4-glucuronide formation, causing a decline in serum thyroxine and fT4, and resulting in increased serum thyroid-stimulating hormone (TSH). Serum TSH was also increased in animals that received 7.5 μg PCB126/kg; no other HPT axis alterations were found in these animals. When pretreated with PCB126, the ClO4− dose trends disappeared, suggesting a less than additive effect on the HPT axis. In dosing study II, animals were given lower doses of PCB126 (0, 0.075, 0.75, or 7.5 μg/kg) on day 0, and followed with ClO4− (0 or 0.01 mg/kg day) in drinking water beginning on day 1 and continuing for several days to explore transient HPT axis effects. No statistical effects were seen for PCB126 or ClO4− alone, and no perturbations were found when administered sequentially in dosing study II. In conclusion, these studies demonstrate that HPT axis disturbances following exposure to ClO4− are less than additive when pretreated with relatively high doses of PCB126. At relatively low doses, at or near the no-observed-effect-level for PCB126 and ClO4−, no interactions between the chemicals occur.</description><identifier>ISSN: 1096-6080</identifier><identifier>EISSN: 1096-0929</identifier><identifier>DOI: 10.1093/toxsci/kfm063</identifier><identifier>PMID: 17379623</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animals ; Body Weight - drug effects ; Dose-Response Relationship, Drug ; Drug Interactions ; Hormones - blood ; Hypothalamo-Hypophyseal System - drug effects ; Iodides - metabolism ; Liver - drug effects ; Liver - enzymology ; Male ; Organ Size - drug effects ; PCB126 ; perchlorate ; Perchlorates - toxicity ; Polychlorinated Biphenyls - toxicity ; Quaternary Ammonium Compounds - toxicity ; rat ; Rats ; Rats, Sprague-Dawley ; Symporters - biosynthesis ; Symporters - physiology ; thyroid ; Thyroid Gland - drug effects ; Thyroid Gland - metabolism ; Thyroid Gland - pathology ; Thyrotropin - blood ; TSH ; UDPGT</subject><ispartof>Toxicological sciences, 2007-06, Vol.97 (2), p.308-317</ispartof><rights>The Author 2007. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-840d47fafdf2246a6de870e7ad61909361f5b0f44d45ed9518ac884e58dff1d23</citedby><cites>FETCH-LOGICAL-c393t-840d47fafdf2246a6de870e7ad61909361f5b0f44d45ed9518ac884e58dff1d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17379623$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McLanahan, Eva D.</creatorcontrib><creatorcontrib>Campbell, Jerry L.</creatorcontrib><creatorcontrib>Ferguson, Duncan C.</creatorcontrib><creatorcontrib>Harmon, Barry</creatorcontrib><creatorcontrib>Hedge, Joan M.</creatorcontrib><creatorcontrib>Crofton, Kevin M.</creatorcontrib><creatorcontrib>Mattie, David R.</creatorcontrib><creatorcontrib>Braverman, Lewis</creatorcontrib><creatorcontrib>Keys, Deborah A.</creatorcontrib><creatorcontrib>Mumtaz, Moiz</creatorcontrib><creatorcontrib>Fisher, Jeffrey W.</creatorcontrib><title>Low-Dose Effects of Ammonium Perchlorate on the Hypothalamic-Pituitary-Thyroid Axis of Adult Male Rats Pretreated with PCB126</title><title>Toxicological sciences</title><addtitle>Toxicol Sci</addtitle><description>The objective of this research was to characterize the disturbances in the hypothalamic-pituitary-thyroid (HPT) axis resulting from exposure to a binary mixture, 3,3′,4,4′,5-pentachlorobiphenyl (PCB126) and perchlorate (ClO4−), known to cause hypothyroidism by different modes of action. Two studies were conducted to determine the HPT axis effects of ClO4− on adult male Sprague-Dawley rats pretreated with PCB126. In dosing study I, rats were administered a single oral dose of PCB126 (0, 7.5, or 75 μg/kg) on day 0 and 9 days later ClO4− (0, 0.01, 0.1, or 1 mg/kg day) was added to the drinking water until euthanasia on day 22. Significant dose-dependent trends were found for all thyroid function indices measured following ClO4− in drinking water for 14 days. Seventy-five micrograms PCB126/kg resulted in a significant increase in hepatic T4-glucuronide formation, causing a decline in serum thyroxine and fT4, and resulting in increased serum thyroid-stimulating hormone (TSH). Serum TSH was also increased in animals that received 7.5 μg PCB126/kg; no other HPT axis alterations were found in these animals. When pretreated with PCB126, the ClO4− dose trends disappeared, suggesting a less than additive effect on the HPT axis. In dosing study II, animals were given lower doses of PCB126 (0, 0.075, 0.75, or 7.5 μg/kg) on day 0, and followed with ClO4− (0 or 0.01 mg/kg day) in drinking water beginning on day 1 and continuing for several days to explore transient HPT axis effects. No statistical effects were seen for PCB126 or ClO4− alone, and no perturbations were found when administered sequentially in dosing study II. In conclusion, these studies demonstrate that HPT axis disturbances following exposure to ClO4− are less than additive when pretreated with relatively high doses of PCB126. At relatively low doses, at or near the no-observed-effect-level for PCB126 and ClO4−, no interactions between the chemicals occur.</description><subject>Animals</subject><subject>Body Weight - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Interactions</subject><subject>Hormones - blood</subject><subject>Hypothalamo-Hypophyseal System - drug effects</subject><subject>Iodides - metabolism</subject><subject>Liver - drug effects</subject><subject>Liver - enzymology</subject><subject>Male</subject><subject>Organ Size - drug effects</subject><subject>PCB126</subject><subject>perchlorate</subject><subject>Perchlorates - toxicity</subject><subject>Polychlorinated Biphenyls - toxicity</subject><subject>Quaternary Ammonium Compounds - toxicity</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Symporters - biosynthesis</subject><subject>Symporters - physiology</subject><subject>thyroid</subject><subject>Thyroid Gland - drug effects</subject><subject>Thyroid Gland - metabolism</subject><subject>Thyroid Gland - pathology</subject><subject>Thyrotropin - blood</subject><subject>TSH</subject><subject>UDPGT</subject><issn>1096-6080</issn><issn>1096-0929</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1P3DAQQK2qiI8tx14rnyouATsfTnxctsBWWiBtt1LVi2XiseKSrLe2I3YP_PcaJaJHTh5ZT280D6GPlJxTwrOLYHe-MRePuicse4eO4ydLCE_5-2lmpCJH6MT7P4RQygg_REe0zErO0uwYPa_sU_LFesBXWkMTPLYaz_vebszQ4xpc03bWyQDYbnBoAS_3Wxta2cneNEltwmCCdPtk3e6dNQrPd2ZUqKEL-FZ2gL_LaK0dBAfRo_CTCS2uF5c0ZR_QgZadh9PpnaGf11frxTJZ3d98XcxXSZPxLCRVTlReaqmVTtOcSaagKgmUUjHKYwRGdfFAdJ6rvADFC1rJpqpyKCqlNVVpNkOfR-_W2b8D-CB64xvoOrkBO3hBOWM8jbtmKBnBxlnvHWixdaaPBwpKxEtvMfYWY-_If5rEw0MP6j89BY7A2QjYYfuma9ptfIDdKyzdo2BRV4jlr99iXZNvd8vbS_Ej-wdkApwB</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>McLanahan, Eva D.</creator><creator>Campbell, Jerry L.</creator><creator>Ferguson, Duncan C.</creator><creator>Harmon, Barry</creator><creator>Hedge, Joan M.</creator><creator>Crofton, Kevin M.</creator><creator>Mattie, David R.</creator><creator>Braverman, Lewis</creator><creator>Keys, Deborah A.</creator><creator>Mumtaz, Moiz</creator><creator>Fisher, Jeffrey W.</creator><general>Oxford University Press</general><scope>BSCLL</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>7TK</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20070601</creationdate><title>Low-Dose Effects of Ammonium Perchlorate on the Hypothalamic-Pituitary-Thyroid Axis of Adult Male Rats Pretreated with PCB126</title><author>McLanahan, Eva D. ; Campbell, Jerry L. ; Ferguson, Duncan C. ; Harmon, Barry ; Hedge, Joan M. ; Crofton, Kevin M. ; Mattie, David R. ; Braverman, Lewis ; Keys, Deborah A. ; Mumtaz, Moiz ; Fisher, Jeffrey W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-840d47fafdf2246a6de870e7ad61909361f5b0f44d45ed9518ac884e58dff1d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Body Weight - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Interactions</topic><topic>Hormones - blood</topic><topic>Hypothalamo-Hypophyseal System - drug effects</topic><topic>Iodides - metabolism</topic><topic>Liver - drug effects</topic><topic>Liver - enzymology</topic><topic>Male</topic><topic>Organ Size - drug effects</topic><topic>PCB126</topic><topic>perchlorate</topic><topic>Perchlorates - toxicity</topic><topic>Polychlorinated Biphenyls - toxicity</topic><topic>Quaternary Ammonium Compounds - toxicity</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Symporters - biosynthesis</topic><topic>Symporters - physiology</topic><topic>thyroid</topic><topic>Thyroid Gland - drug effects</topic><topic>Thyroid Gland - metabolism</topic><topic>Thyroid Gland - pathology</topic><topic>Thyrotropin - blood</topic><topic>TSH</topic><topic>UDPGT</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McLanahan, Eva D.</creatorcontrib><creatorcontrib>Campbell, Jerry L.</creatorcontrib><creatorcontrib>Ferguson, Duncan C.</creatorcontrib><creatorcontrib>Harmon, Barry</creatorcontrib><creatorcontrib>Hedge, Joan M.</creatorcontrib><creatorcontrib>Crofton, Kevin M.</creatorcontrib><creatorcontrib>Mattie, David R.</creatorcontrib><creatorcontrib>Braverman, Lewis</creatorcontrib><creatorcontrib>Keys, Deborah A.</creatorcontrib><creatorcontrib>Mumtaz, Moiz</creatorcontrib><creatorcontrib>Fisher, Jeffrey W.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McLanahan, Eva D.</au><au>Campbell, Jerry L.</au><au>Ferguson, Duncan C.</au><au>Harmon, Barry</au><au>Hedge, Joan M.</au><au>Crofton, Kevin M.</au><au>Mattie, David R.</au><au>Braverman, Lewis</au><au>Keys, Deborah A.</au><au>Mumtaz, Moiz</au><au>Fisher, Jeffrey W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low-Dose Effects of Ammonium Perchlorate on the Hypothalamic-Pituitary-Thyroid Axis of Adult Male Rats Pretreated with PCB126</atitle><jtitle>Toxicological sciences</jtitle><addtitle>Toxicol Sci</addtitle><date>2007-06-01</date><risdate>2007</risdate><volume>97</volume><issue>2</issue><spage>308</spage><epage>317</epage><pages>308-317</pages><issn>1096-6080</issn><eissn>1096-0929</eissn><abstract>The objective of this research was to characterize the disturbances in the hypothalamic-pituitary-thyroid (HPT) axis resulting from exposure to a binary mixture, 3,3′,4,4′,5-pentachlorobiphenyl (PCB126) and perchlorate (ClO4−), known to cause hypothyroidism by different modes of action. Two studies were conducted to determine the HPT axis effects of ClO4− on adult male Sprague-Dawley rats pretreated with PCB126. In dosing study I, rats were administered a single oral dose of PCB126 (0, 7.5, or 75 μg/kg) on day 0 and 9 days later ClO4− (0, 0.01, 0.1, or 1 mg/kg day) was added to the drinking water until euthanasia on day 22. Significant dose-dependent trends were found for all thyroid function indices measured following ClO4− in drinking water for 14 days. Seventy-five micrograms PCB126/kg resulted in a significant increase in hepatic T4-glucuronide formation, causing a decline in serum thyroxine and fT4, and resulting in increased serum thyroid-stimulating hormone (TSH). Serum TSH was also increased in animals that received 7.5 μg PCB126/kg; no other HPT axis alterations were found in these animals. When pretreated with PCB126, the ClO4− dose trends disappeared, suggesting a less than additive effect on the HPT axis. In dosing study II, animals were given lower doses of PCB126 (0, 0.075, 0.75, or 7.5 μg/kg) on day 0, and followed with ClO4− (0 or 0.01 mg/kg day) in drinking water beginning on day 1 and continuing for several days to explore transient HPT axis effects. No statistical effects were seen for PCB126 or ClO4− alone, and no perturbations were found when administered sequentially in dosing study II. In conclusion, these studies demonstrate that HPT axis disturbances following exposure to ClO4− are less than additive when pretreated with relatively high doses of PCB126. At relatively low doses, at or near the no-observed-effect-level for PCB126 and ClO4−, no interactions between the chemicals occur.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>17379623</pmid><doi>10.1093/toxsci/kfm063</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Body Weight - drug effects Dose-Response Relationship, Drug Drug Interactions Hormones - blood Hypothalamo-Hypophyseal System - drug effects Iodides - metabolism Liver - drug effects Liver - enzymology Male Organ Size - drug effects PCB126 perchlorate Perchlorates - toxicity Polychlorinated Biphenyls - toxicity Quaternary Ammonium Compounds - toxicity rat Rats Rats, Sprague-Dawley Symporters - biosynthesis Symporters - physiology thyroid Thyroid Gland - drug effects Thyroid Gland - metabolism Thyroid Gland - pathology Thyrotropin - blood TSH UDPGT |
title | Low-Dose Effects of Ammonium Perchlorate on the Hypothalamic-Pituitary-Thyroid Axis of Adult Male Rats Pretreated with PCB126 |
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