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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Veröffentlicht in:Toxicological sciences 2007-06, Vol.97 (2), p.308-317
Hauptverfasser: 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.
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container_end_page 317
container_issue 2
container_start_page 308
container_title Toxicological sciences
container_volume 97
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. 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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. 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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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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
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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