Elevated plasma corticosterone levels and histopathology of the adrenals and thymuses in 2,3,7,8-tetrachlorodibenzo- p-dioxin-treated rats
The relationship between thymic atrophy and plasma corticosterone levels was examined in 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD)-treated, pair-fed and ad libitum-fed male Sprague - Dawley rats given a usually lethal (125 μg/kg) or non-lethal (25 μg/kg dose of TCDD. At both dosages, corticosteron...
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description | The relationship between thymic atrophy and plasma corticosterone levels was examined in 2,3,7,8-tetrachlorodibenzo-
p-dioxin (TCDD)-treated, pair-fed and ad libitum-fed male Sprague - Dawley rats given a usually lethal (125 μg/kg) or non-lethal (25 μg/kg dose of TCDD. At both dosages, corticosterone levels in TCDD-treated animals begun to rise as early as day 4 after treatment. At later time points corticosterone levels were 5–7 times higher in rats given the non-lethal dose, and 6 – 10 times higher in rats administered the lethal dose than the levels observed in ad libitum-fed controls. Corticosterone levels in control rats pair-fed to the lethal dose group (as a result of the severe reduction in feed intake) were similarly elevated as in TCDD-treated rats but this was not the case in pair-fed rats of the non-lethal TCDD dosage (due to an essentially unchanged feed intake). At both dosages, relative thymus weights of TCDD-treated rats started decreasing by day 4 and continued to decline for the most part of the study. Relative thymus weights of rats pair-fed to the non-lethal TCDD dosage were not different from ad libitum-fed rats. However, the decrease in relative thymus weights of rats pair-fed to the lethal TCDD dosage paralleled that of TCDD-treated rats with an apparent 8-day lag period. Morphologically, the thymus as well as the adrenal revealed differential changes in TCDD-treated rats from those observable in pair-fed rats. These results suggest that either TCDD exerts a direct effect on the thymus and the adrenals or it causes an additional stress (e.g., a metabolic stress) over and above the starvation stress, which may be responsible for the differential morphological changes in these glands. |
doi_str_mv | 10.1016/0300-483X(88)90233-8 |
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p-dioxin (TCDD)-treated, pair-fed and ad libitum-fed male Sprague - Dawley rats given a usually lethal (125 μg/kg) or non-lethal (25 μg/kg dose of TCDD. At both dosages, corticosterone levels in TCDD-treated animals begun to rise as early as day 4 after treatment. At later time points corticosterone levels were 5–7 times higher in rats given the non-lethal dose, and 6 – 10 times higher in rats administered the lethal dose than the levels observed in ad libitum-fed controls. Corticosterone levels in control rats pair-fed to the lethal dose group (as a result of the severe reduction in feed intake) were similarly elevated as in TCDD-treated rats but this was not the case in pair-fed rats of the non-lethal TCDD dosage (due to an essentially unchanged feed intake). At both dosages, relative thymus weights of TCDD-treated rats started decreasing by day 4 and continued to decline for the most part of the study. Relative thymus weights of rats pair-fed to the non-lethal TCDD dosage were not different from ad libitum-fed rats. However, the decrease in relative thymus weights of rats pair-fed to the lethal TCDD dosage paralleled that of TCDD-treated rats with an apparent 8-day lag period. Morphologically, the thymus as well as the adrenal revealed differential changes in TCDD-treated rats from those observable in pair-fed rats. These results suggest that either TCDD exerts a direct effect on the thymus and the adrenals or it causes an additional stress (e.g., a metabolic stress) over and above the starvation stress, which may be responsible for the differential morphological changes in these glands.</description><identifier>ISSN: 0300-483X</identifier><identifier>EISSN: 1879-3185</identifier><identifier>DOI: 10.1016/0300-483X(88)90233-8</identifier><identifier>PMID: 3201474</identifier><identifier>CODEN: TXICDD</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>2,3,7,8-Tetrachlorodibenzo- p-dioxin(TCDD) ; Adrenal changes ; Adrenal Glands - drug effects ; Adrenal Glands - pathology ; Animals ; Biological and medical sciences ; Body Weight - drug effects ; Chemical and industrial products toxicology. Toxic occupational diseases ; Corticosterone ; Corticosterone - blood ; Dioxins - toxicity ; Dose-Response Relationship, Drug ; Eating ; Male ; Medical sciences ; Organ Size - drug effects ; Polychlorinated Dibenzodioxins - toxicity ; Rats ; Rats, Inbred Strains ; Thymmic atrophy ; Thymus Gland - drug effects ; Thymus Gland - pathology ; Toxicology ; Various organic compounds</subject><ispartof>Toxicology (Amsterdam), 1988-12, Vol.53 (1), p.19-32</ispartof><rights>1988</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-13ec9b03464d5e195e76dd0058d6cd99742b0b7ca59ccf15137938869fa3486d3</citedby><cites>FETCH-LOGICAL-c332t-13ec9b03464d5e195e76dd0058d6cd99742b0b7ca59ccf15137938869fa3486d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0300-483X(88)90233-8$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7230065$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3201474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gorski, Joel R.</creatorcontrib><creatorcontrib>Muzi, Giacomo</creatorcontrib><creatorcontrib>Weber, Lutz W.</creatorcontrib><creatorcontrib>Pereira, David W.</creatorcontrib><creatorcontrib>Iatropoulos, Michael J.</creatorcontrib><creatorcontrib>Rozman, Karl</creatorcontrib><title>Elevated plasma corticosterone levels and histopathology of the adrenals and thymuses in 2,3,7,8-tetrachlorodibenzo- p-dioxin-treated rats</title><title>Toxicology (Amsterdam)</title><addtitle>Toxicology</addtitle><description>The relationship between thymic atrophy and plasma corticosterone levels was examined in 2,3,7,8-tetrachlorodibenzo-
p-dioxin (TCDD)-treated, pair-fed and ad libitum-fed male Sprague - Dawley rats given a usually lethal (125 μg/kg) or non-lethal (25 μg/kg dose of TCDD. At both dosages, corticosterone levels in TCDD-treated animals begun to rise as early as day 4 after treatment. At later time points corticosterone levels were 5–7 times higher in rats given the non-lethal dose, and 6 – 10 times higher in rats administered the lethal dose than the levels observed in ad libitum-fed controls. Corticosterone levels in control rats pair-fed to the lethal dose group (as a result of the severe reduction in feed intake) were similarly elevated as in TCDD-treated rats but this was not the case in pair-fed rats of the non-lethal TCDD dosage (due to an essentially unchanged feed intake). At both dosages, relative thymus weights of TCDD-treated rats started decreasing by day 4 and continued to decline for the most part of the study. Relative thymus weights of rats pair-fed to the non-lethal TCDD dosage were not different from ad libitum-fed rats. However, the decrease in relative thymus weights of rats pair-fed to the lethal TCDD dosage paralleled that of TCDD-treated rats with an apparent 8-day lag period. Morphologically, the thymus as well as the adrenal revealed differential changes in TCDD-treated rats from those observable in pair-fed rats. These results suggest that either TCDD exerts a direct effect on the thymus and the adrenals or it causes an additional stress (e.g., a metabolic stress) over and above the starvation stress, which may be responsible for the differential morphological changes in these glands.</description><subject>2,3,7,8-Tetrachlorodibenzo- p-dioxin(TCDD)</subject><subject>Adrenal changes</subject><subject>Adrenal Glands - drug effects</subject><subject>Adrenal Glands - pathology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Corticosterone</subject><subject>Corticosterone - blood</subject><subject>Dioxins - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Eating</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Organ Size - drug effects</subject><subject>Polychlorinated Dibenzodioxins - toxicity</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Thymmic atrophy</subject><subject>Thymus Gland - drug effects</subject><subject>Thymus Gland - pathology</subject><subject>Toxicology</subject><subject>Various organic compounds</subject><issn>0300-483X</issn><issn>1879-3185</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc-KFDEQxoMo67j6Bgo5iChMNOn0n-SyIMu6Kyx4UfAW0km1HelO2iSz7PgIPrWZnWaOe6rD96uvqr5C6DWjHxll7SfKKSW14D_fC_FB0opzIp6gDROdJJyJ5inanJDn6EVKvyktVN2eoTNeUVZ39Qb9u5rgTmeweJl0mjU2IWZnQsoQgwdcVJgS1t7i0aUcFp3HMIVfexwGnEfA2kbwekXyuJ93CRJ2Hldbvu22gmTIUZtxCjFY14P_GwheiHXh3nmSIzwMjzqnl-jZUIzg1VrP0Y8vV98vb8jtt-uvl59vieG8yoRxMLKn5Y7aNsBkA11rLaWNsK2xUnZ11dO-M7qRxgysYbyTXIhWDprXorX8HL07-i4x_NlBymp2ycA0aQ9hlxRrqkq2LStgfQRNDClFGNQS3azjXjGqDi9Qh3zVIV8lhHp4gRKl7c3qv-tnsKemNfOiv111nYyehqi9cemEdVUxbZuCXRyxkj_cOYgqGQfegHURTFY2uMf3-A_zb6QF</recordid><startdate>19881216</startdate><enddate>19881216</enddate><creator>Gorski, Joel R.</creator><creator>Muzi, Giacomo</creator><creator>Weber, Lutz W.</creator><creator>Pereira, David W.</creator><creator>Iatropoulos, Michael J.</creator><creator>Rozman, Karl</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Science</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>19881216</creationdate><title>Elevated plasma corticosterone levels and histopathology of the adrenals and thymuses in 2,3,7,8-tetrachlorodibenzo- p-dioxin-treated rats</title><author>Gorski, Joel R. ; Muzi, Giacomo ; Weber, Lutz W. ; Pereira, David W. ; Iatropoulos, Michael J. ; Rozman, Karl</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-13ec9b03464d5e195e76dd0058d6cd99742b0b7ca59ccf15137938869fa3486d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>2,3,7,8-Tetrachlorodibenzo- p-dioxin(TCDD)</topic><topic>Adrenal changes</topic><topic>Adrenal Glands - drug effects</topic><topic>Adrenal Glands - pathology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Corticosterone</topic><topic>Corticosterone - blood</topic><topic>Dioxins - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Eating</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Organ Size - drug effects</topic><topic>Polychlorinated Dibenzodioxins - toxicity</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Thymmic atrophy</topic><topic>Thymus Gland - drug effects</topic><topic>Thymus Gland - pathology</topic><topic>Toxicology</topic><topic>Various organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gorski, Joel R.</creatorcontrib><creatorcontrib>Muzi, Giacomo</creatorcontrib><creatorcontrib>Weber, Lutz W.</creatorcontrib><creatorcontrib>Pereira, David W.</creatorcontrib><creatorcontrib>Iatropoulos, Michael J.</creatorcontrib><creatorcontrib>Rozman, Karl</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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicology (Amsterdam)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gorski, Joel R.</au><au>Muzi, Giacomo</au><au>Weber, Lutz W.</au><au>Pereira, David W.</au><au>Iatropoulos, Michael J.</au><au>Rozman, Karl</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elevated plasma corticosterone levels and histopathology of the adrenals and thymuses in 2,3,7,8-tetrachlorodibenzo- p-dioxin-treated rats</atitle><jtitle>Toxicology (Amsterdam)</jtitle><addtitle>Toxicology</addtitle><date>1988-12-16</date><risdate>1988</risdate><volume>53</volume><issue>1</issue><spage>19</spage><epage>32</epage><pages>19-32</pages><issn>0300-483X</issn><eissn>1879-3185</eissn><coden>TXICDD</coden><abstract>The relationship between thymic atrophy and plasma corticosterone levels was examined in 2,3,7,8-tetrachlorodibenzo-
p-dioxin (TCDD)-treated, pair-fed and ad libitum-fed male Sprague - Dawley rats given a usually lethal (125 μg/kg) or non-lethal (25 μg/kg dose of TCDD. At both dosages, corticosterone levels in TCDD-treated animals begun to rise as early as day 4 after treatment. At later time points corticosterone levels were 5–7 times higher in rats given the non-lethal dose, and 6 – 10 times higher in rats administered the lethal dose than the levels observed in ad libitum-fed controls. Corticosterone levels in control rats pair-fed to the lethal dose group (as a result of the severe reduction in feed intake) were similarly elevated as in TCDD-treated rats but this was not the case in pair-fed rats of the non-lethal TCDD dosage (due to an essentially unchanged feed intake). At both dosages, relative thymus weights of TCDD-treated rats started decreasing by day 4 and continued to decline for the most part of the study. Relative thymus weights of rats pair-fed to the non-lethal TCDD dosage were not different from ad libitum-fed rats. However, the decrease in relative thymus weights of rats pair-fed to the lethal TCDD dosage paralleled that of TCDD-treated rats with an apparent 8-day lag period. Morphologically, the thymus as well as the adrenal revealed differential changes in TCDD-treated rats from those observable in pair-fed rats. These results suggest that either TCDD exerts a direct effect on the thymus and the adrenals or it causes an additional stress (e.g., a metabolic stress) over and above the starvation stress, which may be responsible for the differential morphological changes in these glands.</abstract><cop>Shannon</cop><cop>Amsterdam</cop><pub>Elsevier Ireland Ltd</pub><pmid>3201474</pmid><doi>10.1016/0300-483X(88)90233-8</doi><tpages>14</tpages></addata></record> |
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subjects | 2,3,7,8-Tetrachlorodibenzo- p-dioxin(TCDD) Adrenal changes Adrenal Glands - drug effects Adrenal Glands - pathology Animals Biological and medical sciences Body Weight - drug effects Chemical and industrial products toxicology. Toxic occupational diseases Corticosterone Corticosterone - blood Dioxins - toxicity Dose-Response Relationship, Drug Eating Male Medical sciences Organ Size - drug effects Polychlorinated Dibenzodioxins - toxicity Rats Rats, Inbred Strains Thymmic atrophy Thymus Gland - drug effects Thymus Gland - pathology Toxicology Various organic compounds |
title | Elevated plasma corticosterone levels and histopathology of the adrenals and thymuses in 2,3,7,8-tetrachlorodibenzo- p-dioxin-treated rats |
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