Effect of dietary fluoride on selenite toxicity in the rat
Three factorial experiments were conducted to determine if high dietary fluoride (F) would inhibit selenite toxicity in rats. Initially, three levels of selenite (0.05, 3, and 5 mg/kg diet) were matched against three levels of F (2, 75, and 150 mg/kg diet). Fluoride failed to prevent the depressive...
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Veröffentlicht in: | Biological trace element research 1992-09, Vol.34 (3), p.265-278 |
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description | Three factorial experiments were conducted to determine if high dietary fluoride (F) would inhibit selenite toxicity in rats. Initially, three levels of selenite (0.05, 3, and 5 mg/kg diet) were matched against three levels of F (2, 75, and 150 mg/kg diet). Fluoride failed to prevent the depressive effect of selenite on 8-wk food intake and body wt gain. Selenium (Se) concentration of plasma and kidney and enzymatic activity of whole blood glutathione peroxidase (GSH-Px) were also unaffected by F. Liver Se concentration, however, was slightly (12%) but significantly (p < 0.025) reduced when the highest F and Se levels were combined. Fluoride (150 mg/kg) appeared to reduce liver selenite toxicity (5 mg/kg). Therefore, further study focused on liver histology with treatments that eliminated the middle levels of selenite and F. Fluoride prevented the hepatic necrosis seen in selenite-toxic rats. Similar histological lesions were not observed for kidney or heart. Fluoride partially (26%) but significantly (p < 0.025) reduced thiobarbituric-reactive substances in selenite-toxic rats, but there was no F effect on intracellular distribution of liver Se, glutathione levels in liver and kidney, or on liver xanthine oxidase activity. Overall, the protective effect of F on selenite toxicity appears to be confined to liver pathology. The exact mechanism for this effect, however, remains unclear. |
doi_str_mv | 10.1007/BF02783682 |
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Therefore, further study focused on liver histology with treatments that eliminated the middle levels of selenite and F. Fluoride prevented the hepatic necrosis seen in selenite-toxic rats. Similar histological lesions were not observed for kidney or heart. Fluoride partially (26%) but significantly (p < 0.025) reduced thiobarbituric-reactive substances in selenite-toxic rats, but there was no F effect on intracellular distribution of liver Se, glutathione levels in liver and kidney, or on liver xanthine oxidase activity. Overall, the protective effect of F on selenite toxicity appears to be confined to liver pathology. The exact mechanism for this effect, however, remains unclear.</description><identifier>ISSN: 0163-4984</identifier><identifier>EISSN: 1559-0720</identifier><identifier>DOI: 10.1007/BF02783682</identifier><identifier>PMID: 1384617</identifier><identifier>CODEN: BTERDG</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Animals ; Biological and medical sciences ; Chemical and Drug Induced Liver Injury ; Chemical and industrial products toxicology. Toxic occupational diseases ; Diet ; Eating - drug effects ; Fluorides - administration & dosage ; Fluorides - pharmacology ; Glutathione Peroxidase - blood ; Kidney - drug effects ; Kidney - metabolism ; Liver - drug effects ; Liver - metabolism ; Liver Diseases - diet therapy ; Liver Diseases - pathology ; Male ; Medical sciences ; Metals and various inorganic compounds ; Rats ; Rats, Sprague-Dawley ; Selenium - antagonists & inhibitors ; Selenium - metabolism ; Selenium - toxicity ; Toxicology</subject><ispartof>Biological trace element research, 1992-09, Vol.34 (3), p.265-278</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-12dec44ced3ba69c5e2c75aaa8cef9c7864e00f0cd7823e9c1a4a219e09990843</citedby><cites>FETCH-LOGICAL-c311t-12dec44ced3ba69c5e2c75aaa8cef9c7864e00f0cd7823e9c1a4a219e09990843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4456463$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1384617$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>QING YU</creatorcontrib><creatorcontrib>CERKLEWSKI, F. L</creatorcontrib><creatorcontrib>WHANGER, P. D</creatorcontrib><creatorcontrib>HEDSTROM, O</creatorcontrib><creatorcontrib>RIDLINGTON, J. W</creatorcontrib><title>Effect of dietary fluoride on selenite toxicity in the rat</title><title>Biological trace element research</title><addtitle>Biol Trace Elem Res</addtitle><description>Three factorial experiments were conducted to determine if high dietary fluoride (F) would inhibit selenite toxicity in rats. Initially, three levels of selenite (0.05, 3, and 5 mg/kg diet) were matched against three levels of F (2, 75, and 150 mg/kg diet). Fluoride failed to prevent the depressive effect of selenite on 8-wk food intake and body wt gain. Selenium (Se) concentration of plasma and kidney and enzymatic activity of whole blood glutathione peroxidase (GSH-Px) were also unaffected by F. Liver Se concentration, however, was slightly (12%) but significantly (p < 0.025) reduced when the highest F and Se levels were combined. Fluoride (150 mg/kg) appeared to reduce liver selenite toxicity (5 mg/kg). Therefore, further study focused on liver histology with treatments that eliminated the middle levels of selenite and F. Fluoride prevented the hepatic necrosis seen in selenite-toxic rats. Similar histological lesions were not observed for kidney or heart. Fluoride partially (26%) but significantly (p < 0.025) reduced thiobarbituric-reactive substances in selenite-toxic rats, but there was no F effect on intracellular distribution of liver Se, glutathione levels in liver and kidney, or on liver xanthine oxidase activity. Overall, the protective effect of F on selenite toxicity appears to be confined to liver pathology. The exact mechanism for this effect, however, remains unclear.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chemical and Drug Induced Liver Injury</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Diet</subject><subject>Eating - drug effects</subject><subject>Fluorides - administration & dosage</subject><subject>Fluorides - pharmacology</subject><subject>Glutathione Peroxidase - blood</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Liver Diseases - diet therapy</subject><subject>Liver Diseases - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metals and various inorganic compounds</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Selenium - antagonists & inhibitors</subject><subject>Selenium - metabolism</subject><subject>Selenium - toxicity</subject><subject>Toxicology</subject><issn>0163-4984</issn><issn>1559-0720</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFj0tLAzEUhYMotVY37oUsXAmjN4_Jw52WVoWCG10PaeYGI9OZkqRg_72VFrs6i_NxOB8h1wzuGYB-eJ4D10Yow0_ImNW1rUBzOCVjYEpU0hp5Ti5y_gZgmlsxIiMmjFRMj8njLAT0hQ6BthGLS1saus2QYot06GnGDvtYkJbhJ_pYtjT2tHwhTa5ckrPguoxXh5yQz_nsY_paLd5f3qZPi8oLxkrFeIteSo-tWDplfY3c69o5ZzwG67VREgEC-FYbLtB65qTjzCJYa8FIMSF3-12fhpwThmad4mr3tGHQ_Pk3R_8dfLOH15vlCtsjuhfe9beH3mXvupBc72P-x6SslVRC_AJAM2E7</recordid><startdate>19920901</startdate><enddate>19920901</enddate><creator>QING YU</creator><creator>CERKLEWSKI, F. L</creator><creator>WHANGER, P. D</creator><creator>HEDSTROM, O</creator><creator>RIDLINGTON, J. W</creator><general>Springer</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></search><sort><creationdate>19920901</creationdate><title>Effect of dietary fluoride on selenite toxicity in the rat</title><author>QING YU ; CERKLEWSKI, F. L ; WHANGER, P. D ; HEDSTROM, O ; RIDLINGTON, J. W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-12dec44ced3ba69c5e2c75aaa8cef9c7864e00f0cd7823e9c1a4a219e09990843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chemical and Drug Induced Liver Injury</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Diet</topic><topic>Eating - drug effects</topic><topic>Fluorides - administration & dosage</topic><topic>Fluorides - pharmacology</topic><topic>Glutathione Peroxidase - blood</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Liver Diseases - diet therapy</topic><topic>Liver Diseases - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metals and various inorganic compounds</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Selenium - antagonists & inhibitors</topic><topic>Selenium - metabolism</topic><topic>Selenium - toxicity</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>QING YU</creatorcontrib><creatorcontrib>CERKLEWSKI, F. L</creatorcontrib><creatorcontrib>WHANGER, P. D</creatorcontrib><creatorcontrib>HEDSTROM, O</creatorcontrib><creatorcontrib>RIDLINGTON, J. W</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><jtitle>Biological trace element research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>QING YU</au><au>CERKLEWSKI, F. L</au><au>WHANGER, P. D</au><au>HEDSTROM, O</au><au>RIDLINGTON, J. W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of dietary fluoride on selenite toxicity in the rat</atitle><jtitle>Biological trace element research</jtitle><addtitle>Biol Trace Elem Res</addtitle><date>1992-09-01</date><risdate>1992</risdate><volume>34</volume><issue>3</issue><spage>265</spage><epage>278</epage><pages>265-278</pages><issn>0163-4984</issn><eissn>1559-0720</eissn><coden>BTERDG</coden><abstract>Three factorial experiments were conducted to determine if high dietary fluoride (F) would inhibit selenite toxicity in rats. Initially, three levels of selenite (0.05, 3, and 5 mg/kg diet) were matched against three levels of F (2, 75, and 150 mg/kg diet). Fluoride failed to prevent the depressive effect of selenite on 8-wk food intake and body wt gain. Selenium (Se) concentration of plasma and kidney and enzymatic activity of whole blood glutathione peroxidase (GSH-Px) were also unaffected by F. Liver Se concentration, however, was slightly (12%) but significantly (p < 0.025) reduced when the highest F and Se levels were combined. Fluoride (150 mg/kg) appeared to reduce liver selenite toxicity (5 mg/kg). Therefore, further study focused on liver histology with treatments that eliminated the middle levels of selenite and F. Fluoride prevented the hepatic necrosis seen in selenite-toxic rats. Similar histological lesions were not observed for kidney or heart. Fluoride partially (26%) but significantly (p < 0.025) reduced thiobarbituric-reactive substances in selenite-toxic rats, but there was no F effect on intracellular distribution of liver Se, glutathione levels in liver and kidney, or on liver xanthine oxidase activity. Overall, the protective effect of F on selenite toxicity appears to be confined to liver pathology. The exact mechanism for this effect, however, remains unclear.</abstract><cop>Heidelberg</cop><pub>Springer</pub><pmid>1384617</pmid><doi>10.1007/BF02783682</doi><tpages>14</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Chemical and Drug Induced Liver Injury Chemical and industrial products toxicology. Toxic occupational diseases Diet Eating - drug effects Fluorides - administration & dosage Fluorides - pharmacology Glutathione Peroxidase - blood Kidney - drug effects Kidney - metabolism Liver - drug effects Liver - metabolism Liver Diseases - diet therapy Liver Diseases - pathology Male Medical sciences Metals and various inorganic compounds Rats Rats, Sprague-Dawley Selenium - antagonists & inhibitors Selenium - metabolism Selenium - toxicity Toxicology |
title | Effect of dietary fluoride on selenite toxicity in the rat |
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