Induction of light hydrocarbon nephropathy by p-dichlorobenzene
In order to clarify the etiology of a dose-related increase in the incidence of tubular cell adenocarcinomas of the kidney in male rats, the nephrotoxicity of p-dichlorobenzene (p-DCB) was investigated in a subchronic study. Groups of ten male and ten female Fischer 344 rats were dosed by gavage wit...
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Veröffentlicht in: | Archives of toxicology 1988-06, Vol.61 (6), p.433-439 |
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description | In order to clarify the etiology of a dose-related increase in the incidence of tubular cell adenocarcinomas of the kidney in male rats, the nephrotoxicity of p-dichlorobenzene (p-DCB) was investigated in a subchronic study. Groups of ten male and ten female Fischer 344 rats were dosed by gavage with 0 (controls), 75, 150, 300 or 600 mg p-DCB/kg/day in corn oil. Half of the animals were sacrificed after 4 weeks and the remainder after 13 weeks. Increased urinary LDH and epithelial cell excretion and exacerbation of hyaline droplet accumulation in the cytoplasm of renal cortical cells were observed in male rats over the entire dose range investigated. Tubular single cell necrosis, dilated tubules with granular cast formation in the outer zone of the medulla, were evident in male rats after 4 and 13 weeks of treatment with doses of 150-600 mg/kg/day. In female rats there was no indication of a nephrotoxic action of p-DCB. The effects on the kidney, both in their morphological characteristics and the fact that they occur exclusively in male animals, correspond to the light hydrocarbon nephropathy observed as a result of short-term treatment with a number of aliphatic and cyclic hydrocarbons. The development of cortical renal tumors seems to be associated with this kind of kidney damage which is unique to male rats. The literature on this subject generally regards these renal effects as not predictive for man. |
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Groups of ten male and ten female Fischer 344 rats were dosed by gavage with 0 (controls), 75, 150, 300 or 600 mg p-DCB/kg/day in corn oil. Half of the animals were sacrificed after 4 weeks and the remainder after 13 weeks. Increased urinary LDH and epithelial cell excretion and exacerbation of hyaline droplet accumulation in the cytoplasm of renal cortical cells were observed in male rats over the entire dose range investigated. Tubular single cell necrosis, dilated tubules with granular cast formation in the outer zone of the medulla, were evident in male rats after 4 and 13 weeks of treatment with doses of 150-600 mg/kg/day. In female rats there was no indication of a nephrotoxic action of p-DCB. The effects on the kidney, both in their morphological characteristics and the fact that they occur exclusively in male animals, correspond to the light hydrocarbon nephropathy observed as a result of short-term treatment with a number of aliphatic and cyclic hydrocarbons. The development of cortical renal tumors seems to be associated with this kind of kidney damage which is unique to male rats. The literature on this subject generally regards these renal effects as not predictive for man.</description><identifier>ISSN: 0340-5761</identifier><identifier>EISSN: 1432-0738</identifier><identifier>DOI: 10.1007/bf00293688</identifier><identifier>PMID: 2903729</identifier><identifier>CODEN: ARTODN</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Acetylglucosaminidase - urine ; Adenocarcinoma - chemically induced ; Adenocarcinoma - pathology ; Adenocarcinoma - ultrastructure ; Aminopeptidases - urine ; Animals ; Biological and medical sciences ; CD13 Antigens ; Chlorobenzenes - toxicity ; Domestic and cosmetic products toxicology ; Female ; Kidney Neoplasms - chemically induced ; Kidney Neoplasms - pathology ; Kidney Neoplasms - ultrastructure ; L-Lactate Dehydrogenase - urine ; Male ; Medical sciences ; Microscopy, Electron ; Organ Size - drug effects ; Rats ; Rats, Inbred F344 ; Sex Factors ; Toxicology</subject><ispartof>Archives of toxicology, 1988-06, Vol.61 (6), p.433-439</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-1597b3cb55f55455c571a2ee41c22204f4284ed7b9848adbefe755d0891da57e3</citedby><cites>FETCH-LOGICAL-c323t-1597b3cb55f55455c571a2ee41c22204f4284ed7b9848adbefe755d0891da57e3</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=7130981$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2903729$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BOMHARD, E</creatorcontrib><creatorcontrib>LUCKHAUS, G</creatorcontrib><creatorcontrib>VOIGT, W.-H</creatorcontrib><creatorcontrib>LOESER, E</creatorcontrib><title>Induction of light hydrocarbon nephropathy by p-dichlorobenzene</title><title>Archives of toxicology</title><addtitle>Arch Toxicol</addtitle><description>In order to clarify the etiology of a dose-related increase in the incidence of tubular cell adenocarcinomas of the kidney in male rats, the nephrotoxicity of p-dichlorobenzene (p-DCB) was investigated in a subchronic study. Groups of ten male and ten female Fischer 344 rats were dosed by gavage with 0 (controls), 75, 150, 300 or 600 mg p-DCB/kg/day in corn oil. Half of the animals were sacrificed after 4 weeks and the remainder after 13 weeks. Increased urinary LDH and epithelial cell excretion and exacerbation of hyaline droplet accumulation in the cytoplasm of renal cortical cells were observed in male rats over the entire dose range investigated. Tubular single cell necrosis, dilated tubules with granular cast formation in the outer zone of the medulla, were evident in male rats after 4 and 13 weeks of treatment with doses of 150-600 mg/kg/day. In female rats there was no indication of a nephrotoxic action of p-DCB. The effects on the kidney, both in their morphological characteristics and the fact that they occur exclusively in male animals, correspond to the light hydrocarbon nephropathy observed as a result of short-term treatment with a number of aliphatic and cyclic hydrocarbons. The development of cortical renal tumors seems to be associated with this kind of kidney damage which is unique to male rats. The literature on this subject generally regards these renal effects as not predictive for man.</description><subject>Acetylglucosaminidase - urine</subject><subject>Adenocarcinoma - chemically induced</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma - ultrastructure</subject><subject>Aminopeptidases - urine</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CD13 Antigens</subject><subject>Chlorobenzenes - toxicity</subject><subject>Domestic and cosmetic products toxicology</subject><subject>Female</subject><subject>Kidney Neoplasms - chemically induced</subject><subject>Kidney Neoplasms - pathology</subject><subject>Kidney Neoplasms - ultrastructure</subject><subject>L-Lactate Dehydrogenase - urine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microscopy, Electron</subject><subject>Organ Size - drug effects</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Sex Factors</subject><subject>Toxicology</subject><issn>0340-5761</issn><issn>1432-0738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kL1Lw0AAxQ9Raq0u7kIGcRCi99m7m0SL1ULBRedwnyaS5uJdMsS_3khjpwfv_XjDD4BLBO8QhPxeewixJEshjsAcUYJzyIk4BnNIKMwZX6JTcJbSF4QIC0lmYIYlJBzLOXjYNLY3XRWaLPisrj7LLisHG4NRUY9l49oyhlZ15ZDpIWtzW5myDjFo1_y4xp2DE6_q5C6mXICP9fP76jXfvr1sVo_b3BBMuhwxyTUxmjHPGGXMMI4Udo4igzGG1FMsqLNcS0GFstp5xxmzUEhkFeOOLMDN_reN4bt3qSt2VTKurlXjQp8KRKUUTMARvN2DJoaUovNFG6udikOBYPFnq3ha_9sa4avptdc7Zw_opGfcr6ddJaNqH1VjqnTAOCJQCkR-AYM0cNk</recordid><startdate>198806</startdate><enddate>198806</enddate><creator>BOMHARD, E</creator><creator>LUCKHAUS, G</creator><creator>VOIGT, W.-H</creator><creator>LOESER, E</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><scope>7T2</scope><scope>7U2</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>198806</creationdate><title>Induction of light hydrocarbon nephropathy by p-dichlorobenzene</title><author>BOMHARD, E ; LUCKHAUS, G ; VOIGT, W.-H ; LOESER, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-1597b3cb55f55455c571a2ee41c22204f4284ed7b9848adbefe755d0891da57e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Acetylglucosaminidase - urine</topic><topic>Adenocarcinoma - chemically induced</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma - ultrastructure</topic><topic>Aminopeptidases - urine</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CD13 Antigens</topic><topic>Chlorobenzenes - toxicity</topic><topic>Domestic and cosmetic products toxicology</topic><topic>Female</topic><topic>Kidney Neoplasms - chemically induced</topic><topic>Kidney Neoplasms - pathology</topic><topic>Kidney Neoplasms - ultrastructure</topic><topic>L-Lactate Dehydrogenase - urine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microscopy, Electron</topic><topic>Organ Size - drug effects</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Sex Factors</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BOMHARD, E</creatorcontrib><creatorcontrib>LUCKHAUS, G</creatorcontrib><creatorcontrib>VOIGT, W.-H</creatorcontrib><creatorcontrib>LOESER, E</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>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><jtitle>Archives of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BOMHARD, E</au><au>LUCKHAUS, G</au><au>VOIGT, W.-H</au><au>LOESER, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of light hydrocarbon nephropathy by p-dichlorobenzene</atitle><jtitle>Archives of toxicology</jtitle><addtitle>Arch Toxicol</addtitle><date>1988-06</date><risdate>1988</risdate><volume>61</volume><issue>6</issue><spage>433</spage><epage>439</epage><pages>433-439</pages><issn>0340-5761</issn><eissn>1432-0738</eissn><coden>ARTODN</coden><abstract>In order to clarify the etiology of a dose-related increase in the incidence of tubular cell adenocarcinomas of the kidney in male rats, the nephrotoxicity of p-dichlorobenzene (p-DCB) was investigated in a subchronic study. Groups of ten male and ten female Fischer 344 rats were dosed by gavage with 0 (controls), 75, 150, 300 or 600 mg p-DCB/kg/day in corn oil. Half of the animals were sacrificed after 4 weeks and the remainder after 13 weeks. Increased urinary LDH and epithelial cell excretion and exacerbation of hyaline droplet accumulation in the cytoplasm of renal cortical cells were observed in male rats over the entire dose range investigated. Tubular single cell necrosis, dilated tubules with granular cast formation in the outer zone of the medulla, were evident in male rats after 4 and 13 weeks of treatment with doses of 150-600 mg/kg/day. In female rats there was no indication of a nephrotoxic action of p-DCB. The effects on the kidney, both in their morphological characteristics and the fact that they occur exclusively in male animals, correspond to the light hydrocarbon nephropathy observed as a result of short-term treatment with a number of aliphatic and cyclic hydrocarbons. The development of cortical renal tumors seems to be associated with this kind of kidney damage which is unique to male rats. The literature on this subject generally regards these renal effects as not predictive for man.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>2903729</pmid><doi>10.1007/bf00293688</doi><tpages>7</tpages></addata></record> |
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subjects | Acetylglucosaminidase - urine Adenocarcinoma - chemically induced Adenocarcinoma - pathology Adenocarcinoma - ultrastructure Aminopeptidases - urine Animals Biological and medical sciences CD13 Antigens Chlorobenzenes - toxicity Domestic and cosmetic products toxicology Female Kidney Neoplasms - chemically induced Kidney Neoplasms - pathology Kidney Neoplasms - ultrastructure L-Lactate Dehydrogenase - urine Male Medical sciences Microscopy, Electron Organ Size - drug effects Rats Rats, Inbred F344 Sex Factors Toxicology |
title | Induction of light hydrocarbon nephropathy by p-dichlorobenzene |
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