DNA single strand breakage, DNA adducts, and sister chromatid exchange in lymphocytes and phenanthrene and pyrene metabolites in urine of coke oven workers

OBJECTIVES: To investigate the specificity of biological monitoring variables (excretion of phenanthrene and pyrene metabolites in urine) and the usefulness of some biomarkers of effect (alkaline filter elution, 32P postlabelling assay, measurement of sister chromatid exchange) in workers exposed to...

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Veröffentlicht in:Occupational and environmental medicine (London, England) England), 1997-03, Vol.54 (3), p.176-183
Hauptverfasser: Popp, W, Vahrenholz, C, Schell, C, Grimmer, G, Dettbarn, G, Kraus, R, Brauksiepe, A, Schmeling, B, Gutzeit, T, von Bülow, J, Norpoth, K
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container_title Occupational and environmental medicine (London, England)
container_volume 54
creator Popp, W
Vahrenholz, C
Schell, C
Grimmer, G
Dettbarn, G
Kraus, R
Brauksiepe, A
Schmeling, B
Gutzeit, T
von Bülow, J
Norpoth, K
description OBJECTIVES: To investigate the specificity of biological monitoring variables (excretion of phenanthrene and pyrene metabolites in urine) and the usefulness of some biomarkers of effect (alkaline filter elution, 32P postlabelling assay, measurement of sister chromatid exchange) in workers exposed to polycyclic aromatic hydrocarbons (PAHs). METHODS: 29 coke oven workers and a standardised control group were investigated for frequencies of DNA single strand breakage, DNA protein cross links (alkaline filter elution assay), sister chromatid exchange, and DNA adducts (32P postlabelling assay) in lymphocytes. Phenanthrene and pyrene metabolites were measured in 24 hour urine samples. 19 different PAHs (including benzo(a)pyrene, pyrene, and phenanthrene) were measured at the workplace by personal air monitoring. The GSTT1 activity in erythrocytes and lymphocyte subpopulations in blood was also measured. RESULTS: Concentrations of phenanthrene, pyrene, and benzo(a)pyrene in air correlated well with the concentration of total PAHs in air; they could be used for comparisons of different workplaces if the emission compositions were known. The measurement of phenanthrene metabolites in urine proved to be a better biological monitoring variable than the measurement of 1-hydroxypyrene. Significantly more DNA strand breaks in lymphocytes of coke oven workers were found (alkaline filter elution assay); the DNA adduct rate was not significantly increased in workers, but correlated with exposure to PAHs in a semiquantitative manner. The number of sister chromatid exchanges was lower in coke oven workers but this was not significant; thus counting sister chromatid exchanges was not a good variable for biomonitoring of coke oven workers. Also, indications for immunotoxic influences (changes in lymphocyte subpopulations) were found. CONCLUSIONS: The measurement of phenanthrene metabolites in urine seems to be a better biological monitoring variable for exposure to PAHs than measurement of hydroxypyrene. The alkaline filter elution assay proved to be the most sensitive biomarker for genotoxic damage, whereas the postlabelling assay was the only one with some specificity for DNA alterations caused by known compounds.
doi_str_mv 10.1136/oem.54.3.176
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METHODS: 29 coke oven workers and a standardised control group were investigated for frequencies of DNA single strand breakage, DNA protein cross links (alkaline filter elution assay), sister chromatid exchange, and DNA adducts (32P postlabelling assay) in lymphocytes. Phenanthrene and pyrene metabolites were measured in 24 hour urine samples. 19 different PAHs (including benzo(a)pyrene, pyrene, and phenanthrene) were measured at the workplace by personal air monitoring. The GSTT1 activity in erythrocytes and lymphocyte subpopulations in blood was also measured. RESULTS: Concentrations of phenanthrene, pyrene, and benzo(a)pyrene in air correlated well with the concentration of total PAHs in air; they could be used for comparisons of different workplaces if the emission compositions were known. The measurement of phenanthrene metabolites in urine proved to be a better biological monitoring variable than the measurement of 1-hydroxypyrene. Significantly more DNA strand breaks in lymphocytes of coke oven workers were found (alkaline filter elution assay); the DNA adduct rate was not significantly increased in workers, but correlated with exposure to PAHs in a semiquantitative manner. The number of sister chromatid exchanges was lower in coke oven workers but this was not significant; thus counting sister chromatid exchanges was not a good variable for biomonitoring of coke oven workers. Also, indications for immunotoxic influences (changes in lymphocyte subpopulations) were found. CONCLUSIONS: The measurement of phenanthrene metabolites in urine seems to be a better biological monitoring variable for exposure to PAHs than measurement of hydroxypyrene. The alkaline filter elution assay proved to be the most sensitive biomarker for genotoxic damage, whereas the postlabelling assay was the only one with some specificity for DNA alterations caused by known compounds.</description><identifier>ISSN: 1351-0711</identifier><identifier>EISSN: 1470-7926</identifier><identifier>DOI: 10.1136/oem.54.3.176</identifier><identifier>PMID: 9155778</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>Adult ; Biological and medical sciences ; Biomarkers - urine ; Biomonitoring ; Case-Control Studies ; Chemical and industrial products toxicology. Toxic occupational diseases ; Cigarette smoking ; Coke ; Coke furnaces ; Deoxyribonucleic acid ; DNA ; DNA adducts ; DNA Adducts - analysis ; DNA Damage ; DNA, Single-Stranded - drug effects ; Elution ; Emission measurements ; Humans ; Lymphocytes ; Lymphocytes - drug effects ; Male ; Medical sciences ; Metabolites ; Middle Aged ; Occupational Exposure ; Phenanthrene ; Phenanthrenes ; Phenanthrenes - urine ; Polycyclic aromatic hydrocarbons ; Pyrene ; Pyrenes - metabolism ; Sensitivity and Specificity ; Sister chromatid exchange ; Sister Chromatid Exchange - drug effects ; Subpopulations ; Toxicology ; Urine ; Various organic compounds</subject><ispartof>Occupational and environmental medicine (London, England), 1997-03, Vol.54 (3), p.176-183</ispartof><rights>1997 INIST-CNRS</rights><rights>Copyright BMJ Publishing Group LTD Mar 1997</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b688t-679b44e486d3f3a563143dfcc997f6442b1b1fc991a1e51f47ccaa58710024523</citedby><cites>FETCH-LOGICAL-b688t-679b44e486d3f3a563143dfcc997f6442b1b1fc991a1e51f47ccaa58710024523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/27730706$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/27730706$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2592748$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9155778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Popp, W</creatorcontrib><creatorcontrib>Vahrenholz, C</creatorcontrib><creatorcontrib>Schell, C</creatorcontrib><creatorcontrib>Grimmer, G</creatorcontrib><creatorcontrib>Dettbarn, G</creatorcontrib><creatorcontrib>Kraus, R</creatorcontrib><creatorcontrib>Brauksiepe, A</creatorcontrib><creatorcontrib>Schmeling, B</creatorcontrib><creatorcontrib>Gutzeit, T</creatorcontrib><creatorcontrib>von Bülow, J</creatorcontrib><creatorcontrib>Norpoth, K</creatorcontrib><title>DNA single strand breakage, DNA adducts, and sister chromatid exchange in lymphocytes and phenanthrene and pyrene metabolites in urine of coke oven workers</title><title>Occupational and environmental medicine (London, England)</title><addtitle>Occup Environ Med</addtitle><description>OBJECTIVES: To investigate the specificity of biological monitoring variables (excretion of phenanthrene and pyrene metabolites in urine) and the usefulness of some biomarkers of effect (alkaline filter elution, 32P postlabelling assay, measurement of sister chromatid exchange) in workers exposed to polycyclic aromatic hydrocarbons (PAHs). METHODS: 29 coke oven workers and a standardised control group were investigated for frequencies of DNA single strand breakage, DNA protein cross links (alkaline filter elution assay), sister chromatid exchange, and DNA adducts (32P postlabelling assay) in lymphocytes. Phenanthrene and pyrene metabolites were measured in 24 hour urine samples. 19 different PAHs (including benzo(a)pyrene, pyrene, and phenanthrene) were measured at the workplace by personal air monitoring. The GSTT1 activity in erythrocytes and lymphocyte subpopulations in blood was also measured. RESULTS: Concentrations of phenanthrene, pyrene, and benzo(a)pyrene in air correlated well with the concentration of total PAHs in air; they could be used for comparisons of different workplaces if the emission compositions were known. The measurement of phenanthrene metabolites in urine proved to be a better biological monitoring variable than the measurement of 1-hydroxypyrene. Significantly more DNA strand breaks in lymphocytes of coke oven workers were found (alkaline filter elution assay); the DNA adduct rate was not significantly increased in workers, but correlated with exposure to PAHs in a semiquantitative manner. The number of sister chromatid exchanges was lower in coke oven workers but this was not significant; thus counting sister chromatid exchanges was not a good variable for biomonitoring of coke oven workers. Also, indications for immunotoxic influences (changes in lymphocyte subpopulations) were found. CONCLUSIONS: The measurement of phenanthrene metabolites in urine seems to be a better biological monitoring variable for exposure to PAHs than measurement of hydroxypyrene. The alkaline filter elution assay proved to be the most sensitive biomarker for genotoxic damage, whereas the postlabelling assay was the only one with some specificity for DNA alterations caused by known compounds.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - urine</subject><subject>Biomonitoring</subject><subject>Case-Control Studies</subject><subject>Chemical and industrial products toxicology. 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Toxic occupational diseases</topic><topic>Cigarette smoking</topic><topic>Coke</topic><topic>Coke furnaces</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA adducts</topic><topic>DNA Adducts - analysis</topic><topic>DNA Damage</topic><topic>DNA, Single-Stranded - drug effects</topic><topic>Elution</topic><topic>Emission measurements</topic><topic>Humans</topic><topic>Lymphocytes</topic><topic>Lymphocytes - drug effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolites</topic><topic>Middle Aged</topic><topic>Occupational Exposure</topic><topic>Phenanthrene</topic><topic>Phenanthrenes</topic><topic>Phenanthrenes - urine</topic><topic>Polycyclic aromatic hydrocarbons</topic><topic>Pyrene</topic><topic>Pyrenes - metabolism</topic><topic>Sensitivity and Specificity</topic><topic>Sister chromatid exchange</topic><topic>Sister Chromatid Exchange - drug effects</topic><topic>Subpopulations</topic><topic>Toxicology</topic><topic>Urine</topic><topic>Various organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Popp, W</creatorcontrib><creatorcontrib>Vahrenholz, C</creatorcontrib><creatorcontrib>Schell, C</creatorcontrib><creatorcontrib>Grimmer, G</creatorcontrib><creatorcontrib>Dettbarn, G</creatorcontrib><creatorcontrib>Kraus, R</creatorcontrib><creatorcontrib>Brauksiepe, A</creatorcontrib><creatorcontrib>Schmeling, B</creatorcontrib><creatorcontrib>Gutzeit, T</creatorcontrib><creatorcontrib>von Bülow, J</creatorcontrib><creatorcontrib>Norpoth, K</creatorcontrib><collection>Istex</collection><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>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>ProQuest Health &amp; 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METHODS: 29 coke oven workers and a standardised control group were investigated for frequencies of DNA single strand breakage, DNA protein cross links (alkaline filter elution assay), sister chromatid exchange, and DNA adducts (32P postlabelling assay) in lymphocytes. Phenanthrene and pyrene metabolites were measured in 24 hour urine samples. 19 different PAHs (including benzo(a)pyrene, pyrene, and phenanthrene) were measured at the workplace by personal air monitoring. The GSTT1 activity in erythrocytes and lymphocyte subpopulations in blood was also measured. RESULTS: Concentrations of phenanthrene, pyrene, and benzo(a)pyrene in air correlated well with the concentration of total PAHs in air; they could be used for comparisons of different workplaces if the emission compositions were known. The measurement of phenanthrene metabolites in urine proved to be a better biological monitoring variable than the measurement of 1-hydroxypyrene. Significantly more DNA strand breaks in lymphocytes of coke oven workers were found (alkaline filter elution assay); the DNA adduct rate was not significantly increased in workers, but correlated with exposure to PAHs in a semiquantitative manner. The number of sister chromatid exchanges was lower in coke oven workers but this was not significant; thus counting sister chromatid exchanges was not a good variable for biomonitoring of coke oven workers. Also, indications for immunotoxic influences (changes in lymphocyte subpopulations) were found. CONCLUSIONS: The measurement of phenanthrene metabolites in urine seems to be a better biological monitoring variable for exposure to PAHs than measurement of hydroxypyrene. The alkaline filter elution assay proved to be the most sensitive biomarker for genotoxic damage, whereas the postlabelling assay was the only one with some specificity for DNA alterations caused by known compounds.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><pmid>9155778</pmid><doi>10.1136/oem.54.3.176</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1351-0711
ispartof Occupational and environmental medicine (London, England), 1997-03, Vol.54 (3), p.176-183
issn 1351-0711
1470-7926
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1128680
source PubMed (Medline); MEDLINE; Alma/SFX Local Collection; JSTOR; EZB Electronic Journals Library
subjects Adult
Biological and medical sciences
Biomarkers - urine
Biomonitoring
Case-Control Studies
Chemical and industrial products toxicology. Toxic occupational diseases
Cigarette smoking
Coke
Coke furnaces
Deoxyribonucleic acid
DNA
DNA adducts
DNA Adducts - analysis
DNA Damage
DNA, Single-Stranded - drug effects
Elution
Emission measurements
Humans
Lymphocytes
Lymphocytes - drug effects
Male
Medical sciences
Metabolites
Middle Aged
Occupational Exposure
Phenanthrene
Phenanthrenes
Phenanthrenes - urine
Polycyclic aromatic hydrocarbons
Pyrene
Pyrenes - metabolism
Sensitivity and Specificity
Sister chromatid exchange
Sister Chromatid Exchange - drug effects
Subpopulations
Toxicology
Urine
Various organic compounds
title DNA single strand breakage, DNA adducts, and sister chromatid exchange in lymphocytes and phenanthrene and pyrene metabolites in urine of coke oven workers
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