Biological fractionation of lead isotopes in Sprague-Dawley rats lead poisoned via the respiratory tract.

It was considered that lead isotope ratios did not change during physical, chemical, or biological processes. Thus, lead isotope ratios have been used as fingerprints to identify possible lead sources. However, recent evidence has shown that the lead isotope ratios among different biological samples...

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Main Authors: Jing Wu, Duojian Liu, Qing Xie, Jingyu Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3530463?pdf=render
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spelling doaj-803eb6b6c1d94ea8a95e28a0c04a487b2020-11-24T22:17:52ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5246210.1371/journal.pone.0052462Biological fractionation of lead isotopes in Sprague-Dawley rats lead poisoned via the respiratory tract.Jing WuDuojian LiuQing XieJingyu WangIt was considered that lead isotope ratios did not change during physical, chemical, or biological processes. Thus, lead isotope ratios have been used as fingerprints to identify possible lead sources. However, recent evidence has shown that the lead isotope ratios among different biological samples in human are not always identical from its lead origins in vitro. An animal experiment was conducted to explore the biological fractionation of lead isotopes in biological systems.24 male Sprague-Dawley (SD) rats were divided into groups that received acute lead exposure (0, 0.02, 0.2, or 2 mg/kg body weight of lead acetate) via the respiratory route every day for 5 days. Biological samples (i.e., blood, urine, and feces) were collected for comparison with the lead acetate (test substance) and the low-lead animal feed (diet) administered to the rats. The lead isotope ratios were determined by inductively coupled plasma mass spectrometry (ICP-MS).There are significant differences (p<0.05) in lead isotope ratios between blood, urine, and feces. Moreover, a nonlinear relationship between the blood lead concentration and the blood lead isotope ratios was observed. There is also a threshold effect to the fractionation function. Only the blood isotope ratio of (204)Pb/(206)Pb matches the test substance well. As for feces, when (204)Pb/(206)Pb ratio is considered, there is no significant difference between feces-test substance pairs in medium and high dose group.The biological fractionation of lead isotopes in SD rats was observed. Moreover, there might be a threshold for the biological fractionation of lead isotopes which is depending on whole blood lead level. It is considered to be more reliable that we compared the isotope ratios of potential lead hazards with both blood and feces lead fingerprints especially for (204)Pb/(206)Pb ratio under high-dose exposure.http://europepmc.org/articles/PMC3530463?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jing Wu
Duojian Liu
Qing Xie
Jingyu Wang
spellingShingle Jing Wu
Duojian Liu
Qing Xie
Jingyu Wang
Biological fractionation of lead isotopes in Sprague-Dawley rats lead poisoned via the respiratory tract.
PLoS ONE
author_facet Jing Wu
Duojian Liu
Qing Xie
Jingyu Wang
author_sort Jing Wu
title Biological fractionation of lead isotopes in Sprague-Dawley rats lead poisoned via the respiratory tract.
title_short Biological fractionation of lead isotopes in Sprague-Dawley rats lead poisoned via the respiratory tract.
title_full Biological fractionation of lead isotopes in Sprague-Dawley rats lead poisoned via the respiratory tract.
title_fullStr Biological fractionation of lead isotopes in Sprague-Dawley rats lead poisoned via the respiratory tract.
title_full_unstemmed Biological fractionation of lead isotopes in Sprague-Dawley rats lead poisoned via the respiratory tract.
title_sort biological fractionation of lead isotopes in sprague-dawley rats lead poisoned via the respiratory tract.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description It was considered that lead isotope ratios did not change during physical, chemical, or biological processes. Thus, lead isotope ratios have been used as fingerprints to identify possible lead sources. However, recent evidence has shown that the lead isotope ratios among different biological samples in human are not always identical from its lead origins in vitro. An animal experiment was conducted to explore the biological fractionation of lead isotopes in biological systems.24 male Sprague-Dawley (SD) rats were divided into groups that received acute lead exposure (0, 0.02, 0.2, or 2 mg/kg body weight of lead acetate) via the respiratory route every day for 5 days. Biological samples (i.e., blood, urine, and feces) were collected for comparison with the lead acetate (test substance) and the low-lead animal feed (diet) administered to the rats. The lead isotope ratios were determined by inductively coupled plasma mass spectrometry (ICP-MS).There are significant differences (p<0.05) in lead isotope ratios between blood, urine, and feces. Moreover, a nonlinear relationship between the blood lead concentration and the blood lead isotope ratios was observed. There is also a threshold effect to the fractionation function. Only the blood isotope ratio of (204)Pb/(206)Pb matches the test substance well. As for feces, when (204)Pb/(206)Pb ratio is considered, there is no significant difference between feces-test substance pairs in medium and high dose group.The biological fractionation of lead isotopes in SD rats was observed. Moreover, there might be a threshold for the biological fractionation of lead isotopes which is depending on whole blood lead level. It is considered to be more reliable that we compared the isotope ratios of potential lead hazards with both blood and feces lead fingerprints especially for (204)Pb/(206)Pb ratio under high-dose exposure.
url http://europepmc.org/articles/PMC3530463?pdf=render
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