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Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels?

BACKGROUND: In the Arctic, polar bears (Ursus maritimus) bio-accumulate mercury as they prey on polluted ringed seals (Phoca hispida) and bearded seals (Erignathus barbatus). Studies have shown that polar bears from East Greenland are among the most mercury polluted species in the Arctic. It is unkn...

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Autores principales: Sonne, Christian, Dietz, Rune, Leifsson, Pall S, Asmund, Gert, Born, Erik W, Kirkegaard, Maja
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1855925/
https://www.ncbi.nlm.nih.gov/pubmed/17439647
http://dx.doi.org/10.1186/1476-069X-6-11
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author Sonne, Christian
Dietz, Rune
Leifsson, Pall S
Asmund, Gert
Born, Erik W
Kirkegaard, Maja
author_facet Sonne, Christian
Dietz, Rune
Leifsson, Pall S
Asmund, Gert
Born, Erik W
Kirkegaard, Maja
author_sort Sonne, Christian
collection PubMed
description BACKGROUND: In the Arctic, polar bears (Ursus maritimus) bio-accumulate mercury as they prey on polluted ringed seals (Phoca hispida) and bearded seals (Erignathus barbatus). Studies have shown that polar bears from East Greenland are among the most mercury polluted species in the Arctic. It is unknown whether these levels are toxic to liver and kidney tissue. METHODS: We investigated the histopathological impact from anthropogenic long-range transported mercury on East Greenland polar bear liver (n = 59) and kidney (n = 57) tissues. RESULTS: Liver mercury levels ranged from 1.1–35.6 μg/g wet weight and renal levels ranged from 1–50 μg/g wet weight, of which 2 liver values and 9 kidney values were above known toxic threshold level of 30 μg/g wet weight in terrestrial mammals. Evaluated from age-correcting ANCOVA analyses, liver mercury levels were significantly higher in individuals with visible Ito cells (p < 0.02) and a similar trend was found for lipid granulomas (p = 0.07). Liver mercury levels were significantly lower in individuals with portal bile duct proliferation/fibrosis (p = 0.007) and a similar trend was found for proximal convoluted tubular hyalinisation in renal tissue (p = 0.07). CONCLUSION: Based on these relationships and the nature of the chronic inflammation we conclude that the lesions were likely a result of recurrent infections and ageing but that long-term exposure to mercury could not be excluded as a co-factor. The information is important as it is likely that tropospheric mercury depletion events will continue to increase the concentrations of this toxic heavy metal in the Sub Arctic and Arctic marine food webs.
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spelling pubmed-18559252007-04-26 Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels? Sonne, Christian Dietz, Rune Leifsson, Pall S Asmund, Gert Born, Erik W Kirkegaard, Maja Environ Health Research BACKGROUND: In the Arctic, polar bears (Ursus maritimus) bio-accumulate mercury as they prey on polluted ringed seals (Phoca hispida) and bearded seals (Erignathus barbatus). Studies have shown that polar bears from East Greenland are among the most mercury polluted species in the Arctic. It is unknown whether these levels are toxic to liver and kidney tissue. METHODS: We investigated the histopathological impact from anthropogenic long-range transported mercury on East Greenland polar bear liver (n = 59) and kidney (n = 57) tissues. RESULTS: Liver mercury levels ranged from 1.1–35.6 μg/g wet weight and renal levels ranged from 1–50 μg/g wet weight, of which 2 liver values and 9 kidney values were above known toxic threshold level of 30 μg/g wet weight in terrestrial mammals. Evaluated from age-correcting ANCOVA analyses, liver mercury levels were significantly higher in individuals with visible Ito cells (p < 0.02) and a similar trend was found for lipid granulomas (p = 0.07). Liver mercury levels were significantly lower in individuals with portal bile duct proliferation/fibrosis (p = 0.007) and a similar trend was found for proximal convoluted tubular hyalinisation in renal tissue (p = 0.07). CONCLUSION: Based on these relationships and the nature of the chronic inflammation we conclude that the lesions were likely a result of recurrent infections and ageing but that long-term exposure to mercury could not be excluded as a co-factor. The information is important as it is likely that tropospheric mercury depletion events will continue to increase the concentrations of this toxic heavy metal in the Sub Arctic and Arctic marine food webs. BioMed Central 2007-04-17 /pmc/articles/PMC1855925/ /pubmed/17439647 http://dx.doi.org/10.1186/1476-069X-6-11 Text en Copyright © 2007 Sonne et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Sonne, Christian
Dietz, Rune
Leifsson, Pall S
Asmund, Gert
Born, Erik W
Kirkegaard, Maja
Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels?
title Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels?
title_full Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels?
title_fullStr Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels?
title_full_unstemmed Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels?
title_short Are liver and renal lesions in East Greenland polar bears (Ursus maritimus) associated with high mercury levels?
title_sort are liver and renal lesions in east greenland polar bears (ursus maritimus) associated with high mercury levels?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1855925/
https://www.ncbi.nlm.nih.gov/pubmed/17439647
http://dx.doi.org/10.1186/1476-069X-6-11
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