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Is dietary mercury of neurotoxicological concern to wild polar bears ( Ursus maritimus )?
Author(s) -
Basu Niladri,
Scheuhammer Anton M.,
Sonne Christian,
Letcher Robert J.,
Born Erik W.,
Dietz Rune
Publication year - 2009
Publication title -
environmental toxicology and chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.1
H-Index - 171
eISSN - 1552-8618
pISSN - 0730-7268
DOI - 10.1897/08-251.1
Subject(s) - ursus maritimus , mercury (programming language) , polar , mercury exposure , zoology , biology , ecology , biomonitoring , arctic , computer science , programming language , physics , astronomy
Polar bears ( Ursus maritimus ) are exposed to high concentrations of mercury because they are apex predators in the Arctic ecosystem. Although mercury is a potent neurotoxic heavy metal, it is not known whether current exposures are of neurotoxicological concern to polar bears. We tested the hypotheses that polar bears accumulate levels of mercury in their brains that exceed the estimated lowest observable adverse effect level (20 μg/g dry wt) for mammalian wildlife and that such exposures are associated with subtle neurological damage, as determined by measuring neurochemical biomarkers previously shown to be disrupted by mercury in other high‐trophic wildlife. Brain stem (medulla oblongata) tissues from 82 polar bears subsistence hunted in East Greenland were studied. Despite surprisingly low levels of mercury in the brain stem region (total mercury = 0.36 ±0.12 μg/g dry wt), a significant negative correlation was measured between N ‐methyl‐D‐aspartate (NMDA) receptor levels and both total mercury ( r = —0.34, p < 0.01) and methylmercury ( r = —0.89, p < 0.05). No relationships were observed among mercury, selenium, and several other neurochemical biomarkers (dopamine‐2, gamma‐aminobutyric acid type A, muscarinic cholinergic, and nicotinic cholinergic receptors; cholinesterase and monoamine oxidase enzymes). These data show that East Greenland polar bears do not accumulate high levels of mercury in their brain stems. However, decreased levels of NMDA receptors could be one of the most sensitive indicators of mercury's subclinical and early effects.

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