Application of Neurochemical Markers for Assessing Health Effects after Developmental Methylmercury and PCB Coexposure
Cholinergic muscarinic receptors (MRs) and monoamine oxidase activity (MAO-B), expressed both in brain and blood cells, were investigated in animals and exposed subjects to assess (i) MeHg (0.5–1 mg/kg/day GD7-PD7) and/or PCB153 (20 mg/kg/day GD10–GD16) effects on cerebellar MAO-B and MRs, and lymph...
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| Format: | Article |
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Wiley
2012-01-01
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| Series: | Journal of Toxicology |
| Online Access: | http://dx.doi.org/10.1155/2012/216032 |
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| author | E. Roda L. Manzo T. Coccini |
| author_facet | E. Roda L. Manzo T. Coccini |
| author_sort | E. Roda |
| collection | DOAJ |
| description | Cholinergic muscarinic receptors (MRs) and monoamine oxidase activity (MAO-B), expressed both in brain and blood cells, were investigated in animals and exposed subjects to assess (i) MeHg (0.5–1 mg/kg/day GD7-PD7) and/or PCB153 (20 mg/kg/day GD10–GD16) effects on cerebellar MAO-B and MRs, and lymphocyte MRs, in dams and offspring 21 days postpartum; (ii) MAO-B in platelets and MRs in lymphocytes of a Faroese 7-year-old children cohort, prenatally exposed to MeHg/PCBs. Animal Data. MAO-B was altered in male cerebellum by MeHg, PCB153, and their combination (35%, 45%, and 25% decrease, resp.). Cerebellar MRs were enhanced by MeHg alone in dams (87%) and male pups (27%). PCB153 alone and in mixture did not modify cerebellar MRs. Similarly to brain, lymphocyte MRs were enhanced in both dams and offspring by MeHg alone. All changes were caused by 1 MeHg mg/kg/day, the lower dose was ineffective. Human Data. Both biomarkers showed homogeneous distributions within the cohort (MRs, range 0.1–36.78 fmol/million cells; MAO-B, 0.95–14.95 nmol/mg protein/h). No correlation was found between the two biomarkers and neurotoxicant concentrations in blood (pre- and postnatally). |
| format | Article |
| id | doaj-art-a19ab80a94654b39b671f5c366a0647e |
| institution | Kabale University |
| issn | 1687-8191 1687-8205 |
| language | English |
| publishDate | 2012-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Journal of Toxicology |
| spelling | doaj-art-a19ab80a94654b39b671f5c366a0647e2025-02-03T06:07:28ZengWileyJournal of Toxicology1687-81911687-82052012-01-01201210.1155/2012/216032216032Application of Neurochemical Markers for Assessing Health Effects after Developmental Methylmercury and PCB CoexposureE. Roda0L. Manzo1T. Coccini2Laboratory of Clinical Toxicology, Salvatore Maugeri Foundation IRCCS, Institute of Pavia, 27100 Pavia, ItalyLaboratory of Clinical Toxicology, Salvatore Maugeri Foundation IRCCS, Institute of Pavia, 27100 Pavia, ItalyLaboratory of Clinical Toxicology, Salvatore Maugeri Foundation IRCCS, Institute of Pavia, 27100 Pavia, ItalyCholinergic muscarinic receptors (MRs) and monoamine oxidase activity (MAO-B), expressed both in brain and blood cells, were investigated in animals and exposed subjects to assess (i) MeHg (0.5–1 mg/kg/day GD7-PD7) and/or PCB153 (20 mg/kg/day GD10–GD16) effects on cerebellar MAO-B and MRs, and lymphocyte MRs, in dams and offspring 21 days postpartum; (ii) MAO-B in platelets and MRs in lymphocytes of a Faroese 7-year-old children cohort, prenatally exposed to MeHg/PCBs. Animal Data. MAO-B was altered in male cerebellum by MeHg, PCB153, and their combination (35%, 45%, and 25% decrease, resp.). Cerebellar MRs were enhanced by MeHg alone in dams (87%) and male pups (27%). PCB153 alone and in mixture did not modify cerebellar MRs. Similarly to brain, lymphocyte MRs were enhanced in both dams and offspring by MeHg alone. All changes were caused by 1 MeHg mg/kg/day, the lower dose was ineffective. Human Data. Both biomarkers showed homogeneous distributions within the cohort (MRs, range 0.1–36.78 fmol/million cells; MAO-B, 0.95–14.95 nmol/mg protein/h). No correlation was found between the two biomarkers and neurotoxicant concentrations in blood (pre- and postnatally).http://dx.doi.org/10.1155/2012/216032 |
| spellingShingle | E. Roda L. Manzo T. Coccini Application of Neurochemical Markers for Assessing Health Effects after Developmental Methylmercury and PCB Coexposure Journal of Toxicology |
| title | Application of Neurochemical Markers for Assessing Health Effects after Developmental Methylmercury and PCB Coexposure |
| title_full | Application of Neurochemical Markers for Assessing Health Effects after Developmental Methylmercury and PCB Coexposure |
| title_fullStr | Application of Neurochemical Markers for Assessing Health Effects after Developmental Methylmercury and PCB Coexposure |
| title_full_unstemmed | Application of Neurochemical Markers for Assessing Health Effects after Developmental Methylmercury and PCB Coexposure |
| title_short | Application of Neurochemical Markers for Assessing Health Effects after Developmental Methylmercury and PCB Coexposure |
| title_sort | application of neurochemical markers for assessing health effects after developmental methylmercury and pcb coexposure |
| url | http://dx.doi.org/10.1155/2012/216032 |
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