This project investigates the neurobehavioral effects of ingested aluminum (Al). Brain Al accumulation and changes in neurobehavioral indices have been described after dietary exposure to Al in both adult and developing mice. In addition, alterations in tissue Mn and Fe have been documented after developmental but not adult exposure. During the current project period, the behavioral work will be extended to characterize progression/ reversal of effects on neurobehavioral indices (reflexes, activity level, auditory startle) after discontinuation of exposure and possible delayed onset of effects late in the lifespan. In addition, possible deficits in spatial task performance and changes in food motivation suggested by recently completed operant studies will be investigated. Work on brain Al accumulation will involve regional Al localization in the central nervous system (CNS) during development using a guinea pig model. To follow up findings of altered tissue Fe and Mn, developmental indices dependent on these trace elements will be studied. Also, effects of dietary Al on Fe and Mn absorption and tissue distribution will be addressed. As an initial approach to identifying targets of action, CNS cell types (neurons and glia) will be studied in cell culture. These studies will also be designed to determine the biological actions of Al-transferrin (Al-Trf), the predominate Al species in serum, which might be relevant to toxicological effects at the cellular level. Fe and Mn uptake, transferrin receptor number and affinity and transferrin mRNA will be measured in cells exposed to Al-transferrin. Through this work we hope to further clarify potential human health risks associated with ingestion of aluminum in food, water and pharmaceuticals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
2R01ES004190-07A1
Application #
2153600
Study Section
Pharmacology A Study Section (PHRA)
Project Start
1987-02-01
Project End
1996-12-31
Budget Start
1994-02-01
Budget End
1995-01-31
Support Year
7
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of California Davis
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Golub, Mari S; Zhang, Wei; Keen, Carl L et al. (2002) Cellular actions of Al at low (1.25 microM) concentrations in primary oligodendrocyte culture. Brain Res 941:82-90
Golub, M S; Germann, S L (2001) Long-term consequences of developmental exposure to aluminum in a suboptimal diet for growth and behavior of Swiss Webster mice. Neurotoxicol Teratol 23:365-72
Golub, M S; Germann, S L; Han, B et al. (2000) Lifelong feeding of a high aluminum diet to mice. Toxicology 150:107-17
Kwik-Uribe, C L; Golub, M S; Keen, C L (2000) Chronic marginal iron intakes during early development in mice alter brain iron concentrations and behavior despite postnatal iron supplementation. J Nutr 130:2040-8
Kwik-Uribe, C L; Gietzen, D; German, J B et al. (2000) Chronic marginal iron intakes during early development in mice result in persistent changes in dopamine metabolism and myelin composition. J Nutr 130:2821-30
Golub, M S (2000) Adolescent health and the environment. Environ Health Perspect 108:355-62
Kwik-Uribe, C L; Golubt, M S; Keen, C L (1999) Behavioral consequences of marginal iron deficiency during development in a murine model. Neurotoxicol Teratol 21:661-72
Golub, M S; Keen, C L (1999) Effects of dietary aluminum on pubertal mice. Neurotoxicol Teratol 21:595-602
Golub, M S; Han, B; Keen, C L (1999) Aluminum uptake and effects on transferrin mediated iron uptake in primary cultures of rat neurons, astrocytes and oligodendrocytes. Neurotoxicology 20:961-70
Golub, M S; Tarara, R P (1999) Morphometric studies of myelination in the spinal cord of mice exposed developmentally to aluminum. Neurotoxicology 20:953-9

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