Abstract
In order to study age-related differences in striatal electrophysiological activity in freely-moving animals, multi-wire electrode arrays were chronically implanted in the striatum of young (6-8 months) and aged (24-26 months) Fischer 344 rats. After recording baseline activity, d-amphetamine (D-AMPH; 1.0 mg/kg) and apomorphine (APO; 0.5 mg/kg) were administered to the two age groups. For both the D-AMPH and APO series, the percentage of striatal neurons that increased firing rates as a result of the DA agonists was 19% higher in the old animals than in the young animals. In addition, D-AMPH increased the firing rates of D-AMPH-excited neurons to a greater extent in the old animals than in the young animals. While the rate-increasing effects of APO did not differ significantly as a function of age, its effects were slightly greater in the old animals as well. These results suggest that age-related decreases in nigrostriatal DA function may result in alterations in the way in which the striatum integrates corticostriatal and nigrostriatal inputs to influence motor function.
Original language | English |
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Pages (from-to) | 263-270 |
Number of pages | 8 |
Journal | Neurobiology of Aging |
Volume | 23 |
Issue number | 2 |
DOIs | |
State | Published - 2002 |
Bibliographical note
Funding Information:This work was supported by grants from USPHS AG06434, AG13494, NS39787, and a level II Research Scientist Award (MH01245) to G. Gerhardt.
Funding
This work was supported by grants from USPHS AG06434, AG13494, NS39787, and a level II Research Scientist Award (MH01245) to G. Gerhardt.
Funders | Funder number |
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Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke Council | P50NS039787 |
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke Council | |
U.S. Public Health Service | AG13494, AG06434, MH01245 |
U.S. Public Health Service |
Keywords
- Aging
- Basal ganglia
- Dopamine
- Electrophysiology
- Freely-moving
- Multiunit
- Striatum
ASJC Scopus subject areas
- General Neuroscience
- Aging
- Clinical Neurology
- Developmental Biology
- Geriatrics and Gerontology