Dose-Dependent Effects of the Dopamine D1 Receptor Agonists A77636 or SKF81297 On Spatial Working Memory in Aged Monkeys1

Abstract

With advancing age, monkeys develop deficits in spatial working memory resembling those induced by lesions of the prefrontal cortex (PFC). Aged monkeys also exhibit marked loss of dopamine from the PFC, a transmitter known to be important for proper PFC cognitive function. Previous results suggest that D1 agonist treatment can improve spatial working memory abilities in aged monkeys. However, this research was limited by the use of drugs with either partial agonist actions or significant D2 receptor actions. In our study, the selective dopamine D1 receptor full agonists A77636 and SKF81297 were examined in aged monkeys for effects on the working memory functions of the PFC. Both compounds produced a significant, dose-related effect on delayed response performance without evidence of side effects: low doses improved performance although higher doses impaired or had no effect on performance. Both the improvement and impairment in performance were reversed by pretreatment with the D1 receptor antagonist, SCH23390. These findings are consistent with previous results demonstrating that there is a narrow range of D1 receptor stimulation for optimal PFC cognitive function, and suggest that very low doses of D1 receptor agonists may have cognitive-enhancing actions in the elderly.

Footnotes

  • Send reprint requests to: Dr. A. F. T. Arnsten, Section of Neurobiology, Yale Medical School, 333 Cedar St., New Haven, CT 06510-8001.

  • 1 This work was supported by The Chinese Academy of Sciences KP-85, KY-85 and NSFC to J.X.C. and Public Health Service Grant AG06036 to A.F.T.A.

  • Abbreviations:
    PFC
    prefrontal cortex
    DA
    dopamine
    6-OHDA
    6-hydroxydopamine
    WGTA
    Wisconsin General Test Apparatus
    1-ANOVA-R
    one-way analysis of variance with repeated measures
    Tdep
    dependent (i.e., paired) t test
    MPTP
    N-methyl-4 phenyl 1,2,5,6 tetrahydropyridine
    • Received March 11, 1997.
    • Accepted June 9, 1997.
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