Abstract
The effects of N-methyl-d-aspartate receptor blockade on two major variants of rabbit eyeblink conditioning were evaluated using a selective noncompetitive antagonist, [5R, 10S]-[+]-5-methyl-10,11-dihydro-5H-dibenzo[a, d] cyclo-hepten-5,10-imine hydrogen maleate; dizocilpine (MK-801) or phencyclidine (PCP), a drug of abuse. Either MK-801 or PCP (given daily) impaired rabbits’ ability to associate tone conditioned stimuli with airpuff unconditioned stimuli, with the severity of impairment exhibiting clear dose and task dependencies. Trace-conditioned rabbits given ≥ 80 μg/kg of MK-801 or ≥1.0 mg/kg of PCP failed to reach a criterion of 80% conditioned responses during training, with significant impairments seen at intermediate doses. Delay-conditioned rabbits, although dose-dependently slowed, successfully acquired the task, even when given doses of MK-801 or PCP that completely blocked acquisition in trace conditioning. Additionally, even low doses of MK-801 (10 μg/kg) or of PCP (0.1 mg/kg) severely altered conditioned response timing in trace but not in delay conditioning, resembling effects observed after hippocampal lesions. Doses of MK-801 or PCP that impaired acquisition also severely impaired extinction of both trace- and delay-conditioned eyeblink responses. However, neither MK-801 nor PCP altered retention or timing of previously learned responses. Higher doses of MK-801 (≥200 μg/kg) or of PCP (≥2.0 mg/kg) dose-dependently impaired unconditioned response performance, although lower doses of MK-801 (≤160 μg/kg) or of PCP (≤1.0 mg/kg) had no effects on unconditioned responses or on nonassociative pseudoconditioned responses. The deficits observed indicate that although not necessary for retention, N-methyl-d-aspartate receptor activation may facilitate acquisition of delay-conditioning. N-methyl-d-aspartate receptor activation appears to be necessary for acquisition of trace conditioning, and for extinction in either paradigm.
Footnotes
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Send reprint requests to: Dr. L. T. Thompson, Department of CM Biology, Northwestern University Medical School, 303 E. Chicago Ave., Chicago, IL 60611-3008.
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↵1 This work was supported by 1 R01 AG08796 and 1 R01 DA07633.
- Abbreviations:
- NMDA
- N-methyl-d-aspartate
- MK-801
- ([5R, 10S]-[+]-5-methyl-10,11-dihydro-5H-dibenzo[a, d] cyclo-hepten-5,10-imine hydrogen maleate
- dizocilpine)
- PCP, phencyclidine (1-[1-phencyclohexyl] piperidine)
- LTP
- long-term potentiation
- AP5
- D-2-amino-phosphonopentanoate
- NMR
- nictitating membrane response
- CS
- conditioned stimulus
- US
- unconditioned stimulus
- CR
- conditioned response
- UR
- unconditioned response
- NZW
- New Zealand white
- ISI
- interstimulus interval
- Received September 16, 1996.
- Accepted January 8, 1997.
- The American Society for Pharmacology and Experimental Therapeutics
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