Abstract
In rats unilaterally lesioned with 6-hydroxydopamine, the D-1 agonist SKF 38393 (3 mg/kg SC) induced contralateral turning only after priming with a dopaminergic agonist such as apomorphine. Administration of the N-methyl-d-aspartate receptor antagonist (+) MK 801 (0.1 mg/kg IP) 15 min before apomorphine (0.1 mg/kg SC) prevented the ability of apomorphine to act as a primer while potentiating its acute contralateral turning effects. The inactive isomer (−) MK 801 was without effect. The results indicate that the N-methyl-d-aspartate receptor exerts a permissive role on priming.
References
Collingridge GL, Bliss TVP (1987) NMDA receptors their role in long-term potentiation. Trends Neurosci 10:288–293
Morelli M, Di Chiara G (1987) Agonist-induced homologous and heterologous sensitization to D-1 and D-2 dependent contraversive turning. Eur J Pharmacol 141:101–107
Morelli M, Fenu S, Garau L, Di Chiara G (1989) Time and dose dependence of the “priming” of the expression of dopamine receptor supersensitivity. Eur J Pharmacol 162:329–335
Morris RGM, Anderson E, Lynch GS, Baudry M (1986) Selective impairment of learning and blockade of long-term potentiation by an N-methyl-d-aspartate-receptor antagonist, AP5. Nature 319:774–776
Robinson TE (1988) Stimulant drugs and stress: factors influencing individual differences in the susceptibility to sensitization. In: Kalivas PW, Barnes C (eds) Sensitization of the nervous system. Telford Press, Caldwell, N.J., pp 145–173
Wong EHF, Knight AR, Woodruff GN (1988) [3H]MK-801 labels a site on the N-methyl-d-aspartate receptor channel complex in rat brain membranes. J Neurochem 50:274
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Morelli, M., Di Chiara, G. Stereospecific blockade of N-methyl-d-aspartate transmission by MK 801 prevents priming of SKF 38393-induced turning. Psychopharmacology 101, 287–288 (1990). https://doi.org/10.1007/BF02244143
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DOI: https://doi.org/10.1007/BF02244143