Effects of the non-competitive NMDA-receptor antagonist memantine on morphine- and cocaine-induced potentiation of lateral hypothalamic brain stimulation reward

Citation
Tm. Tzschentke et Wj. Schmidt, Effects of the non-competitive NMDA-receptor antagonist memantine on morphine- and cocaine-induced potentiation of lateral hypothalamic brain stimulation reward, PSYCHOPHAR, 149(3), 2000, pp. 225-234
Citations number
70
Categorie Soggetti
Neurosciences & Behavoir
Journal title
Volume
149
Issue
3
Year of publication
2000
Pages
225 - 234
Database
ISI
SICI code
Abstract
Rationale: NMDA-receptor antagonists may be of potential therapeutic use in several states of disease. It has been reported that drugs like MK-801 can potentiate the rewarding effects of other drugs, which may complicate the therapeutic use of this class of drugs. However, since MK-801 appears to be an "atypical" drug in several respects, other NMDA-receptor antagonists ma y not share this effect of MK-801. Objectives. We tested the effects of mem antine, a clinically used NMDA-receptor antagonist, in a paradigm that has previously shown the reward-potentiating effects of MK-801 to see if this d rug would yield qualitatively comparable results. Methods: The effects of m emantine on morphine- and cocaine-induced potentiation of brain stimulation reward were examined, using the rate-free curve-shift paradigm. Results: L ow doses of morphine (2.5 mg/kg) and cocaine (5 mg/kg) produced moderate de creases in the reward threshold frequency reflected in moderate leftward sh ifts of the function relating response rate to stimulation frequency. These effects were not altered by co-administration of an intermediate dose of m emantine (5 mg/kg), but maximum response rate was significantly increased b y these drug combinations. Higher doses of morphine (7.5 mg/kg) and cocaine (10 mg/kg) had stronger effects on the rate-frequency function and reward threshold. These effects were enhanced by co-administration of a high dose of memantine (10 mg/kg), while the effects on maximum response rate were le ss pronounced. Conclusions: These results demonstrate that fairly high dose s of memantine and morphine or cocaine have to be combined in order to obse rve an enhancement of the latter drugs' potentiation of brain stimulation r eward. In this respect, memantine differs markedly from MK-801, another non -competitive NMDA-receptor antagonist which has been shown to interact with morphine and cocaine at very low doses.