Behavioural and neurochemical adaptations to nicotine in rats: influence of NMDA antagonists

1 The repeated co‐administration of the non‐competitive N‐methyl‐d‐aspartate (NMDA) receptor antagonist dizocilpine (0.1 and 0.3 mg kg−1, i.p.) with nicotine (0.4 mg kg−1, s.c.) attenuated the development of tolerance to the locomotor depressant effect of the nicotine in rats. 2 The repeated co‐administration of the competitive NMDA antagonist d‐CPPene (SDZ EAA 494; 3‐(2‐carboxypiperazin‐4‐yl)‐1‐propenyl‐1‐phosphonic acid, 2 and 8 mg kg−1, i.p.) also attenuated tolerance to the locomotor depressant effect of nicotine. 3 Dizocilpine (0.3 mg kg−1, i.p.) pretreatment attenuated sensitization to the locomotor stimulant effect of nicotine (0.4 mg kg−1, s.c.) and prevented sensitization of nicotine‐induced dopamine release in the nucleus accumbens. However, pretreatment with dizocilpine alone caused a modest enhancement of the behavioural response to a subsequent acute dose of nicotine. 4 d‐CPPene (2.0 mg kg−1, i.p.) pretreatment prevented sensitization to the nicotine‐induced dopamine release in the nucleus accumbens. There was no enhanced locomotor response that could be attributed to nicotine pretreatment when d‐CPPene was co‐administered with nicotine. However, pretreatment with d‐CPPene alone enhanced the locomotor response to an acute dose of nicotine. 5 The results suggest the involvement of NMDA receptors in adaptations of the behavioural and neurochemical effects of nicotine that occur as a result of repeated administration of the drug.