ANTICONFLICT EFFECT OF MK-801 IN RATS - TIME-COURSE AND CHRONIC TREATMENT STUDIES

The present study examined the time course and chronic treatment effec ts of the noncompetitive N-methyl-D-aspartate (NMDA) antagonist, MK-80 1 (dizocilpine), an conflict behavior in the conditioned suppression o f drinking (CSD) paradigm, a repeated-measures conflict task. Tn daily 10-min sessions, water-restricted rats drank from a tube that was occ asionally electrified (0.25- or 0.5-mA shocks signaled by a tone). Tra ined subjects (4 weeks of CSD testing) exhibited stable baselines for both punished responding and unpunished responding. In the first exper iment, the effects of MK-801 administered IP were determined in female and male rats following a range of pretreatment intervals (i.e., 0.5- 48 h). In female rats, 0.2 mg/kg MK-801 exerted an anticonflict effect at pretreatment intervals of 10-36 h, but not before 10 h or after 36 h. In male rats, qualitatively similar results were obtained; MK-801 (0.4 mg/kg) exerted anticonflict effects following pretreatment interv als of 6-14 h, but not before 6 or after 14 h. In the second experimen t, chronic treatment of female rats with 0.04, 0.1, or 0.2 mg/kg MK-80 1 resulted in a dose-dependent anticonflict effect in CSD paradigm, wh ich remained stable over the course of 5 weeks of chronic treatment. P unished responding returned to pretreatment levels within 2-3 days aft er discontinuation of chronic treatment with MK-801. These data sugges t that MK-801 exerts a delayed anticonflict effect in both female and male rats with a qualitatively similar pattern, and that there is no t olerance to the anticonflict effect of MK-801 with chronic treatment.