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Inhibition of morphine withdrawal by the NMDA receptor antagonist MK‐801 in rat is age‐dependent
Author(s) -
Zhu Hongbo,
Barr Gordon A.
Publication year - 2001
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.1051
Subject(s) - nmda receptor , morphine , saline , naltrexone , antagonist , opiate , dizocilpine , kindling , physical dependence , receptor antagonist , morphine sulfate , chemistry , litter , anesthesia , endocrinology , medicine , pharmacology , receptor , biology , stimulation , agronomy
This study investigated the effects of the NMDA receptor antagonist MK‐801 on the development of morphine dependence in 7‐, 14‐, and 21‐day‐old rat pups. For 6.5 days, starting at 1, 8, or 15 days of age, rats were pretreated with MK‐801 (0.03 or 0.1 mg/kg, bid) or saline; 15 min later, morphine sulfate (10 mg/kg) or saline was injected to induce opiate dependence. On the afternoon of the seventh day, pups were injected with MK‐801 (0.1 mg/kg) or saline and 15 min later with naltrexone (1 mg/kg) to precipitate withdrawal. Pups were then placed in a warm chamber with the litter and their behavior scan‐sampled every 15 sec for a total of 15 min. MK‐801 failed to inhibit morphine withdrawal in the 7‐day‐old rat, but did attenuate the development of morphine dependence in both the 14‐ and 21‐day‐old rats. These results suggest that the NMDA receptor is not functionally active in opiate withdrawal until around the second to third week of postnatal life in the rat and that there exists a transition period for the NMDA receptor to play a role in the development of opiate dependence and withdrawal. Synapse 40:282–293, 2001. © 2001 Wiley‐Liss, Inc.