• 1 January 1977
    • journal article
    • research article
    • Vol. 201 (1), 44-54
Abstract
Rats were trained to press a lever (respond) under a fixed-ratio 20 schedule for food presentation. Administration of 10 or 25 mg of naloxone (NX)/kg i.p. to drug-naive rats suppressed responding whereas 1 mg of NX/kg was without effect. Administration of 0.25 mg of NX/kg to rats which had received 10 or 15 mg of morphine sulfate/kg 48 h previously induced small, but statistically reliable, decrements in responding. Rats implanted with 1 pellet containing 75 mg of morphine base displayed tolerance to the depressant effects of the morphine pellet within 2 days after implantation. A systematic study of the effects of naloxone given to morphine tolerant-dependent rats revealed good concordance between the amount of weight loss and the severity of behavioral disruption, within the same subject, after administration of the antagonist. Although 0.03 mg of NX/kg given 3-6 days after pellet implantation significantly suppressed responding, 0.1 mg of NX/kg was required to produce a significant reduction in body weight. Semiweekly injections of 1 mg of NX/kg continued to suppress responding up to 4 wk after implantation of a single morphine pellet. The body weight changes were significant only up to 3 wk after implantation. Disruption of fixed-ratio responding is a sensitive indicator of antagonist-precipitated morphine withdrawal.