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Discriminative stimulus effects of morphine: central versus peripheral training
J P Cleary1, E O'Hare, J D Pomonis
1Department of Psychology, University of Minnesota, Minneapolis, USA.
Brain Research
|November 24, 1999
Summary
Rats learned to distinguish direct brain morphine injections from saline. Peripheral morphine injections generalized to brain-trained cues, but not vice versa, indicating distinct drug discrimination pathways.
Area of Science:
- Neuroscience
- Pharmacology
- Behavioral Science
Background:
- Rats can differentiate peripheral morphine from saline.
- Discrimination of direct brain-site morphine injections from saline has not been previously studied.
Purpose of the Study:
- To train rats to discriminate direct brain-site injections of morphine from saline.
- To investigate the generalization of morphine's effects between central and peripheral administration routes.
- To examine the role of naloxone in blocking morphine discrimination.
Main Methods:
- Rats were trained to discriminate morphine (0.3 microgram) from saline injected into the perifornical area of the hypothalamus (PFA).
- Dose-response generalization curves were generated for both PFA and intraperitoneal (i.p.) morphine injections.
- Naloxone was administered centrally (PFA) and peripherally to assess its blocking effects on discrimination.
Main Results:
- Rats learned to discriminate PFA-injected morphine in approximately 37 sessions.
- Peripheral morphine injections generalized to PFA-trained morphine cues, but PFA injections did not generalize to i.p.-trained cues.
- Naloxone administered centrally or peripherally blocked discrimination in PFA-trained rats, but not in i.p.-trained rats when co-administered with i.p. morphine.
Conclusions:
- Morphine discrimination differs depending on the injection site (central vs. peripheral).
- Peripheral morphine administration shares some discriminative stimulus effects with centrally administered morphine.
- The study highlights distinct neural pathways involved in central and peripheral morphine perception.