Abstract
Effects of low (butorphanol, nalbuphine)-, intermediate (buprenorphine)-, and high (morphine, levorphanol)-efficacy μ opioids were examined in F344, Sprague-Dawley (SD), Long-Evans (LE), and Lewis rats using a tail withdrawal and a drug discrimination procedure. In the tail withdrawal procedure using low (50°C), intermediate (52°C), and high (56°C) water temperatures, morphine and levorphanol produced maximal effects in each of the strains and were most potent in F344 and least potent in Lewis. Similar differences across strains were obtained with buprenorphine, and at the high intensity, maximal effects were not obtained in Lewis. At the low intensity, butorphanol produced maximal effects in F344 and SD at relatively low doses, half-maximal effects in LE at very high doses, and no effect in Lewis. Nalbuphine produced near maximal effects in F344 and SD when tested with the low intensity and no effect in the LE and Lewis. Similar results were obtained at the intermediate intensity for these opioids, although the absolute level of antinociception was lower. These results indicate that there are profound differences to the antinociceptive effects of μ opioids across rat strains. The magnitude of these differences increased with higher stimulus intensities and when tested with lower efficacy opioids. In rats trained to discriminate morphine (3.0 or 5.6 mg/kg) from water, there were no consistent differences across rat strains to the effects of these μ opioids. Possible reasons for differences between the results obtained in the tail withdrawal and drug discrimination procedures are discussed.
Footnotes
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Send reprint requests to: Mitchell J. Picker, University of North Carolina, Department of Psychology, CB#3270, Davie Hall, Chapel Hill, NC 27599-3270. E-mail:mjpicker{at}emailunc.edu
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↵1 This work was supported by National Institute on Drug Abuse Grant DA10277.
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↵2 Supported by National Institute on Drug Abuse Predoctoral Fellowship DA05669. This manuscript partially fulfills the requirements for the Doctor of Philosophy Degree from the University of North Carolina at Chapel Hill. Present address: Department of Physiology and Pharmacology, Center for the Neurobiological Investigation of Drug Abuse, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC.
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↵3 Supported by National Institute on Drug Abuse Training Grant DA07244.
- Abbreviations:
- LE
- Long-Evans
- FR
- fixed ratio schedule
- SD
- Sprague-Dawley
- Received June 29, 1998.
- Accepted January 12, 1999.
- The American Society for Pharmacology and Experimental Therapeutics
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