A Potent Mu-Opioid Receptor Agonist, Dihydroetorphine, Fails to Produce the Conditioned Place Preference in Mice.
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- Tokuyama Shogo
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Nagasaki University
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- Nakamura Fumihiro
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Nagasaki University
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- Nakao Kaoru
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Nagasaki University
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- Takahashi Masakatsu
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Nagasaki University
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- Kaneto Hiroshi
- Department of Pharmacology, Faculty of Pharmaceutical Sciences, Nagasaki University
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Abstract
Reinforcing effects of dihydroetorphine (DHE) and morphine were evaluated by the conditioned place preference paradigm. Both DHE and morphine produced an antinociceptive effect in a dose-dependent manner. On the other hand, DHE (0.1, 1, 3 and 10 μg/kg, i.p.) failed to induce the conditioned preference, while morphine (0.1, 1, 3 and 10 mg/kg, i.p.) caused a dose-dependent preference for the drug-paired place. Thus, these characteristic properties of DHE make it attractive for development as a novel potent analgesic compound that has less dependence liability.
Journal
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- The Japanese Journal of Pharmacology
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The Japanese Journal of Pharmacology 71 (4), 357-360, 1996
The Japanese Pharmacological Society
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Details 詳細情報について
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- CRID
- 1390282679264459008
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- NII Article ID
- 10008189416
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- NII Book ID
- AA00691188
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- COI
- 1:CAS:528:DyaK28XltlKls7o%3D
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- ISSN
- 13473506
- 00215198
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- PubMed
- 8886936
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- Text Lang
- en
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- Data Source
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed