The Antinociceptive Effects of Intrathecally Administered Levonantradol and Desacetyllevonantradol in the Rat

Journal of Clinical Pharmacology - Tập 21 Số S1 - 1981
Tony L. Yaksh1
1Department of Neurosurgical Research, Mayo Clinic, Rochester, Minn. 55901.

Tóm tắt

Abstract: Levonantradol and its desacetylated metabolite (desacetyllevonantradol) produced a dose‐dependent increase in the hot plate and tail flick response latencies following intrathecal administration in a dose range from 4 to 40 μg. No difference in potency between the two drugs was observed, as defined by the ED50 values obtained in either test. The duration of the effect of either drug was also dose dependent, ranging from 30 to 120 minutes. No effect on placing, stepping or righting reflexes or the ability of the rats to negotiate a 60° inclined plane was observed at these doses. At the highest doses, however, an exaggerated myoclonic response to abrupt muscle stretch was observed. None of those effects was antagonized by naloxone (2 mg/kg) administered intraperitoneally before or after levonantradol.

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Tài liệu tham khảo

10.1007/BF00426745

Brunk SF, 1975, The analgesic effect of Δ9‐tetrahydrocannabinol, J Clin Pharmacol., 15, 554

Dewey WL, 1972, Some pharmacological and toxicological effects of 1‐trans‐Δ8‐tetrahydrocannabinol and 1‐trans‐Δ9‐tetrahydrocannabinol in laboratory rodents, Arch Int Pharmacodyn Therap., 196, 133

10.1002/cpt197518184

10.1007/BF00432273

10.1002/j.1552-4604.1981.tb02609.x

Milne GM, 1980, Problems of Drug Dependence, 1979., 84

10.1016/B978-0-08-025488-3.50095-7

Goldstein A., 1968, Biostatistics.

10.1016/0031-9384(76)90029-9