Portal de Periódicos da CAPES

TRK-820, a Selective κ-Opioid Agonist, Produces Potent Antinociception in Cynomolgus Monkeys

2001; Japanese Pharmacological Society; Volume: 85; Issue: 3 Linguagem: Inglês

10.1254/jjp.85.282

1347-3506

Takashi Endoh, Atsushi Tajima, Naoki Izumimoto, Tomohiko Suzuki, Akiyoshi Saitoh, Tsutomu Suzuki, Minora Narita, Junzo Kamei, Leon F. Tseng, Hirokazu Mizoguchi, Hiroshi Nagase,

Receptor Mechanisms and Signaling

TRK-820 ((-)-17-cyclopropylmethyl-3,14b-dihydroxy-4,5a-epoxy-6b-[N-methyl-tra«s-3-(3-furyl)acrylamide]morphinan hydrochloride) has been shown to be a potent opioid κ-receptor agonist with pharmacological properties different from those produced by κ1-opioid receptor agonists in rodents. To ascertain whether or not these properties of TRK-820 would be extended to primates, the antinociceptive effect of TRK-820 was evaluated in cynomolgus monkeys by the hot-water tail-withdrawal procedure. TRK-820 given intramuscularly (i.m.) produced a potent antinociceptive effect that was 295- and 495-fold more potent than morphine with the 50°C and 55°C hot-water tests, respectively, and 40-fold more potent than U-50,488H and 1,000-fold more potent than pentazocine in the 50°C hot-water test. The duration of antinociceptive effects of TRK-820 treatment (0.01 and 0.03 mg/kg, i.m.) lasted more than 6 h, which was much longer than those of U-50,488H. The antinociception produced by the higher dose (0.03 mg /kg, i.m.) of TRK-820 was not inhibited by nor-binaltorphimine (3.2 and 10 mg /kg, s.c.) or by naloxone (0.1 mg /kg, s.c.), although the antinociception induced by a lower dose of TRK-820 (0.01 mg/kg, i.m.) was inhibited by nor-binaltorphimine (10 mg/kg, s.c.). The same doses of nor-binaltorphimine and naloxone effectively inhibited the antinociception induced by the higher doses ofU-50,488H (1.0 mg /kg, i.m.) and morphine (10 mg/kg, i.m.), respectively. These results indicate that the antinociception induced by TRK-820 is less sensitive to nor-binaltorphimine and suggest that it is mediated by the stimulation of a subtype of κ-opioid receptor different from the κ1-opioid receptor in cynomolgus monkeys.