Tamura T, Ogawa J, Taniguchi T, Waki I
Central Research Laboratories, Nihon Iyakuhin Kogyo Co., Ltd., Toyama, Japan.
Nihon Yakurigaku Zasshi. 1990 Jan;95(1):41-6. doi: 10.1254/fpj.95.1_41.
Actions of eptazocine, a novel analgesic, on isolated smooth muscle preparations were investigated. Eptazocine (10(-5) M) slightly inhibited electrically-driven twitch-tension in guinea pig ileum preparations sensitive to mu- and kappa-agonists, and this effect was antagonized by 10(-7) M naloxone. Eptazocine (10(-5)-10(-4) M) inhibited such an effect by the mu-agonist morphine. In mouse vas deferens preparations having delta-, mu- and kappa-receptors, eptazocine (10(-7) M-) inhibited the twitch-tension in a dose-dependent manner, being hardly inhibited by naloxone. On the other hand, MR-2266 (10(-6) M), a relatively selective kappa-receptor antagonist, inhibited the eptazocine effect. The Ke (equilibrium dissociation constant) value of naloxone against eptazocine was 325 nM and the Ke value of MR-2266 against eptazocine was 33.2 nM, showing that MR-2266 was 9.79-fold more effective than naloxone. These results suggest that eptazocine acted as a mu-receptor antagonist and as a kappa-receptor preferential agonist in isolated smooth muscle preparations.
研究了新型镇痛药依他佐辛对离体平滑肌制剂的作用。依他佐辛(10⁻⁵ M)对豚鼠回肠制剂中对μ和κ激动剂敏感的电驱动抽搐张力有轻微抑制作用,且此作用被10⁻⁷ M纳洛酮拮抗。依他佐辛(10⁻⁵ - 10⁻⁴ M)抑制μ激动剂吗啡的这种作用。在具有δ、μ和κ受体的小鼠输精管制剂中,依他佐辛(10⁻⁷ M -)以剂量依赖性方式抑制抽搐张力,几乎不被纳洛酮抑制。另一方面,相对选择性的κ受体拮抗剂MR - 2266(10⁻⁶ M)抑制依他佐辛的作用。纳洛酮对依他佐辛的Ke(平衡解离常数)值为325 nM,MR - 2266对依他佐辛的Ke值为33.2 nM,表明MR - 2266的效力比纳洛酮高9.79倍。这些结果表明,在离体平滑肌制剂中,依他佐辛起μ受体拮抗剂和κ受体优先激动剂的作用。