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[新型镇痛药依托唑啉在离体豚鼠回肠和小鼠输精管制剂中与阿片受体的优先作用]

[Preferential action of eptazocine, a novel analgesic, with opioid receptors in isolated guinea pig ileum and mouse vas deferens preparations].

作者信息

Tamura T, Ogawa J, Taniguchi T, Waki I

机构信息

Central Research Laboratories, Nihon Iyakuhin Kogyo Co., Ltd., Toyama, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1990 Jan;95(1):41-6. doi: 10.1254/fpj.95.1_41.

Abstract

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.

摘要

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。

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