Department of Anesthesiology, First Affiliated Hospital of Sun Yat-sen University, 58 Zhongshan 2nd Road, Guangzhou, Guangdong, 510080, China.
J Pharmacol Exp Ther. 2011 Aug;338(2):579-87. doi: 10.1124/jpet.111.179879. Epub 2011 May 4.
Pentazocine is a widely used mixed agonist-antagonist opioid. Previous animal studies have demonstrated that pentazocine-induced antinociception displayed a ceiling effect characterized by biphasic dose response with a increasing and then descending analgesia like a bell-shaped curve. This study attempted to clarify the mechanisms underlying such dose-response relationships. ddY and C57BL/6J mice received subcutaneous injection of saline or pentazocine (3, 10, 30, 56, or 100 mg · kg(-1)), at 120 min after subcutaneous injection of saline, a μ-opioid receptor antagonist clocinnamox mesylate (C-CAM) (5 mg · kg(-1)), a κ-opioid receptor antagonist nor-binaltorphimine (nor-BNI) (10 mg · kg(-1)), or the combination of C-CAM and nor-BNI. The antinociceptive effects of pentazocine were evaluated using tail pressure, hot plate, tail flick, and acetic acid writhing tests. Without pretreatment with an opioid receptor antagonist, the antinociceptive effects of pentazocine exhibited biphasic bell-shaped dose-response curves peaking at 30 mg · kg(-1). C-CAM completely and partly antagonized the antinociception induced by pentazocine at low (3-30 mg · kg(-1)) and high (56-100 mg · kg(-1)) doses, respectively. nor-BNI enhanced the antinociception by pentazocine at high doses and turned the later descending portion of the biphasic dose-response curves into a sigmoid curve. The combination of C-CAM and nor-BNI completely abolished the antinociception by pentazocine at all doses. Our results suggest pentazocine produces antinociception primarily via activation of μ-opioid receptors, but at high doses, this μ-opioid receptor-mediated antinociception is antagonized by concomitant activation of κ-opioid receptors. This provides the first reasonable hypothesis to explain the ceiling effects of pentazocine analgesia characterized by a biphasic dose response.
喷他佐辛是一种广泛使用的混合激动-拮抗剂阿片类药物。先前的动物研究表明,喷他佐辛诱导的镇痛作用表现出双相剂量反应,呈钟形曲线样的增加和随后的镇痛下降。本研究试图阐明这种剂量反应关系的机制。ddY 和 C57BL/6J 小鼠接受皮下注射生理盐水或喷他佐辛(3、10、30、56 或 100mg·kg(-1)),在皮下注射生理盐水后 120 分钟,给予 μ-阿片受体拮抗剂氯环苯甲肟甲磺酸盐(C-CAM)(5mg·kg(-1))、κ-阿片受体拮抗剂诺宾那替林(nor-BNI)(10mg·kg(-1))或 C-CAM 和 nor-BNI 的组合。使用尾部压力、热板、尾部闪烁和醋酸扭体试验评估喷他佐辛的镇痛作用。在没有预先给予阿片受体拮抗剂的情况下,喷他佐辛的镇痛作用呈双相钟形剂量反应曲线,在 30mg·kg(-1)时达到峰值。C-CAM 完全和部分拮抗低(3-30mg·kg(-1))和高(56-100mg·kg(-1))剂量喷他佐辛诱导的镇痛作用。nor-BNI 增强高剂量喷他佐辛的镇痛作用,并将双相剂量反应曲线的后期下降部分转变为 S 形曲线。C-CAM 和 nor-BNI 的组合完全消除了所有剂量的喷他佐辛的镇痛作用。我们的结果表明,喷他佐辛主要通过激活 μ-阿片受体产生镇痛作用,但在高剂量下,这种 μ-阿片受体介导的镇痛作用被 κ-阿片受体的同时激活所拮抗。这为解释喷他佐辛镇痛的双相剂量反应特征的封顶效应提供了第一个合理的假设。