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μ-阿片受体激动剂和拮抗剂与丁丙诺啡对小鼠镇痛作用的相互作用。

Interaction of mu-opioid receptor agonists and antagonists with the analgesic effect of buprenorphine in mice.

作者信息

Kögel Babette, Christoph Thomas, Strassburger Wolfgang, Friderichs Elmar

机构信息

Department of Pharmacology, Biomedical Research, Grünenthal GmbH, Zieglerstr. 6, 52099 Aachen, Germany.

出版信息

Eur J Pain. 2005 Oct;9(5):599-611. doi: 10.1016/j.ejpain.2005.02.002.

Abstract

Buprenorphine is a potent opioid analgesic with partial agonistic properties at mu-opioid receptors. This study investigated the interaction potential with several full mu-agonists in the tail-flick test in mice. We further examined the reversibility of buprenorphine antinociception by different mu-opioid receptor antagonists. Combination of buprenorphine with morphine, oxycodone, hydromorphone and fentanyl in the analgesic dose range resulted in additive or synergistic effects. When given after the decline of the acute buprenorphine effect, both morphine and fentanyl also showed full efficacy. A moderate antagonistic effect according to the partial mu-agonistic properties of buprenorphine was only seen when high doses exceeding the therapeutic dose ranges were combined. Under these conditions antinociception of morphine was reduced to the effect of buprenorphine alone. Prophylactic administration of naloxone (10 mg/kg i.v.), naltrexone (1 mg/kg i.v.) and clocinnamox (5 mg/kg s.c.) fully and persistently blocked the antinociception of a high dose of buprenorphine. An established effect of buprenorphine was less sensitive, although repeated administration of naloxone induced complete antagonism, as did the irreversible antagonist clocinnamox under prophylactic and curative treatment conditions. Our results suggest that the antinociceptive effect of buprenorphine is mainly, if not exclusively, mediated by activation of mu-opioid receptors. They confirm clinical experience that in the analgesic dose range a switch between buprenorphine and full mu-agonists is possible without loss of analgesic efficacy and without a refractory period between the termination of buprenorphine analgesia and the onset of action of the new mu-opioid treatment. Antinociception of buprenorphine is sensitive towards mu-opioid receptor antagonists and incomplete inhibition can be improved by increasing the dose or repetitive dosing.

摘要

丁丙诺啡是一种强效阿片类镇痛药,对μ-阿片受体具有部分激动特性。本研究在小鼠甩尾试验中研究了其与几种完全μ-激动剂的相互作用潜力。我们进一步研究了不同μ-阿片受体拮抗剂对丁丙诺啡镇痛作用的可逆性。丁丙诺啡与吗啡、羟考酮、氢吗啡酮和芬太尼在镇痛剂量范围内联合使用会产生相加或协同作用。在丁丙诺啡急性作用消退后给予吗啡和芬太尼,它们也均显示出完全疗效。仅在联合使用超过治疗剂量范围的高剂量时,才会根据丁丙诺啡的部分μ-激动特性出现中度拮抗作用。在这些条件下,吗啡的镇痛作用减弱至仅丁丙诺啡的作用水平。预防性静脉注射纳洛酮(10 mg/kg)、纳曲酮(1 mg/kg)和皮下注射氯辛那明(5 mg/kg)可完全且持续地阻断高剂量丁丙诺啡的镇痛作用。丁丙诺啡已确立的作用不太敏感,尽管重复注射纳洛酮可诱导完全拮抗作用,在预防性和治疗性给药条件下不可逆拮抗剂氯辛那明也能如此。我们的结果表明,丁丙诺啡的镇痛作用主要(如果不是唯一)由μ-阿片受体的激活介导。它们证实了临床经验,即在镇痛剂量范围内,丁丙诺啡与完全μ-激动剂之间可以切换,而不会损失镇痛效果,且在丁丙诺啡镇痛作用终止与新的μ-阿片类治疗起效之间没有不应期。丁丙诺啡的镇痛作用对μ-阿片受体拮抗剂敏感,增加剂量或重复给药可改善不完全抑制作用。

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