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纳洛酮可阻断左啡诺在豹蛙体内的镇痛作用,但对右啡烷的镇痛作用无影响。

Naloxone blocks the analgesic action of levorphanol but not of dextrorphan in the leopard frog.

作者信息

Stevens C W, Pezalla P D

出版信息

Brain Res. 1984 May 28;301(1):171-4. doi: 10.1016/0006-8993(84)90418-9.

DOI:10.1016/0006-8993(84)90418-9
PMID:6329442
Abstract

Intraspinal injection of levorphanol (3 micrograms) at the lumbar area of the leopard frog, Rana pipiens, induced analgesia which was completely blocked by co-injection of naloxone (3 micrograms), whereas dextrorphan (3 micrograms) induced analgesia which was unaffected by naloxone. Subcutaneous levorphanol (20 or 80 mg/kg) induced a dose-dependent analgesia which was blocked by concurrent naloxone (2 mg/kg), while only the higher dose of dextrorphan (80 mg/kg) induced analgesia which was unaffected by concurrent naloxone at 8 or 80 mg/kg. These data are the first to indicate naloxone-insensitive, dextrorphan-induced analgesia.

摘要

在豹蛙(北美豹蛙)腰椎区域脊髓内注射左啡诺(3微克)可诱导产生镇痛作用,而同时注射纳洛酮(3微克)可完全阻断该镇痛作用;相反,右啡烷(3微克)诱导产生的镇痛作用不受纳洛酮影响。皮下注射左啡诺(20或80毫克/千克)可诱导产生剂量依赖性镇痛作用,同时注射纳洛酮(2毫克/千克)可阻断该作用;而只有较高剂量的右啡烷(80毫克/千克)诱导产生的镇痛作用不受同时注射的8或80毫克/千克纳洛酮的影响。这些数据首次表明了右啡烷诱导产生的纳洛酮不敏感的镇痛作用。

相似文献

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Naloxone blocks the analgesic action of levorphanol but not of dextrorphan in the leopard frog.纳洛酮可阻断左啡诺在豹蛙体内的镇痛作用,但对右啡烷的镇痛作用无影响。
Brain Res. 1984 May 28;301(1):171-4. doi: 10.1016/0006-8993(84)90418-9.
2
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引用本文的文献

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Opioid research in amphibians: an alternative pain model yielding insights on the evolution of opioid receptors.两栖动物的阿片类药物研究:一种揭示阿片受体进化的替代性疼痛模型。
Brain Res Brain Res Rev. 2004 Oct;46(2):204-15. doi: 10.1016/j.brainresrev.2004.07.003.
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Testing and comparison of non-opioid analgesics in amphibians.两栖动物中非阿片类镇痛药的测试与比较
Contemp Top Lab Anim Sci. 2001 Jul;40(4):23-7.
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Selective opioid agonist and antagonist competition for [3H]-naloxone binding in amphibian spinal cord.选择性阿片类激动剂和拮抗剂在两栖动物脊髓中对[3H]-纳洛酮结合的竞争。
Brain Res. 2000 Nov 24;884(1--2):184-91. doi: 10.1016/s0006-8993(00)02967-x.
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Supraspinal administration of opioids with selectivity for mu-, delta- and kappa-opioid receptors produces analgesia in amphibians.对μ、δ和κ阿片受体有选择性的阿片类药物经脊髓上给药可在两栖动物中产生镇痛作用。
Eur J Pharmacol. 1997 Jul 16;331(1):15-21. doi: 10.1016/s0014-2999(97)01026-1.