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关于小鼠苯醌镇痛试验中各种药物作用所涉及受体的研究。

Studies on the receptors involved in the action of the various agents in the phenylbenzoquinone analgesic assay in mice.

作者信息

Smits S E, Takemori A E

出版信息

Br J Pharmacol. 1970 Jul;39(3):639-46. doi: 10.1111/j.1476-5381.1970.tb10371.x.

Abstract
  1. Tolerance to the activity of several narcotic analgesics (morphine, levorphanol, and methadone) and several narcotic-antagonist analgesics (pentazocine, cyclazocine, and nalorphine) was studied in the mouse phenylbenzoquinone stretching test. Virtually complete tolerance was induced by chronic treatment with each of the narcotic agents, while no apparent tolerance was induced by the narcotic antagonists.2. In morphine-tolerant mice there was a high degree of cross-tolerance to the effects of not only the other narcotic drugs but also to those of the narcotic antagonists, acetylsalicylic acid, and physostigmine.3. The effects of morphine and pentazocine were antagonized by naloxone but not by atropine, while the effects of physostigmine were antagonized by atropine but not by naloxone. Neither atropine nor naloxone antagonized the effect of acetylsalicylic acid.4. The results of the tolerance study suggest that there is a fundamental difference in the consequences of receptor interaction for the narcotic and the narcotic-antagonist analgesics. Morphine-tolerant mice exhibit cross-tolerance non-specifically. The selectivity of naloxone and atropine differentiates the narcotic and narcotic-analgesics from the other two agents used in this analgesic test.
摘要
  1. 在小鼠苯醌伸展试验中研究了对几种麻醉性镇痛药(吗啡、左啡诺和美沙酮)以及几种麻醉性拮抗镇痛药(喷他佐辛、环唑辛和烯丙吗啡)活性的耐受性。每种麻醉药的长期治疗均可诱导出几乎完全的耐受性,而麻醉性拮抗剂则未诱导出明显的耐受性。

  2. 在吗啡耐受的小鼠中,不仅对其他麻醉药的作用,而且对麻醉性拮抗剂、乙酰水杨酸和毒扁豆碱的作用都有高度的交叉耐受性。

  3. 吗啡和喷他佐辛的作用可被纳洛酮拮抗,但不能被阿托品拮抗,而毒扁豆碱的作用可被阿托品拮抗,但不能被纳洛酮拮抗。阿托品和纳洛酮均不能拮抗乙酰水杨酸的作用。

  4. 耐受性研究结果表明,麻醉性镇痛药和麻醉性拮抗镇痛药在受体相互作用的后果上存在根本差异。吗啡耐受的小鼠表现出非特异性的交叉耐受性。纳洛酮和阿托品的选择性将麻醉性镇痛药和麻醉性拮抗镇痛药与该镇痛试验中使用的其他两种药物区分开来。

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The interaction of morphine and nalorphine on respiration.吗啡与烯丙吗啡对呼吸的相互作用。
Clin Pharmacol Ther. 1968 Mar-Apr;9(2):152-61. doi: 10.1002/cpt196892152.

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