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小鼠中阿片类药物散瞳作用的拮抗作用。

Antagonism of opiate mydriasis in mice.

作者信息

Korczyn A D, Rock M

出版信息

Br J Pharmacol. 1981 Aug;73(4):807-10. doi: 10.1111/j.1476-5381.1981.tb08732.x.

Abstract

1 Morphine-induced mydriasis in mice is antagonized by nalorphine, levallorphan and naloxone in a dose-dependent manner. 2 The relative potency of the three agents is 10:56: 134 respectively, thus being in accordance with other tests of narcotic antagonism. Naloxone has the shortest duration of action. 3 When injected into naive animals, nalorphine (but not levallorphan or naloxone) produces a slight mydriasis. 4 Measurement of the diameter of the pupil in mice seems to be a precise, simple and rapid test for studying narcotic antagonist as well as agonist action and has several advantages over standard methods used for this purpose.

摘要

1 纳洛芬、左洛啡烷和纳洛酮能以剂量依赖方式拮抗吗啡引起的小鼠瞳孔散大。2 这三种药物的相对效价分别为10:56:134,因此与其他麻醉拮抗试验结果一致。纳洛酮的作用持续时间最短。3 当注射到未用过药的动物体内时,纳洛芬(而非左洛啡烷或纳洛酮)会引起轻微瞳孔散大。4 测量小鼠瞳孔直径似乎是一种精确、简单且快速的试验,可用于研究麻醉拮抗剂以及激动剂的作用,与用于此目的的标准方法相比有几个优点。

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Antagonism of opiate mydriasis in mice.小鼠中阿片类药物散瞳作用的拮抗作用。
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Mydriatic activity of analgesics in mice.镇痛药对小鼠的散瞳作用。
Experientia. 1956 Aug 15;12(8):293-4. doi: 10.1007/BF02159614.
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Naloxone, naltrexone, and related noroxymorphones.
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Interactions of narcotic antagonists and antagonist-analgesics.
J Pharm Pharmacol. 1968 Jul;20(7):547-52. doi: 10.1111/j.2042-7158.1968.tb09803.x.
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