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阿片受体亚型特异性交叉耐受性对吗啡对小鼠定时控制行为的影响

Opioid receptor subtype-specific cross-tolerance to the effects of morphine on schedule-controlled behavior in mice.

作者信息

Solomon R E, Goodrich J E, Katz J L

机构信息

Department of Pharmacology, University of Michigan Medical School, Ann Arbor 48109.

出版信息

Psychopharmacology (Berl). 1988;96(2):218-22. doi: 10.1007/BF00177563.

DOI:10.1007/BF00177563
PMID:2852820
Abstract

Key-press responding of mice was maintained under a fixed-ratio (FR) 30-response schedule of food presentation. Successive 3-min periods during which the experimental chamber was illuminated and the schedule was in effect were preceded by 10-min time-out (TO) periods during which all lights were out and responses had no scheduled consequences. Intraperitoneal (IP) injections of saline or of cumulative doses of drugs were given at the start of each TO period. Successive saline injections had little or no effect on response rates, whereas the mu-opioid agonists morphine (0.1-10.0 mg/kg) and levorphanol (0.1-3.0 mg/kg), the kappa-opioid agonist ethylketazocine (0.03-3.0 mg/kg), the mixed mu-/delta-opioid agonist metkephamid (0.1-10.0 mg/kg), and the nonopioid dissociative anesthetic ketamine (1.0-100.0 mg/kg) generally produced dose-related decreases in response rates. Following chronic administration of morphine (100.0 mg/kg/6 h), tolerance developed to the effects of morphine on rates of responding. In addition, a comparable degree of cross-tolerance developed to the effects of levorphanol and metkephamid. On the other hand, there was no evidence of cross-tolerance to the effects of ethylketazocine or ketamine. These results are consistent with the evidence suggesting that different opioid agonists exert their behavioral effects through distinct classes of opioid receptors.

摘要

小鼠的按键反应在固定比率(FR)为30次反应的食物呈现时间表下得以维持。在实验箱被照亮且时间表生效的连续3分钟时间段之前,有10分钟的超时(TO)时间段,在此期间所有灯光熄灭,反应没有预定的结果。在每个TO时间段开始时进行腹腔内(IP)注射生理盐水或累积剂量的药物。连续注射生理盐水对反应率几乎没有影响,而μ-阿片受体激动剂吗啡(0.1 - 10.0毫克/千克)和左啡诺(0.1 - 3.0毫克/千克)、κ-阿片受体激动剂乙基酮唑辛(0.03 - 3.0毫克/千克)、μ/δ混合阿片受体激动剂美他沙酮(0.1 - 10.0毫克/千克)以及非阿片类解离麻醉剂氯胺酮(1.0 - 100.0毫克/千克)通常会使反应率产生剂量相关的下降。在长期给予吗啡(100.0毫克/千克/6小时)后,对吗啡对反应率的影响产生了耐受性。此外,对左啡诺和美他沙酮的影响也产生了相当程度的交叉耐受性。另一方面,没有证据表明对乙基酮唑辛或氯胺酮的影响存在交叉耐受性。这些结果与以下证据一致,即不同的阿片受体激动剂通过不同类别的阿片受体发挥其行为效应。

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Opioid receptor subtype-specific cross-tolerance to the effects of morphine on schedule-controlled behavior in mice.阿片受体亚型特异性交叉耐受性对吗啡对小鼠定时控制行为的影响
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Differential cross-tolerance to mu and kappa opioid agonists in morphine-tolerant rats responding under a schedule of food presentation.在按食物呈现时间表做出反应的吗啡耐受大鼠中,对μ和κ阿片受体激动剂的差异性交叉耐受性。
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本文引用的文献

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Metkephamid effects on operant behavior.美替卡明对操作性行为的影响。
Peptides. 1982 Sep-Oct;3(5):771-3. doi: 10.1016/0196-9781(82)90013-4.
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Discriminative stimulus effects of N-substituted analogs of phencyclidine in rhesus monkeys.苯环利定的N-取代类似物对恒河猴的辨别刺激作用。
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对不同程度μ受体效能的阿片类药物的反应率降低效应存在交叉耐受性和增强敏感性。
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Metkephamid (Tyr-D-ala-Gly-Phe-N(Me)Met-NH2), a potent opioid peptide: receptor binding and analgesic properties.美替法胺(酪氨酰-D-丙氨酰-甘氨酰-苯丙氨酰-N-甲基蛋氨酰胺),一种强效阿片肽:受体结合及镇痛特性
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Cross-tolerance studies distinguish morphine- and metkephamid-induced analgesia.交叉耐受性研究区分了吗啡和美他沙酮诱导的镇痛作用。
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Are there subtypes (isoreceptors) of multiple opiate receptors in the mouse vas deferens?小鼠输精管中是否存在多种阿片受体的亚型(同种受体)?
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Differentiation of opiate receptors in the brain by the selective development of tolerance.通过耐受性的选择性发展对大脑中阿片受体进行分化。
Pharmacol Biochem Behav. 1981 Jan;14(1):75-9. doi: 10.1016/0091-3057(81)90105-2.
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Metkephamid, a systemically active analog of methionine enkephalin with potent opioid alpha-receptor activity.美替法胺,一种蛋氨酸脑啡肽的全身活性类似物,具有强效阿片α受体活性。
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Effects of clonidine and some alpha-adrenergic antagonists alone and in combination on schedule-controlled behavior in pigeons and mice.可乐定和某些α-肾上腺素能拮抗剂单独及联合使用对鸽子和小鼠按程序控制行为的影响。
Psychopharmacology (Berl). 1984;83(1):38-43. doi: 10.1007/BF00427419.
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Mechanisms of multiple cellular adaptation processes in clonal cell lines during chronic opiate treatment.慢性阿片类药物治疗期间克隆细胞系中多种细胞适应过程的机制
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