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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.

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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