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吗啡、乙基酮环唑新、N-烯丙基去甲左啡诺及纳洛酮对家兔活动能力的影响。

Effects of morphine, ethylketocyclazocine, N-allylnormetazocine and naloxone on locomotor activity in the rabbit.

作者信息

Schindler C W, White M F, Goldberg S R

机构信息

NIDA Addiction Research Center, Baltimore, MD 21224.

出版信息

Psychopharmacology (Berl). 1990;101(2):172-7. doi: 10.1007/BF02244122.

DOI:10.1007/BF02244122
PMID:2190257
Abstract

Locomotor activity was studied in the rabbit following injections of morphine, ethylketocyclazocine and N-allylnormetazocine. All three drugs produced only depression of activity. The opioid antagonist naloxone antagonized the effects of both morphine and ethylketocyclazocine. Naloxone (0.1 mg/kg) did not antagonize the effects of N-allylnormetazocine. Naloxone alone depressed locomotor activity at doses above 0.3 mg/kg. This effect of naloxone was partially antagonized by 0.1 mg/kg ethylketocyclazocine, but not by 0.1 mg/kg morphine. The GABA agonist muscimol (0.1 and 1.0 mg/kg) also did not antagonize the effect of naloxone on locomotor activity. Finally, amphetamine did not produce a great deal of locomotor activation in the rabbit, which may indicate that increasing activity in the rabbit by drug intervention may be inherently difficult. These results indicate that the opioids have effects in the rabbit that are clearly different from those observed in rodents, where morphine and N-allylnormetazocine have been reported to produce locomotor activation, and naloxone typically has little effect. In addition, the effects of the opioids on locomotor activity were clearly distinguishable from their effects on learning in the rabbit. While morphine and ethylketocyclazocine were approximately equipotent in depressing locomotor activity, morphine is much less potent than ethylketocyclazocine in retarding acquisition of the classically conditioned nictitating membrane response in the rabbit.

摘要

研究了家兔注射吗啡、乙基酮环唑辛和N-烯丙基去甲左啡诺后的运动活动。这三种药物均只引起活动抑制。阿片类拮抗剂纳洛酮可拮抗吗啡和乙基酮环唑辛的作用。纳洛酮(0.1毫克/千克)不能拮抗N-烯丙基去甲左啡诺的作用。单独使用纳洛酮时,剂量高于0.3毫克/千克会抑制运动活动。纳洛酮的这种作用可被0.1毫克/千克的乙基酮环唑辛部分拮抗,但不能被0.1毫克/千克的吗啡拮抗。γ-氨基丁酸(GABA)激动剂蝇蕈醇(0.1和1.0毫克/千克)也不能拮抗纳洛酮对运动活动的作用。最后,苯丙胺在家兔中并未产生大量的运动激活,这可能表明通过药物干预增加家兔的活动可能本来就很困难。这些结果表明,阿片类药物在家兔中的作用明显不同于在啮齿动物中观察到的作用,在啮齿动物中,据报道吗啡和N-烯丙基去甲左啡诺会产生运动激活,而纳洛酮通常作用很小。此外,阿片类药物对运动活动的作用明显不同于它们对家兔学习的作用。虽然吗啡和乙基酮环唑辛在抑制运动活动方面大致等效,但在延缓家兔经典条件反射性瞬膜反应的获得方面,吗啡的效力远低于乙基酮环唑辛。

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本文引用的文献

1
Selective, naloxone-reversible morphine depression of learned behavioral and hippocampal responses.选择性的、纳洛酮可逆的吗啡对习得性行为和海马反应的抑制作用。
Science. 1982 Apr 23;216(4544):434-6. doi: 10.1126/science.7071592.
2
Acute effects of naloxone and naltrexone, but lack of delayed effects, on exploratory behavior in the rat.纳洛酮和纳曲酮对大鼠探索行为的急性作用,但无延迟效应。
Psychopharmacology (Berl). 1984;84(3):383-7. doi: 10.1007/BF00555217.
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Effects of opioids on accuracy of a fixed-ratio discrimination in monkeys and rats.
Psychopharmacology (Berl). 1992;107(4):581-90. doi: 10.1007/BF02245274.
阿片类药物对猴子和大鼠固定比率辨别准确性的影响。
J Pharmacol Exp Ther. 1984 Sep;230(3):541-9.
4
Naloxone induces multiple effects on aversive Pavlovian conditioning in rabbits.纳洛酮对家兔厌恶性巴甫洛夫条件反射有多种影响。
Behav Neurosci. 1983 Jun;97(3):478-91. doi: 10.1037//0735-7044.97.3.478.
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Locomotor activity and antinociception after putative mu, kappa and sigma opioid receptor agonists in the rat: influence of dopaminergic agonists and antagonists.
J Pharmacol Exp Ther. 1981 May;217(2):451-60.
6
U-50,488: a selective and structurally novel non-Mu (kappa) opioid agonist.U-50,488:一种具有选择性且结构新颖的非μ(κ)阿片类激动剂。
J Pharmacol Exp Ther. 1983 Jan;224(1):7-12.
7
Interactions between narcotic agonists, partial agonists and antagonists evaluated by schedule-controlled behavior.通过程序控制行为评估麻醉激动剂、部分激动剂和拮抗剂之间的相互作用。
J Pharmacol Exp Ther. 1980 Jun;213(3):497-503.
8
Behavioral activating effects of opiates and opioid peptides.阿片类药物和阿片肽的行为激活作用。
Biol Psychiatry. 1980 Feb;15(1):77-86.
9
Behavioral effects of a novel kappa opioid analgesic, U-50488, in rats and rhesus monkeys.新型κ阿片类镇痛药U-50488对大鼠和恒河猴的行为影响。
Psychopharmacology (Berl). 1985;85(3):309-14. doi: 10.1007/BF00428193.
10
Effects of morphine, ethylketocyclazocine, and N-allylnormetazocine on classical conditioning of the rabbit nictitating membrane response.吗啡、乙基酮环唑辛和N-烯丙基去甲左啡诺对兔瞬膜反应经典条件反射的影响。
Behav Neurosci. 1986 Oct;100(5):647-51. doi: 10.1037//0735-7044.100.5.647.