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吗啡与阿扑吗啡的相互作用:行为学和生物化学研究。

Interactions of morphine with apomorphine: behavioural and biochemical studies.

作者信息

Möller H G, Kuschinsky K

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1986 Dec;334(4):452-7. doi: 10.1007/BF00569385.

Abstract

The interactions of morphine with the agonist at dopamine receptors apomorphine were studied on the behavioural and biochemical level. Apomorphine (0.5 mg/kg s.c.) produced stereotyped sniffing and some licking behaviour. Pretreatment with morphine enhanced licking behaviour and, in addition, produced some gnawing behaviour, a sign which is seen after a larger dose of apomorphine alone as well. This enhancement by morphine was maximal after 3.3 mg/kg i.p. and less pronounced after smaller or larger doses of morphine; naloxone (1 mg/kg i.p.) antagonized the enhancement. Morphine did not affect the decrease in the concentration of 3,4-dihydroxyphenylacetic acid (DOPAC) produced by apomorphine in striatum and nucleus accumbens. In contrast, morphine increased the concentration of 3-methoxytyramine (3-MT) in both areas after pretreatment with pargyline (75 mg/kg i.p.), suggesting that it increased the release of dopamine, which might explain the enhancement of apomorphine-induced stereotyped behaviour. The enhancement by morphine of stereotyped behaviour produced by lisuride (2 or 4 mg/kg i.p.), another agonist at dopamine receptors, was much less pronounced than on apomorphine-induced stereotypies.

摘要

在行为和生化水平上研究了吗啡与多巴胺受体激动剂阿扑吗啡之间的相互作用。阿扑吗啡(0.5毫克/千克,皮下注射)会引发刻板的嗅闻和一些舔舐行为。吗啡预处理增强了舔舐行为,此外,还产生了一些啃咬行为,单独使用较大剂量阿扑吗啡后也会出现这种迹象。吗啡的这种增强作用在腹腔注射3.3毫克/千克后最大,在较小或较大剂量的吗啡作用下则不太明显;纳洛酮(1毫克/千克,腹腔注射)可拮抗这种增强作用。吗啡不影响阿扑吗啡在纹状体和伏隔核中引起的3,4 - 二羟基苯乙酸(DOPAC)浓度的降低。相反,在用帕吉林(75毫克/千克,腹腔注射)预处理后,吗啡增加了这两个区域中3 - 甲氧基酪胺(3 - MT)的浓度,表明它增加了多巴胺的释放,这可能解释了吗啡对阿扑吗啡诱导的刻板行为的增强作用。吗啡对多巴胺受体的另一种激动剂利苏瑞得(2或4毫克/千克,腹腔注射)产生的刻板行为的增强作用,比对阿扑吗啡诱导的刻板行为的增强作用要小得多。

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