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吗啡依赖与多巴胺能活性:对单侧黑质损伤大鼠的转圈反应测试

Morphine dependence and dopaminergic activity: tests of circling responses in rats with unilateral nigral lesions.

作者信息

Halliwell J V, Kumar R

出版信息

Br J Pharmacol. 1980 Dec;70(4):545-54. doi: 10.1111/j.1476-5381.1980.tb09773.x.

Abstract

1 Rats with unilateral electrolytic lesions involving both parts of the substantia nigra show dose-related, ipsilateral circling responses to apomorphine which are stable over time. 2 In non-tolerant rats, morphine (up to 10 mg/kg) does not elicit any circling behaviour but as tolerance develops to morphine, initially 10 mg/kg daily and then 100 ng/kg daily for about 4 months, the rats show a progressive tendency to walk more towards the side of the lesion. This behaviour is qualitatively different from apomorphine-induced circling. 3 When apomorphine (0 to 1.0 mg/kg) and morphine (10 or 100 mg/kg) are tested together, the total amounts of 'circling' are increased in an additive manner. However, after 22 h withdrawal from morphine there is a more marked increase in apomorphine-induced circling which is related to the level of dependence. 4 It is suggested that the sensitivity of striatal dopamine receptors is not altered by morphine dependence and that the increased response to apomorphine in abstinence probably reflects changes in the modulating actions of other neurotransmitter systems in the striatum.

摘要
  1. 单侧电解损伤累及黑质两部分的大鼠对阿扑吗啡呈现剂量相关的同侧旋转反应,且该反应随时间稳定。2. 在未产生耐受性的大鼠中,吗啡(高达10毫克/千克)不会引发任何旋转行为,但随着对吗啡产生耐受性,最初每天10毫克/千克,然后每天100毫克/千克,持续约4个月,大鼠表现出逐渐向损伤侧行走更多的趋势。这种行为在性质上与阿扑吗啡诱导的旋转不同。3. 当同时测试阿扑吗啡(0至1.0毫克/千克)和吗啡(10或100毫克/千克)时,“旋转”的总量以相加的方式增加。然而,在停用吗啡22小时后,阿扑吗啡诱导的旋转有更明显的增加,这与依赖程度有关。4. 提示吗啡依赖性不会改变纹状体多巴胺受体的敏感性,戒断时对阿扑吗啡反应的增加可能反映了纹状体中其他神经递质系统调节作用的变化。

相似文献

本文引用的文献

2
Catecholamine biosynthesis in brains of rats treated with morphine.
Science. 1970 May 15;168(3933):854-6. doi: 10.1126/science.168.3933.854.
3
Functional role of the nigro-neostriatal dopamine neurons.黑质 - 新纹状体多巴胺神经元的功能作用。
Acta Pharmacol Toxicol (Copenh). 1966;24(2):263-74. doi: 10.1111/j.1600-0773.1966.tb00389.x.
4

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