Suppr超能文献

伏隔核中应激诱导的多巴胺释放的个体差异受皮质酮影响。

Individual differences in stress-induced dopamine release in the nucleus accumbens are influenced by corticosterone.

作者信息

Rougé-Pont F, Deroche V, Le Moal M, Piazza P V

机构信息

Laboratoire de Psychobiologie des Comportements Adaptatifs, Domaine de Carreire, Bordeaux, France.

出版信息

Eur J Neurosci. 1998 Dec;10(12):3903-7. doi: 10.1046/j.1460-9568.1998.00438.x.

Abstract

Stressful experiences, glucocorticoids hormones and dopaminergic neurons seems to interact in determining a higher propensity to develop drug abuse. In this report, we studied the acute interaction between these three factors. For this purpose, we compared stress-induced dopamine release in intact rats and in rats in which stress-induced corticosterone secretion was experimentally blocked. Ten-minute tail-pinch was used as a stressor and dopamine release estimated in the nucleus accumbens by using the microdialysis technique. Individual differences were also taken into account by comparing rats identified as either predisposed (HRs) or resistant (LRs) to develop self-administration of drugs of abuse, on the basis of their locomotor response to novelty. It was found that suppression of stress-induced corticosterone secretion significantly decreased stress-induced dopamine release. However, such an effect greatly differed between HR and LR rats. When corticosterone secretion was intact HR animals had a higher and longer dopamine release in response to stress than LRs. The blockade of stress-induced corticosterone secretion selectively reduced the dopaminergic response of HRs that did not differ from LRs anymore. These findings strength the idea that glucocorticoids could be involved in determining propensity to develop drug self-administration. In particular, these hormones could play a role in determining the higher dopaminergic activity that characterizes drug proned individuals.

摘要

应激经历、糖皮质激素和多巴胺能神经元似乎在决定药物滥用的更高易感性方面相互作用。在本报告中,我们研究了这三个因素之间的急性相互作用。为此,我们比较了完整大鼠以及实验性阻断应激诱导的皮质酮分泌的大鼠中应激诱导的多巴胺释放情况。使用十分钟的夹尾作为应激源,并通过微透析技术估计伏隔核中的多巴胺释放。还通过比较根据其对新奇事物的运动反应被确定为易发展为滥用药物自我给药(高反应者,HRs)或有抵抗力(低反应者,LRs)的大鼠,来考虑个体差异。结果发现,应激诱导的皮质酮分泌的抑制显著降低了应激诱导的多巴胺释放。然而,这种效应在HR和LR大鼠之间有很大差异。当皮质酮分泌完整时,HR动物对应激的多巴胺释放比LR动物更高且持续时间更长。应激诱导的皮质酮分泌的阻断选择性地降低了HR的多巴胺能反应,此时HR与LR不再有差异。这些发现强化了糖皮质激素可能参与决定药物自我给药易感性的观点。特别是,这些激素可能在决定药物易感性个体特有的更高多巴胺能活性方面发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验