游泳应激对蓝斑核促肾上腺皮质激素释放因子敏感性的长期调节

Long-term regulation of locus ceruleus sensitivity to corticotropin-releasing factor by swim stress.

作者信息

Curtis A L, Pavcovich L A, Valentino R J

机构信息

Department of Psychiatry, Medical College of Pennsylvania and Hahnemann University, Philadelphia, Pennsylvania, USA.

出版信息

J Pharmacol Exp Ther. 1999 Jun;289(3):1211-9.

DOI:
Abstract

Corticotropin-releasing factor (CRF) acts as a putative neurotransmitter in the locus ceruleus (LC) to mediate its activation by certain stressors. In this study, we quantified LC sensitivity to CRF 24 h after swim stress, at a time when behavioral depression that is sensitive to antidepressants is apparent. Rats were placed in a tank with 30 cm (swim stress) or 4 cm water and 24 h later, either behavior was monitored in a forced swim test or LC discharge was recorded. Swim stress rats were more immobile than control animals in the swim test. LC neurons of swim stress rats were sensitized to low doses of CRF (0.1-0.3 microgram i.c.v.) that were ineffective in control animals and were desensitized to higher doses. Swim stress selectively altered LC sensitivity to CRF because neither LC spontaneous discharge nor responses to other agents (e.g., carbachol, vasoactive intestinal peptide) were altered. Finally, the mechanism for sensitization was localized to the LC because neuronal activation by low doses of CRF was prevented by the intracerulear administration of a CRF antagonist. CRF dose-response curves were consistent with a two-site model with similar dissociation constants under control conditions but divergent dissociation constants after swim stress. The results suggest that swim stress (and perhaps other stressors) functionally alters CRF receptors that have an impact on LC activity. Stress-induced regulation of LC sensitivity to CRF may underlie behavioral aspects of stress-related psychiatric disorders.

摘要

促肾上腺皮质激素释放因子(CRF)作为蓝斑(LC)中一种假定的神经递质,介导某些应激源对其的激活作用。在本研究中,我们在游泳应激24小时后对LC对CRF的敏感性进行了量化,此时对抗抑郁药敏感的行为性抑郁表现明显。将大鼠置于30厘米(游泳应激)或4厘米水深的水箱中,24小时后,要么在强迫游泳试验中监测行为,要么记录LC放电情况。在游泳试验中,游泳应激组大鼠比对照组动物更不动。游泳应激组大鼠的LC神经元对低剂量的CRF(0.1 - 0.3微克,脑室内注射)敏感,而这些剂量对对照组动物无效,且对高剂量CRF脱敏。游泳应激选择性地改变了LC对CRF的敏感性,因为LC的自发放电以及对其他药物(如卡巴胆碱、血管活性肠肽)的反应均未改变。最后,致敏机制定位于LC,因为脑室内注射CRF拮抗剂可阻止低剂量CRF引起的神经元激活。CRF剂量 - 反应曲线与一个双位点模型一致,在对照条件下具有相似的解离常数,但在游泳应激后解离常数不同。结果表明,游泳应激(可能还有其他应激源)在功能上改变了对LC活性有影响的CRF受体。应激诱导的LC对CRF敏感性的调节可能是应激相关精神障碍行为方面的基础。

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