Roman Viktor, Hagewoud Roelina, Luiten Paul G M, Meerlo Peter
Department of Molecular Neurobiology, School of Behavioral and Cognitive Neurosciences, University of Groningen, Haren, The Netherlands.
J Sleep Res. 2006 Dec;15(4):386-94. doi: 10.1111/j.1365-2869.2006.00555.x.
Disrupted sleep and stress are often linked to each other, and considered as predisposing factors for psychopathologies such as depression. The depressed brain is associated with reduced serotonergic and enhanced cholinergic neurotransmission. In an earlier study, we showed that chronic sleep restriction by forced locomotion caused a gradual decrease in postsynaptic serotonin-1A receptor sensitivity, whilst chronic forced activity alone, with sufficient sleep time, did not affect receptor sensitivity. The first aim of the present study was to examine whether the sleep loss-induced change in receptor sensitivity is mediated by adrenal stress hormones. The results show that the serotonin-1A receptor desensitization is independent of adrenal hormones as it still occurs in adrenalectomized rats. The second aim of the study was to establish the effects of sleep restriction on cholinergic muscarinic receptor sensitivity. While sleep restriction affected muscarinic receptor sensitivity only slightly, forced activity significantly hypersensitized the muscarinic receptors. This hypersensitization is because of the stressful nature of the forced activity protocol as it did not occur in adrenalectomized rats. Taken together, these data confirm that sleep restriction may desensitize the serotonin-1A receptor system. This is not a generalized effect as sleep restriction did not affect the sensitivity of the muscarinic cholinergic receptor system, but the latter was hypersensitized by stress. Thus, chronic stress and sleep loss may, partly via different pathways, change the brain into a direction as it is seen in mood disorders.
睡眠中断与压力常常相互关联,并被视为诸如抑郁症等精神病理学的诱发因素。抑郁的大脑与血清素能神经传递减少和胆碱能神经传递增强有关。在一项早期研究中,我们发现通过强迫运动导致的慢性睡眠限制会使突触后5-羟色胺-1A受体敏感性逐渐降低,而单独的慢性强迫活动,在有足够睡眠时间的情况下,不会影响受体敏感性。本研究的首要目的是检验受体敏感性的睡眠剥夺诱导变化是否由肾上腺应激激素介导。结果表明,5-羟色胺-1A受体脱敏独立于肾上腺激素,因为它在肾上腺切除的大鼠中仍然会发生。该研究的第二个目的是确定睡眠限制对胆碱能毒蕈碱受体敏感性的影响。虽然睡眠限制仅轻微影响毒蕈碱受体敏感性,但强迫活动会显著使毒蕈碱受体超敏。这种超敏是由于强迫活动方案的应激性质,因为它在肾上腺切除的大鼠中不会发生。综上所述,这些数据证实睡眠限制可能使5-羟色胺-1A受体系统脱敏。这并非普遍效应,因为睡眠限制并未影响毒蕈碱胆碱能受体系统的敏感性,但其会因压力而超敏。因此,慢性压力和睡眠剥夺可能部分通过不同途径,使大脑朝着情绪障碍中所见的方向转变。