Department of Biomedical Sciences, Division of Neuroscience and Clinical Pharmacology, University of Cagliari, Monserrato (CA), Italy.
National Institute of Neuroscience (INN), University of Cagliari, Monserrato, CA, Italy.
J Neuroendocrinol. 2020 Jan;32(1):e12792. doi: 10.1111/jne.12792. Epub 2019 Sep 30.
Sleep deprivation (SD) is associated with a broad spectrum of cognitive and behavioural complications, including emotional lability and enhanced stress reactivity, as well as deficits in executive functions, decision making and impulse control. These impairments, which have profound negative consequences on the health and productivity of many individuals, reflect alterations of the prefrontal cortex (PFC) and its connectivity with subcortical regions. However, the molecular underpinnings of these alterations remain elusive. Our group and others have begun examining how the neurobehavioural outcomes of SD may be influenced by neuroactive steroids, a family of molecules deeply implicated in sleep regulation and the stress response. These studies have revealed that, similar to other stressors, acute SD leads to increased synthesis of the neurosteroid allopregnanolone in the PFC. Whereas this up-regulation is likely aimed at counterbalancing the detrimental impact of oxidative stress induced by SD, the increase in prefrontal allopregnanolone levels contributes to deficits in sensorimotor gating and impulse control, signalling a functional impairment of PFC. This scenario suggests that the synthesis of neuroactive steroids during acute SD may be enacted as a neuroprotective response in the PFC; however, such compensation may in turn set off neurobehavioural complications by interfering with the corticolimbic connections responsible for executive functions and emotional regulation.
睡眠剥夺(SD)与广泛的认知和行为并发症有关,包括情绪不稳定和增强的应激反应,以及执行功能、决策和冲动控制方面的缺陷。这些损伤对许多人的健康和生产力产生了深远的负面影响,反映了前额叶皮层(PFC)及其与皮质下区域的连接的改变。然而,这些改变的分子基础仍然难以捉摸。我们的小组和其他小组已经开始研究 SD 的神经行为结果如何可能受到神经活性类固醇的影响,神经活性类固醇是一组深深涉及睡眠调节和应激反应的分子。这些研究表明,与其他应激源类似,急性 SD 导致 PFC 中神经甾体别孕烯醇酮的合成增加。虽然这种上调可能旨在抵消 SD 诱导的氧化应激的有害影响,但前额叶别孕烯醇酮水平的增加导致感觉运动门控和冲动控制的缺陷,表明 PFC 的功能受损。这种情况表明,急性 SD 期间神经活性类固醇的合成可能在 PFC 中作为一种神经保护反应而发生;然而,这种补偿可能通过干扰负责执行功能和情绪调节的皮质边缘连接而反过来引发神经行为并发症。