Neuronal Circuits Laboratory, Department of Human Anatomy and Embryology, Faculty of Medicine and Odontology, University of Valencia, Valencia 46010, Spain.
Institute of Biomedicine and Biotechnology of Cantabria, IBBTEC (CSIC, Universidad de Cantabria), Santander 39011, Spain; Biomedical Research Networking Centre for Mental Health (CIBERSAM), Santander, Spain.
Neuroscience. 2021 Nov 10;476:72-89. doi: 10.1016/j.neuroscience.2021.09.009. Epub 2021 Sep 17.
Displaying a stress response to threatening stimuli is essential for survival. These reactions must be adjusted to be adaptive. Otherwise, even mental illnesses may develop. Describing the physiological stress response may contribute to distinguishing the abnormal responses that accompany the pathology, which may help to improve the development of both diagnoses and treatments. Recent advances have elucidated many of the processes and structures involved in stress response management; however, there is still much to unravel regarding this phenomenon. The main aim of the present research is to characterize the response of three brain areas deeply involved in the stress response (i.e., to an acute stressful experience). Specifically, the electrophysiological activity of the infralimbic division of the medial prefrontal cortex (IL), the basolateral nucleus of the amygdala (BLA), and the dorsal hippocampus (dHPC) was recorded after the infusion of 0.5 µl of corticosterone-releasing factor into the dorsal raphe nucleus (DRN), a procedure which has been validated as a paradigm to cause acute stress. This procedure induced a delayed reduction in slow waves in the three structures, and an increase in faster oscillations, such as those in theta, beta, and gamma bands. The mutual information at low theta frequencies between the BLA and the IL increased, and the delta and slow wave mutual information decreased. The low theta-mid gamma phase-amplitude coupling increased within BLA, as well as between BLA and IL. This electrical pattern may facilitate the activation of these structures, in response to the stressor, and memory consolidation.
对威胁性刺激表现出应激反应对于生存至关重要。这些反应必须进行调整以适应环境。否则,即使是精神疾病也可能发展。描述生理应激反应可能有助于区分伴随病理学的异常反应,这有助于改善诊断和治疗的发展。最近的进展阐明了许多参与应激反应管理的过程和结构;然而,对于这种现象仍有很多需要研究。本研究的主要目的是描述三个深度参与应激反应的大脑区域(即急性应激体验)的反应。具体来说,在将 0.5µl 皮质酮释放因子注入中缝背核(DRN)后,记录内侧前额叶皮质(IL)的下边缘分区、杏仁核基底外侧核(BLA)和背侧海马(dHPC)的电生理活动,这一程序已被验证为引起急性应激的范例。该程序导致三个结构中的慢波延迟性减少,较快的振荡(如θ、β和γ波段的振荡)增加。BLA 和 IL 之间低频θ的互信息增加,而δ和慢波互信息减少。BLA 内以及 BLA 和 IL 之间的低θ-中γ相位-幅度耦合增加。这种电模式可能促进这些结构的激活,以响应应激源和记忆巩固。