Anisman Hymie, Hayley Shawn, Turrin Nicolas, Merali Zul
Institute of Neuroscience, Carleton University, Ottawa, Ontario, Canada.
Int J Neuropsychopharmacol. 2002 Dec;5(4):357-73. doi: 10.1017/S1461145702003097.
Stressful events have been implicated in the provocation of depressive illness. Inasmuch as immunological challenge, and particularly cytokine administration, engender neuroendocrine and central neurochemical changes reminiscent of those provoked by psychogenic stressors, it was suggested that immune activation may also contribute to affective illness. The present report provides a brief overview of the neurochemical sequelae of acute and repeated interleukin-1beta (IL-1beta), tumour necrosis factor-alpha (TNF-alpha) and IL-2 treatment, describes some of the synergisms associated with these treatments, as well as their potential interactions with psychogenic stressors. In addition, a discussion is provided concerning the fact that cytokines, like stressors, may have time-dependent proactive effects, so that re-exposure to the treatments provoke greatly augmented neurochemical changes (sensitization). Given that the effects of cytokines are evident within hypothalamic, as well as extrahypothalamic sites, including various limbic regions, it is suggested that cytokines may impact on emotional changes, including depression.
应激事件被认为与抑郁症的诱发有关。由于免疫挑战,特别是细胞因子的施用,会引起神经内分泌和中枢神经化学变化,这些变化让人联想到由心理应激源所引发的变化,因此有人提出免疫激活也可能导致情感性疾病。本报告简要概述了急性和重复给予白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)和IL-2治疗后的神经化学后遗症,描述了与这些治疗相关的一些协同作用,以及它们与心理应激源的潜在相互作用。此外,还讨论了细胞因子与应激源一样可能具有时间依赖性的主动作用这一事实,即再次接触这些治疗会引发大大增强的神经化学变化(致敏作用)。鉴于细胞因子在下丘脑以及下丘脑外部位(包括各个边缘区域)的作用是明显的,因此有人提出细胞因子可能会影响情绪变化,包括抑郁。