Mohr David C, Pelletier Daniel
Department of Psychiatry and Neurology, University of California, San Francisco, CA 94131, USA.
Brain Behav Immun. 2006 Jan;20(1):27-36. doi: 10.1016/j.bbi.2005.03.011.
A growing literature reports that stressful life events are associated with exacerbation and the subsequent development of brain lesions in patients with multiple sclerosis (MS). The evolution an MS exacerbation occurs over a period of many months and involves many different biological processes that change over time. Likewise, the experience of stress also occurs over time, with an onset, a shift from acute to chronic in some cases, and resolution. Each of these phases is associated with unique biological features. Thus, the impact of stress on MS exacerbation may depend on the temporal trajectories of stress and MS exacerbation, and when the intersection between these two trajectories occurs. This paper presents a temporal model, along with three different temporal relationships and associated mechanisms by which stress may impact MS exacerbation. These include the onset of a stressor, which may be mediated by mast cell activation, the point that a stressor begins to become chronic, which may be mediated by glucocorticoid resistance in immune cells, and the resolution of the stressor, which may be mediated by a drop in cortisol. These three hypotheses are not necessarily mutually exclusive. Data on psychosocial mediators and moderators are also briefly reviewed and future research directions are discussed.
越来越多的文献报道,生活应激事件与多发性硬化症(MS)患者病情加重及随后脑损伤的发展有关。MS病情加重的演变过程持续数月,涉及许多随时间变化的不同生物学过程。同样,应激体验也随时间发生,有一个起始阶段,在某些情况下会从急性转变为慢性,然后缓解。这些阶段中的每一个都与独特的生物学特征相关。因此,应激对MS病情加重的影响可能取决于应激和MS病情加重的时间轨迹,以及这两条轨迹何时相交。本文提出了一个时间模型,以及应激可能影响MS病情加重的三种不同时间关系和相关机制。这些包括应激源的起始阶段,可能由肥大细胞激活介导;应激源开始变为慢性的阶段,可能由免疫细胞中的糖皮质激素抵抗介导;以及应激源的缓解阶段,可能由皮质醇下降介导。这三种假设不一定相互排斥。还简要回顾了心理社会调节因素和缓和因素的数据,并讨论了未来的研究方向。