Muscatell Keely A, Moieni Mona, Inagaki Tristen K, Dutcher Janine M, Jevtic Ivana, Breen Elizabeth C, Irwin Michael R, Eisenberger Naomi I
Department of Psychology, University of California, Berkeley, United States.
Department of Psychology, University of California, Los Angeles, United States.
Brain Behav Immun. 2016 Oct;57:21-29. doi: 10.1016/j.bbi.2016.03.022. Epub 2016 Mar 28.
Inflammation, part of the body's innate immune response, can lead to "sickness behaviors," as well as alterations in social and affective experiences. Elevated levels of pro-inflammatory cytokines have been associated with increased neural sensitivity to social rejection and social threat, but also decreased neural sensitivity to rewards. However, recent evidence suggests that inflammation may actually enhance sensitivity to certain social rewards, such as those that signal support and care. Despite a growing interest in how inflammation influences neural reactivity to positive and negative social experiences, no known studies have investigated these processes in the same participants, using a similar task. To examine this issue, 107 participants were randomly assigned to receive either placebo or low-dose endotoxin, which safely triggers an inflammatory response. When levels of pro-inflammatory cytokines were at their peak, participants were scanned using fMRI while they received positive, negative, and neutral feedback from an "evaluator" (actually a confederate) about how they came across in an audio-recorded interview. In response to negative feedback (vs. neutral), participants in the endotoxin condition showed heightened neural activity in a number of threat-related neural regions (i.e., bilateral amygdala, dorsal anterior cingulate cortex) and a key mentalizing-related region (i.e., dorsomedial PFC), compared to placebo participants. Interestingly, when receiving positive feedback (vs. neutral), endotoxin (vs. placebo) led to greater neural activity in the ventral striatum and ventromedial PFC, regions often implicated in processing reward, as well as greater activity in dorsomedial PFC. Together, these results reveal that individuals exposed to an inflammatory challenge are more "neurally sensitive" to both negative and positive social feedback, suggesting that inflammation may lead to a greater vigilance for both social threats and social rewards.
炎症作为身体固有免疫反应的一部分,可导致“疾病行为”以及社交和情感体验的改变。促炎细胞因子水平升高与对社交排斥和社交威胁的神经敏感性增加有关,但也与对奖励的神经敏感性降低有关。然而,最近的证据表明,炎症实际上可能增强对某些社交奖励的敏感性,比如那些表示支持和关爱的奖励。尽管人们越来越关注炎症如何影响对积极和消极社交体验的神经反应,但尚无已知研究在同一参与者中使用类似任务来探究这些过程。为了研究这个问题,107名参与者被随机分配接受安慰剂或低剂量内毒素,后者可安全触发炎症反应。当促炎细胞因子水平达到峰值时,参与者在接受来自“评估者”(实际上是一名同伙)关于他们在一段录音采访中的表现的积极、消极和中性反馈时,使用功能磁共振成像(fMRI)进行扫描。与安慰剂组参与者相比,在内毒素组中,参与者在面对消极反馈(与中性反馈相比)时,在一些与威胁相关的神经区域(即双侧杏仁核、背侧前扣带回皮质)和一个与心理理论相关的关键区域(即背内侧前额叶皮质)表现出增强的神经活动。有趣的是,当接受积极反馈(与中性反馈相比)时,内毒素组(与安慰剂组相比)在腹侧纹状体和腹内侧前额叶皮质(这些区域通常与奖励处理有关)表现出更强的神经活动,同时在背内侧前额叶皮质也有更强的活动。总之,这些结果表明,受到炎症挑战的个体对消极和积极社交反馈都更“神经敏感”,这表明炎症可能导致对社交威胁和社交奖励都有更高的警惕性。