Department of Integrative Physiology and Center for Neuroscience, University of Colorado Boulder, 1725 Pleasant Street, Boulder, CO, 80309-0354, USA.
School of Psychology and Public Health, La Trobe University, Melbourne, VIC, Australia, 3086.
Cell Mol Neurobiol. 2018 Jan;38(1):289-304. doi: 10.1007/s10571-017-0564-3. Epub 2017 Nov 13.
Peripheral immune activation can have profound physiologic and behavioral effects. One mechanism through which immune activation may affect physiology and behavior is through actions on brainstem neuromodulatory systems, such as serotonergic systems. To test this hypothesis, in Experiment 1, adult male BALB/c mice were implanted with telemetric recording devices and then immunized with Mycobacterium vaccae NCTC 11659 (0.1 mg, s.c.; Days - 28, - 14; N = 36). On Day 1, mice received an acute challenge with M. vaccae (0.1 mg, s.c.) or borate-buffered saline vehicle. Core body temperature and locomotor activity recordings were conducted during a 36 h period beginning 24 h prior to challenge; 12 h following acute challenge, mice were either tested in a 6-min forced swim test, or served as home cage controls (n = 9 per group). In Experiment 2, the protocol was repeated, but with the aim of assessing c-Fos expression in brainstem serotonergic neurons, assessed 90 min following exposure to forced swim (N = 32; n = 8 per group). In Experiment 1, acute M. vaccae challenge in M. vaccae-immunized mice, relative to vehicle-challenged controls, decreased locomotor activity and core body temperature measured 3 h following challenge, as measured by continuous telemetric recordings, and decreased immobility in the forced swim test measured 12 h following challenge. In Experiment 2, acute M. vaccae challenge in M. vaccae-immunized mice decreased home cage locomotion, in alignment with findings in Experiment 1, as measured by video-based behavioral analysis, and, among mice exposed to the forced swim test, increased c-Fos expression in subsets of serotonergic neurons within the dorsal raphe nucleus (DR) measured 13.5 h following challenge. Together, these data are consistent with the hypothesis that acute peripheral immune activation with a heat-killed preparation of M. vaccae transiently induces mild hypothermia in association with suppression of locomotor activity, activates subsets of serotonergic neurons in the DR, and induces antidepressant-like behavioral responses.
外周免疫激活会对生理和行为产生深远影响。免疫激活影响生理和行为的一种机制是通过作用于脑干神经调制系统,如 5-羟色胺能系统。为了验证这一假设,在实验 1 中,成年雄性 BALB/c 小鼠植入遥测记录设备,然后用结核分枝杆菌 NCTC 11659(0.1mg,皮下;-28 天,-14 天;N=36)免疫。在第 1 天,小鼠接受一次急性结核分枝杆菌挑战(0.1mg,皮下)或硼酸缓冲盐水载体。核心体温和运动活动记录在挑战前 24 小时开始的 36 小时期间进行;急性挑战后 12 小时,小鼠要么在 6 分钟强制游泳测试中进行测试,要么作为笼内对照(每组 9 只)。在实验 2 中,重复了该方案,但目的是评估暴露于强制游泳后 90 分钟脑干 5-羟色胺能神经元中的 c-Fos 表达(N=32;每组 8 只)。在实验 1 中,与载体对照相比,急性结核分枝杆菌挑战在结核分枝杆菌免疫小鼠中,相对于载体对照,在挑战后 3 小时通过连续遥测记录测量的运动活动和核心体温减少,在挑战后 12 小时通过强制游泳测试测量的不动性减少。在实验 2 中,急性结核分枝杆菌挑战在结核分枝杆菌免疫小鼠中,相对于载体对照,减少了视频行为分析测量的笼内运动,与实验 1 的发现一致,并且,在暴露于强制游泳测试的小鼠中,增加了 5-羟色胺能神经元亚群的 c-Fos 表达背侧中缝核(DR)中的 13.5 小时后挑战。总的来说,这些数据与以下假设一致,即用热灭活的结核分枝杆菌制剂进行急性外周免疫激活会暂时引起轻度体温过低,同时抑制运动活动,激活 DR 中的 5-羟色胺能神经元亚群,并诱导抗抑郁样行为反应。