Hotchkiss Brain Institute, Cumming School of Medicine, Mathison Center for Mental Health, University of Calgary, 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada; Department of Neuroscience, University of Calgary, 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada.
Hotchkiss Brain Institute, Cumming School of Medicine, Mathison Center for Mental Health, University of Calgary, 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada.
Brain Behav Immun. 2017 Jul;63:176-185. doi: 10.1016/j.bbi.2016.11.022. Epub 2016 Nov 22.
A large body of evidence has been brought forward connecting developmental immune activation to abnormal fear and anxiety levels. Anxiety disorders have extremely high lifetime prevalence, yet susceptibility factors that contribute to their emergence are poorly understood. In this research we investigated whether an inflammatory insult early in life can alter the response to fear conditioning in adulthood. Fear learning and extinction are important and adaptive behaviors, mediated largely by the amygdala and its interconnectivity with cortico-limbic circuits. Male and female rat pups were given LPS (100μg/kg i.p.) or saline at postnatal day 14; LPS activated cFos expression in the central amygdala 2.5h after exposure, but not the basal or lateral nuclei. When tested in adulthood, acquisition of an auditory cued or contextual learned fear memory was largely unaffected as was the extinction of fear to a conditioned context. However, we detected a deficit in auditory fear extinction in male and female rats that experienced early-life inflammation, such that there is a significant delay in fear extinction processes resulting in more sustained fear behaviors in response to a conditioned cue. This response was specific to extinction training and did not persist into extinction recall. The effect could not be explained by differences in pain threshold (unaltered) or in baseline anxiety, which was elevated in adolescent females only and unaltered in adolescent males and adult males and females. This research provides further evidence for the involvement of the immune system during development in the shaping of fear and anxiety related behaviors.
大量证据表明,发育中的免疫激活与异常的恐惧和焦虑水平有关。焦虑障碍的终身患病率极高,但导致其出现的易感因素仍知之甚少。在这项研究中,我们研究了生命早期的炎症是否会改变成年后对恐惧条件反射的反应。恐惧学习和消退是重要的适应性行为,主要由杏仁核及其与皮质-边缘回路的相互连接介导。雄性和雌性幼鼠在出生后第 14 天分别给予 LPS(100μg/kg 腹腔注射)或生理盐水;LPS 在暴露后 2.5 小时激活了中央杏仁核中的 cFos 表达,但不激活基底核或外侧核。当在成年期进行测试时,听觉线索或情境习得性恐惧记忆的获得基本不受影响,对条件性情境的恐惧消退也不受影响。然而,我们在经历过早期生活炎症的雄性和雌性大鼠中检测到听觉恐惧消退的缺陷,即恐惧消退过程明显延迟,导致对条件性线索的恐惧行为持续时间更长。这种反应是特定于消退训练的,不会持续到消退回忆中。这种效应不能用痛阈(未改变)或基线焦虑来解释,后者仅在青春期雌性中升高,而在青春期雄性和成年雄性和雌性中未改变。这项研究进一步证明了免疫系统在发育过程中的参与在塑造与恐惧和焦虑相关的行为方面的作用。