Interleukin-1 receptor null mutant mice show decreased anxiety-like behavior and enhanced fear memory

被引:118
作者
Koo, Ja Wook [2 ]
Duman, Ronald S. [1 ]
机构
[1] Yale Univ, Sch Med, Div Mol Psychiat, New Haven, CT 06508 USA
[2] Mt Sinai Sch Med, Dept Neurosci, New York, NY 10029 USA
关键词
IL-1; beta; Anxiety; Fear; IL-1RI KO mice; ELEVATED PLUS-MAZE; NECROSIS-FACTOR-ALPHA; LIGHT-DARK PARADIGM; NEUROTROPHIC FACTOR; ANIMAL-MODELS; BASOLATERAL AMYGDALA; VENTRAL HIPPOCAMPUS; SICKNESS BEHAVIOR; RESTRAINT STRESS; SOCIAL-ISOLATION;
D O I
10.1016/j.neulet.2009.03.068
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
IL-1 beta is a proinflammatory cytokine that contributes to psychological stress responses and has been implicated in various psychiatric disorders most notably depression. Preclinical studies also demonstrate that IL-1 beta modulates anxiety- and fear-related behaviors, although these findings are difficult to assess because IL-1 beta infusions influence locomotor activity and nociception. Here we demonstrate that IL-1RI null mice exhibit a behavioral phenotype consistent with a decrease in anxiety-related behaviors. This includes significant effects in the elevated plus maze, light-dark, and novelty-induced hypophagia tests compared to wild-type mice, with no differences in locomotor activity. With regard to fear conditioning, IL-1RI null mice showed more freezing in auditory and contextual fear conditioning tests, and there was no effect on pain sensitivity. Taken together, the results indicate that the IL-1 beta/IL-1RI signaling pathway induces anxiety-related behaviors and impairs fear memory. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:39 / 43
页数:5
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