Section on Fundamental Neuroscience, National Institute of Mental Health/National Institutes of Health, Bethesda, MD 20892, USA.
Genes Brain Behav. 2011 Feb;10(1):90-9. doi: 10.1111/j.1601-183X.2010.00643.x. Epub 2010 Sep 29.
Tuberoinfundibular peptide of 39 residues (TIP39) is a neuropeptide localized to neural circuits subserving emotional processing. Recent work showed that mice with null mutation for the gene coding TIP39 (TIP39-KO mice) display increased susceptibility to environmental provocation. Based on this stressor-dependent phenotype, the neuroanatomical distribution of TIP39, and knowledge that novelty-induced arousal modulates memory functions via noradrenergic activation, we hypothesized that exposure to a novel environment differently affects memory performance of mice with or without TIP39 signaling, potentially by differences in sensitivity of the noradrenergic system. We tested TIP39-KO mice and mice with null mutation of its receptor, the parathyroid hormone 2 receptor (PTH2-R), in tasks of short-term declarative and social memory (object recognition and social recognition tests, respectively), and of working memory (Y-maze test) under conditions of novelty-induced arousal or acclimation to the test conditions. Mice lacking TIP39 signaling showed memory impairment selectively under conditions of novelty-induced arousal. Acute administration of a PTH2-R antagonist in wild-type mice had a similar effect. The restoration of memory functions in TIP39-KO mice after injection of a β-adrenoreceptor-blocker, propranolol, suggested involvement of the noradrenergic system. Collectively, these results suggest that the TIP39/PTH2-R system modulates the effects of novelty exposure on memory performance, potentially by acting on noradrenergic signaling.
39 个氨基酸的 Tuberoinfundibular 肽 (TIP39) 是一种神经肽,定位于情绪处理的神经回路中。最近的研究表明,编码 TIP39 基因缺失突变的小鼠 (TIP39-KO 小鼠) 对环境刺激的易感性增加。基于这种应激依赖性表型、TIP39 的神经解剖分布以及新异诱发唤醒通过去甲肾上腺素能激活调节记忆功能的知识,我们假设暴露于新环境会以不同的方式影响具有或不具有 TIP39 信号的小鼠的记忆表现,可能是通过去甲肾上腺素能系统的敏感性差异。我们在短期陈述性和社交记忆任务(物体识别和社交识别测试)以及工作记忆任务(Y 迷宫测试)中测试了 TIP39-KO 小鼠和其受体甲状旁腺素 2 受体 (PTH2-R) 缺失突变的小鼠,分别在新异诱发唤醒或适应测试条件下。缺乏 TIP39 信号的小鼠仅在新异诱发唤醒条件下表现出记忆障碍。在野生型小鼠中急性给予 PTH2-R 拮抗剂具有相似的效果。在 TIP39-KO 小鼠中注射β-肾上腺素受体阻滞剂普萘洛尔后,记忆功能得到恢复,表明涉及去甲肾上腺素能系统。总之,这些结果表明 TIP39/PTH2-R 系统调节了新异暴露对记忆表现的影响,可能通过作用于去甲肾上腺素能信号。