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在味觉增强的厌恶回避检索后,嗅觉线索是否会在老年大鼠的大脑中激活相同的网络?

Does the olfactory cue activate the same brain network during aging in the rat after taste potentiated odor aversion retrieval?

机构信息

Centre Européen des Sciences du Goût, CNRS UMR 5170, 15 rue Hugues Picardet, 21000 Dijon, France.

出版信息

Neurobiol Learn Mem. 2010 Jan;93(1):137-50. doi: 10.1016/j.nlm.2009.09.004. Epub 2009 Sep 15.

DOI:10.1016/j.nlm.2009.09.004
PMID:19761859
Abstract

Depending on the brain networks involved, aging is not accompanied by a general decrease in learning and memory capabilities. We demonstrated previously that learning and retrieval of taste potentiated odor aversion (TPOA) is preserved, and even slightly improved, in senescent rats showing some memory deficiencies in cognitive tasks (Dardou, Datiche, & Cattarelli, 2008). TPOA is a particular behavior in which the simultaneous presentation of odor and taste cues followed by a delayed visceral illness leads to a robust aversion towards both conditioned stimuli, which permits diet selection and animal survival. The present experiment was performed in order to investigate the stability or the evolution of the brain network underlying TPOA retrieval during aging. By using immunocytochemical detection of Fos and Egr1 proteins we mapped the cerebral activation induced by TPOA retrieval elicited by the odor presentation in the young, the adult and the senescent rats. The pattern of brain activation changed and the number of activated areas decreased with age. Nevertheless, the piriform cortex and the basolateral amygdala nucleus were always activated and seemed essential for TPOA retrieval. The hippocampus and the neocortical areas could have different implications in TPOA memory in relation to age. The patterns of expression of Fos and Egr1 were different, suggesting their differential involvement in TPOA retrieval. Data are discussed according to the possible roles of the brain areas studied and a model of schematic brain network subtending TPOA retrieval induced by the odor cue is proposed.

摘要

根据涉及的大脑网络,衰老并不会伴随学习和记忆能力的普遍下降。我们之前已经证明,在表现出一些认知任务记忆缺陷的衰老大鼠中,味觉增强的嗅觉厌恶(TPOA)的学习和检索得到保留,甚至略有改善(Dardou、Datiche 和 Cattarelli,2008)。TPOA 是一种特殊的行为,同时呈现气味和味觉线索,随后出现内脏疾病,会导致对两种条件刺激物产生强烈的厌恶,从而促进饮食选择和动物生存。本实验旨在研究在衰老过程中,TPOA 检索所涉及的大脑网络的稳定性或演变。通过免疫细胞化学检测 Fos 和 Egr1 蛋白,我们绘制了在年轻、成年和衰老大鼠中,由于气味呈现而引起的 TPOA 检索所诱导的大脑激活图。大脑激活模式发生变化,激活区域数量随年龄增长而减少。然而,梨状皮层和基底外侧杏仁核核始终被激活,似乎对 TPOA 检索至关重要。海马体和新皮层区域可能与年龄有关,在 TPOA 记忆中具有不同的作用。Fos 和 Egr1 的表达模式不同,这表明它们在 TPOA 检索中的参与程度不同。根据所研究的大脑区域的可能作用,讨论了数据,并提出了一个示意性大脑网络模型,该模型可以支持由气味线索引起的 TPOA 检索。

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