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神经营养因子-3 注入脑岛皮层可增强条件性味觉厌恶记忆。

Neurotrophin-3 into the insular cortex strengthens conditioned taste aversion memory.

机构信息

División de Investigación y Estudios de Posgrado, Facultad de Psicología, Universidad Nacional Autónoma de México 04510, Mexico.

División de Investigación y Estudios de Posgrado, Facultad de Psicología, Universidad Nacional Autónoma de México 04510, Mexico.

出版信息

Behav Brain Res. 2024 Mar 12;461:114857. doi: 10.1016/j.bbr.2024.114857. Epub 2024 Jan 9.

Abstract

Memory consolidation is an essential process of long-term memory formation. Neurotrophins have been suggested as key regulators of activity dependent changes in the synaptic efficacy and morphology, which are considered the downstream mechanisms of memory consolidation. The neurotrophin 3 (NT-3), a member of the neurotrophin family, and its high affinity receptor TrkC, are widely expressed in the insular cortex (IC), a region with a critical role in the consolidation of the conditioned taste aversion (CTA) paradigm, in which an animal associates a novel taste with nausea. Nevertheless, the role of this neurotrophin in the cognitive processes that the IC mediates remains unexamined. To answer whether NT-3 is involved in memory consolidation at the IC, adult male Wistar rats were administered with NT-3 or NT-3 in combination with the Trk receptors inhibitor K252a into the IC, immediately after CTA acquisition under two different conditions: a strong-CTA (0.2 M lithium chloride i.p.) or a weak-CTA (0.1 M lithium chloride i.p.). Our results show that NT-3 strengthens the memory trace of CTA, transforming a weak conditioning into a strong one, in a Trk-dependent manner. The present evidence suggests that NT-3 has a key role in the consolidation process of an aversive memory in a neocortical region.

摘要

记忆巩固是长期记忆形成的一个必要过程。神经营养因子被认为是突触效能和形态的活动依赖性变化的关键调节因子,这些变化被认为是记忆巩固的下游机制。神经生长因子 3(NT-3)是神经营养因子家族的一员,其高亲和力受体 TrkC,广泛表达于脑岛皮层(IC),在条件味觉厌恶(CTA)范式的巩固中具有关键作用,在此范式中,动物将一种新的味觉与恶心联系起来。然而,该神经营养因子在 IC 介导的认知过程中的作用仍未被研究。为了回答 NT-3 是否参与 IC 中的记忆巩固,成年雄性 Wistar 大鼠在 CTA 获得后立即在 IC 内给予 NT-3 或 NT-3 与 Trk 受体抑制剂 K252a 联合使用,在两种不同条件下进行:强 CTA(0.2 M 氯化锂腹腔内注射)或弱 CTA(0.1 M 氯化锂腹腔内注射)。我们的结果表明,NT-3 以 Trk 依赖性的方式增强了 CTA 的记忆痕迹,将弱条件转化为强条件。目前的证据表明,NT-3 在新皮层区域的厌恶记忆巩固过程中起着关键作用。

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