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本文引用的文献

1
Aging is not equal across memory systems.衰老在记忆系统中并不均衡。
Neurobiol Learn Mem. 2020 Jul;172:107232. doi: 10.1016/j.nlm.2020.107232. Epub 2020 Apr 18.
2
Using a memory systems lens to view the effects of estrogens on cognition: Implications for human health.从记忆系统的视角审视雌激素对认知的影响:对人类健康的启示
Physiol Behav. 2018 Apr 1;187:67-78. doi: 10.1016/j.physbeh.2017.11.022. Epub 2017 Dec 5.
3
Training-induced elevations in extracellular lactate in hippocampus and striatum: Dissociations by cognitive strategy and type of reward.训练引起的海马体和纹状体细胞外乳酸水平升高:认知策略和奖励类型的分离
Neurobiol Learn Mem. 2017 Jan;137:142-153. doi: 10.1016/j.nlm.2016.12.001. Epub 2016 Dec 2.
4
Differential Arc expression in the hippocampus and striatum during the transition from attentive to automatic navigation on a plus maze.在从注意力集中的十字迷宫导航过渡到自动导航过程中,海马体和纹状体中Arc基因的差异表达。
Neurobiol Learn Mem. 2016 May;131:36-45. doi: 10.1016/j.nlm.2016.03.008. Epub 2016 Mar 11.
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Memory Systems and the Addicted Brain.记忆系统与成瘾大脑
Front Psychiatry. 2016 Feb 25;7:24. doi: 10.3389/fpsyt.2016.00024. eCollection 2016.
6
Neurocognitive Aging and the Hippocampus across Species.跨物种的神经认知衰老与海马体
Trends Neurosci. 2015 Dec;38(12):800-812. doi: 10.1016/j.tins.2015.10.003. Epub 2015 Nov 19.
7
Estrogens and cognition: Friends or foes?: An evaluation of the opposing effects of estrogens on learning and memory.雌激素与认知:朋友还是敌人?:评估雌激素对学习和记忆的相反作用
Horm Behav. 2015 Aug;74:105-15. doi: 10.1016/j.yhbeh.2015.06.017. Epub 2015 Jul 3.
8
Differential effects of massed and spaced training on place and response learning: A memory systems perspective.集中训练和间隔训练对位置学习与反应学习的不同影响:记忆系统视角
Behav Processes. 2015 Sep;118:85-9. doi: 10.1016/j.beproc.2015.06.004. Epub 2015 Jun 3.
9
Older adults report moderately more detailed autobiographical memories.老年人报告的自传体记忆适度更详细。
Front Psychol. 2015 May 19;6:631. doi: 10.3389/fpsyg.2015.00631. eCollection 2015.
10
Forgetfulness during aging: an integrated biology.衰老过程中的健忘:综合生物学。
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在老年大鼠中使纹状体失活可恢复其学习海马敏感空间导航任务的能力。

Inactivation of the striatum in aged rats rescues their ability to learn a hippocampus-sensitive spatial navigation task.

机构信息

Department of Biology, Syracuse University, 107 College Place, 329 Life Science Complex, Syracuse, NY 13244, USA.

Department of Biology, Syracuse University, 107 College Place, 329 Life Science Complex, Syracuse, NY 13244, USA.

出版信息

Neurobiol Learn Mem. 2020 Jul;172:107231. doi: 10.1016/j.nlm.2020.107231. Epub 2020 Apr 17.

DOI:10.1016/j.nlm.2020.107231
PMID:32305514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8915206/
Abstract

Studies of age-related changes in learning and memory often focus on hippocampus-sensitive tasks and reveal age-associated impairments across numerous species and contexts. However, cognitive decline with advanced age is not all-encompassing; for example, forms of striatum-sensitive learning are conserved or enhanced with age. Under certain conditions, hippocampal and striatal memory systems function in opposition. In young adult rodents, disruption of one structure can enhance learning on tasks dependent on the other, suggesting that competitive interactions across memory systems contribute to learning and memory abilities. This report examines whether imbalances across memory systems might contribute to cognitive aging. We inactivated the striatum using central infusions of lidocaine (sodium channel blocker) prior to hippocampus-sensitive spatial (place) training in young (3-4-month-old) and old (24-25-month-old) F344 male rats. Consistent with prior work, vehicle-infused old rats exhibited place learning impairments relative to young rats. Additionally, striatal inactivation enhanced learning in old rats, but not young rats, abolishing the age-related impairment. These findings suggest that age-related declines in learning tasks thought to engage the hippocampus may stem from exaggerated interference from other memory systems and that interventions to target the striatum may reverse some age-related learning decrements.

摘要

研究学习和记忆随年龄变化的相关内容通常集中在海马体敏感任务上,揭示了在众多物种和环境中与年龄相关的认知损伤。然而,随着年龄的增长,认知能力的下降并不是全面的;例如,纹状体敏感的学习形式在随着年龄的增长而保持或增强。在某些条件下,海马体和纹状体记忆系统会相互对抗。在年轻成年啮齿动物中,破坏一个结构可以增强对依赖另一个结构的任务的学习,这表明记忆系统之间的竞争相互作用有助于学习和记忆能力。本报告探讨了记忆系统之间的不平衡是否可能导致认知老化。我们在年轻(3-4 个月大)和老年(24-25 个月大)F344 雄性大鼠的海马体敏感空间(位置)训练之前,使用利多卡因(钠离子通道阻滞剂)对纹状体进行中枢内注射以使其失活。与之前的研究一致,与年轻大鼠相比,接受载体注射的老年大鼠表现出位置学习损伤。此外,纹状体失活增强了老年大鼠的学习能力,但没有增强年轻大鼠的学习能力,从而消除了与年龄相关的损伤。这些发现表明,在被认为与海马体相关的学习任务中,与年龄相关的学习下降可能源于其他记忆系统的干扰过大,而针对纹状体的干预措施可能会逆转一些与年龄相关的学习下降。