4.6 Article

Activation of 5-HT1A and 5-HT7 receptors enhanced a positively reinforced long-term memory

期刊

BEHAVIOURAL BRAIN RESEARCH
卷 397, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.bbr.2020.112932

关键词

Memory; 5-HT; Autoshaping; 8-OH-DPAT; LP 211

资金

  1. Consejo Nacional de Ciencia y Tecnologia, Mexico [277701]

向作者/读者索取更多资源

Memory is a crucial aspect of individuality, with retrieval posing a challenge for patients with memory deficits. The neurotransmitter 5-hydroxytryptamine (5-HT) is involved in memory processes, and activation of 5-HT1A and 5-HT7 receptors has been shown to enhance memory retrieval, making them potential therapeutic targets for improving long-term memory retrieval.
Memory is one of the most important capabilities of our mind since it determines our individuality. Memory formation involves different stages: acquisition, consolidation and retrieval. There are many studies about early stages, however little is known about memory retrieval. Retrieval is the use of learned information and represents a big problem in patients with memory deficits where the main issue is that they can learn but cannot remember. Previous findings have demonstrated that 5-hydroxytryptamine (5-HT) is a neurotransmitter involved in memory process. Hence, here we are exploring the role of 5-HT in memory retrieval by using its metabolic precursor L-tryptophan and several ligands at 5-HT1A and 5-HT7 receptors. Experimental protocol consisted of evaluating conditioned responses (%CR) after one week of interruption following autoshaping sessions for memory formation; a decrease of %CR was interpreted as memory decay. Systemic administration of: (1) L-tryptophan (50 and 100 mg/kg), (2) 5-HT 1A receptor agonist 8-OH-DPAT (0.031 and 0.062 mg/kg), (3) the selective antagonist 5-HT1A receptor WAY 100635 (0.3 and 0.6 mg/kg), (4) the 5-HT7 receptor agonist, LP 211, in a dose-dependent manner (1, 2.5, 5.0 and 10.0 mg/kg) enhanced memory retrieval. Further, the 5-HT7 receptor antagonist, SB 269970 (10.0 mg/kg), had no effect. Finally, SB 269970 (10.0 mg/kg) significantly blocked memory retrieval enhancement produced by 10.0 mg/kg LP 211, but not that induced by 2.5 mg/kg LP 211.These results, taken together, suggest that activation of 5-HT1A and 5-HT7 receptors enhanced memory retrieval and these receptors may be therapeutic targets to improve long-term memory retrieval.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据