Dopamine and serotonin interplay for valence-based spatial learning

被引:11
作者
Wert-Carvajal, Carlos [1 ,2 ,3 ]
Reneaux, Melissa [1 ]
Tchumatchenko, Tatjana [2 ,3 ,4 ]
Clopath, Claudia [1 ]
机构
[1] Imperial Coll London, Bioengn Dept, London SW7 2AZ, England
[2] Max Planck Inst Brain Res, Theory Neural Dynam Grp, D-60438 Frankfurt, Germany
[3] Univ Bonn, Med Ctr, Life & Brain Ctr, Inst Expt Epileptol & Cognit Res, D-53127 Bonn, Germany
[4] Johannes Gutenberg Univ Mainz, Med Ctr, Inst Physiol Chem, D-55131 Mainz, Germany
来源
CELL REPORTS | 2022年 / 39卷 / 02期
基金
英国工程与自然科学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
MORRIS WATER MAZE; LONG-TERM POTENTIATION; SYNAPTIC PLASTICITY; RECEPTOR; MEMORY; ANTAGONIST; PREDICTION; 5-HT2A; DRUG; CA1;
D O I
10.1016/j.celrep.2022.110645
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dopamine (DA) and serotonin (5-HT) are important neuromodulators of synaptic plasticity that have been linked to learning from positive or negative outcomes or valence-based learning. In the hippocampus, both affect long-term plasticity but play different roles in encoding uncertainty or predicted reward. DA has been related to positive valence, from reward consumption or avoidance behavior, and 5-HT to aversive encoding. We propose DA produces overall LTP while 5-HT elicits LTD. Here, we compare two reward -modulated spike timing-dependent plasticity (R-STDP) rules to describe the action of these neuromodulators. We examined their role in cognitive performance and flexibility for computational models of the Morris water maze task and reversal learning. Our results show that the interplay of DA and 5-HT improves learning performance and can explain experimental evidence. This study reinforces the importance of neuromodulation in determining the direction of plasticity.
引用
收藏
页数:16
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