Differential transcriptome profile underlying risky choice in a rat gambling task

被引:1
|
作者
Kwak, Myung Ji [1 ]
Kim, Wha Young [2 ]
Jung, Seung-Hyun [3 ,4 ,5 ]
Chung, Yeun-Jun [4 ,5 ,6 ]
Kim, Jeong-Hoon [1 ,2 ]
机构
[1] Yonsei Univ, Grad Sch Med Sci, Dept Med Sci, Brain Korea Project 21,Coll Med, Seoul 03722, South Korea
[2] Yonsei Univ, Dept Physiol, Coll Med, Seoul 03722, South Korea
[3] Catholic Univ Korea, Canc Evolut Res Ctr, Dept Biochem, Coll Med, Seoul 06591, South Korea
[4] Catholic Univ Korea, Dept Biomed & Hlth Sci, Coll Med, Seoul 06591, South Korea
[5] Catholic Univ Korea, Precis Med Res Ctr, Coll Med, Seoul 06591, South Korea
[6] Catholic Univ Korea, Dept Microbiol, IRCGP, Coll Med, Seoul 06591, South Korea
基金
新加坡国家研究基金会;
关键词
rat gambling task; risky choice; medial prefrontal cortex; transcriptome; GENOME-WIDE ASSOCIATION; DECISION-MAKING; FEAR MEMORY; CHANNEL; VULNERABILITIES; MECHANISMS; TENEURIN-4; DISORDERS; ADDICTION; BEHAVIORS;
D O I
10.1556/2006.2022.00068
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background and aims: Proper measurement of expected risk is important for making rational decisions, and maladaptive decision making may underlie various psychiatric disorders. However, differentially expressed genetic profiling involved in this process is still largely unknown. A rodent version of the gambling task (rGT) has been developed to measure decision-making by adopting the same principle of Iowa Gambling Task in humans. In the present study, we examined using next-generation sequencing (NGS) technique whether there are differences in gene expression profiles in the medial prefrontal cortex (mPFC) and the nucleus accumbens (NAc) when rats make different choices toward risk in rGT. Methods: Rats were trained in a touch screen chamber to learn the relationships between 4 different light signals on the window of the screen and accompanied reward outcomes or punishments set up with different magnitudes and probabilities. Once they showed a stabilized pattern of preference upon free choice, rats were classified into risk-averse or risk-seeking groups. After performing the rGT, rats were decapitated, the mPFC and the NAc was dissected out, and NGS was performed with the total RNA extracted. Results: We found that 477 and 36 genes were differentially expressed (approximately 75 and 83% out of them were downregulated) in the mPFC and the NAc, respectively, in risk-seeking compared to risk-averse rats. Among those, we suggested a few top ranked genes that may contribute to promoting risky choices. Discussion and conclusions: Our findings provide insights into transcriptional components underlying risky choices in rats.
引用
收藏
页码:845 / 857
页数:13
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