Modeling risky decision-making in nonhuman animals: shared core features

被引:14
|
作者
Heilbronner, Sarah R. [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Dept Pharmacol & Physiol, 601 Elmwood Ave,Box 711, Rochester, NY 14642 USA
基金
美国国家卫生研究院;
关键词
DOPAMINERGIC MODULATION; CINGULATE CORTEX; SEX-DIFFERENCES; RAT MODEL; REWARD; PREFERENCES; NEURONS; CHOICE; PERFORMANCE; RESPONSES;
D O I
10.1016/j.cobeha.2017.03.001
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Understanding the neural mechanisms of risky decision-making is critical to developing appropriate treatments for psychiatric disorders, problem gambling, and addiction to drugs of abuse. Probing neurobiological mechanisms requires the use of nonhuman animal models (particularly rhesus macaques, rats, and mice). However, there is considerable variation across species in risk preferences. Nevertheless, there are shared core features of risky decision-making present across species. As demonstrated with a wide variety of behavioral paradigms, modulators of risk preference observed in humans are readily replicated in model species. Thus, risky decision-making represents an important implementation of reward-guided decision-making that is feasibly modeled across species.
引用
收藏
页码:23 / 29
页数:7
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