Aberg Kristoffer C, Paz Rony
Department of Brain Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.
Department of Brain Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.
Cell Rep. 2024 Mar 26;43(3):113880. doi: 10.1016/j.celrep.2024.113880. Epub 2024 Feb 27.
Exploration is typically motivated by gaining information, with previous research showing that potential information gains drive a "directed" type of exploration. Yet, this research usually studies exploration in the context of learning paradigms and does not directly manipulate multiple levels of information gain. Here, we present a task that isolates learning from decision-making and controls the magnitude of prospective information gains. As predicted, participants explore more with larger future information gains. Both value gains and information gains, at a trial-by-trial level, engage the ventromedial prefrontal cortex (vmPFC), the ventral striatum (VStr), the amygdala, the dorsal anterior cingulate cortex (dACC), and the anterior insula (aINS). Moreover, individual sensitivities to value gains and information gains modulate the vmPFC, dACC, and aINS, but the amygdala and VStr are modulated only by individual sensitivities to information gains. Overall, we identify the neural circuitry of information-based exploration and its relationship with inter-individual exploration biases.
探索通常是由获取信息所驱动的,先前的研究表明潜在的信息获取会驱动一种“定向”类型的探索。然而,这项研究通常是在学习范式的背景下研究探索,并没有直接操纵多个层次的信息获取。在这里,我们提出了一项将学习与决策分离并控制预期信息获取量的任务。正如预测的那样,参与者在未来信息获取量更大时会进行更多的探索。在逐个试验的层面上,价值获取和信息获取都会激活腹内侧前额叶皮层(vmPFC)、腹侧纹状体(VStr)、杏仁核、背侧前扣带回皮层(dACC)和前脑岛(aINS)。此外,个体对价值获取和信息获取的敏感性会调节vmPFC、dACC和aINS,但杏仁核和VStr仅受个体对信息获取敏感性的调节。总体而言,我们确定了基于信息的探索的神经回路及其与个体间探索偏差的关系。