Department of Psychiatry, Kyoto University Graduate School of Medicine, Kyoto 606-8507, Japan.
J Neurosci. 2010 Dec 8;30(49):16567-72. doi: 10.1523/JNEUROSCI.3933-10.2010.
Misestimating risk could lead to disadvantaged choices such as initiation of drug use (or gambling) and transition to regular drug use (or gambling). Although the normative theory in decision-making under risks assumes that people typically take the probability-weighted expectation over possible utilities, experimental studies of choices among risks suggest that outcome probabilities are transformed nonlinearly into subjective decision weights by a nonlinear weighting function that overweights low probabilities and underweights high probabilities. Recent studies have revealed the neurocognitive mechanism of decision-making under risk. However, the role of modulatory neurotransmission in this process remains unclear. Using positron emission tomography, we directly investigated whether dopamine D₁ and D₂ receptors in the brain are associated with transformation of probabilities into decision weights in healthy volunteers. The binding of striatal D₁ receptors is negatively correlated with the degree of nonlinearity of weighting function. Individuals with lower striatal D₁ receptor density showed more pronounced overestimation of low probabilities and underestimation of high probabilities. This finding should contribute to a better understanding of the molecular mechanism of risky choice, and extreme or impaired decision-making observed in drug and gambling addiction.
风险估计错误可能导致不利的选择,例如开始使用药物(或赌博)和过渡到常规药物(或赌博)使用。尽管风险下的决策规范理论假设人们通常会对可能的效用进行概率加权预期,但对风险之间的选择进行的实验研究表明,结果概率通过非线性加权函数非线性地转换为主观决策权重,该函数对低概率进行过度加权,对高概率进行低估。最近的研究揭示了风险下决策的神经认知机制。然而,调节性神经传递在这个过程中的作用尚不清楚。使用正电子发射断层扫描,我们直接研究了大脑中的多巴胺 D₁ 和 D₂ 受体是否与健康志愿者将概率转换为决策权重有关。纹状体 D₁ 受体的结合与加权函数的非线性程度呈负相关。纹状体 D₁ 受体密度较低的个体对低概率的高估和对高概率的低估更为明显。这一发现有助于更好地理解风险选择的分子机制,以及药物和赌博成瘾中观察到的极端或受损的决策。