Neuropharmacology involvement of dopamine D3 receptor in impulsive choice decision-making in male rats

IF 4.6 2区 医学 Q1 NEUROSCIENCES Neuropharmacology Pub Date : 2024-06-23 DOI:10.1016/j.neuropharm.2024.110051
Hui Shen , Zilu Ma , Emma Hans , Ying Duan , Guo-Hua Bi , Yurim C. Chae , Alessandro Bonifazi , Francisco O. Battiti , Amy Hauck Newman , Zheng-Xiong Xi , Yihong Yang
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Abstract

Impulsive decision-making has been linked to impulse control disorders and substance use disorders. However, the neural mechanisms underlying impulsive choice are not fully understood. While previous PET imaging and autoradiography studies have shown involvement of dopamine and D2/3 receptors in impulsive behavior, the roles of distinct D1, D2, and D3 receptors in impulsive decision-making remain unclear. In this study, we used a food reward delay-discounting task (DDT) to identify low- and high-impulsive rats, in which low-impulsive rats exhibited preference for large delayed reward over small immediate rewards, while high-impulsive rats showed the opposite preference. We then examined D1, D2, and D3 receptor gene expression using RNAscope in situ hybridization assays. We found that high-impulsive male rats exhibited lower levels of D2 and D3, and particularly D3, receptor expression in the nucleus accumbens (NAc), with no significant changes in the insular, prelimbic, and infralimbic cortices. Based on these findings, we further explored the role of the D3 receptor in impulsive decision-making. Systemic administration of a selective D3 receptor agonist (FOB02-04) significantly reduced impulsive choices in high-impulsive rats but had no effects in low-impulsive rats. Conversely, a selective D3 receptor antagonist (VK4-116) produced increased both impulsive and omission choices in both groups of rats. These findings suggest that impulsive decision-making is associated with a reduction in D3 receptor expression in the NAc. Selective D3 receptor agonists, but not antagonists, may hold therapeutic potentials for mitigating impulsivity in high-impulsive subjects.

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神经药理学 多巴胺 D3 受体对雄性大鼠冲动性选择决策的影响
冲动决策与冲动控制障碍和药物使用障碍有关。然而,人们对冲动选择的神经机制尚未完全了解。虽然之前的 PET 成像和自显影研究显示多巴胺和 D2/3 受体参与了冲动行为,但不同的 D1、D2 和 D3 受体在冲动决策中的作用仍不清楚。在这项研究中,我们使用食物奖励延迟折现任务(DDT)来识别低冲动大鼠和高冲动大鼠,其中低冲动大鼠表现出对大额延迟奖励的偏好,而不是对小额即时奖励的偏好,而高冲动大鼠则表现出相反的偏好。然后,我们使用 RNAscope 原位杂交测定法检测了 D1、D2 和 D3 受体基因的表达。我们发现,高冲动性雄性大鼠的脑核(NAc)中 D2 和 D3 受体表达水平较低,尤其是 D3 受体,而在岛叶、前边缘和下边缘皮质中则无明显变化。基于这些发现,我们进一步探讨了 D3 受体在冲动决策中的作用。全身给药选择性 D3 受体激动剂(FOB02-04)可显著减少高冲动性大鼠的冲动性选择,但对低冲动性大鼠没有影响。相反,选择性 D3 受体拮抗剂(VK4-116)会增加两组大鼠的冲动选择和遗漏选择。这些发现表明,冲动性决策与 NAc 中 D3 受体表达的减少有关。选择性 D3 受体激动剂(而非拮抗剂)可能具有减轻高冲动性受试者冲动性的治疗潜力。
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来源期刊
Neuropharmacology
Neuropharmacology 医学-神经科学
CiteScore
10.00
自引率
4.30%
发文量
288
审稿时长
45 days
期刊介绍: Neuropharmacology publishes high quality, original research and review articles within the discipline of neuroscience, especially articles with a neuropharmacological component. However, papers within any area of neuroscience will be considered. The journal does not usually accept clinical research, although preclinical neuropharmacological studies in humans may be considered. The journal only considers submissions in which the chemical structures and compositions of experimental agents are readily available in the literature or disclosed by the authors in the submitted manuscript. Only in exceptional circumstances will natural products be considered, and then only if the preparation is well defined by scientific means. Neuropharmacology publishes articles of any length (original research and reviews).
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