多巴胺D2受体的神经调节改变眼窝额叶神经元活动并减少炎症性疼痛雄性大鼠的风险倾向行为。

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-07-01 Epub Date: 2025-02-22 DOI:10.1007/s12035-025-04781-0
Margarida Dourado, Helder Cardoso-Cruz, Clara Monteiro, Vasco Galhardo
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引用次数: 0

摘要

在基于风险的决策过程中,多巴胺(DA)在维持啮齿动物眶额皮质(OFC)网络的完整性方面起着至关重要的作用。慢性疼痛状况可导致能量信号受损,进而可能影响基于风险的反应的动机控制。然而,这种不稳定性背后的神经机制尚不清楚。在这项研究中,我们旨在研究这种损伤是否依赖于DA D2受体(D2r)的活性。为了验证这一假设,我们将双侧多电极基质植入雄性大鼠的OFC,并记录了它们在进行食物强化啮齿动物赌博任务(rGT)时的神经活动。我们在诱导炎症性疼痛模型-完全弗氏辅助(CFA)模型之前和之后评估行为表现和神经活动模式。我们的研究结果显示,CFA治疗的大鼠在rGT表现中表现出对大/不确定奖励的异常偏好。这种改变的行为选择特征可以通过先前全身给予D2r配体(0.05 mg/kg,喹匹罗或氯氯pride)来逆转,这表明D2r在该任务所需的决策过程中具有潜在作用。这些配体在特定剂量下的使用不会影响疼痛反应,但会导致OFC神经元活动的显著改变,从而支持rGT中目标导向的选择反应。最后,我们发现证据表明,cfa处理大鼠表现出OFC功能改变,即DA D1受体(D1r)上调和DA β -羟化酶(DH)下调。这些结果表明,在疼痛条件下,大脑网络中能量平衡的破坏对于高风险决策档案的发展至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuromodulation of Dopamine D2 Receptors Alters Orbitofrontal Neuronal Activity and Reduces Risk-Prone Behavior in Male Rats with Inflammatory Pain.

Dopamine (DA) is believed to play a crucial role in maintaining the integrity of the rodent orbitofrontal cortex (OFC) networks during risk-based decision-making processes. Chronic pain conditions can lead to impaired DAergic signaling, which, in turn, may affect the motivational control of risk-based responses. Nevertheless, the neural mechanisms underlying this instability are poorly understood. In this study, we aimed to investigate whether this impairment is dependent on the activity of the DA D2 receptor (D2r). To address this hypothesis, we implanted bilateral matrices of multielectrodes into the OFC of male rats and recorded the neural activity while they performed a food-reinforced rodent gambling task (rGT). We evaluated behavioral performance and neural activity patterns before and after inducing a model of inflammatory pain - complete Freund's adjuvant (CFA) model. Our findings revealed that rats treated with CFA exhibited an abnormal preference for the large/uncertain reward during rGT performance. This altered behavioral choice profile could be reversed by prior systemic administration of D2r ligands (0.05 mg/kg, quinpirole or raclopride), indicating a potential role of D2r in the decision-making process required for this task. The administration of these ligands at the specified dosages did not affect pain responses, but lead to a significant alteration of OFC neuronal activity that support goal-directed choice responses in the rGT. Finally, we found evidence that CFA-treated rats exhibit OFC functional changes, namely an upregulation of DA D1 receptor (D1r) and a downregulation of DA beta-hydroxylase (DH). These results demonstrate that the disruption of DAergic balance in the brain networks is crucial for the development of high-risk decision profiles during painful conditions.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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