Department of Psychiatry, University of Puerto Rico School of Medicine, San Juan, Puerto Rico.
Biol Psychiatry. 2010 Dec 1;68(11):1055-60. doi: 10.1016/j.biopsych.2010.08.014.
Fear extinction is dependent on plasticity in the infralimbic prefrontal cortex, an area heavily innervated by midbrain dopaminergic inputs. Dopamine D2 receptors are concentrated in infralimbic output neurons that are involved in the suppression of conditioned fear after extinction. Here, we examined the specific role of infralimbic D2 receptors in mediating associative learning underlying fear extinction using the selective D2 antagonist raclopride.
Raclopride was administered systemically or infused into the infralimbic prefrontal cortex before fear extinction, and extinction retention was tested the following day. Rats were also prepared for single-unit recording in the infralimbic prefrontal cortex to assess the effect of raclopride on firing properties.
We found that systemic injection of raclopride given before extinction impaired retrieval of extinction when rats were tested drug-free the next day but also induced catalepsy during extinction training. To determine whether impaired extinction was due to impaired motor function or disruption of extinction consolidation, we infused raclopride directly into the infralimbic prefrontal cortex. Raclopride infused immediately before extinction training did not produce motor deficits but impaired recall of extinction when tested drug-free. Furthermore, in animals that underwent extinction training, systemic raclopride reduced the tone responsiveness of infralimbic prefrontal cortex neurons in layers 5/6, with no changes in average firing rate.
We suggest that D2 receptors facilitate extinction by increasing the signal-to-noise of infralimbic prefrontal cortex neurons that consolidate extinction.
恐惧的消除依赖于边缘下前额皮质的可塑性,该区域受到中脑多巴胺能传入的强烈支配。多巴胺 D2 受体集中在边缘下输出神经元中,这些神经元参与了恐惧消退后的条件性恐惧抑制。在这里,我们使用选择性 D2 拮抗剂氯丙嗪检查了边缘下 D2 受体在介导恐惧消退的联想学习中的特定作用。
在恐惧消退前,氯丙嗪通过系统给药或输注到边缘下前额皮质中,然后在第二天测试消退保留。还准备了大鼠进行边缘下前额皮质中的单细胞记录,以评估氯丙嗪对放电特性的影响。
我们发现,在消退前给予氯丙嗪系统注射会损害大鼠在第二天无药物测试时对消退的检索,但也会在消退训练期间引起僵住。为了确定消退受损是由于运动功能受损还是消退巩固中断引起的,我们将氯丙嗪直接输注到边缘下前额皮质中。在消退训练前立即输注氯丙嗪不会导致运动缺陷,但在无药物测试时会损害消退的回忆。此外,在进行了消退训练的动物中,系统给予氯丙嗪会降低边缘下前额皮质第 5/6 层神经元对音调的反应性,而平均放电率没有变化。
我们认为 D2 受体通过增加巩固消退的边缘下前额皮质神经元的信号噪声来促进消退。