Kabitzke Patricia A, Barr Gordon A, Chan Thomas, Shair Harry N, Wiedenmayer Christoph P
1] Department of Psychiatry, Columbia University, New York, NY, USA [2] Division of Developmental Neuroscience, New York State Psychiatric Institute, New York, NY, USA.
Department of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia and the University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Neuropsychopharmacology. 2014 Jul;39(8):1924-32. doi: 10.1038/npp.2014.40. Epub 2014 Feb 19.
To survive, all mammalian species must recognize and respond appropriately to threatening stimuli. In adults, the prelimbic medial prefrontal cortex (mPFC) appears to be involved in fear expression, whereas the infralimbic mPFC mediates fear extinction. In juvenile rats (PN26), the mPFC receives information on potential predators but does not act on it. To test whether the prefrontal cortex is capable of fear regulation in the young organism, we exposed juvenile rats to a threatening or nonthreatening stimulus and assessed fear and brain Fos activation of the mPFC subdivisions, amygdala and periaqueductal gray (PAG). In response to the threat, juveniles froze more, spent more time far from the threat, and had elevated numbers of Fos-positive cells in the prelimbic mPFC, the medial amygdala, and ventral PAG. To test the hypothesis that the mPFC has a dual role in modulating the amygdala and PAG in juveniles, we pharmacologically disinhibited each of the two subdivisions of the mPFC and assessed freezing and downstream activation to the threat. Juvenile rats infused with picrotoxin into the prelimbic mPFC and exposed to a threatening stimulus froze less, spent less time far from the threat, and increased Fos expression. Infusion of picrotoxin into the infralimbic mPFC also reduced fear responding to the threatening stimulus but had no effect on Fos expression. In sum, it appears that the mPFC can process threatening stimuli in juveniles at this age, even though it is normally not involved in the fear responses.
为了生存,所有哺乳动物物种都必须识别并对威胁性刺激做出适当反应。在成年动物中,前额叶内侧前额叶皮质(mPFC)似乎参与恐惧表达,而边缘下mPFC介导恐惧消退。在幼年大鼠(出生后第26天)中,mPFC接收有关潜在捕食者的信息,但并不对其做出反应。为了测试前额叶皮质在幼年生物体中是否能够调节恐惧,我们将幼年大鼠暴露于威胁性或非威胁性刺激下,并评估了mPFC各亚区、杏仁核和导水管周围灰质(PAG)的恐惧和脑Fos激活情况。对威胁的反应中,幼年大鼠僵住的时间更多,远离威胁的时间更长,并且在前额叶内侧mPFC、内侧杏仁核和腹侧PAG中Fos阳性细胞数量增加。为了测试mPFC在调节幼年大鼠杏仁核和PAG中具有双重作用的假设,我们对mPFC的两个亚区分别进行了药理学去抑制,并评估了对威胁的僵住反应和下游激活情况。向前额叶内侧mPFC注射印防己毒素并暴露于威胁性刺激下的幼年大鼠僵住的时间减少,远离威胁的时间减少,并且Fos表达增加。向边缘下mPFC注射印防己毒素也减少了对威胁性刺激的恐惧反应,但对Fos表达没有影响。总之,似乎在这个年龄段,mPFC能够处理幼年大鼠的威胁性刺激,尽管它通常不参与恐惧反应。