Department of Neurobiology, Yale Medical School, 333 Cedar St, New Haven, CT 06510, USA.
Expert Rev Neurother. 2010 Oct;10(10):1595-605. doi: 10.1586/ern.10.133.
Neuropsychiatric disorders involve dysfunction of the prefrontal cortex (PFC), a highly evolved brain region that mediates executive functioning. The dorsolateral PFC is specialized for regulating attention and behavior, while the ventromedial PFC is specialized for regulating emotion. These abilities arise from PFC pyramidal cell networks that excite each other to maintain goals and rules 'in mind'. Imaging studies have shown reduced PFC gray matter, weaker PFC connections and altered PFC function in patients with attention-deficit/hyperactivity disorder. Thus, medications that strengthen PFC network connections may be particularly useful for the treatment of attention-deficit/hyperactivity disorder and related disorders. Recent data show that compounds such as guanfacine can enhance PFC function by stimulating postsynaptic α-2A receptors on the dendritic spines of PFC pyramidal cells where networks interconnect. Stimulation of these receptors inhibits cAMP signaling, thus closing potassium channels and strengthening physiological connections. These actions may benefit patients with weak PFC function.
神经精神疾病涉及前额叶皮层(PFC)的功能障碍,PFC 是一个高度进化的大脑区域,介导执行功能。背外侧前额叶皮层专门用于调节注意力和行为,而腹内侧前额叶皮层专门用于调节情绪。这些能力源于 PFC 锥体神经元网络,它们相互兴奋以保持目标和规则“在头脑中”。成像研究表明,注意力缺陷/多动障碍患者的 PFC 灰质减少、PFC 连接减弱和 PFC 功能改变。因此,增强 PFC 网络连接的药物可能对治疗注意力缺陷/多动障碍和相关疾病特别有用。最近的数据表明,胍法辛等化合物可以通过刺激 PFC 锥体神经元树突棘上的突触后α-2A 受体来增强 PFC 功能,这些网络相互连接。这些受体的刺激抑制 cAMP 信号转导,从而关闭钾通道并增强生理连接。这些作用可能有益于 PFC 功能较弱的患者。