The use of α-2A adrenergic agonists for the treatment of attention-deficit/hyperactivity disorder

被引:47
作者
Arnsten, Amy F. T. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06510 USA
关键词
alpha-2A adrenoceptors; attention-deficit/hyperactivity disorder; benzedrine; cAMP signaling; clonidine; dopamine; guanfacine; norepinephrine; prefrontal cortex; stimulants; DEFICIT HYPERACTIVITY DISORDER; WORKING-MEMORY PERFORMANCE; GUANFACINE EXTENDED-RELEASE; DORSOLATERAL PREFRONTAL CORTEX; DOPAMINE-BETA-HYDROXYLASE; CORTICAL COGNITIVE FUNCTION; D1 RECEPTOR ACTIONS; ALPHA-2-ADRENERGIC AGONIST; LOCUS-COERULEUS; ORBITOFRONTAL CORTEX;
D O I
10.1586/ERN.10.133
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 alpha-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.
引用
收藏
页码:1595 / 1605
页数:11
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