The pharmacology of amphetamine and methylphenidate: Relevance to the neurobiology of attention-deficit/hyperactivity disorder and other psychiatric comorbidities

被引:408
作者
Faraone, Stephen V. [1 ,2 ,3 ]
机构
[1] SUNY Upstate Med Univ, Dept Psychiat, Syracuse, NY 13210 USA
[2] SUNY Upstate Med Univ, Dept Neurosci & Physiol, Syracuse, NY 13210 USA
[3] Univ Bergen, KG Jebsen Ctr Res Neuropsychiat Disorders, Bergen, Norway
关键词
Amphetamine; Attention-deficit/hyperactivity disorder; Methylphenidate; Pharmacology; DEFICIT HYPERACTIVITY DISORDER; INDUCED DOPAMINE RELEASE; POSITRON-EMISSION-TOMOGRAPHY; LISDEXAMFETAMINE DIMESYLATE AUGMENTATION; SERIOUS CARDIOVASCULAR EVENTS; MONOAMINE-OXIDASE INHIBITORS; MAJOR DEPRESSIVE DISORDER; ENDOGENOUS OPIOID RELEASE; DL-THREO-METHYLPHENIDATE; BLOOD-FLOW RESPONSE;
D O I
10.1016/j.neubiorev.2018.02.001
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
010107 [宗教学]; 030301 [社会学]; 070906 [古生物学及地层学(含古人类学)];
摘要
Psychostimulants, including amphetamines and methylphenidate, are first-line pharmacotherapies for individuals with attention-deficit/hyperactivity disorder (ADHD). This review aims to educate physicians regarding differences in pharmacology and mechanisms of action between amphetamine and methylphenidate, thus enhancing physician understanding of psychostimulants and their use in managing individuals with ADHD who may have comorbid psychiatric conditions. A systematic literature review of PubMed was conducted in April 2017, focusing on cellular- and brain system level effects of amphetamine and methylphenidate. The primary pharmacologic effect of both amphetamine and methylphenidate is to increase central dopamine and norepinephrine activity, which impacts executive and attentional function. Amphetamine actions include dopamine and norepinephrine transporter inhibition, vesicular monoamine transporter 2 (VMAT-2) inhibition, and monoamine oxidase activity inhibition. Methylphenidate actions include dopamine and norepinephrine transporter inhibition, agonist activity at the serotonin type 1A receptor, and redistribution of the VMAT-2. There is also evidence for interactions with glutamate and opioid systems. Clinical implications of these actions in individuals with ADHD with comorbid depression, anxiety, substance use disorder, and sleep disturbances are discussed.
引用
收藏
页码:255 / 270
页数:16
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