Musco Shaina, McAllister Vivian, Caudle Ian
Department of Clinical Sciences, High Point University Fred Wilson School of Pharmacy, One University Parkway, High Point, NC 27262, USA.
High Point University David R. Hayworth College of Arts and Sciences, One University Parkway, High Point, NC, USA.
Ther Adv Psychopharmacol. 2020 Aug 27;10:2045125320937575. doi: 10.1177/2045125320937575. eCollection 2020.
Dopamine-receptor blocking agent-associated akathisia (DRBA-A) is an adverse effect that can significantly limit the use of these important medications for the treatment of a variety of psychiatric diseases, yet there is no unifying theory regarding its pathophysiology. This knowledge gap limits clinicians' ability to effectively manage DRBA-A and mitigate negative outcomes in an already vulnerable patient population. Based on a review of the current literature on the subject, it is hypothesized that dopaminergic and noradrenergic signaling is perturbed in DRBA-A. Accordingly, it is proposed that the optimal agent to manage this extrapyramidal symptom should increase dopamine signaling in the affected areas of the brain and counteract compensatory noradrenergic signaling antagonism of adrenergic or serotonergic receptors.
多巴胺受体阻断剂相关的静坐不能(DRBA - A)是一种不良反应,它会显著限制这些重要药物用于治疗多种精神疾病,然而关于其病理生理学尚无统一的理论。这一知识空白限制了临床医生有效管理DRBA - A并减轻本就脆弱的患者群体中负面结果的能力。基于对该主题当前文献的综述,推测在DRBA - A中多巴胺能和去甲肾上腺素能信号传导受到干扰。因此,有人提出,管理这种锥体外系症状的最佳药物应增加大脑受影响区域的多巴胺信号传导,并抵消去甲肾上腺素能信号传导的代偿性肾上腺素能或5-羟色胺能受体拮抗作用。