"Behavior and Basal Ganglia" Research Unit (EA 4712), University of Rennes 1, Rennes, France.
Movement Disorders Unit, Neurology Department, Pontchaillou University Hospital, Rennes, France.
Clin Drug Investig. 2018 Apr;38(4):287-312. doi: 10.1007/s40261-018-0619-3.
The present paper consists of a comprehensive review of the literature on apomorphine pharmacological properties and its usefulness in Parkinson's disease (PD). The chemistry, structure-activity relationship, pharmacokinetics and pharmacodynamics of apomorphine are described with regard to its effects on PD symptoms, drug interactions, interindividual variability and adverse events. Apomorphine chemical structure accounts for most of its beneficial and deleterious properties, both dopaminergic and non-dopaminergic. Its pharmacokinetics and pharmacodynamics are complex and subject to interindividual variability, particularly for subcutaneous absorption and metabolism. Subcutaneous apomorphine, either as injections or infusion, is particularly useful for the treatment of PD motor symptoms and growing evidence supports its clinical value for nonmotor disorders. Owing to interindividual variability and sensitivity, apomorphine treatment must be tailored to each patient. While the subcutaneous route has been the gold standard for decades, the search for alternative routes is ongoing, with promising results from studies of pulmonary, sublingual and transdermal routes. In addition, the potential of apomorphine as a disease-modifying therapy deserves to be investigated, as well as its ability to induce brain plasticity through chronic infusion. Moreover, the ongoing progress in the development of analytical methods should be accompanied by new pharmacokinetic and pharmacodynamic studies of apomorphine metabolism and sites of action in humans, as its biochemistry has yet to be fully described.
本文对阿扑吗啡的药理学特性及其在帕金森病(PD)中的应用进行了全面综述。本文描述了阿扑吗啡的化学结构、构效关系、药代动力学和药效动力学,以及其对 PD 症状、药物相互作用、个体间差异和不良反应的影响。阿扑吗啡的化学结构决定了其大部分有益和有害的特性,包括多巴胺能和非多巴胺能特性。其药代动力学和药效动力学复杂,受个体间差异的影响,特别是皮下吸收和代谢的影响。皮下注射阿扑吗啡,无论是注射还是输注,对治疗 PD 的运动症状特别有用,越来越多的证据支持其对非运动障碍的临床价值。由于个体间的差异和敏感性,阿扑吗啡的治疗必须根据每个患者的情况进行调整。虽然皮下给药途径几十年来一直是金标准,但人们仍在寻找替代途径,肺部、舌下和透皮途径的研究取得了有希望的结果。此外,阿扑吗啡作为一种疾病修饰治疗的潜力值得研究,以及它通过慢性输注诱导大脑可塑性的能力也值得研究。此外,在开发分析方法方面取得的进展,应该伴随着对阿扑吗啡代谢和作用部位的新的药代动力学和药效动力学研究,因为其生化特性尚未完全描述。