Silva-Carvalho Mariana, Barbosa Daniel José, Dias da Silva Diana, Dinis-Oliveira Ricardo Jorge
Associate Laboratory i4HB-Institute for Health and Bioeconomy, University Institute of Health Sciences-IUCS-CESPU, Gandra, Portugal.
UCIBIO-Research Unit on Applied Molecular Biosciences, Translational Toxicology Research Laboratory (1H-TOXRUN), University Institute of Health Sciences (IUCS-CESPU), Gandra, Portugal.
Basic Clin Pharmacol Toxicol. 2025 Nov;137(5):e70111. doi: 10.1111/bcpt.70111.
Lisdexamfetamine (LDX), a prodrug of d-amphetamine, is widely used in the pharmacological treatment of neuropsychiatric disorders such as attention-deficit/hyperactivity disorder (ADHD) and binge eating disorder (BED). Chemically, it consists of the amino acid lysine linked to d-amphetamine. Its enzymatic conversion to d-amphetamine sets the stage for a prolonged and controlled release, influencing its clinical profile and differentiating it from other stimulant medications. As a central nervous system stimulant, LDX primarily acts by increasing the release of neurotransmitters, particularly dopamine and noradrenaline, in the brain. Clinically, this enhanced availability of neurotransmitters is believed to contribute to improvements in attention, focus and impulse control in individuals with ADHD. The side effects of LDX include insomnia, decreased appetite, weight loss and xerostomia. This work reviews the pharmacological mechanisms, clinical applications and forensic considerations associated with its use. It is expected that clinicians, researchers and policymakers have a comprehensive understanding of the pharmacological and toxicological aspects of LDX.
赖右苯丙胺(LDX),即右旋苯丙胺的前体药物,广泛用于治疗诸如注意力缺陷多动障碍(ADHD)和暴饮暴食症(BED)等神经精神疾病的药物治疗。从化学结构上看,它由与右旋苯丙胺相连的氨基酸赖氨酸组成。其酶促转化为右旋苯丙胺为长效和控释奠定了基础,影响其临床特征并使其有别于其他兴奋剂药物。作为一种中枢神经系统兴奋剂,LDX主要通过增加大脑中神经递质,特别是多巴胺和去甲肾上腺素的释放来发挥作用。临床上,神经递质可用性的提高被认为有助于改善ADHD患者的注意力、专注力和冲动控制能力。LDX的副作用包括失眠、食欲减退、体重减轻和口干。本文综述了与其使用相关的药理机制、临床应用和法医学考量。期望临床医生、研究人员和政策制定者对LDX的药理和毒理学方面有全面的了解。