A Translational Model‐Based Meta‐Analysis to Predict Tremor Incidence Associated with Serotonin Reuptake Transporter Inhibition

血清素转运体 血清素 再摄取抑制剂 药理学 5-羟色胺再摄取抑制剂 抗抑郁药 再摄取 运输机 5-羟色胺质膜转运蛋白 5-羟色胺摄取抑制剂 医学 心理学 内科学 生物 氟西汀 海马体 生物化学 受体 基因
作者
Sheetal Panday,Benjamin Lang,G Kapitanov,Kalyanasundaram Subramanian,Lena Klopp‐Schulze,Karthik Venkatakrishnan,Anup Zutshi,Abed E. Alnaif
出处
期刊:Clinical Pharmacology & Therapeutics [Wiley]
卷期号:118 (3): 588-592
标识
DOI:10.1002/cpt.3696
摘要

The serotonin reuptake transporter (SERT) is responsible for the removal and recycling of the neurotransmitter serotonin from neuronal synapses and is an important pharmacological target for treating a variety of CNS disorders. However, excessive levels of extrasynaptic serotonin resulting from SERT inhibition can lead to serotonin toxicity, which manifests as a spectrum of adverse events (AEs) termed “serotonin syndrome” (SS), ranging in severity from mild to life‐threatening. We hypothesized that, by performing a model‐based meta‐analysis (MBMA) of the data in the literature, the dose at which tremors (a characteristic manifestation of SS) occur could be predicted based on the pharmacokinetic properties and SERT inhibitory potency of a given drug. To investigate the relationship between tremors and the predicted relative strength of SERT inhibition, a literature survey was performed to collate observed tremor data, pharmacokinetic parameters, and SERT potency data for known SERT inhibitors. Using these data for 20 SERT inhibitors, an E max model relationship between tremor incidence and the ratio between brain unbound exposure and SERT IC50 was observed. The identified relationship provides a valuable tool to predict the likelihood of tremor incidence for investigational drugs with SERT inhibitory activity and to inform safety assessment and dose selection.
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