Abou Farha Khalid, Bruggeman Richard, Baljé-Volkers Corine
Rob Giel Research Centre, Department of Psychiatry, University Medical Centre Groningen (UMCG), Hanzeplein 1, 9713 GZ Groningen, The Netherlands.
Department of Epidemiology (Medical Statistics), University Medical Centre Groningen (UMCG), Hanzeplein 1, 9713 GZ Groningen, The Netherlands.
ISRN Psychiatry. 2014 Mar 4;2014:652750. doi: 10.1155/2014/652750. eCollection 2014.
Metabotropic Glutamate Receptor 5 (mGluR5) negative allosteric modulators (NAMs) may play a role in some psychiatric disorders such as anxiety and depression. The pharmacokinetic profile and pharmacodynamics effects of mGluR5-NAMs have been previously reported. We performed a post hoc analysis of pharmacological and clinical data obtained from 18 young healthy female subjects who received a mGluR5-NAM in the context of a phase I drug-drug interaction study between a mGluR5 NAM and a monophasic oral contraceptive. mGluR5-NAM was administered in an escalating bidaily dose level design. There was no interaction between the OC and mGluR5-NAM. Higher morning mGluR5-NAM plasma concentrations were found compared to evening concentrations. Most of the observed clinically significant neuropsychiatric adverse reactions occurred nocturnally and included visual (pseudo) hallucinations, insomnia accompanied by secondary behavioural disorders, and cognitive dysfunction symptoms of sufficient severity to interfere with daily functioning. Circadian rhythm-related physiological variations in drug absorption and disposition may explain this pharmacokinetics-pharmacodynamics apparently disproportionate relationship. We suggest that clinical trials evaluating basic pharmacokinetic properties of psychiatric medications consider potential drug's chronopharmacokinetics. This may assist with dose optimization and minimize serious neuropsychiatric adverse reactions in the vulnerable psychiatric patient.
代谢型谷氨酸受体5(mGluR5)负变构调节剂(NAMs)可能在某些精神疾病如焦虑和抑郁中发挥作用。mGluR5-NAMs的药代动力学特征和药效学作用此前已有报道。我们对18名年轻健康女性受试者的数据进行了事后分析,这些受试者在一项mGluR5-NAM与单相口服避孕药的I期药物相互作用研究中接受了mGluR5-NAM。mGluR5-NAM采用每日两次剂量递增设计给药。口服避孕药(OC)与mGluR5-NAM之间没有相互作用。与晚上的浓度相比,早晨的mGluR5-NAM血浆浓度更高。观察到的大多数具有临床意义的神经精神不良反应发生在夜间,包括视觉(假性)幻觉、伴有继发性行为障碍的失眠,以及严重到足以干扰日常功能的认知功能障碍症状。药物吸收和处置中与昼夜节律相关的生理变化可能解释了这种药代动力学-药效学明显不成比例的关系。我们建议,评估精神药物基本药代动力学特性的临床试验应考虑潜在药物的时辰药代动力学。这可能有助于优化剂量,并将脆弱的精神科患者严重神经精神不良反应降至最低。