Development of a non-human primate model to support CNS translational research: Demonstration with D-amphetamine exposure and dopamine response

• Published in: Journal of neuroscience methods Vol. 317; pp. 71 - 81
• Main Authors: Folgering, Joost H., Choi, Minha, Schlumbohm, Christina, van Gaalen, Marcel M., Stratford Jr, Robert E.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.04.2019
• Subjects: Amphetamine; Dopamine; Microdialysis; Non-human primate; Population modeling; Translational sciences; ADHD; BBB; Dopamine; Translational sciences; MRI; CNS; ECF; PBPKPD; PFC; BCSFB; Amphetamine; Microdialysis; CSF; NHP; Non-human primate; SEM; Population modeling
• ISSN: 0165-0270; 1872-678X; 1872-678X
• DOI: 10.1016/j.jneumeth.2019.02.005

•Measurement of drug and biomarker levels in primate brain achieved by microdialysis.•Population pharmacokinetic modeling reduces animal requirements.•Primate sourced modeling approach improves confidence in translational predictions.•Temporal effects of D-amphetamine on dopamine translationally conserved from rodent to primate. Challenges specific to the discovery and development of candidate CNS drugs have led to implementation of various in silico, in vitro and in vivo approaches to improve the odds for commercialization of novel treatments. Advances in analytical methodology and microdialysis probe design have enabled development of a non-human primate model capable of measuring concentrations of drugs or endogenous chemicals in brain extracellular fluid (ECF) and cerebrospinal fluid (CSF). Linking these to population modeling reduces animal numbers to support predictive translational sciences in primates. Application to measure D-amphetamine exposure and dopamine response in ECF and CSF demonstrate the approach. Following a 0.1 mg/kg intravenous bolus dose of D-amphetamine, a population approach was used to build a plasma compartmental-based and brain physiologic-based pharmacokinetic (PK) model linking drug concentrations in plasma to brain ECF and CSF concentrations. Dopamine was also measured in brain ECF. The PK model was used to simulate the relationship between D-amphetamine exposure and dopamine response in ECF over a wide dose range. Ability to co-sample and measure drug and endogenous substances in blood, brain ECF and/or CSF, coupled with population modeling, provides an in vivo approach to evaluate CNS drug penetration and effect in non-human primates. A method to measure drug and endogenous neurochemicals in non-human primate brain fluids is demonstrated. Its basis in non-human primates merits improved confidence regarding predictions of drug exposure and target engagement in human CNS.