A pharmacokinetic/pharmacodynamic investigation: Assessment of edivoxetine and atomoxetine on systemic and central 3,4-dihydroxyphenylglycol, a biochemical marker for norepinephrine transporter inhibition

• Published in: European neuropsychopharmacology Vol. 25; no. 3; pp. 377 - 385
• Main Authors: Kielbasa, William, Pan, Alan, Pereira, Alvaro
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.03.2015
• Subjects: Adrenergic Uptake Inhibitors - pharmacokinetics; Adult; Atomoxetine; Atomoxetine Hydrochloride - blood; Atomoxetine Hydrochloride - cerebrospinal fluid; Atomoxetine Hydrochloride - pharmacokinetics; Chromatography, High Pressure Liquid; DHPG; Dose-Response Relationship, Drug; Edivoxetine; Electrochemical Techniques; Female; Humans; Internal Medicine; Male; Methoxyhydroxyphenylglycol - analogs & derivatives; Methoxyhydroxyphenylglycol - blood; Methoxyhydroxyphenylglycol - cerebrospinal fluid; Morpholines - blood; Morpholines - cerebrospinal fluid; Morpholines - pharmacokinetics; Pharmacodynamics; Pharmacokinetic; Phenylethyl Alcohol - analogs & derivatives; Phenylethyl Alcohol - blood; Phenylethyl Alcohol - cerebrospinal fluid; Phenylethyl Alcohol - pharmacokinetics; Psychiatry; Time Factors; Young Adult; Pharmacodynamics; Edivoxetine; DHPG; Atomoxetine; Pharmacokinetic
• DOI: 10.1016/j.euroneuro.2014.12.009
• ISSN: 0924-977X; 1873-7862

Inhibition of norepinephrine (NE) reuptake into noradrenergic nerves is a common therapeutic target in the central nervous system (CNS). In noradrenergic nerves, NE is oxidized by monoamine oxidase to 3,4-dihydroxyphenylglycol (DHPG). In this study, 40 healthy male subjects received the NE transporter (NET) inhibitor edivoxetine (EDX) or atomoxetine (ATX), or placebo. The pharmacokinetic and pharmacodynamic profile of these drugs in plasma and cerebrospinal fluid (CSF) was assessed. In Part A, subjects received EDX once daily (QD) for 14 or 15 days at targeted doses of 6mg or 9mg. In Part B, subjects received 80mg ATX QD for 14 or 15 days. Each subject received a lumbar puncture before receiving drug and after 14 or 15 days of dosing. Plasma and urine were collected at baseline and after 14 days of dosing. Edivoxetine plasma and CSF concentrations increased dose dependently. The time to maximum plasma concentration of EDX was 2h, and the half-life was 9h. At the highest EDX dose of 9mg, DHPG concentrations were reduced from baseline by 51% at 8h postdose in CSF, and steady-state plasma and urine DHPG concentrations decreased by 38% and 26%, respectively. For 80mg ATX, the decrease of plasma, CSF, or urine DHPG was similar to EDX. Herein we provide clinical evidence that EDX and ATX decrease DHPG concentrations in the periphery and CNS, presumably via NET inhibition. EDX and ATX concentrations measured in the CSF confirmed the availability of those drugs in the CNS.