Functional neurotoxicity evaluation of noribogaine using video-EEG in cynomolgus monkeys

被引:9
作者
Authier, Simon [1 ,2 ]
Accardi, Michael V. [1 ]
Paquette, Dominique [3 ]
Pouliot, Mylene [1 ]
Arezzo, Joseph [4 ,5 ]
Stubbs, R. John [6 ]
Gerson, Ronald J.
Friedhoff, Lawrence T. [7 ]
Weis, Holger [8 ]
机构
[1] CiToxLAB North Amer, 445 Armand Frappier, Laval, PQ H7V 4B3, Canada
[2] Univ Montreal, Fac Med Vet, POB 5000, St Hyacinthe, PQ J2S 7C6, Canada
[3] Ctr Vet DMV, 2300 54e Ave, Lachine, PQ H8T 3R2, Canada
[4] Albert Einstein Coll Med, Dept Neurosci, New York, NY USA
[5] Albert Einstein Coll Med, Dept Neurol, New York, NY USA
[6] Stubbs & Hensel Pharma Consulting LLC, POB 935, Blue Bell, PA 19422 USA
[7] Pharmaceut Special Projects Grp, Ft Lauderdale, FL USA
[8] DemeRx Inc, Ft Lauderdale, FL USA
关键词
Noribogaine; Electroencephalography; EEG; Cynomolgus monkey; Pentylenetetrazol; PRIMARY METABOLITE; IBOGAINE; 12-HYDROXYIBOGAMINE; SAFETY; 18-METHOXYCORONARIDINE; TELEMETRY; EFFICACY; MORPHINE; LIGANDS; 18-MC;
D O I
10.1016/j.vascn.2016.04.012
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Continuous video-electroencephalographic (EEG) monitoring remains the gold standard for seizure liability assessments in preclinical drug safety assessments. EEG monitored by telemetry was used to assess the behavioral and EEG effects of noribogaine hydrochloride (noribogaine) in cynomolgus monkeys. Noribogaine is an iboga alkaloid being studied for the treatment of opioid dependence. Methods: Six cynomolgus monkeys (3 per gender) were instrumented with EEG telemetry transmitters. Noribogaine was administered to each monkey at both doses (i.e., 160 and 320 mg/kg, PO) with an interval between dosing of at least 6 days, and the resulting behavioral and EEG effects were evaluated. IV pentylenetetrazol (PTZ), served as a positive control for induced seizures. Results: The administration of noribogaine at either of the doses evaluated was not associated with EEG evidence of seizure or with EEG signals known to be premonitory signs of increased seizure risk (e.g., sharp waves, unusual synchrony, shifts to high-frequency patterns). Noribogaine was associated with a mild reduction in activity levels, increased scratching, licking and chewing, and some degree of poor coordination and related clinical signs. A single monkey exhibited brief myoclonic movements that increased in frequency at the high dose, but which did not appear to generalize, cluster or to be linked with EEG abnormalities. Noribogaine was also associated with emesis and partial anorexia. In contrast, PTZ was associated with substantial pre-ictal EEG patterns including large amplitude, repetitive sharp waves leading to generalized seizures and to typical post-ictal EEG frequency attenuation. Interpretation: EEG patterns were within normal limits following administration of noribogaine at doses up to 320 mg/kg with concurrent clinical signs that correlated with plasma exposures and resolved by the end of the monitoring period. PTZ was invariably associated with EEG paroxysmal activity leading to ictal EEG. In the current study, a noribogaine dose of 320 mg/kg was considered to be the EEG no observed adverse effect level (NOAEL) in conscious freely moving cynomolgus monkeys. (C) 2016 The Authors. Published by Elsevier Inc.
引用
收藏
页码:306 / 312
页数:7
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