Chronic continuous cocaine infusion in rats: Effect on urine cocaine, ecgonine methylester and benzoylecgonine concentrations and bolus-dose cocaine pharmacokinetics

Citation
B. Mets et al., Chronic continuous cocaine infusion in rats: Effect on urine cocaine, ecgonine methylester and benzoylecgonine concentrations and bolus-dose cocaine pharmacokinetics, J PHARM PHA, 52(4), 2000, pp. 389-395
Citations number
26
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF PHARMACY AND PHARMACOLOGY
ISSN journal
00223573 → ACNP
Volume
52
Issue
4
Year of publication
2000
Pages
389 - 395
Database
ISI
SICI code
0022-3573(200004)52:4<389:CCCIIR>2.0.ZU;2-V
Abstract
The aim of this study was to determine the effect of chronic cocaine infusi on on urine cocaine, ecgonine methylester and benzoylecgonine concentration s to establish if they varied with dose and duration of cocaine administrat ion. Male rats were continuously infused with cocaine at either 6 or 18 mg kg(-1 ) daily for 13 days. Three urine samples taken over the course of the infus ion period showed that cocaine, ecgonine methylester and benzoylecgonine co ncentrations varied with the dose administered and the duration of administ ration. Cocaine, ecgonine methylester and benzoylecgonine concentrations we re 2-3 times greater in the high-dose group than the low-dose group at each sampling time point. These decreased, respectively, from 7.0+/-1.1, 26.7+/ - 4.5 and 29.5+/-5.4 mu g mL(-1) to 2.5+/-0.5, 10.5+/-1.8 and 11.8+/-1.5 mu g mL(-1) in the high-dose group and from 1.0+/-0.2, 7.8+/-1.5 and 6.3+/-0. 1 mu g mL(-1) to 0.5+/-0.1, 4.0+/-0.6 and 3.1+/-0.4 mu g mL(-1) in the low- dose group (P < 0.05) over the infusion period. We also studied the pharmac okinetic and metabolic profile of an intravenous bolus dose of 2.5 mg kg(-1 ) cocaine hydrochloride after a similar cocaine infusion in rats. Cocaine p harmacokinetics and the profile of ecgonine methylester, benzoylecgonine an d norcocaine were no different from rats chronically infused with saline fo r the same period. Altered cocaine metabolism could not explain the effect of the duration of cocaine infusion on altered metabolite concentrations in urine. Ecgonine methylester/benzoylecgonine urine concentration ratios did not alter with duration of infusion (1.2+/-0.2 and 1.1+/-0.2 in the high-d ose group at the first and last time point) and were not affected by the do se of cocaine (1.3+/-0.6 and 1.2+/-0.1 at corresponding times in the low-do se group (P > 0.05)). We conclude that chronic cocaine infusion does not alter cocaine metabolism . This was not reflected by absolute cocaine metabolite urine concentration s, which varied with time, but was represented by urine ecgonine methyleste r/benzoylecgonine concentration ratios.