PHARMACOKINETICS AND ANTICONVULSANT EFFECT OF A NEW HYPNOTIC, CL-284,846, IN RATS

被引:12
作者
GAUDREAULT, J
VARIN, F
POLLACK, GM
机构
[1] UNIV N CAROLINA, SCH PHARM, DIV PHARMACEUT, CHAPEL HILL, NC 27599 USA
[2] UNIV MONTREAL, FAC PHARM, MONTREAL, PQ H3C 3J7, CANADA
关键词
ANTICONVULSANT; CL 284,846; CL 284,859; PENTYLENETETRAZOL; PHARMACOKINETICS; PHARMACODYNAMICS;
D O I
10.1023/A:1016224629614
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. CL 284,846 (CL846) is an investigational non-benzodiazepine agent with hypnotic, anxiolytic, myorelaxant and anticonvulsant properties. This study assessed the pharmacokinetics and anticonvulsant action of CL846 in female Sprague-Dawley rats. Methods. CL846 pharmacokinetics were examined after either an iv bolus dose (2.5 mg/kg) or a 6-hr infusion (0.4 mg/kg/hr). CL846 pharmacodynamics were evaluated with a pentylenetetrazol (PTZ) infusion 5 min after a CL846 in bolus dose (0 to 10 mg/kg). CL846 and the derived metabolite CL 284,859 (CL859) concentrations in serum and brain tissue were determined by HPLC with fluorescence detection. Results. Both the steady-state volume of distribution (1636 +/- 162 and 1804 +/- 293 ml/kg, after bolus and infusion administration, respectively) and systemic clearance (19.1 +/- 7.1 and 22.2 +/- 4.3 ml/min/kg for bolus and infusion administration, respectively) were high. No differences in pharmacokinetic parameters were noted between the two modes of administration. The relationship between anticonvulsant effect and brain/serum concentrations was well described by an E(max) model. CL846 was as effective as triazolam in antagonizing PTZ-induced seizures. Conclusions. Under theconditions of the present study, CL846 pharmacokinetics were linear and stationary. Further evaluation of the anticonvulsant properties of CL846 is warranted, including the potential development of tolerance, which is well known for benzodiazepines.
引用
收藏
页码:1592 / 1597
页数:6
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