Distribution of gacyclidine enantiomers after experimental spinal cord injury in rats: possible involvement of an active transport system.

Abstract

The pharmacokinetics of gacyclidine enantiomers, a noncompetitive N-methyl-D-aspartate (NMDA) antagonist, were studied in plasma and spinal cord extracellular fluid (ECF) after experimental spinal cord injury in rats. Spinal cord trauma was produced by introducing an inflatable balloon in the dorsal subdural space. Upon implantation of microdialysis probes in spinal cord (T9) and intravenous (iv) bolus administration of (+/-)-gacyclidine (2.5 mg/kg), concentrations in plasma and ECF were monitored over 5 h and analyzed by a stereospecific gas chromatography-mass spectrometry (GC-MS) assay. In plasma, concentrations of (+)-gacyclidine were approximately 25% higher than those of (-)-gacyclidine over the duration of the experiment and decayed in parallel (t(1/2 alpha) approximately 7 min; t(1/2 beta) approximately 90 min) with no significant difference between the two enantiomers. Clearance (CL) and volume of distribution (Vd) of (-)-gacyclidine were approximately 20% higher than those of its optical antipode (CL: 285 versus 236 mL. kg(-1). min(-1); Vd(beta): 39.3 versus 31.2 l/kg). Protein binding (approximately 91%) was not stereoselective. In spinal cord ECF, both enantiomers were quantifiable within 10 min after drug administration, and their concentration remained stable over the duration of the experiment in spite of changing blood concentrations. Repeated iv bolus injections of gacyclidine did not modify these profiles. Areas under the curves (AUCs) of concentration in ECF versus time were similar for both enantiomers and not correlated with AUCs in plasma. Penetration of (-)-gacyclidine was, however, significantly higher (approximately 30%) than that of (+)-gacyclidine. In summary, the disposition of gacyclidine enantiomers is stereoselective. Both enantiomers exhibit a high affinity for spinal cord tissue, and the drug exchange between plasma and spinal cord ECF involves an active transport system. These findings contribute to the explanation of the discrepancy between drug concentrations in plasma and spinal cord ECF.

• Authors: G Hoizey, M L Kaltenbach, S Dukic, D Lamiable, A Lallemand, H Millart, P D'Arbigny, R Vistelle
• Journal: Journal of pharmaceutical sciences (J Pharm Sci) Vol. 90 Issue 1 Pg. 70-8 (Jan 2001) ISSN: 0022-3549 [Print] United States
• PMID: 11064380 (Publication Type: Journal Article)
• Copyright: Copyright 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 90: 70-78, 2001

Chemical References

• Cyclohexanes
• Cyclohexenes
• Neuroprotective Agents
• Piperidines
• gacyclidine

Topics

• Animals
• Biological Transport, Active
• Calibration
• Cyclohexanes (pharmacokinetics)
• Cyclohexenes
• Disease Models, Animal
• Dose-Response Relationship, Drug
• Male
• Neuroprotective Agents (pharmacokinetics)
• Piperidines (pharmacokinetics)
• Protein Binding (drug effects)
• Rats
• Rats, Wistar
• Spinal Cord Injuries (metabolism)
• Stereoisomerism
• Tissue Distribution