Original Investigation


, Volume 170, Issue 1, pp 33-41

First online:

Extracts of kava (Piper methysticum) induce acute anxiolytic-like behavioral changes in mice

  • Kennon M. GarrettAffiliated withDepartment of Physiology, University of Oklahoma Health Sciences Center Email author 
  • , Garo BasmadjianAffiliated withDepartment of Pharmaceutical Sciences, University of Oklahoma Health Sciences Center
  • , Ikhlas A. KhanAffiliated withNational Center for Natural Products Research, School of Pharmacy, University of Mississippi
  • , Brian T. SchanebergAffiliated withNational Center for Natural Products Research, School of Pharmacy, University of Mississippi
  • , Thomas W. SealeAffiliated withDepartment of Pediatrics, University of Oklahoma Health Sciences Center

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Kava has been used for centuries by Pacific Islanders for its tranquilizing and sedative effects. Recent clinical trials suggest that kava has therapeutic value for the treatment of anxiety. Demonstration of kava's anxiolytic effects in animals under controlled conditions would provide additional support for its clinical potential as an anxiolytic and would facilitate investigation of its mechanism(s) of action.


This study systematically characterized the acute dosage-dependent anxiolytic and sedative effects of kava extract in well established quantitative murine behavioral assays and compared kava- and diazepam-induced behavioral changes.


Various doses of an ethanolic extract of kava root or diazepam were administered intraperitoneally to BALB/cByJ inbred mice. Behavioral changes were measured in the mirrored chamber avoidance assay and elevated plus-maze assay. Reduced latency to enter and increased time spent in a normally avoided environment operationally defined anxiolysis. Sedation was defined by a significant decrease in locomotor activity in a circular arena.


Kava extract produced statistically significant dose-dependent anxiolytic-like behavioral changes in both assays of anxiolysis. ED50 values for kava-induced increases in time spent inside the mirrored chamber and on the open arms of the plus maze were 125 mg/kg and 88 mg/kg, respectively. Kava extract also caused a profound decrease in locomotor activity (ED50 of 172 mg/kg). Flumazenil, a competitive benzodiazepine receptor antagonist, blocked both the anxiolytic and sedative effects of diazepam, but had no effect on kava's behavioral actions.


Kava extracts produce significant murine anxiolytic-like behavioral changes and sedation that are not mediated through the benzodiazepine binding site on the GABAA receptor complex.


Kava Anxiety Sedation Mice Benzodiazepines