Abstract
Two extracts of St. John's Wort (Hypericum perforatum) were investigated in the animal
model "Tele-Stereo-EEC" which consisted of continuous recording of intracerebral field
potentials in the freely moving rat. One was a CO2 extract for research purposes containing 30.14 % hyperforin, a phloroglucine derivative
known to occur within the reproductive parts of the plant, and lacking other major
constituents like naphtodianthrones and flavonoids according to HPLC fingerprint.
The other extract was the methanolic extract L1160 S (4.67 % hyperforin). The dosage
schedule was elaborated for the application of identical amounts of hyperforin in
both extracts in each dosing group. Both extracts produced nearly identical patterns
of electrical power changes during the first two hours of recording. These changes
mainly consisted of reproducible power increases within the alphai band of the striatum.
Comparison with earlier data obtained by identical protocols revealed that the early
action was very similar to that following the application of serotonin reuptake inhibitors,
thus matching biochemical in vitro data previously reported. These changes might be
due to the presence of hyperforin. Only LI 160 S developed a late action not seen
with the CO2 extract, consisting in increases in delta activity. This late action of LI 160S matched
data obtained by analysis of the action of NMDA-antagonists like MK 801 or memantine.
Again, these results support previously reported biochemical findings of the interaction
of hypericum extract with the glutamatergic system. In all probability, this action
stems from substances only present in LI 160 S, not in the CO2 extract. Which of the components contained within hypericum extracts are responsible
for the clinical efficacy of St. John's wort in depression remains to be determined.