Extracts of St. John's wort, Hypericum perforatum L (Hypericaceae), are used as a phytotherapeutic antidepressant. A number of clinical
studies demonstrate that their antidepressive potency is comparable to tricyclic antidepressants
(TCA). Although the therapeutic effect of hypericum extracts is well documented, very
little is known about the molecular mode of action. As the improvement of the depressive
symptoms with both TCA and hypericum extracts only occurs significantly after a lag
phase of 10 to 14 days, it is assumed that the medication causes long-term adaptations
within the central nervous system. In this context, serotonergic (5-HT) receptors
are of special interest. Therefore, we investigated possible alterations in affinity
and density of 5-HT1 A and 5-HT2 A receptors caused by long-term treatment of rats
with St. John's wort. The brain without cerebellum and brain stem of rats, treated
daily for 26 weeks with a commercially available hypericum extract (2700 mg/kg LI
160) were used for membrane preparations. Affinity (KD) and amount (Bmax) of serotonergic receptors were determined by employing receptor binding assays using
3 H-8-OH-DPAT and 3H-Ketanserin as selective radioligands for the 5-HT1 A and the 5-HT2 A receptors,
respectively. We found that in hypericum-treated rats the number of both 5-HT1 A and
5-HT2A receptors were significantly increased by 50 % compared to controls, whereas
the affinity of both serotonergic receptors remained unaltered. The data suggest an
upregulation of 5-HT1 A and 5-HT2 A receptors due to prolonged administration of hypericum
extracts. These results are consistent with a modification of the expression levels
of serotonergic receptors caused by synthetic antidepressants.