Neurochemical studies with St. John's wort in vitro

• Published in: Pharmacopsychiatry Vol. 34 Suppl 1; p. S137
• Main Authors: Simmen, U, Higelin, J, Berger-Büter, K, Schaffner, W, Lundstrom, K
• Format: Journal Article
• Language: English
• Published: Germany 01-07-2001
• Subjects: Animals; Cerebellum - chemistry; Cerebellum - drug effects; Cerebellum - metabolism; Female; GTP-Binding Proteins - metabolism; Hypericum; In Vitro Techniques; Male; Plant Extracts - pharmacology; Radioligand Assay; Rats; Rats, Wistar; Receptors, Corticotropin-Releasing Hormone - metabolism; Receptors, Estrogen - metabolism; Receptors, GABA-A - metabolism; Receptors, Histamine - metabolism; Receptors, Metabotropic Glutamate - metabolism; Receptors, Neurokinin-1 - metabolism; Receptors, Serotonin - metabolism
• ISSN: 0176-3679
• DOI: 10.1055/s-2001-15475

The effect of extracts and constituents of St. John's wort, Hypericum perforatum, at various CNS receptors were studied by radioligand binding techniques in order to determine a profile of pharmacological activity in vitro. Binding inhibition was examined for the G-protein coupled opioid, serotonin (5-HT), histamine, neurokinin and corticotropin releasing factor (CRF) receptors, for the steroid estrogen-alpha receptor and for the ligand-gated ionchannel GABA(A) receptor. Hypericin showed the most potent binding inhibiton of all tested constituents to human CRF1 receptor with an IC50 value of 300 nM. Preliminary GTPgamma35S binding studies to CRF1 coupled G-protein indicated an antagonistic action for hypericin. The acylphloroglucinole hyperforin failed to inhibit 125I-astressin binding to hCRF, receptor up to 10 microM. Hyperforin inhibited binding to opioid and serotonin (5-HT) receptors at IC50 values between 0.4 and 3 microM, while hypericin and pseudohypericin inhibited with weaker potency. The biflavonoid I3,II8-biapigenin inhibited 3H-estradiol binding to the estrogen-alpha receptor with an IC50 value of 1 microM. The inhibition of 3H-muscimol binding to the GABA(A) receptor is likely to be exclusively due to GABA present in the extract. We therefore hypothesize that additive or synergistic actions of several ditsinct compounds may be responsible for the beneficial antidepressant effect of St. John's wort.