Hyperforin depletes synaptic vesicles content and induces compartmental redistribution of nerve ending monoamines

• Published in: Life sciences (1973) Vol. 75; no. 23; pp. 2841 - 2850
• Main Authors: Roz, Netta, Rehavi, Moshe
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 22.10.2004
• Subjects: Analysis of Variance; Animals; Biogenic Monoamines - metabolism; Biological Transport; Brain - metabolism; Brain slices; Bridged Bicyclo Compounds - pharmacology; Dopamine; Dopamine - metabolism; Dose-Response Relationship, Drug; Hydrogen-Ion Concentration; Hyperforin; Hypericum perforatum; Monoamines release; Neurotransmitter Uptake Inhibitors - pharmacology; Phloroglucinol - analogs & derivatives; Phloroglucinol - pharmacology; Rats; Serotonin; Serotonin - metabolism; Synaptic Vesicles - drug effects; Terpenes - pharmacology; Time Factors; Tritium; Hyperforin; Brain slices; Monoamines release; Dopamine; Serotonin
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2004.08.004

Hyperforin, a phloroglucinol derivative found in Hypericum perforatum (St. John's wort) extracts has antidepressant properties in depressed patients. Hyperforin has a unique pharmacological profile and it inhibits uptake of biogenic monoamines as well as amino acid transmitters. We have recently showed that the monoamines uptake inhibition exerted by hyperforin is related to its ability to dissipate the pH gradient across the synaptic vesicle membrane thereby interfering with vesicular monoamines storage. In the present study we demonstrate that hyperforin induces dose-dependent efflux of preloaded [ 3H]5HT and [ 3H]DA from rat brain slices. Moreover, we show that hyperforin attenuates depolarization- dependent release of monoamines, while increasing monoamine release by amphetamine or fenfluramine. It is also demonstrated that preincubation of brain slices with reserpine is associated with dose- dependent blunting of efflux due to hyperforin. Our data indicate that hyperforin-induced efflux of [ 3H]5HT and [ 3H]DA reflect elevated cytoplasmic concentrations of the two monoamines secondary to the depletion of the synaptic vesicle content and the compartmental redistribution of nerve ending monoamines.