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Volume 6, Issue 4 (Suppl)

Clin Pharmacol Biopharm, an open access journal

ISSN: 2167-065X

Euro Biopharma & Ethnopharmacology 2017

November 09-11, 2017

Page 12

Notes:

&

6

th

International Conference and Exhibition on

November 09-11, 2017 Vienna, Austria

4

th

EUROPEAN BIOPHARMA CONGRESS

PHARMACOLOGY AND ETHNOPHARMACOLOGY

Joint Event

Reverse pharmacology of

sceletium tortuosum

A

“reverse pharmacology” approach was started with an extract of

Sceletium tortuosum

, currently sold as Zembrin® in

the USA, Canada, Brazil, Malaysia, and South Africa. It is a proprietary extract of a low-alkaloid cultivated selection of

Sceletium tortuosum

, and is used by healthy people for enhancing mood, decreasing anxiety and stress and improving cognitive

function under stressful situations. As test model the hippocampus slice

in vitro

was chosen to compare its effects with four of its

alkaloid constituents, namely Mesembrine, Mesembrenone, Mesembrenol and Mesembranol. Measurement of the amplitude

of population spikes was performed in the presence of single shock stimulation and theta burst stimulation resulting in long

term potentiation (LTP). Rats were treated daily for one week with 5 or 10 mg/kg of Zembrin® before the hippocampus was

taken out for

in vitro

analysis. Amplitudes of the population spikes were dose dependently attenuated. Out of four glutamate

receptor agonists only Fluorowillardine was completely unable to induce its agonistic action. This points to an AMPA receptor

mediated attenuation of hippocampal excitability produced by repetitive dosing of Zembrin®. Superfusing the slices directly

with the alkaloids at nanomolar concentrations (3.5 – 35 nM) resulted in a concentration dependent attenuation of population

spike amplitudes. However, only Mesembrenol and Mesembranol were able to prevent the action of Fluorowillardine, thus

resembling the effect of the whole extract. Comparing now the chemical formula of the alkaloids in terms of a structure activity

relationship, the hydroxy group at C6 instead of a carbonyl group in mesembranol seems to be essential for interaction with

AMPA dependent transmission. Since attenuation of AMPA mediated transmission has been related to successful adjunctive

treatment of epileptic patients, Mesembranol - following the principle and methodology of “reverse pharmacology” - might

serve as chemical lead for the development of new drugs for the treatment of epilepsy.

Biography

Wilfried Dimpfel is Honorary Professor at Justus-Liebig-University Giessen, Germany, since 1983. He is Pharmacologist and got his Neurophysiological Education during

1973-1974 as Max Kade stipend (New York) at the NIH Bethesda from Phil Nelson. Together with Hans-Carlos Hofmann, a Physicist and Mathematician, he developed

quantitative EEG software for research and practice. He is Consultant and CSO at NeuroCode AG, Wetzlar, Germany. He published more than 150 papers in peer-re-

viewed journals.

Wilfried.Dimpfel@pharma.med.uni-giessen.de

s

Wilfried Dimpfel

University of Giessen, Germany

Wilfried Dimpfel, Clin Pharmacol Biopharm 2017, 6:4(Suppl)

DOI: 10.4172/2167-065X-C1-024