Abstract
For centuries the science of pharmacognosy has dominated rational drug development
until it was gradually substituted by target-based drug discovery in the last fifty
years. Pharmacognosy stems from the different systems of traditional herbal medicine
and its “reverse pharmacology” approach has led to the discovery of numerous pharmacologically
active molecules and drug leads for humankind. But do botanical drugs also provide
effective mixtures? Nature has evolved distinct strategies to modulate biological
processes, either by selectively targeting biological macromolecules or by creating
molecular promiscuity or polypharmacology (one molecule binds to different targets).
Widely claimed to be superior over monosubstances, mixtures of bioactive compounds
in botanical drugs allegedly exert synergistic therapeutic effects. Despite evolutionary
clues to molecular synergism in nature, sound experimental data are still widely lacking
to support this assumption. In this short review, the emerging concept of network
pharmacology is highlighted, and the importance of studying ligand-target networks
for botanical drugs is emphasized. Furthermore, problems associated with studying
mixtures of molecules with distinctly different pharmacodynamic properties are addressed.
It is concluded that a better understanding of the polypharmacology and potential
network pharmacology of botanical drugs is fundamental in the ongoing rationalization
of phytotherapy.
Key words
polypharmacology - network pharmacology - drug discovery - synergism - synergy - herbal
medicine - phytotherapy - pharmacodynamics - mixtures - evolution
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Prof. Dr. Jürg Gertsch
Institute of Biochemistry and Molecular Medicine University of Bern
Bühlstrasse 28
3012 Bern
Switzerland
Telefon: +41 3 16 31 41 24
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eMail: gertsch@mci.unibe.ch