The medicinal plant goldenseal (Hydrastis canadensis) has been used historically to treat infection [1], and it is currently among the
top ten best selling botanicals in the US. This plant has demonstrated activity in
vitro against a number of bacteria, including multidrug-resistant Staphylococcus aureus (MRSA) [2]. Previous studies have implicated several alkaloids, including berberine,
in the antibacterial activity of H. canadensis [2, 3]. Recent results from our laboratories, however, have led to the hypothesis
that non-alkaloidal constituents also play an important role. An extract from the
aerial portions of H. canadensis was separated into 12 fractions using flash chromatography. One of these fractions
contained only very low (1000 x < MIC) concentrations of alkaloids, but it enhanced
significantly the antibacterial activity of berberine. LC-MS analysis of all 12 of
the fractions indicated three potential active compounds (thus far unidentified) that
were present at the highest concentration in the active fraction. On the basis of
experiments comparing antibacterial activity against wild type and efflux pump knockout
mutants of S. aureus, the active constituents of the fraction appear to act as efflux pump inhibitors.
Our studies indicate that goldenseal's mechanism of antibacterial activity may be
more complex than previously reported, and suggest that H. canadensis could be useful for the treatment of drug resistant bacterial infections, particularly
as a topical agent. In addition, we demonstrate the effectiveness of combining bioassay
guided fractionation with comprehensive LC-MS analysis to identify potential potentiators/synergists
in medicinal plants.
Acknowledgements:
Bill Burch, Bear Wallow Ginseng, Hendersonville, NC; Research Corporation Cottrell
College Science Award CC6642; NSF-MRI Award 0420292.
References:1. Upton, R., Goldenseal Root (2001) Hydrastis canadensis: Standards of analysis, quality control, and therapeutics. American Herbal Pharmacopoeia.
Santa Cruz; 2. Scazzocchino, F. et. al. (2001) Planta Med. 67: 561–564 3. Gentry, E. J. et. al. (1998)J. Nat. Prod. 61:1187–1193.