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WHO monographs on selected medicinal plants - travolekar.ru

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<str<strong>on</strong>g>WHO</str<strong>on</strong>g> <str<strong>on</strong>g>m<strong>on</strong>ographs</str<strong>on</strong>g> <strong>on</strong> <strong>selected</strong> <strong>medicinal</strong> <strong>plants</strong><br />

phate, arachid<strong>on</strong>ic acid or collagen, in which collagen-induced thromboxane<br />

A 2<br />

synthesis was also inhibited (42). In vivo, the plasma<br />

prostacyclin level was reduced by 34.6% during a 30-min period after<br />

intravenous administrati<strong>on</strong> of 50.0 mg/kg bw of berberine to rabbits.<br />

These results suggest that berberine inhibits arachid<strong>on</strong>ic acid metabolism<br />

in rabbit platelets and endothelial cells at two or more sites: cyclooxygenase<br />

in the arachid<strong>on</strong>ic acid cascade and possibly the enzyme(s) for arachid<strong>on</strong>ic<br />

acid liberati<strong>on</strong> from membrane phospholipids (42).<br />

Antimicrobial activity<br />

A methanol extract of the bark and berberine inhibited the growth of<br />

Helicobacter pylori in vitro. Berberine inhibited the growth of 15 strains<br />

of H. pylori, with a minimum inhibitory c<strong>on</strong>centrati<strong>on</strong> of 12.5 μg/ml<br />

(range 0.78–25.0 μg/ml) (43). The antibacterial activity of berberine against<br />

Staphylococcus aureus at a sub-inhibitory dose was potentiated by the flav<strong>on</strong>es<br />

chrysosplenol-D and chrysoplenetin, from Artemisia annua. The<br />

potentiati<strong>on</strong> is due to the inhibiti<strong>on</strong> of an S. aureus multid<strong>ru</strong>g resistance<br />

pump (44). Berberine had a minimum inhibitory c<strong>on</strong>centrati<strong>on</strong> of 25–<br />

50 μg/ml against S. aureus and Mycobacterium smegmatis (45, 46). The<br />

antimicrobial activity of berberine was evaluated against 17 microorganisms<br />

including two Gram-negative bacteria, Pseudom<strong>on</strong>as ae<strong>ru</strong>ginosa and<br />

Escherichia coli (both resistant and sensitive), two Gram-positive bacteria,<br />

Bacillus subtilis and S. aureus, Zoogloea ramigera, six filamentous<br />

fungi, Penicillium chrysogenum, Aspergillus niger, Aureobasidium pullulans<br />

(black and white strain), Trichoderma viride (original green strain<br />

and brown mutant), Fusarium nivale, Microspo<strong>ru</strong>m gypseum and two<br />

yeasts, Candida albicans and Saccharomyces cerevisiae (47).<br />

The results dem<strong>on</strong>strated that the minimum inhibitory c<strong>on</strong>centrati<strong>on</strong>,<br />

minimum microbicidal c<strong>on</strong>centrati<strong>on</strong> and minimum microbistatic c<strong>on</strong>centrati<strong>on</strong>s<br />

varied c<strong>on</strong>siderably depending <strong>on</strong> the microorganism tested.<br />

In general, the sensitivity of the microorganisms to berberine in decreasing<br />

order was as follows: S. aureus > P. ae<strong>ru</strong>ginosa S (sensitive) > E. coli<br />

(sensitive) > P. ae<strong>ru</strong>ginosa R (resistant) > E. coli (resistant) > B. subtilis<br />

> Z. ramigera > C. albicans > S. cerevisiae > A. pullulans > T. viride<br />

(brown) > M. gypseum > A. niger > F. nivale > P. chrysogenum<br />

> T. viride (green).<br />

Berberine weakly inhibited the growth of Bacillus subtilis and Salm<strong>on</strong>ella<br />

enteritidis in vitro at a c<strong>on</strong>centrati<strong>on</strong> of 1 mg/ml and 0.5 mg/ml, respectively<br />

(48). Berberine also weakly inhibited the growth of Clostridium<br />

perfringens in vitro (150 μg/ml), and, at a c<strong>on</strong>centrati<strong>on</strong> of 1.0 mg/ml,<br />

weakly inhibited the growth of Entamoeba histolytica, Giardia lamblia<br />

36

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