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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 />

The effect of the f<strong>ru</strong>it <strong>on</strong> the expressi<strong>on</strong> of P-fimbriae of E. coli was assessed<br />

by growing P-fimbriated E. coli in solid media c<strong>on</strong>taining cranberry<br />

juice. Cranberry c<strong>on</strong>centrate at pH 7.0 was added to the medium to achieve<br />

a final c<strong>on</strong>centrati<strong>on</strong> of 25%. E. coli strains JR1 and DS17 were plated <strong>on</strong><br />

to this medium, with a plain medium c<strong>on</strong>trol, and incubated at 37 °C. Cultures<br />

were tested for ability to agglutinate P-receptor-specific beads. The<br />

results dem<strong>on</strong>strated that for E. coli strain JR1, P-fimbrial agglutinati<strong>on</strong><br />

was inhibited after the third plating and strain DS17 was fully inhibited<br />

after the sec<strong>on</strong>d plating. Fully inhibited bacteria had a 100% reducti<strong>on</strong> in<br />

expressi<strong>on</strong> of fimbriae (25). Two compounds in cranberry juice inhibited<br />

lectin-mediated adherence of E. coli to mucosal cells. One of these compounds<br />

was f<strong>ru</strong>ctose and the other was a n<strong>on</strong>dialysable polymeric compound<br />

(25). Further investigati<strong>on</strong>s have found that exposure of pathogenic<br />

bacteria to the n<strong>on</strong>dialysable polymeric compound in either the gut or<br />

bladder produces a bacteriostatic effect by inhibiting the expressi<strong>on</strong> of<br />

specific adhesins present <strong>on</strong> the pili <strong>on</strong> the bacterial surface (26, 28).<br />

The proanthocyanidin fracti<strong>on</strong>, isolated from an ethyl acetate extract<br />

of the f<strong>ru</strong>it, was assessed for its ability to prevent adherence of E. coli by<br />

measuring the ability to prevent agglutinati<strong>on</strong> of both isolated P-receptor<br />

resin-coated beads and human erythrocytes. The proanthocyanidin fracti<strong>on</strong>,<br />

at a c<strong>on</strong>centrati<strong>on</strong> as low as 75.0 mg/ml, exhibited potent antiadherence<br />

activity in uropathogenic isolates of P-fimbriated E. coli bacteria to<br />

cellular surfaces c<strong>on</strong>taining alpha-Gal(14)beta-Gal receptor sequences<br />

similar to those <strong>on</strong> epithelial cells in the urinary tract. The chemical st<strong>ru</strong>ctures<br />

of the proanthocyanidins c<strong>on</strong>sisted predominantly of epicatechin<br />

units c<strong>on</strong>taining at least <strong>on</strong>e A-type linkage. The procyanidin A2 was the<br />

most comm<strong>on</strong> terminating unit, occurring about four times as frequently<br />

as the epicatechin m<strong>on</strong>omer (29). Isolated A-type proanthocyanidins isolated<br />

from cranberry juice cocktail had anti-adhesive activity at 60 g/ml,<br />

while the B-type exhibited weak activity at 1.2 mg/ml (30).<br />

A high-molecular-weight c<strong>on</strong>stituent of the f<strong>ru</strong>it, named n<strong>on</strong>dialysable<br />

material, at c<strong>on</strong>centrati<strong>on</strong>s of 100.0 μg/ml, inhibited the adhesi<strong>on</strong> of<br />

Helicobacter pylori strain BZMC-25 to human gastric mucosal cells. The<br />

inhibiti<strong>on</strong> of adhesi<strong>on</strong> by n<strong>on</strong>dialysable material was dose-dependent,<br />

and the 50% inhibitory c<strong>on</strong>centrati<strong>on</strong> was strain-dependent, the c<strong>on</strong>centrati<strong>on</strong>s<br />

being 37.0, 125.0 and 305.0 μg/ml for H. pylori strains BZMC-25,<br />

EHL-65 and 17874, respectively (31).<br />

In <strong>on</strong>e study, uropathogenic P-fimbriated E. coli isolates were obtained<br />

from the urine of women with clinically diagnosed, culture-c<strong>on</strong>firmed<br />

urinary tract infecti<strong>on</strong>s and incubated for 20 minutes in urine collected<br />

over a 12-hour period from healthy women before and after c<strong>on</strong>sumpti<strong>on</strong><br />

154

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