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WHO monographs on selected medicinal plants - travolekar.ru

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F<strong>ru</strong>ctus Macrocarp<strong>on</strong>ii<br />

Medicinal uses<br />

Uses supported by clinical data<br />

Orally as adjunct therapy for the preventi<strong>on</strong> and symptomatic treatment<br />

of urinary tract infecti<strong>on</strong>s in adults (8–20). Two clinical trials have assessed<br />

the effect of the f<strong>ru</strong>it juice in paediatric populati<strong>on</strong>s (17, 21), but<br />

the results were negative. Results from clinical trials involving the use of<br />

cranberry for the treatment of children with neurogenic bladder were also<br />

negative and do not support the use of cranberry products in paediatric<br />

populati<strong>on</strong>s (22).<br />

Uses described in pharmacopoeias and well established documents<br />

No informati<strong>on</strong> was found.<br />

Uses described in traditi<strong>on</strong>al medicine<br />

Treatment of asthma, fever, loss of appetite, scurvy and stomach ailments,<br />

as well as gallbladder and liver disease and for treatment of wounds (3, 23).<br />

Pharmacology<br />

Experimental pharmacology<br />

Antimicrobial and antiadhesive activity<br />

A c<strong>on</strong>centrated extract of the juice of the c<strong>ru</strong>de d<strong>ru</strong>g was tested for activity<br />

against the following pathogens: Alcaligenes faecalis, Clostridium perfringens,<br />

Enterococcus faecalis, Escherichia coli, Mycobacterium phlei,<br />

Pseudom<strong>on</strong>as ae<strong>ru</strong>ginosa, Salm<strong>on</strong>ella california, Salm<strong>on</strong>ella enteritidis,<br />

Salm<strong>on</strong>ella typhimurium, Shigella s<strong>on</strong>nei, Staphylococcus aureus and methicillin-resistant<br />

S. aureus, as well as Candida albicans. The c<strong>ru</strong>de d<strong>ru</strong>g<br />

c<strong>on</strong>centrate did not inhibit the growth of C. albicans, but had variable<br />

activity against the bacteria at diluti<strong>on</strong>s of 1:5 and 1:10 (24).<br />

Early investigati<strong>on</strong>s of the mechanism of cranberry’s bacteriostatic activity<br />

suggested that acidificati<strong>on</strong> of the urine may be resp<strong>on</strong>sible for its<br />

activity. However, more recent studies have dem<strong>on</strong>strated that urinary<br />

acidificati<strong>on</strong> is not the mechanism by which cranberry exerts its effects,<br />

but it does so through a mechanism that involves the inhibiti<strong>on</strong> of bacterial<br />

adherence (25–27). In vitro studies have shown that, in the 77 clinical<br />

isolates tested, cranberry juice decreased bacterial adherence of E. coli to<br />

uroepithelial cells by 60% when compared with saline soluti<strong>on</strong> (28). Furthermore,<br />

cranberry juice inhibited the adherence of E. coli to human urinary<br />

epithelial cells three times more st<strong>on</strong>gly than E. coli isolated from<br />

other clinical sources (27, 28). One study dem<strong>on</strong>strated that cranberry<br />

juice dose-dependently inhibited the haemagglutinati<strong>on</strong> activity of E. coli<br />

urinary isolates expressing type I and P adhesi<strong>on</strong> (27).<br />

153

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