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WHO monographs on selected medicinal plants - travolekar.ru

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Flos Trifolii<br />

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

Topical treatment of dermatological disorders such as psoriasis and eczema,<br />

as well as orally for the treatment of asthma and cough (5).<br />

Pharmacology<br />

Experimental pharmacology<br />

Much of the experimental pharmacology for Flos Trifolii is based <strong>on</strong> informati<strong>on</strong><br />

from pure compounds isolated from the c<strong>ru</strong>de d<strong>ru</strong>g, or from<br />

extracts of the aerial parts of the plant. Therefore, how these data apply to<br />

the c<strong>ru</strong>de d<strong>ru</strong>g needs to be further investigated.<br />

Anti-inflammatory activity<br />

Genistein has been found to provide protecti<strong>on</strong> from oxidative damage<br />

induced by ultraviolet (UV) radiati<strong>on</strong> both in vitro and following dietary<br />

administrati<strong>on</strong>. One in vivo study assessed the potential of a number of<br />

isoflav<strong>on</strong>es isolated from the c<strong>ru</strong>de d<strong>ru</strong>g, as well as some metabolically<br />

related compounds, to offer protecti<strong>on</strong> against UV irradiati<strong>on</strong>. The results<br />

were assessed in hairless mice after topical applicati<strong>on</strong> of the extract<br />

or isoflav<strong>on</strong>es in combinati<strong>on</strong> with UV exposure. Daidzein, biochanin A<br />

and form<strong>on</strong><strong>on</strong>etin were not active, while 20 μM loti<strong>on</strong>s of genistein and<br />

the metabolites equol, isoequol and dehydroequol reduced oedema and<br />

inflammati<strong>on</strong>, as well as suppressing hypersensitivity induced by moderate<br />

doses of artificial UV radiati<strong>on</strong>. The protective effect of equol was<br />

c<strong>on</strong>centrati<strong>on</strong>-dependent and 5 μM equol markedly reduced UV-induced<br />

inflammati<strong>on</strong> (20).<br />

Inhibiti<strong>on</strong> of cell proliferati<strong>on</strong><br />

Isoflav<strong>on</strong>es inhibit the growth of some types of tumour cells, including<br />

prostate adenocarcinoma. In the prostate cancer cell line, LNCaP, and xenografts,<br />

the mechanism of the antiproliferative effects of biochanin A was<br />

determined (18). LNCaP cells were treated with varying c<strong>on</strong>centrati<strong>on</strong>s of<br />

biochanin A to evaluate viability, DNA synthesis and DNA fragmentati<strong>on</strong><br />

by terminal deoxynucleotidyltransferase dUTP nick end labelling<br />

(TUNEL) analysis. Regulati<strong>on</strong> of gene expressi<strong>on</strong> was determined using<br />

Western immunoblotting and cDNA microarrays. Antiproliferative effects<br />

were evaluated by using athymic mice with LNCaP flank tumours.<br />

Biochanin A induced a dose-dependent inhibiti<strong>on</strong> of LNCaP cell proliferati<strong>on</strong><br />

and tritiated thymidine incorporati<strong>on</strong> that correlated with increased<br />

DNA fragmentati<strong>on</strong>, indicative of apoptosis. Western blot analyses<br />

of cell cycle regulatory proteins revealed that biochanin A significantly<br />

decreased expressi<strong>on</strong> of cyclin B and p21, whereas flow cytometry showed<br />

that cells were accumulating in the G(0)/G(1) phase. cDNA microarray<br />

339

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