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WHO monographs on selected medicinal plants - travolekar.ru

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Radix Panacis Quinquefolii<br />

estradiol (10 −9 M) induced the expressi<strong>on</strong> of pS2 RNA and protein in<br />

MCF-7 cells, whereas tamoxifen suppressed expressi<strong>on</strong>. Neither the extract<br />

nor estradiol induced increased pS2 expressi<strong>on</strong> in T-47D or BT-<br />

20 cell lines. Although estradiol exhibited a proliferative effect and tamoxifen<br />

had an inhibitory effect, the extract of the c<strong>ru</strong>de d<strong>ru</strong>g had no<br />

significant effect <strong>on</strong> cell proliferati<strong>on</strong>. Because the extract does not exhibit<br />

a proliferative effect, it may play a protective role against breast cancer<br />

rather than serving as a mitogen (32).<br />

Intragastric administrati<strong>on</strong> of the powdered root, at a dose of 100.0 mg/<br />

kg bw for 28 days, enhanced mounting behaviour of male rats and increased<br />

sperm counts in rabbit testes (33, 34). The effect of ginsenoside-<br />

Rb1 <strong>on</strong> the secreti<strong>on</strong> of luteinizing horm<strong>on</strong>e was investigated in vivo and<br />

in vitro. Male rats were orchidectomized 2 weeks or subjected to swim<br />

training for 1 week before catheterizati<strong>on</strong> via the right jugular vein. They<br />

were intravenously injected with ginsenoside-Rb1 (10.0 μg/kg bw) or saline<br />

15 minutes before a challenge with g<strong>on</strong>adotropin-releasing horm<strong>on</strong>e<br />

or a 10 minute-swim. Blood samples were collected at several time intervals<br />

following intravenous injecti<strong>on</strong> of ginsenoside-Rb1. In the in vitro<br />

experiment, male rats were decapitated and their anterior pituitary glands<br />

were either bisected or enzymatically dispersed. The dispersed anterior<br />

pituitary gland cells were primed with dihydrotestoster<strong>on</strong>e for 3 days,<br />

and then challenged with ginsenoside-Rbl (10.0 and 100.0 μM, n = 8) for<br />

3 h. The c<strong>on</strong>centrati<strong>on</strong>s of luteinizing horm<strong>on</strong>e or testoster<strong>on</strong>e in samples<br />

were measured by radioimmunoassay. Administrati<strong>on</strong> of ginsenoside-<br />

Rb1 did not alter the levels of plasma luteinizing horm<strong>on</strong>e in either intact<br />

or orchidectomized rats, but significantly increased c<strong>on</strong>centrati<strong>on</strong> of<br />

plasma luteinizing horm<strong>on</strong>e at the terminati<strong>on</strong> of the 10-minute swimming<br />

exercise. Administrati<strong>on</strong> of ginsenoside-Rb1 resulted in a lower testoster<strong>on</strong>e<br />

resp<strong>on</strong>se to g<strong>on</strong>adotropin-releasing horm<strong>on</strong>e challenge or<br />

swimming exercise than seen in saline-treated rats. Ginsenoside-Rb1<br />

dose-dependently increased the release of luteinizing horm<strong>on</strong>e from both<br />

hemi-anterior pituitary gland tissues and the dihydrotestoster<strong>on</strong>e-primed<br />

dispersed anterior pituitary gland cells in vitro. These results suggest that<br />

ginsenoside-Rb1 increases secreti<strong>on</strong> of luteinizing horm<strong>on</strong>e by acting directly<br />

<strong>on</strong> cells of rat anterior pituitary gland (34).<br />

Immune stimulati<strong>on</strong> effects<br />

The immunostimulatory activities of an aqueous extract (1 g in 10 ml water)<br />

and a methanol extract (1 g in 200 ml methanol) of the root were assessed in<br />

rat alveolar macrophages. Tumour necrosis factor alpha (TNF-) producti<strong>on</strong><br />

was used as a measure of activity. The aqueous extracts (1.0–100.0 μg/<br />

ml) significantly stimulated alveolar macrophage TNF- release. By c<strong>on</strong>-<br />

233

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