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WHO monographs on selected medicinal plants - travolekar.ru

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Radix Panacis Quinquefolii<br />

Two-way ANOVA showed that the main effects of treatment and administrati<strong>on</strong><br />

time were significant (p < 0.05). Glycaemia was lower over the last<br />

45 minutes of the test after doses of 1, 2 or 3 g than after placebo (p < 0.05);<br />

there were no significant differences between the three doses. The reducti<strong>on</strong>s<br />

in the areas under the curve for these three doses were 14.4 ± 6.5%,<br />

10.6 ± 4.0% and 9.1 ± 6%, respectively. Glycaemia in the last hour of the<br />

test and area under the curve were lower when the c<strong>ru</strong>de d<strong>ru</strong>g was administered<br />

40 minutes before the challenge than when it was administered 20,<br />

10 or 0 minutes before the challenge (p < 0.05). Thus, doses of the c<strong>ru</strong>de<br />

d<strong>ru</strong>g within the range of 1–3 g were equally effective (22).<br />

Adverse reacti<strong>on</strong>s<br />

No adverse reacti<strong>on</strong>s have been reported.<br />

C<strong>on</strong>traindicati<strong>on</strong>s<br />

Radix Panacis Quinquefolii is c<strong>on</strong>traindicated in cases of known allergy<br />

or hypersensitivity to the plant material.<br />

Warnings<br />

No informati<strong>on</strong> available.<br />

Precauti<strong>on</strong>s<br />

D<strong>ru</strong>g interacti<strong>on</strong>s<br />

While no d<strong>ru</strong>g interacti<strong>on</strong>s have been reported, an extract of the root<br />

(c<strong>on</strong>taining 10% ginsenosides) inhibited the activity of cytochrome<br />

P450 isozymes CYP1A1, CYP1A2 and CYP1B1 in vitro in human liver<br />

microsomes (45). Thus, there is a potential for interacti<strong>on</strong>s with other<br />

d<strong>ru</strong>gs that are metabolized by these enzymes.<br />

Radix Panacis Quinquefolii and its preparati<strong>on</strong>s may lower blood sugar<br />

levels. Interacti<strong>on</strong>s with antidiabetic d<strong>ru</strong>gs are possible, but this subject<br />

has not been sufficiently investigated.<br />

Carcinogenesis, mutagenesis, impairment of fertility<br />

At c<strong>on</strong>centrati<strong>on</strong>s up to 36.0 mg/ml, neither an aqueous nor a butanol<br />

extract of the c<strong>ru</strong>de d<strong>ru</strong>g was mutagenic in the Salm<strong>on</strong>ella microsome assay<br />

using S. typhimurium strain TM677 in the presence or absence of a<br />

metabolic activating mix S9 (47).<br />

Pregnancy: n<strong>on</strong>-teratogenic effects<br />

Due to a lack of safety data, use of the c<strong>ru</strong>de d<strong>ru</strong>g during pregnancy is not<br />

recommended.<br />

239

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