WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru
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 />
Precauti<strong>on</strong>s<br />
General<br />
Use with cauti<strong>on</strong> in patients with high blood pressure, diabetes, glaucoma<br />
or a history of cardiovascular disease.<br />
D<strong>ru</strong>g interacti<strong>on</strong>s<br />
Berberine is reported to upregulate the expressi<strong>on</strong> of the human multid<strong>ru</strong>g<br />
resistance gene coding for multid<strong>ru</strong>g resistance transporter (PGP-<br />
170); thus the treatment of tumours with berberine may result in reduced<br />
retenti<strong>on</strong> of chemotherapeutic agents such as paclitaxel (71, 72). Berberine<br />
has been reported to interact with cyclosporin in renal transplant patients<br />
(73). Blood c<strong>on</strong>centrati<strong>on</strong>s of cyclosporin were enhanced by 75% after<br />
co-administrati<strong>on</strong> of berberine hydrochloride in renal transplant patients,<br />
but this did not increase the toxicity of cyclosporin (73).<br />
D<strong>ru</strong>g and laboratory test interacti<strong>on</strong>s<br />
N<strong>on</strong>e reported.<br />
Carcinogenesis, mutagenesis, impairment of fertility<br />
The genotoxic effects of berberine in prokaryotic cells were assessed in<br />
the SOS chromotest in Saccharomyces cerevisiae (74). No genotoxic activity<br />
with or without metabolic activati<strong>on</strong> was observed, and no cytotoxic<br />
or mutagenic effects were seen under n<strong>on</strong>growth c<strong>on</strong>diti<strong>on</strong>s. However, in<br />
dividing cells, the alkaloid induced cytotoxic and cytostatic effects in proficient<br />
and repair-deficient Saccharomyces cerevisiae. In dividing cells, the<br />
inducti<strong>on</strong> of frameshift and mitoch<strong>on</strong>drial mutati<strong>on</strong>s, as well as crossing<br />
over, showed that the compound is not a potent mutagen (74).<br />
Pregnancy: teratogenic effects<br />
No informati<strong>on</strong> was found.<br />
Pregnancy: n<strong>on</strong>-teratogenic effects<br />
Due to a lack of safety data, the use of the c<strong>ru</strong>de d<strong>ru</strong>g during pregnancy is<br />
not recommended.<br />
Nursing mothers<br />
Due to a lack of safety data, the use of the c<strong>ru</strong>de d<strong>ru</strong>g during breastfeeding<br />
is not recommended.<br />
Paediatric use<br />
Due to a lack of safety data, the use of the c<strong>ru</strong>de d<strong>ru</strong>g in children under<br />
the age of 12 years is not recommended.<br />
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