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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Cortex Phellodendr<strong>on</strong><br />
flammatory cytokine, interleukin-8, in rectal mucosal cells in vitro at a<br />
c<strong>on</strong>centrati<strong>on</strong> of 10 −5 M (41). Treatment of a human oesophageal squamous<br />
cell carcinoma cell line (YES-2) with berberine (8.0–32.0 μM) for 24 hours<br />
reduced the expressi<strong>on</strong> of messenger rib<strong>on</strong>ucleic acid for the inflammatory<br />
cytokine, interleukin-6 (42).<br />
Antimicrobial and antitrypanosomal activities<br />
A hot aqueous extract of the c<strong>ru</strong>de d<strong>ru</strong>g inhibited the growth of Escherichia<br />
coli and Staphylococcus aureus (43); Streptococcus mutans (44); Candida<br />
albicans, C. glabrata and C. tropicalis (45). Berberine inhibited the<br />
growth of Helicobacter pylori in vitro. The median inhibitory c<strong>on</strong>centrati<strong>on</strong><br />
ranged from 0.625–40.00 μg/ml (46, 47). Berberine also inhibited the<br />
growth of Staphylococcus aureus and Mycobacterium smegmatis, with a<br />
minimum inhibitory c<strong>on</strong>centrati<strong>on</strong> of 25.0–50.0 μg/ml (48, 49). Berberine<br />
inhibited the growth of Bacillus subtilis and Salm<strong>on</strong>ella enteritidis in vitro<br />
at a c<strong>on</strong>centrati<strong>on</strong> of 1.0 mg/ml and 0.5 mg/ml, respectively (50). Berberine<br />
also inhibited the growth of Clostridium perfringens in vitro<br />
(150.0 μg/ml), and at a c<strong>on</strong>centrati<strong>on</strong> of 1.0 mg/ml significantly inhibited<br />
the growth of Entamoeba histolytica, Giardia lamblia and Trichom<strong>on</strong>as<br />
vaginalis and induced morphological changes in the parasites (p < 0.001)<br />
(51). At a c<strong>on</strong>centrati<strong>on</strong> of 250.0 μg/ml, a methanol extract of the c<strong>ru</strong>de<br />
d<strong>ru</strong>g inhibited the growth of Trypanosoma c<strong>ru</strong>zi in vitro (52).<br />
Antiulcer activity<br />
Intragastric administrati<strong>on</strong> of a berberine-free fracti<strong>on</strong> of a bark extract<br />
(at a dose of 1.0 g/kg bw) reduced ulcer formati<strong>on</strong> in rodents (15). The<br />
fracti<strong>on</strong> significantly inhibited the formati<strong>on</strong> of ulcers induced by ethanol<br />
or aspirin, and of pylo<strong>ru</strong>s-ligated ulcer in rats, as well as that of stress ulcer<br />
in restrained and water-immersed mice (p < 0.05). In additi<strong>on</strong>, secreti<strong>on</strong><br />
of gastric acid in pylo<strong>ru</strong>s-ligated rats was significantly reduced by the<br />
fracti<strong>on</strong> when administered subcutaneously or intraduodenally, but not<br />
when it was administered orally (15).<br />
Subcutaneous administrati<strong>on</strong> of the same berberine-free fracti<strong>on</strong> to<br />
rats at a dose of 20.0 mg/kg bw prevented ethanol-induced ulcers and<br />
those induced by pylo<strong>ru</strong>s-ligati<strong>on</strong> (15). In rats, a hot aqueous extract of<br />
the c<strong>ru</strong>de d<strong>ru</strong>g (dose 100.0 mg/kg bw) inhibited gastric secreti<strong>on</strong> induced<br />
by administrati<strong>on</strong> of pentagastrin (53).<br />
Effects <strong>on</strong> smooth muscle<br />
Berberine, at a c<strong>on</strong>centrati<strong>on</strong> of 1.0 μM, induced relaxati<strong>on</strong> of norepinephrine-prec<strong>on</strong>tracted<br />
isolated rat aorta (54). At a c<strong>on</strong>centrati<strong>on</strong> of 10 −5 M,<br />
berberine induced relaxati<strong>on</strong> in isolated prec<strong>on</strong>tracted rat mesenteric ar-<br />
249