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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 />

In cultured hippocampal neur<strong>on</strong>s from ne<strong>on</strong>atal mice, hydrogen peroxide-induced<br />

neur<strong>on</strong>al damage was significantly reduced after treatment<br />

of the cells with 80 g/ml of the c<strong>ru</strong>de d<strong>ru</strong>g (27). A methanol extract of<br />

the c<strong>ru</strong>de d<strong>ru</strong>g protected against N-methyl-D-aspartate-induced excitotoxicity<br />

in cultured rat hippocampus slices at a c<strong>on</strong>centrati<strong>on</strong> of 100 g/<br />

ml (28).<br />

Antihypertensive activity<br />

An alkaloid-c<strong>on</strong>taining extract of the c<strong>ru</strong>de d<strong>ru</strong>g reduced blood pressure<br />

in rats when administered by gavage at a dose of 50.0 mg/kg bw for<br />

20 days, or when administered by intravenous injecti<strong>on</strong> to cats at a dose<br />

of 20.0 mg/kg bw for 20 days (29). A 50% methanol extract of the c<strong>ru</strong>de<br />

d<strong>ru</strong>g inhibited the activity of angiotensin-c<strong>on</strong>verting enzyme isolated<br />

from pig kidney at a c<strong>on</strong>centrati<strong>on</strong> of 200.0 μg/ml in vitro (30).<br />

An infusi<strong>on</strong> of the c<strong>ru</strong>de d<strong>ru</strong>g inhibited norepinephrine-induced c<strong>on</strong>tracti<strong>on</strong>s<br />

of isolated rat aorta at a c<strong>on</strong>centrati<strong>on</strong> of 0.12 mg/ml (31). Endothelium-dependent<br />

relaxati<strong>on</strong> induced by the extract of the c<strong>ru</strong>de d<strong>ru</strong>g<br />

was inhibited by N-m<strong>on</strong>omethyl-L-arginine, but not indometacin or atropine,<br />

and was decreased when the endothelium was not present. The authors<br />

c<strong>on</strong>cluded that the extract relaxes the prec<strong>on</strong>tracted rat aorta through<br />

an endothelium-dependent mechanism involving nitric oxide (31).<br />

Anti-inflammatory activity<br />

A decocti<strong>on</strong> of the c<strong>ru</strong>de d<strong>ru</strong>g suppressed carrageenan-induced footpad<br />

oedema in rats when administered by subcutaneous injecti<strong>on</strong> at a dose of<br />

10.0 ml/kg bw (32). An infusi<strong>on</strong> of the c<strong>ru</strong>de d<strong>ru</strong>g inhibited the activity of<br />

prostaglandin synthetase in rabbit microsomes at a c<strong>on</strong>centrati<strong>on</strong> of<br />

750.0 μg/ml (33).<br />

Antimicrobial activity<br />

An ethanol extract of the c<strong>ru</strong>de d<strong>ru</strong>g was not active against Bacillus subtilis,<br />

Candida albicans, Escherichia coli or Streptococcus pneum<strong>on</strong>iae in<br />

vitro at c<strong>on</strong>centrati<strong>on</strong>s up to 500.0 mg/disc (34).<br />

Antioxidant activity<br />

Intraperit<strong>on</strong>eal administrati<strong>on</strong> of an ethanol extract of the c<strong>ru</strong>de d<strong>ru</strong>g at a<br />

dose of 1.0 g/kg bw to rats inhibited an increase in lipid peroxidati<strong>on</strong> in<br />

the ipsilateral cortex induced by the injecti<strong>on</strong> of ferric chloride into the<br />

lateral cortex (35). The extract also induced an increase in the activity of<br />

superoxide dismutase in the mitoch<strong>on</strong>drial fracti<strong>on</strong> of the ipsilateral cortex<br />

(35). A methanol extract of the c<strong>ru</strong>de d<strong>ru</strong>g inhibited kainic acidinduced<br />

lipid peroxidati<strong>on</strong> in rat brain tissues in vitro (21). An aqueous<br />

extract of the c<strong>ru</strong>de d<strong>ru</strong>g, at a c<strong>on</strong>centrati<strong>on</strong> of 50.0 μg/ml, had str<strong>on</strong>g<br />

358

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