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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Rhizoma Picrorhizae<br />
transaminases, sorbitol dehydrogenase, glutamate dehydrogenase, lactate<br />
dehydrogenase, acid phosphatase, alkaline phosphatase and bili<strong>ru</strong>bin in<br />
the se<strong>ru</strong>m of aflatoxin B1-treated rats (31).<br />
The mechanism of acti<strong>on</strong> of an iridoid glycoside extract of the rhizome<br />
<strong>on</strong> hepatocellular injury and redox status was investigated in a haemorrhage-resuscitati<strong>on</strong><br />
injury in adult rats (32). Anaesthetized rats were subjected<br />
to haemorrhagic shock by bleeding 30 ml/kg bw. After 60 minutes<br />
of shock, rats were resuscitated with twice the shed blood volume of lactated<br />
Ringer’s soluti<strong>on</strong> and were killed 2 hours after resuscitati<strong>on</strong>. Pretreatment<br />
with the extract (12 mg/kg bw), given orally for 7 days, resulted<br />
in a significant decrease in se<strong>ru</strong>m aspartate transaminase and -glutamyl<br />
transpeptidase levels. The extract also inhibited the lipid peroxidati<strong>on</strong> and<br />
nitric oxide release that occurred after haemorrhage-resuscitati<strong>on</strong> and altered<br />
the activity of glutathi<strong>on</strong>e reductase in a favourable manner. The<br />
extract down-regulated the stress-sensitive transcripti<strong>on</strong> factor activator<br />
protein 1 and decreased the level of c-fos mRNA as well as c-jun and c-fos<br />
proteins in liver tissue, indicating that its acti<strong>on</strong>s could be mediated<br />
through AP1 and associated signal transducti<strong>on</strong> pathways (32).<br />
Anti-inflammatory activity<br />
Intragastric administrati<strong>on</strong> of a 95% ethanol extract of the rhizome to<br />
rats, at a dose of 100.0 mg/kg bw for 3 days, reduced carrageenan-induced<br />
pedal oedema (32, 33). Co-administrati<strong>on</strong> of the anti-inflammatory antag<strong>on</strong>ists,<br />
propranolol or timolol with the 95% ethanol extract of the rhizome<br />
reduced its effects.<br />
Choleretic activity<br />
Intragastric administrati<strong>on</strong> of a glycoside mixture (picroside-1 and kutkoside<br />
1:1.5, isolated from the rhizome) to guinea-pigs, at a dose of<br />
1.5 mg/kg bw, reduced paracetamol-induced cholestasis by 59.2%; at<br />
3 mg/kg bw, treatment reduced ethynylestradiol-induced cholestasis by<br />
77%. At a dose of 6.0 mg/kg bw the same mixture increased bile flow by<br />
120% (34). Intragastric administrati<strong>on</strong> of an extract of the c<strong>ru</strong>de d<strong>ru</strong>g at a<br />
dose of 2.0 mg/kg bw increased bile secreti<strong>on</strong> (35). Intragastric administrati<strong>on</strong><br />
of an unspecified extract (no further details available) of the rhizome<br />
to guinea-pigs at a dose of 6.0 mg/kg bw for 7 days prior to thiacetamide<br />
administrati<strong>on</strong> prevented cholestasis and hepatotoxicity (37).<br />
Diuretic activity<br />
Intraperit<strong>on</strong>eal administrati<strong>on</strong> of an aqueous ethanol extract (1:1) of the rhizome<br />
to rats at a dose of 250.0 mg/kg bw increased the amount of urine produced<br />
over a 4-hour period, in animals preloaded with saline soluti<strong>on</strong> (38).<br />
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