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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 />

Uses described in pharmacopoeias and well established documents<br />

Orally for the treatment of atherosclerosis and kidney dysfuncti<strong>on</strong>s (diuretic)<br />

(5).<br />

One study has indicated that the c<strong>ru</strong>de d<strong>ru</strong>g may be of benefit for the<br />

treatment of irritable bowel syndrome (28), but further randomized c<strong>on</strong>trolled<br />

clinical trials are needed before any therapeutic recommendati<strong>on</strong>s<br />

can be made.<br />

Uses described in traditi<strong>on</strong>al medicine<br />

Oral treatment of anaemia, diabetes, fever, gout, rheumatism and urinary<br />

st<strong>on</strong>es (7, 9, 29).<br />

Pharmacology<br />

Experimental pharmacology<br />

Antiatherosclerotic and antihypercholesterolaemic activities<br />

A dried aqueous extract of the leaves (4.5:1) inhibited cholesterol biosynthesis<br />

from 14 C-acetate in primary cultured rat hepatocytes in a c<strong>on</strong>centrati<strong>on</strong>-dependent<br />

biphasic manner with moderate inhibiti<strong>on</strong> (approximately<br />

20%) being noted between 0.007 and 0.1 mg/ml and str<strong>on</strong>ger inhibiti<strong>on</strong> at<br />

1 mg/ml (80%). Replacement of 14 C-acetate by 14 C-meval<strong>on</strong>ate largely<br />

prevented the inhibitory effects of the extracts, indicating inhibiti<strong>on</strong> of the<br />

activity of hydroxyl-methyl-glutaryl-CoA-reductase. Stimulati<strong>on</strong> of hydroxyl-methyl-glutaryl-CoA-reductase<br />

activity by insulin was efficiently<br />

blocked by the extract. Cynaroside and its aglyc<strong>on</strong>e luteolin, c<strong>on</strong>stituents<br />

of the extract, were mainly resp<strong>on</strong>sible for enzyme inhibiti<strong>on</strong> (30). The<br />

effect of an extract of the leaves in vivo was investigated in four groups of<br />

10 rats each fed an atherosclerogenic diet. Group <strong>on</strong>e was administered<br />

110 mg/kg body weight (bw) powdered leaves; group two, 80.0 mg/kg bw<br />

powdered Cynara cardunculus; group three, 10.0 mg/kg bw heparaxal;<br />

and group four served as the c<strong>on</strong>trol. Examinati<strong>on</strong> of tissue after 120 days<br />

showed that the leaf extract prevented formati<strong>on</strong> of atherosclerotic changes,<br />

prevented se<strong>ru</strong>m cholesterol increase, caused a decrease in lipid phosphate,<br />

slightly increased the level of glycoproteins in the blood, prevented<br />

an increase in se<strong>ru</strong>m -globulin, decreased albumin, glycoproteins and<br />

liver cholesterol, and increased -globulin and -globulin fracti<strong>on</strong>s. Cynara<br />

cardunculus showed a similar but weaker activity (31). A methanol<br />

extract of the leaves was shown to reduce se<strong>ru</strong>m triglyceride levels in olive<br />

oil-loaded mice. Oral administrati<strong>on</strong> of the extract, at doses between 125<br />

and 500.0 mg/kg bw, significantly suppressed se<strong>ru</strong>m triglyceride elevati<strong>on</strong><br />

2 h after administrati<strong>on</strong> of olive oil. In c<strong>on</strong>trast, 6 h after administrati<strong>on</strong> of<br />

olive oil, increases in triglyceride level were observed in the groups that<br />

96

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