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WHO monographs on selected medicinal plants - travolekar.ru

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Gummi Boswellii<br />

H 3 C CH 3<br />

H<br />

CH 3 CH 3<br />

CH 3<br />

R<br />

O<br />

H H CH 3<br />

H<br />

H 3 C CO 2 H<br />

H CH 3<br />

H<br />

H 3 C<br />

X<br />

CH 3 CH 3<br />

H CH 3<br />

R<br />

O<br />

H H CH 3<br />

H<br />

H 3 C CO 2 H<br />

-Boswellic acid<br />

R = H<br />

3-O-Acetyl--boswellic acid<br />

R = CO-CH 3<br />

-Boswellic acid<br />

R = H X = H 2<br />

3-O-Acetyl--boswellic acid<br />

R = CO-CH 3 X = H 2<br />

11-Oxo--boswellic acid<br />

R = H X = O<br />

3-O-Acetyl-11-oxo--boswellic acid<br />

R = CO-CH 3 X = O<br />

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

Treatment of abdominal pain, asthma, coughs, dysentery, fever, jaundice,<br />

kidney st<strong>on</strong>es, pimples, sores and stomach disorders (5). Also used as an<br />

antivenin and an emmenagogue (24, 25).<br />

Pharmacology<br />

Experimental pharmacology<br />

Analgesic activity<br />

Intragastric administrati<strong>on</strong> of the gum at doses ranging from 100.0–<br />

500.0 mg/kg body weight (bw) had no analgesic effects in dogs, rabbits or<br />

rats (26–28). However, administrati<strong>on</strong> of a n<strong>on</strong>-phenolic fracti<strong>on</strong> of the<br />

c<strong>ru</strong>de d<strong>ru</strong>g produced analgesia in 60% of rats treated with a dose of<br />

60.0 mg/kg bw. A dose of 150.0 mg/kg bw induced analgesia in 70% of<br />

rats (29). The degree of analgesia was comparable to a dose of 3–4.5 mg/<br />

kg bw of morphine. A dose of 150.0 mg/kg bw also caused a 70% reducti<strong>on</strong><br />

in sp<strong>on</strong>taneous motor activity that lasted for 2 hours (29).<br />

Anticomplementary activity<br />

Boswellic acids exhibited anticomplementary activity in vitro, as assessed<br />

by the reducti<strong>on</strong> of immune-induced haemolysis of antibody-coated<br />

sheep erythrocytes by pooled guinea-pig se<strong>ru</strong>m (30). The decrease in immune-induced<br />

haemolysis was due to inhibiti<strong>on</strong> of C3-c<strong>on</strong>vertase of the<br />

classical complement pathway. The threshold c<strong>on</strong>centrati<strong>on</strong> for inhibiting<br />

C3-c<strong>on</strong>vertase was found to be 100.0 μg/ml (30).<br />

51

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