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NIS - libdoc.who.int - World Health Organization

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WHO monographs on medicinal plants commonly used in the Newly Independent States (<strong>NIS</strong>)<br />

ergy production (59). Other constituents of Radix Ginseng, such as vanillic<br />

and salicylic acid, have also been reported to have “antifatigue” activity<br />

in rats (68). Furthermore, the antioxidant activity of ginseng was<br />

associated with both the ginsenosides and the flavonoid constituents (31,<br />

69). The ginsenosides protected pulmonary vascular endothelium against<br />

free-radical-induced injury (69).<br />

Mice given ginseng extract or ginsenosides Rb 1<br />

and Rg 2<br />

orally during<br />

passive avoidance response tests showed an improvement in learning ability<br />

which was negatively influenced by stress (30), and rats showed improved<br />

retention of learned behaviour (70). Ginsenosides Rg 1<br />

and Rb 1<br />

are the active<br />

nootropic constituents of the drug (66), and improve memory and learning<br />

in normal as well as cognition-impaired animals. The mode of action involves<br />

an increase in the synthesis and release of acetylcholine, and a decrease<br />

of brain serotonin levels (66). In cerebral and coronary blood vessels,<br />

extracts of Radix Ginseng produced vasodilatation, which improved brain<br />

and coronary blood flow (71). The vasodilatory activity of the ginsenosides<br />

appears to be primarily due to relaxation of vascular smooth muscles. The<br />

ginsenosides block the constricting effects of norepinephrine in isolated<br />

aorta strips, and inhibit the uptake of 45 Ca 2+ in the membrane and sarcolemma<br />

of rabbit heart tissue. Inhibition of Ca 2+ uptake in the muscle membrane<br />

contributes to the mechanism of vasodilatation (71).<br />

A number of polypeptides and glycans isolated from Radix Ginseng,<br />

named GP and panaxans A–E, respectively, have demonstrated hypoglycaemic<br />

activity when given <strong>int</strong>raperitoneally to mice (72, 73). Two of the<br />

glycans, panaxans A and B, have been shown to stimulate hepatic glucose<br />

utilization by increasing the activity of glucose-6-phosphate 1-dehydrogenase,<br />

phosphorylase a, and phosphofructokinase (72). Panaxan A did<br />

not affect plasma insulin levels or insulin sensitivity, but panaxan B elevated<br />

the plasma insulin level by stimulating insulin secretion from pancreatic<br />

islets, and further enhanced insulin sensitivity by increasing insulin<br />

binding to receptors (72). The panaxans are not active after oral administration.<br />

Administration of GP (<strong>int</strong>ravenously or subcutaneously) to mice<br />

or rats decreased blood glucose and liver glycogen levels (73). Radix Ginseng<br />

also contains a number of other constituents with hypoglycaemic<br />

activity (72, 74). Adenosine, isolated from a water extract of Radix Ginseng,<br />

enhanced lipogenesis and cyclic AMP accumulation of adipocytes,<br />

and some of the ginsenosides inhibited ACTH-induced lipolysis, suppressed<br />

insulin-stimulated lipogenesis, and stimulated the release of insulin<br />

from cultured islets (72).<br />

Subcutaneous administration of a ginseng extract enhanced the mating<br />

behaviour of male rats (75). The drug further stimulated spermatogenesis<br />

148

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