WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru WHO monographs on selected medicinal plants - travolekar.ru
Radix Panacis Quinquefolii water as a placebo in a similar fashion. A two-phase formalin test was performed in both groups. Although there was no difference between groups in the first phase, mice treated with the extract spent significantly less time in licking and biting of the injured paws in the second phase, indicating analgesic effects (39). The pseudoginsenoside-F11, an ocotillol-type saponin isolated from the roots has been shown to have antagonistic actions on morphine-induced behavioural changes in mice. Pseudoginsenoside-F11 antagonizes morphine-induced intracellular production of cyclic adenosine monophosphate (cAMP) and antagonizes morphine-induced decreases in dopamine levels in the limbic area of rat. The antagonistic effects of pseudoginsenoside-F11 on methamphetamine-induced behavioural and neurochemical toxicities were studied in mice. Methamphetamine was administered intraperitoneally at a dose of 10.0 mg/kg bw four times at 2-hourly intervals, and pseudoginsenoside-F11 was orally administered at doses of 4.0 and 8.0 mg/kg bw twice at 4-hourly intervals, 60 min prior to methamphetamine administration. The results showed that pseudoginsenoside-F11 ameliorated the anxiety-like behaviour induced by methamphetamine in the light–dark box task, but the change was not statistically significant. In the forced swimming task, pseudoginsenoside-F11 also shortened the prolonged immobility time induced by methamphetamine. In the appetitive-motivated T-maze task, pseudoginsenoside-F11 greatly shortened methamphetamine-induced prolonged latency and decreased the error counts. Similar results were also observed in the Morris water maze task, where administration of pseudoginsenoside-F11 shortened the escape latency prolonged by methamphetamine. There were significant decreases in the contents of dopamine, 3,4-dihydroxyphenacetic acid, homovanillic acid and 5-hydroxyindoacetic acid in the brain of methamphetamine-treated mice (40). Memory effects The effect of an alcohol extract of the roots on memory was assessed in the scopolamine-induced memory and performance deficits in a spatial learning task. Long-term oral administration of the extract protected against scopolamine-induced amnesia and increased choline uptake in synaptosomal preparations. Treatment with the extract did not alter brain concentrations of norepinephrine, dopamine, 5-HT (serotonin), 3,4-hydroxyphenylacetic acid or 5-hydroxyindoleacetic acid. The extract weakly inhibited the activity of monoamine oxidase in vitro (41). Ginsenoside Rb1, a saponin of the crude drug was found to exert beneficial effects on memory and learning, putatively through its actions on the cholinergic system. In situ hybridization studies show that ginsenoside Rb1 increases 235
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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 />
trast, a methanol extract c<strong>on</strong>taining ginsenosides (but no polysaccharides),<br />
and pure ginsenoside-Rb1 were not active. Significant TNF- stimulating<br />
activity was found in the extractable polysaccharide fracti<strong>on</strong> (24).<br />
The effect of an aqueous extract of the powdered root, c<strong>on</strong>taining<br />
mainly oligosaccharides and polysaccharides was assessed for immune<br />
stimulatory activity in murine spleen cells and perit<strong>on</strong>eal macrophages.<br />
The extract (5.0–500.0 μg/ml) stimulated the proliferati<strong>on</strong> of normal<br />
mouse spleen cells, primarily B lymphocytes. The extract activated perit<strong>on</strong>eal<br />
exudate macrophages leading to enhanced producti<strong>on</strong> of interleukin-1,<br />
interleukin-6, TNF- and nitric oxide (35).<br />
Neurological effects<br />
The neuroprotective effects of a hot aqueous extract of the root (no further<br />
descripti<strong>on</strong> available) <strong>on</strong> sodium channels were assessed, as neur<strong>on</strong>al<br />
damage during ischaemic episodes has been associated with abnormal sodium<br />
fluxes. An aqueous extract of the root was evaluated in tsA201 cells<br />
transfected with cDNA expressing alpha subunits of the brain (2a) sodium<br />
channel using the whole-cell patch clamp technique. The extract<br />
(3.0 mg/ml) t<strong>on</strong>ically and reversibly blocked the sodium channel in a c<strong>on</strong>centrati<strong>on</strong>-<br />
and voltage-dependent manner. It shifted the voltage-dependence<br />
of inactivati<strong>on</strong> by 14 mV (3.0 mg/ml) in the hyperpolarizing directi<strong>on</strong><br />
and delayed recovery from inactivati<strong>on</strong>, whereas activati<strong>on</strong> of the<br />
channel was unaffected. Ginsenoside Rb1, a major c<strong>on</strong>stituent of the extract,<br />
produced similar effects at a c<strong>on</strong>centrati<strong>on</strong> of 150 μM (36).<br />
Brainstem neur<strong>on</strong>s receiving subdiaphragmatic vagal inputs were recorded<br />
in an in vitro ne<strong>on</strong>atal rat brainstem–gastric preparati<strong>on</strong>. Aqueous<br />
extracts of the root were added to the gastric compartment or to the brainstem<br />
compartment of the bath chamber to evaluate the peripheral gut and<br />
central brain effects of the extracts <strong>on</strong> brainstem unitary activity. After<br />
additi<strong>on</strong> of the extract (30.0 μg/ml) to the gastric or brainstem compartment,<br />
a c<strong>on</strong>centrati<strong>on</strong>-related inhibiti<strong>on</strong> of neur<strong>on</strong>al discharge frequency<br />
in the brainstem unitary activity (38.2%, p < 0.01) was observed, suggesting<br />
that extract may play an important role in regulating the digestive<br />
process and modulating brain functi<strong>on</strong> (37). In a subsequent study, the<br />
pharmacological effects of P. quinquefolius cultivated in Wisc<strong>on</strong>sin and of<br />
P. quinquefolius cultivated in Illinois were compared. The results showed<br />
that P. quinquefolius cultivated in Illinois had both a str<strong>on</strong>ger peripheral<br />
gastric and a str<strong>on</strong>ger central brain modulating effect <strong>on</strong> brainstem neur<strong>on</strong>al<br />
activity. The data indicated that this discrepancy was due to a different<br />
ginsenoside profile (38).<br />
In a formalin-induced nocicepti<strong>on</strong> test, mice were force-fed an aqueous<br />
extract of the roots for 4 days. Another group of mice were fed with<br />
234