WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru WHO monographs on selected medicinal plants - travolekar.ru
Fructus Momordicae number of beta cells in treated animals, as compared with untreated diabetic rats, but their number was still significantly smaller than that obtained for normal rats. There was also a significant (p < 0.006) increase in the number of delta cells in rats with streptozotocin-induced diabetes compared to non-diabetic rats, but the number of alpha cells did not change. These data indicate that oral administration of the crude drug may renew the beta cells in rats with streptozotocin-induced diabetes or alternatively may permit the recovery of partially destroyed beta cells (41). The effect of the fruit juice on rats fed a hyperinsulinaemic high-fat diet was investigated. In a dose–response study (0.375, 0.75 and 1.5% freeze-dried juice administered in rations), oral glucose tolerance was improved in rats fed a high fat (30%) diet supplemented with freeze-dried juice at a dose of 0.75% or higher (p < 0.05). At the highest dose, treated rats had lower energy efficiency (p < 0.05) and tended to have a lower visceral fat mass (p = 0.10). In a subsequent experiment, rats habitually fed a high fat diet either continued to consume the diet or were switched to a high fat + fruit juice, low fat (7%), or low fat + fruit juice (0.75%) diet for 7 weeks. Rats which had been switched to the high fat + fruit juice diet gained less weight and had less visceral fat than those fed the high fat diet (p < 0.05). Supplementation of the high fat diet with the crude drug improved insulin resistance, lowered serum insulin and leptin, but raised free fatty acid concentration in the serum (p < 0.05) (42). Antihypercholesterolaemic activity A long-term (10-week) feeding experiment measured the effect of a fruit extract (10 ml 100% fruit juice/kg bw) on blood plasma and tissue lipid profiles in normal rats and rats with streptozotocin-induced type 1 diabetes. The results showed a significant (p < 0.05) increase in plasma nonesterified cholesterol, triglycerides and phospholipids in rats with streptozotocin-induced diabetes, accompanied by a decrease in high-density lipoprotein-cholesterol. A moderate increase in the plasma lipid peroxidase product, malondialdehyde, and about a twofold increase in kidney plasma lipid peroxidase was also observed. The treatment of diabetic rats with the fruit extract over a 10-week period returned these levels to normal. In addition, the extract exhibited an inhibitory effect on membrane plasma lipid peroxidase under in vitro conditions (43). The effects of a freeze-dried powder of the fruit on serum glucose levels and lipid parameters of the serum and liver were studied in rats fed diets supplemented with cholesterol and without cholesterol. For 14 days, rats were fed the diets either containing the freeze-dried powder at 0.5, 1 or 3% without added dietary cholesterol (experiment 1) or containing 1% powder with or without 0.5% cholesterol and 0.15% bile acid (ex- 199
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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 />
gated in KK-Ay mice. The extract in combinati<strong>on</strong> with exercise reduced<br />
the blood glucose c<strong>on</strong>centrati<strong>on</strong> of KK-Ay mice 5 weeks after oral administrati<strong>on</strong><br />
daily for 5 weeks (p < 0.001), and also significantly lowered<br />
the plasma insulin of KK-Ay mice under similar c<strong>on</strong>diti<strong>on</strong>s (p < 0.01).<br />
The blood glucose c<strong>on</strong>centrati<strong>on</strong> following treatment with the extract<br />
plus exercise was lower than that following treatment with the extract<br />
<strong>on</strong>ly or exercise <strong>on</strong>ly, 5 weeks after the administrati<strong>on</strong>. Administrati<strong>on</strong> of<br />
the extract combined with exercise decreased blood glucose in a glucose<br />
tolerance test (38).<br />
Effect <strong>on</strong> insulin resistance<br />
In a study in rats, the effect of the c<strong>ru</strong>de d<strong>ru</strong>g <strong>on</strong> insulin resistance, a<br />
major c<strong>on</strong>tributor to the development of hyperglycaemia, was assessed<br />
in vivo. The effects of different doses (100.0, 200.0 and 400.0 mg per day)<br />
of alcohol extracts or aqueous extracts of the f<strong>ru</strong>its (1 kg of f<strong>ru</strong>it to 500 ml<br />
ethanol) <strong>on</strong> the metabolic parameters (body weight and se<strong>ru</strong>m glucose<br />
insulin and triglyceride levels) of rats fed f<strong>ru</strong>ctose were studied. Feeding<br />
f<strong>ru</strong>ctose for 15 days increased se<strong>ru</strong>m glucose and insulin levels markedly<br />
and triglyceride levels marginally when compared with the c<strong>on</strong>trols<br />
(75.46 versus 55.59 mg/dl, 6.26 versus 15.04 mg/dl and 50.93 versus<br />
41.1 mg/dl, respectively). Treatment with 400.0 mg/day of aqueous<br />
extract (1 kg in 500 ml water) for 15 days substantially reduced hyperglycaemia<br />
and hyperinsulinaemia induced by a diet high in f<strong>ru</strong>ctose (39).<br />
The antidiabetic activity of an aqueous extract of the f<strong>ru</strong>it was investigated<br />
in KK-Ay mice, an animal model having type 2 diabetes with<br />
hyperinsulinaemia. Intragastric administrati<strong>on</strong> of an aqueous extract of<br />
the f<strong>ru</strong>it reduced the blood glucose of KK-Ay mice after 3 weeks of intragastric<br />
administrati<strong>on</strong> (p < 0.01) and also significantly lowered the se<strong>ru</strong>m<br />
insulin (p < 0.01). However, the extract did not affect the blood glucose<br />
in normal mice. Blood glucose in treated KK-Ay mice was<br />
significantly decreased in an insulin tolerance test (p < 0.01) (37).<br />
The activity of the f<strong>ru</strong>it juice was assessed in vitro <strong>on</strong> streptozotocintreated<br />
RIN cells and isolated islet cells, and in vivo in mice. It was found<br />
that feeding juice caused a reducti<strong>on</strong> in streptozotocin-induced hyperglycaemia<br />
in mice. The juice reduced the streptozotocin-induced lipid peroxidati<strong>on</strong><br />
in pancreas of mice, RIN cells and islets. It also reduced the<br />
streptozotocin-induced apoptosis in RIN cells indicating the mode of<br />
protecti<strong>on</strong> of the juice <strong>on</strong> RIN cells, islet cells and pancreatic beta-cells<br />
(40). The activity of the f<strong>ru</strong>it juice <strong>on</strong> the distributi<strong>on</strong> and number of alpha,<br />
beta and delta cells in the pancreas of rats with streptozotocin-induced<br />
diabetes was determined using immunohistochemical methods. The<br />
results suggested that there was a significant (p < 0.004) increase in the<br />
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