2006
DOI: 10.1159/000497588
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Medicinal plants with potential antidiabetic activity - A review of ten years of herbal medicine research (1990-2000)

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Cited by 268 publications
(156 citation statements)
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“…19 In the present study, the dysregulation of glucose metabolism observed in STZ-diabetic rats was overcome following treatment with either the PRF-Th or glibenclamide, which is an oral sulfonylurea antidiabetic preparation widely used as a reference drug in tests of antidiabetic activity. 20 Moreover, in the present study, PRF-Th significantly decreased systolic arterial pressure similar to the effects observed for captopril. Captopril is an angiotensin-converting enzyme inhibitor that blocks the conversion of the prohormone angiotensin I to the active hormone angiotensin II.…”
Section: Discussionsupporting
confidence: 87%
“…19 In the present study, the dysregulation of glucose metabolism observed in STZ-diabetic rats was overcome following treatment with either the PRF-Th or glibenclamide, which is an oral sulfonylurea antidiabetic preparation widely used as a reference drug in tests of antidiabetic activity. 20 Moreover, in the present study, PRF-Th significantly decreased systolic arterial pressure similar to the effects observed for captopril. Captopril is an angiotensin-converting enzyme inhibitor that blocks the conversion of the prohormone angiotensin I to the active hormone angiotensin II.…”
Section: Discussionsupporting
confidence: 87%
“…Sitosterol-d-glucoside present in the bark of Ficus religiosa is believed to elicit hypoglycemic activity in rabbits [14]. The bioactive components present in Ficus are leucocyandin 3-O-beta-d-galactosyl cellobioside, leucopelargonidin-3-O-alpha-L rhamnoside [15, 16]. The phytoconstituents present in Ficus can impart a significant antidiabetic effect.…”
Section: Indian Medicinal Plants With Antidiabetic Potentialmentioning
confidence: 99%
“…For long time, plants were used in treatment of many diseases especially in the East region countries [13]. In addition, Lycium barbarum protects mice liver from carbon tetrachloride-induced oxidative stress and necroinflammation by reducing the hepatic necrosis and the serum alanine aminotransferase (ALT) level induced by CCl4 intoxication, inhibiting cytochrome P450 2E1 expression, and restoring the expression levels of antioxidant enzymes and decreasing the level of nitric oxide metabolism and lipid peroxidation induced by CCl4 [14].…”
Section: Introductionmentioning
confidence: 99%