Key result
Phanoside, a novel saponin isolated from Gynostemma pentaphyllum, stimulated insulin release in isolated rat pancreatic islets and improved glucose tolerance in rats.
Why the study?
Does phanoside stimulate insulin release in isolated rat pancreatic islets and improve glucose tolerance in rats?
Does phanoside stimulate insulin release in isolated rat pancreatic islets and improve glucose tolerance in rats?
Phanoside, a novel saponin isolated from Gynostemma pentaphyllum, stimulates insulin release in vitro and improves glucose tolerance in vivo, suggesting potential as a hypoglycemic agent.
Hypothesis-generating for phanoside in diabetes; human studies needed before clinical consideration.
Extracts from Gynostemma pentaphyllum Makino (Cucurbitaceae), a Southeast Asian herb, has been reported to affect numerous activities resulting in antitumor, cholesterol-lowering, immunopotentiating, antioxidant, and hypoglycemic effects. We have isolated one active compound by ethanol extraction, distribution in n-butyl alcohol/water, solid phase extraction/separation, and several rounds of reverse phase high pressure liquid chromatography. We have shown by NMR and mass spectrometry that this active compound is a novel saponin, a gypenoside, which we have named phanoside (21-,23-epoxy-,3beta-,20-,21-trihydroxydammar-24-ene-3-O-([alpha-d-rhamnopyranosyl(1-->2)]-[beta-d-glycopyranosyl(1-->3)]-beta-d-lyxopyranoside)), with a molecular mass of 914.5 Da. Phanoside is a dammarane-type saponin, and four stereoisomers differing in configurations at positions 21 and 23 were identified, each of which were found to stimulate insulin release from isolated rat pancreatic islets. We have also found that the stereoisomers are interconvertible. Dose-dependent insulin-releasing activities at 3.3 and 16.7 mM glucose levels were determined for the racemic mixture containing all four stereoisomers. Phanoside at 500 microM stimulates insulin release in vitro 10-fold at 3.3 mM glucose and potentiates the release almost 4-fold at 16.7 mM glucose. At these glucose levels, 2 microm glibenclamide stimulates insulin release only 2-fold. Interestingly, beta-cell sensitivity to phanoside is higher at 16.7 mM than at 3.3 mM glucose, although insulin responses were significantly increased by phanoside below 125 microM only at high glucose levels. Also when given orally to rats, phanoside (40 and 80 mg/ml) improved glucose tolerance and enhanced plasma insulin levels at hyperglycemia.
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Norberg et al. (2004) studied hyperglycemia. Phanoside vs. glibenclamide was evaluated on insulin release. Phanoside, a novel saponin isolated from Gynostemma pentaphyllum, stimulated insulin release in isolated rat pancreatic islets and improved glucose tolerance in rats.
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