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Effects of Syzygium aromaticum ‐derived oleanolic acid on glucose transport and glycogen synthesis in the rat small intestine (丁香衍生物齐墩果酸对大鼠小肠中的葡萄糖转运以及糖原合成的影响)
Author(s) -
KHATHI Andile,
MASOLA Bubuya,
MUSABAYANE Cephas T.
Publication year - 2013
Publication title -
journal of diabetes
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.949
H-Index - 43
eISSN - 1753-0407
pISSN - 1753-0393
DOI - 10.1111/j.1753-0407.2012.00230.x
Subject(s) - glycogen , medicine , endocrinology , phlorizin , maltase , glycogenesis , metformin , insulin , diabetes mellitus , carbohydrate metabolism , streptozotocin , small intestine , glucose transporter , postprandial , oleanolic acid , glycogen synthase , chemistry , biochemistry , enzyme , alternative medicine , pathology
Abstract Background:  In the present study, we investigated the effects of oleanolic acid (OA), which has hypoglycemic properties, on glucose transport and glycogen synthesis in the small intestine, an organ that secretes enzymes involved in carbohydrate metabolism. Methods:  The OA was isolated from Syzygium aromaticum ethyl acetate‐soluble fractions followed by recrystallization with ethanol. It was diluted to required concentrations in freshly prepared dimethyl sulfoxide (2 mL) and normal saline (19 mL) before being administered to rats (p.o.). Glycogen concentrations were determined in isolated small intestines from fasted and non‐fasted non‐diabetic and streptozotocin‐diabetic rats after 18 h treatment with 80 mg/kg, p.o., OA or standard hypoglycemic drugs (i.e. 100 μg/kg, s.c., insulin; 500 mg/kg, p.o., metformin). In a separate series of experiments, the effects of 30‐min incubation with graded concentrations of OA (0.82–6.56 mmol/L) on d ‐glucose were evaluated by monitoring changes in glucose concentrations inside and outside of intestinal sacs isolated from fasted, non‐diabetic rats and mounted in an organ bath containing Krebs–Henseleit bicarbonate buffer. Results:  All in vivo treatments increased the glycogen concentration in rat small intestine, although the effects of metformin treatment in non‐fasted diabetic rats failed to reach statistical significance. In vitro , both OA (1.64–6.56 mmol/L) and phlorizin (10 −5 –10 −3  mol/L) decreased glucose transport from the mucosa to the serosa. Conclusion:  The data suggest that OA may be a potential alternative drug treatment for postprandial hyperglycemia because of its inhibition of glucose uptake across the small intestine and its concomitant conversion of glucose to glycogen in the intestinal wall.

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