KMID : 0043320170400010037
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Archives of Pharmacal Research 2017 Volume.40 No. 1 p.37 ~ p.48
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Prunin is a highly potent flavonoid from Prunus davidiana stems that inhibits protein tyrosine phosphatase 1B and stimulates glucose uptake in insulin-resistant HepG2 cells
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Jung Hyun-Ah
Ali Md. Yousof Bhakta Himanshu Kumar Min Byung-Sun Choi Jae-Sue
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Abstract
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Prunin is the main flavonoid in Prunus davidiana stems and improves hyperglycemia and hyperlipidemia in streptozotocin-induced diabetic rats. The aim of this study was to investigate the in vitro anti-diabetic potential of prunin via the inhibition of protein tyrosine phosphatase 1B (PTP1B), ¥á-glucosidase, peroxynitrite (ONOO?)-mediated tyrosine nitration, and stimulation of glucose uptake in insulin-resistant hepatocytes. In addition, a molecular docking simulation was performed to predict specific prunin binding modes during PTP1B inhibition. Prunin showed strong inhibitory activity against PTP1B, with an IC50 value of 5.5 ¡¾ 0.29 ¥ìM, and significant inhibitory activity against ¥á-glucosidase, with an IC50 value of 317 ¡¾ 2.12 ¥ìM. Moreover, a kinetics study revealed that prunin inhibited PTP1B (Ki = 8.66) and ¥á-glucosidase (Ki = 189.56) with characteristics typical of competitive and mixed type inhibitors, respectively. Docking simulations showed that prunin selectively inhibited PTP1B by targeting its active site and exhibited good binding affinity, with a docking score of ?9 kcal/mol. Furthermore, prunin exhibited dose-dependent inhibitory activity against ONOO?-mediated tyrosine nitration and stimulated glucose uptake by decreasing PTP1B expression level in insulin-resistant HepG2 cells. These results indicate that prunin has significant potential as a selective PTP1B inhibitor and may possess anti-diabetic properties by improving insulin resistance.
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KEYWORD
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Prunin, Protein tyrosine phosphatase 1B, Anti-diabetic, Glucose uptake, HepG2 cell, Molecular docking
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