Hesperetin stimulates cholecystokinin secretion in enteroendocrine STC-1 cells

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Abstract

Hesperetin (3',5,7-trihydroxy 4'-methoxyflavanone) and its glycoside hesperidin (hesperetin 7-rhamnoglucoside) in oranges have been reported to possess pharmacological effects related to anti-obesity. However, hesperetin and hesperidin have not been studied on suppressive effects on appetite. This study examined that hesperetin and hesperidin can stimulate the release of cholecystokinin (CCK), one of appetite-regulating hormones, from the enteroendocrine STC-1 cells, and then examined the mechanisms involved in the CCK release. Hesperetin significantly and dose-dependently stimulated CCK secretion with an EC50 of 0.050 mM and increased the intracellular Ca2+ concentrations ([Ca2+]i) compared to the untreated control. The stimulatory effect by hesperetin was mediated via the entry of extracellular Ca2+ and the activation of TRP channels including TRPA1. These results suggest that hesperetin can be a candidate biomolecule for the suppression of appetite and eventually for the therapeutics of obesity. © 2013 The Korean Society of Applied Pharmacology.

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Kim, H. Y., Park, M., Kim, K., Lee, Y. M., & Rhyu, M. R. (2013). Hesperetin stimulates cholecystokinin secretion in enteroendocrine STC-1 cells. Biomolecules and Therapeutics, 21(2), 121–125. https://doi.org/10.4062/biomolther.2012.077

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