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Hu Z, Qu G, Yu X, Jiang H, Teng XL, Ding L, et al

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In mice, intragastric administration of a mixture of BTR agonists (including DB, phenylthiocarbamide (PTC), quinine and D-[-]salicin) was shown to increase plasma total ghrelin and octanoyl ghrelin levels without affecting ghrelin mRNA expression ( CCK Initial evidence to support the potential for BTR-evoked CCK secretion was reported in STC-1 cells, where both DB and PTC increased intracellular Ca 2+ and stimulated CCK secretion in a dose-dependent manner ( Hoodia gordonii [which tastes bitter, and has potent appetite-suppressant effects in both animals and humans ( ex vivo from rat intestine, and from HuTu-80 cells ( ad libitum meal in healthy young individuals ( GLP-1 and PYY Underpinned by the successful clinical application of GLP-1 receptor agonists and dipeptidyl peptisase-4 inhibitors to the management of type 2 diabetes ( At the cellular level, numerous bitter compounds have been reported to induce GLP-1 secretion from enteroendocrine cells via BTR pathways