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Key Research Areas Gastrointestinal mucosal protection BPC-157 is studied in gut tissue models for its interaction with gastric mucosal repair pathways, including protection against NSAID-induced lesions and inflammatory bowel disease models Tendon and ligament biology Investigated in in-vitro and rodent models for its influence on fibroblast activity, collagen synthesis, and tendon-to-bone attachment repair Angiogenesis Studied for its promotion of VEGF expression and new blood vessel formation in wound healing and ischaemia models Neuroprotection Referenced in studies examining dopamine and serotonin system modulation
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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
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