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Administration of semaglutide at the dose regimen of ~ 90 g/kg/day failed to evidence significant weight loss but more importantly, led to alteration of cortical bone microarchitecture, represented by lower cortical thickness, and ultimately to a significant decrease in bone strength [69]

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[2] [16] In the stomach, GLP-1 inhibits gastric emptying, acid secretion and motility, which collectively decrease appetite

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It is notable that in a study performed by Bernardo, some human GLP-1 could bind to a functional receptor in rat MC3T3-E1 cells with a dependence on time and temperature, but independent of the type of cAMP-linked G protein receptor