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Each session consisted of 15 gap trials and 15 no-gap trials, presented in random paired order with variable intervals between trials (1723 s)

At steady state, average blood levels are higher and more stable than after the first dose, which often translates into smoother appetite and glucose effectsand sometimes more noticeable GI side effects during dose increases

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Trnblom et al., 2012), disturbances in gut-brain interaction, and psychological distress

GLP-1 blocks glucagon (a hormone that works to raise blood sugar) and signals to the pancreas to release insulin