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[3] [4] These medications work by mimicking the incretin hormone glucagon-like peptide-1, which enhances insulin secretion, suppresses glucagon release, and significantly reduces appetite primarily through central satiety pathways, with some slowing of gastric emptying (an effect that may attenuate over time)

d-Allulose treatment at 3 g kg 1 day 1 for 10 days significantly reduced the elevated basal blood glucose levels and tended to attenuate hyperinsulinemia in HFD-fed mice fasted 4 h (Fig

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