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This stimulation prompts the body to secrete its own GLP-1, GIP, and PYY hormones naturally, as part of its normal satiety signaling process
In many cases, only 10% to 20% of a standard oral dose makes it into the bloodstream
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These modifications enhance its stability and prolong its interaction with receptors in experimental systems, distinguishing it from native GLP-1, which is rapidly degraded in the body
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