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We next repeated this experimental paradigm in Gipr hypo-KO and Gipr hypo-GFP mice, combining the initiation of HFD with a combination of LIRA (or VEH) alone or LIRA (or VEH) plus GIPR antagonist peptide (GIPR-antag)

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Yet a question remains whether their effect on gastric emptying might modulate the rate of drug absorption (maximal plasma drug concentration, [ C max ], and time to maximal concentration, [ t max ])

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