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First, MafA controls Glp1r expression [10]

For example, we observed that both GLP-1 and its presumed inert metabolite GLP-1(936) showed coronary and mesenteric artery vasodilation, as well as cardioprotection from IRI ex vivo, in isolated tissues from both WT and Glp1r -KO ( Glp1r / ) mice, whereas the nondegradable GLP-1R agonist exenatide did not have these effects in the absence of a functional GLP-1R (4, 21)

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All data is from a research context, not a guide to personal use: GI adverse events were dose-dependent and most pronounced during dose escalation