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Consistent with these findings, previous in vitro studies showed that OXM is a full agonist at the GCGR and GLP-1R but is 3-fold less potent at the GCGR than native glucagon and 100-fold less potent at the GLP-1R than native GLP-1, in terms of activating cAMP accumulation ( Despite convincing data suggesting the central role of GLP-1R signalling in the food intake reduction effects of OXM, there were still some unexplained effects of the gut hormone including increased energy expenditure, suggesting a GLP-1R independent mechanism of action ( in vitro in addition to enhanced metabolic rate in humans had been previously shown ( Glp1r -/- mice, suggesting that both GLP-1R and GCGR are required for weight loss to occur

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The thermic effect of food decreases

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