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It is studied as a melanocortin receptor (MC1R/MC4R) agonist with documented anti-inflammatory activity in mucosal, epithelial, and wound-healing models

Consistently, we found that administration of CA, an endogenous FXR agonist, could not only significantly attenuate the T3-induced elevation of GLP-1 and insulin levels but also attenuate the glucose-lowering effect of T3 in MMI mice (Fig

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