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GLP-1 medications substantially decrease appetite, and many patients inadvertently consume far fewer calories than their body requires for optimal energy levels
BBR was delivered to DIO mice through dietary supplementation for 8 weeks to establish the metabolic impact in the DIO model
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Despite the loss of its insulinotropic effect, the GLP-1 products of DPP-4 catalysis exert other actions, such as suppression of hepatic glucose production and antioxidant activity in the cardiovascular system [14]
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