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The GLP-1 analogs, semaglutide and liraglutide, delay the progression of atherosclerosis by regulating inflammatory pathways in low-density lipoprotein receptor-deficient (LDLr -/- ) and apolipoprotein E-deficient (ApoE -/- ) mice [16]

Most patients who accidentally administer a single dose of expired semaglutide are unlikely to experience adverse effects beyond potentially reduced blood glucose control or diminished appetite suppression

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In early-stage HUA experiments, 32 mice were randomly divided into a blank group and a model group