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Impact of endocrine disrupting chemicals on neurodevelopment: the need for better testing strategies for endocrine disruption-induced developmental neurotoxicity

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Semaglutide, a GLP-1 receptor agonist, was administered subcutaneously at a dose of 0.052 mg/kg/day for 4 weeks, starting 4 weeks after PAB

TCF7L2 , a transcription factor tied to glucose homeostasis and GLP-1 secretion, and MC4R , a melanocortin receptor central to satiety, help describe the terrain a GLP-1 compound acts on