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The pathways linking GLP-1RAs to psychiatric and neurodevelopmental conditions remain underexplored for conditions such as PTSD and OCD

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triagonism) on energy expenditure, glucose regulation, food intake, and weight loss in a well-established DIO mouse model in comparison to clinically relevant GLP1 receptor agonists [83]

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These medications slow gastric emptying, enhance insulin secretion in response to glucose, and signal satiety to the brain's appetite centers