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The distinction that matters is whether GLP-1 receptor agonists cause a disproportionate loss of muscle relative to fat

This movement is caused by cellular swelling and a relative narrowing of extracellular gaps, which in turn generate slow-conducting waves of depolarization in multiple neurons and glial cells, resulting in the temporary inhibition of synaptic activity ( 2+ overload induces a transient oxidative stress in the organism and promotes the generation of ROS, which activate injurious signaling through transient receptor potential subtype anchor protein 1 channels ( 2+ lead to the opening of neuronal pannexin 1 channels to open and activate cystatinase 1, followed by the release of high mobility group box-1 protein and the activation of nuclear factor kappa-B signaling pathway in astrocytes (Figure 1B)