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The GLP-1 receptor herbal agonist morroniside attenuates neuropathic pain via spinal microglial expression of IL-10 and beta-endorphin

GLP-1 receptor agonist initiation was associated with a reduced risk for exacerbation in the obese group, with a risk ratio of 0.790 and a risk difference of 12.2 percent

Controlled endocrine investigations demonstrate stable cortisol or corticosterone concentrations despite measurable growth hormone pulses, supporting limited hypothalamic-pituitary-adrenal axis engagement in experimental models