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Furthermore, dynamic disulfide exchange reactions have been harnessed to construct poly(disulfide)-based hydrogels exhibiting ultra-fast self-healing, adjustable mechanical strength, and redox-controlled therapeutic release mechanistic features directly translatable to HAGSH scaffolds

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Comparative metabolic and hepatic effects of GLP-1-based mono-, dual-, and triple-agonist therapies GLP-1 receptor signaling Intestinal L-cells serve as the primary source of GLP-1 synthesis, which operates via G-protein coupled receptors present in pancreatic beta cells, gastrointestinal and central neural systems, cardiac tissues, and kidneys [26]

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