Hepatic effects that are considered adverse include death, abnormal clinical chemistry parameters, obvious functional organ impairment, DNA and mitochondrial alteration, glutathione depletion, hepatocyte necrosis, enhanced replicative DNA synthesis, generation of reactive oxygen species, and increased peroxisome proliferation (in rodents) (Williams and Iatropoulos 2002)
Future research should aim to harmonize differentiation protocols, stem cell sources, and treatment concentrations to better define the therapeutic window and mechanisms of GLP-1-RA in regenerative applications
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