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Idiopathic Pulmonary Fibrosis (IPF) IPF is a fatal and irreversible interstitial lung disease characterized by the involvement of ROSs in specific fibrotic processes, including macrophage polarization, immunosenescence, alveolar epithelial cell apoptosis, myofibroblast differentiation, and alterations in the acellular extracellular matrix [101]

Hypoglycaemia results in the sympathetic and parasympathetic nervous systems mediating glucagon secretion from islet alpha-cells

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10.1016/j.freeradbiomed.2010.03.026 63 HuangK.ZhangJ.ONeillK