Irisin preserves mitochondrial integrity and function in tubular epithelial cells after ischemia–reperfusion‐induced acute kidney injury - Cui, Yu; Yu, Lu; Cong, Wenqi; Jiang, Shan; Qiu, Xingyu; Wei, Chunchun; Zheng, Gui; Mao, Jianhua; Liu, Ruisheng; Patzak, Andreas; Persson, Pontus B.; Chen, Jianghua; et al. (Acta Physiologica, 2024)
Keywords: acute kidney injury; Acute Kidney Injury - metabolism; Acute Kidney Injury - pathology; Animals; Autophagy; Confocal microscopy; Creatinine; Epithelial cells; Epithelial Cells - metabolism; Female; Fibronectins - metabolism; Gelatinase; Humans; Immunohistochemistry; inflammasome activation; irisin; Ischemia; Kidney Tubules - metabolism; Kidney Tubules - pathology; Kidneys; Kinases; Leukocytes (neutrophilic); Lipocalin; Male; Membrane proteins; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondria - metabolism; mitochondrial autophagy; Movement disorders; Neurodegenerative diseases; Parkinson's disease; Proteins; Proximal tubules; PTEN protein; PTEN-induced putative kinase; Renal function; renal ischemia–reperfusion; Reperfusion; Reperfusion Injury - metabolism; Reperfusion Injury - pathology; Skeletal muscle; Translocase; inflammasome activation; mitochondrial autophagy; acute kidney injury; irisin; renal ischemia–reperfusion