homeostasis/metabolism
• reduced following 50 minutes of ischemia and 24 hours reperfusion compared with wild-type mice
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• reduced deposition of C3d in the kidney following 30 or 50 minutes of ischemia and 24 hours reperfusion compared with wild-type mice
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• following 50 minutes of ischemia and 24 hours reperfusion, mice exhibit reduced tubule necrosis, inflammatory cell infiltration (neutrophils and macrophages), deposition of complement (Cd3d) and blood urea nitrogen levels compared with wild-type mice
• following 30 minutes of ischemia and 24 hours reperfusion, mice exhibit reduced loss of renal function, preservation of renal architecture and reduced leukocyte infiltration and tubular deposition of complement compared with wild-type mice
• transplanted kidneys subjected to ischemia and reperfusion exhibit improved structure and function compared with wild-type kidneys
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renal/urinary system
• following 50 minutes of ischemia and 24 hours reperfusion, mice exhibit reduced tubule necrosis, inflammatory cell infiltration (neutrophils and macrophages), deposition of complement (Cd3d) and blood urea nitrogen levels compared with wild-type mice
• following 30 minutes of ischemia and 24 hours reperfusion, mice exhibit reduced loss of renal function, preservation of renal architecture and reduced leukocyte infiltration and tubular deposition of complement compared with wild-type mice
• transplanted kidneys subjected to ischemia and reperfusion exhibit improved structure and function compared with wild-type kidneys
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• reduced tubule necrosis and inflammation following 30 or 50 minutes of ischemia and 24 hours reperfusion compared with wild-type mice
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immune system
• reduced deposition of C3d in the kidney following 30 or 50 minutes of ischemia and 24 hours reperfusion compared with wild-type mice
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