부산대학교 도서관

Disruption of the renal endothelial integrity is pivotal for the development of a vascular leak, tissue edema and consequently acute kidney injury. Kidney ischemia amplifies endothelial activation and up-regulation of pro-inflammatory mechanisms. After restoring a sufficient blood flow, the kidney is damaged through complex pathomechanisms that are classically referred to as ischemia and reperfusion injury, where the disruption of the inter-endothelial connections seems to be a crucial step in this pathomechanism. Focusing on the molecular cell-cell interaction, the fibrinopeptide B[beta].sub.15-42 prevents vascular leakage by stabilizing these inter-endothelial junctions. The peptide associates with vascular endothelial-cadherin, thus preventing early kidney dysfunction by preserving blood perfusion efficacy, edema formation and thus organ dysfunction. We intended to demonstrate the early therapeutic benefit of intravenously administered B[beta].sub.15-42 in a mouse model of renal ischemia and reperfusion. After 30 minutes of ischemia, the fibrinopeptide B[beta].sub.15-42 was administered intravenously before reperfusion was commenced for 1 and 3 hours. We show that B[beta].sub.15-42 alleviates early functional and morphological kidney damage as soon as 1 h and 3 h after ischemia and reperfusion. Mice treated with B[beta].sub.15-42 displayed a significantly reduced loss of VE-cadherin, indicating a conserved endothelial barrier leading to less neutrophil infiltration which in turn resulted in significantly reduced structural renal damage. The significant reduction in tissue and serum neutrophil gelatinase-associated lipocalin levels reinforced our findings. Moreover, renal perfusion analysis by color duplex sonography revealed that B[beta].sub.15-42 treatment preserved resistive indices and even improved blood velocity. Our data demonstrate the efficacy of early therapeutic intervention using the fibrinopeptide B[beta].sub.15-42 in the treatment of acute kidney injury resulting from ischemia and reperfusion. In this context B[beta].sub.15-42 may act as a potent renoprotective agent by preserving the endothelial and vascular integrity.
Author(s): Anja Urbschat 1,*, Kai Zacharowski 2, Nicholas Obermüller 3, Katrin Rupprecht 2, Daniela Penzkofer 4, Carla Jennewein 2, Nguyen Tran 2, Bertram Scheller 2, Stefanie Dimmeler 4, Patrick Paulus [...]