exploring the mechanism of septic acute kidney injury(Fostering Joint International Research)
Project/Area Number |
15KK0346
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Research Category |
Fund for the Promotion of Joint International Research (Fostering Joint International Research)
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Allocation Type | Multi-year Fund |
Research Field |
General pharmacology
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Research Institution | Kagawa University |
Principal Investigator |
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Research Collaborator |
Titze Jens Vanderbilt大学, Department of Clinical Pharmacology, 教授
Wiig Helge Bergen大学, The Department of Biomedicine, 教授
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Project Period (FY) |
2016 – 2017
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥14,560,000 (Direct Cost: ¥11,200,000、Indirect Cost: ¥3,360,000)
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Keywords | 敗血症 / 急性腎障害 / Acute kidney injury |
Outline of Final Research Achievements |
The project examined the mechanism for the onset of septic acute kidney injury (AKI). The study explored that the pattern-recognition receptors in the proximal tubules plays essential roles for the early-phase changes of lipopolysaccharide-induced AKI. Triggering this mechanism induced early-phase AKI; however, it works as a compensatory protective factor against the further progression of AKI that is induced mainly by hemodynamic changes, including glomerular filtration decline. Monocyte/macrophage showed a contribution to the early phase AKI and the effect was either protective or deteriorative; active phagocyte population protected kidney against lipopolysaccharide-induced AKI, and monocytes/macrophage with poor phagocytic activity made AKI more severe.
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Report
(3 results)
Research Products
(4 results)
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[Journal Article] Guanylyl cyclase A in both renal proximal tubular and vascular endothelial cells protects the kidney against acute injury in rodent experimental endotoxemia models.2018
Author(s)
Kidney against Acute Injury in Rodent Experimental Endotoxemia Models. Kitamura H, Nakano D, Sawanobori Y, Asaga T, Yokoi H, Yanagita M, Mukoyama M, Tokudome T, Kangawa K, Shirakami G, Nishiyama A.
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Journal Title
Anesthesiology
Volume: 印刷中
Issue: 2
Pages: 296-310
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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