Delayed inhibition of p38 mitogen-activated protein kinase ameliorates renal fibrosis in obstructive nephropathy
M Nishida, Y Okumura, H Sato… - Nephrology Dialysis …, 2008 - academic.oup.com
M Nishida, Y Okumura, H Sato, K Hamaoka
Nephrology Dialysis Transplantation, 2008•academic.oup.comBackground. The p38 mitogen-activated protein kinase (MAPK) pathway is an important
intracellular signalling pathway involved in the production of proinflammatory and profibrotic
mediators. Previous reports indicated the role of p38 MAPK activation in renal fibrosis.
Methods. We administered a selective p38α MAPK inhibitor, FR167653, in a mouse model
of unilateral ureteral obstruction (UUO) during the late stage (Days 7–14) after UUO, and the
kidneys were examined at Day 14. p38 and phospho-p38 MAPK protein levels, the degree …
intracellular signalling pathway involved in the production of proinflammatory and profibrotic
mediators. Previous reports indicated the role of p38 MAPK activation in renal fibrosis.
Methods. We administered a selective p38α MAPK inhibitor, FR167653, in a mouse model
of unilateral ureteral obstruction (UUO) during the late stage (Days 7–14) after UUO, and the
kidneys were examined at Day 14. p38 and phospho-p38 MAPK protein levels, the degree …
Abstract
Background. The p38 mitogen-activated protein kinase (MAPK) pathway is an important intracellular signalling pathway involved in the production of proinflammatory and profibrotic mediators. Previous reports indicated the role of p38 MAPK activation in renal fibrosis.
Methods. We administered a selective p38α MAPK inhibitor, FR167653, in a mouse model of unilateral ureteral obstruction (UUO) during the late stage (Days 7–14) after UUO, and the kidneys were examined at Day 14. p38 and phospho-p38 MAPK protein levels, the degree of renal fibrosis, the degree of myofibroblast accumulation and macrophage infiltration, and mRNA levels for TGF-β1 and α1(I) collagen in the kidneys were assessed.
Results. FR167653 treatment caused marked decreases in phospho-p38 MAPK levels along with decreased fibrosis at Day 14 after UUO. Although myofibroblast accumulation and α1(I) collagen mRNA level were decreased, no significant change was observed in the number of interstitial macrophages and TGF-β1 mRNA level with FR167653 treatment.
Conclusions. These results suggest that p38 MAPK blockade is an appealing therapeutic target, even after the emergence of established fibrosis.
Oxford University Press