TY - JOUR
T1 - Nicorandil as a novel therapy for advanced diabetic nephropathy in the eNOS-deficient mouse
AU - Tanabe, Katsuyuki
AU - Lanaspa, Miguel A.
AU - Kitagawa, Wataru
AU - Rivard, Christopher J.
AU - Miyazaki, Makoto
AU - Klawitter, Jelena
AU - Schreiner, George F.
AU - Saleem, Moin A.
AU - Mathieson, Peter W.
AU - Makino, Hirofumi
AU - Johnson, Richard J.
AU - Nakagawa, Takahiko
PY - 2012/5/1
Y1 - 2012/5/1
N2 - Nicorandil is an orally available drug that can act as a nitric oxide donor, an antioxidant, and an ATP-dependent K channel activator. We hypothesized that it may have a beneficial role in treating diabetic nephropathy. We administered nicorandil to a model of advanced diabetic nephropathy (the streptozotocin-induced diabetes in mice lacking endothelial nitric oxide synthase, eNOSKO); controls included diabetic eNOS KO mice without nicorandil and nondiabetic eNOS KO mice treated with either nicorandil or vehicle. Mice were treated for 8 wk. Histology, blood pressure, and renal function were determined. Additional studies involved examining the effects of nicorandil on cultured human podocytes. Here, we found that nicorandil did not affect blood glucose levels, blood pressure, or systemic endothelial function, but significantly reduced proteinuria and glomerular injury (mesangiolysis and glomerulosclerosis). Nicorandil protected against podocyte loss and podocyte oxidative stress. Studies in cultured podocytes showed that nicorandil likely protects against glucose-mediated oxidant stress via the ATP-dependent K channel as opposed to its NO-stimulating effects. In conclusion, nicorandil may be beneficial in diabetic nephropathy by preserving podocyte function. We recommend clinical trials to determine whether nicorandil may benefit diabetic nephropathy or other conditions associated with podocyte dysfunction.
AB - Nicorandil is an orally available drug that can act as a nitric oxide donor, an antioxidant, and an ATP-dependent K channel activator. We hypothesized that it may have a beneficial role in treating diabetic nephropathy. We administered nicorandil to a model of advanced diabetic nephropathy (the streptozotocin-induced diabetes in mice lacking endothelial nitric oxide synthase, eNOSKO); controls included diabetic eNOS KO mice without nicorandil and nondiabetic eNOS KO mice treated with either nicorandil or vehicle. Mice were treated for 8 wk. Histology, blood pressure, and renal function were determined. Additional studies involved examining the effects of nicorandil on cultured human podocytes. Here, we found that nicorandil did not affect blood glucose levels, blood pressure, or systemic endothelial function, but significantly reduced proteinuria and glomerular injury (mesangiolysis and glomerulosclerosis). Nicorandil protected against podocyte loss and podocyte oxidative stress. Studies in cultured podocytes showed that nicorandil likely protects against glucose-mediated oxidant stress via the ATP-dependent K channel as opposed to its NO-stimulating effects. In conclusion, nicorandil may be beneficial in diabetic nephropathy by preserving podocyte function. We recommend clinical trials to determine whether nicorandil may benefit diabetic nephropathy or other conditions associated with podocyte dysfunction.
KW - ATP-dependent K channel
KW - Endothelial dysfunction
KW - Podocyte
KW - Sulfo-nylurea receptor
UR - http://www.scopus.com/inward/record.url?scp=84860540851&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84860540851&partnerID=8YFLogxK
U2 - 10.1152/ajprenal.00596.2011
DO - 10.1152/ajprenal.00596.2011
M3 - Article
C2 - 22338086
AN - SCOPUS:84860540851
SN - 0363-6127
VL - 302
SP - F1151-F1161
JO - American Journal of Physiology - Renal Physiology
JF - American Journal of Physiology - Renal Physiology
IS - 9
ER -