Renal
ischemia-reperfusion injury (IRI), an important cause of
acute kidney injury (AKI), causes increased renal tubular injury and microvascular
inflammation. 1,[Formula: see text]2,[Formula: see text]3,[Formula: see text]4,[Formula: see text]6-
penta-O-galloyl-[Formula: see text]-
D-glucose (
PGG) from
Galla rhois has anticancer, anti-oxidation and
angiogenesis effects. We examined protective effects of
PGG on IRI-induced acute AKI. Clamping both renal arteries for 45[Formula: see text]min induced isechemia and then reperfusion. Treatment with
PGG (10[Formula: see text]mg/kg/day and 50[Formula: see text]mg/kg/day for four days) significantly ameliorated urine volume, urine osmolality,
creatinine clearance (Ccr) and blood
urea nitrogen (BUN). In addition,
PGG increased aquaporine 1/2/3, Na[Formula: see text]-K[Formula: see text]-
ATPase and
urea transporter (UT-B) and decreased
ICAM-1, MCP-1, and HMGB-1 expression. In this histopathologic study,
PGG improved glomerular and tubular damage. Immunohistochemistry results showed that
PGG increased aquaporine 1/2, and Na[Formula: see text]-K[Formula: see text]
ATPase and decreased
ICAM-1 expression. These findings suggest that
PGG ameliorates tubular injury including tubular dysfunction and microvascular
inflammation in IRI-induced AKI rats.