Fig. 2From: Angiopoietin 1 influences ischemic reperfusion renal injury via modulating endothelium survival and regenerationa Expression of Angpt1 mRNA 1, 3, 7, and 14 days after IRI in wild mice. The expression of Angpt1 increased 7 days and 14 days after IRI. (N = 6 per sham and IRI groups at each time point) b The expression of Angpt1 in kidney was significantly suppressed in the Angpt1 knockout mice on the day of IRI and 1, 3, or 7 days after IRI compared to that in the control mice (N = 6, 6, 12, and 17 in knockout group on day 0, 1, 3, and 7 days respectively, N = 6, 6, 12, and 15 in control group on day 0, 1, 3, and 7 days respectively, P < 0.05 or P < 0.01) c & d Western blotting of mouse Angpt1 3 days after IRI. The Angpt1 protein level was lower in the knockout than control mice. (N = 5 for each group, P < 0.05) e Serum creatinine level was higher in the Angpt1 knockout mice 3 and 7 days after IRI. (N = 17 in knockout group, N = 15 in control group, N = 5 in the sham group, *P < 0.05, **P < 0.01) f Serum BUN level was higher in Angpt1 knockout mice 3 days after IRI. (N = 17 in knockout group, N = 15 in control group, N = 5 in the sham group, *P < 0.05) g PAS staining of renal tissue in control, knockout and sham mice. The remaining tubular necrosis was more severe and the renal tubular recovery was less in the knockout mice 7 days after IRI. Arrow indicates recovery tubule. Arrow head indicates necrotic tubule. h Semi-quantitative analysis of the regeneration score in the control and knockout mice. The recovery percentage was lower and the necrosis percentage was higher in the Angpt1 knockout mice 7 days after IRI (N = 17 in the knockout group, N = 15 in the control group)Back to article page