Figures & data
Table 1. The primers used for real-time PCR analysis.
Figure 1. Effects of Curcumin pretreatment on renal function following renal I/R-induced injury. Serum creatinine and BUN were measured to assess the reno-protective effect of Cur against renal I/R. Data are represented as mean ± SEM (n = 10). ***p < .001 (IRI vs. Sham); #p < .005 (IRI vs. Cur).
![Figure 1. Effects of Curcumin pretreatment on renal function following renal I/R-induced injury. Serum creatinine and BUN were measured to assess the reno-protective effect of Cur against renal I/R. Data are represented as mean ± SEM (n = 10). ***p < .001 (IRI vs. Sham); #p < .005 (IRI vs. Cur).](/cms/asset/c3a908e5-7b69-406c-acb7-a36ce77cf6f9/irnf_a_1544565_f0001_b.jpg)
Figure 2. Effects of Curcumin pretreatment on I/R-induced renal histology. Representative microphotographs were taken from the kidneys of the sham, IRI, and Cur groups at the time point of 24 h after renal I/R. Histopathological examination was performed using PAS staining. Semi-quantitative assessment of the histological lesions based on tubular necrosis (B). Data are represented as mean ± SEM (n = 10). ***p < .001 (IRI vs. Sham); #p < .001 (IRI vs. Cur).
![Figure 2. Effects of Curcumin pretreatment on I/R-induced renal histology. Representative microphotographs were taken from the kidneys of the sham, IRI, and Cur groups at the time point of 24 h after renal I/R. Histopathological examination was performed using PAS staining. Semi-quantitative assessment of the histological lesions based on tubular necrosis (B). Data are represented as mean ± SEM (n = 10). ***p < .001 (IRI vs. Sham); #p < .001 (IRI vs. Cur).](/cms/asset/992c056b-596d-4ec8-bdee-704557ed706a/irnf_a_1544565_f0002_c.jpg)
Table 2. Effects of curcumin pretreatment on the mRNA level of TNF-α, IL-6, and IL-8 in the kidney after renal ischemia-reperfusion injury.
Table 3. Effects of curcumin pretreatment on the expression of TNF-α, IL-6, and IL-8 in the serum after renal ischemia-reperfusion injury.
Figure 3. Effects of Curcumin pretreatment on the expression of p65 and p-p65 after renal ischemia-reperfusion injury. Western blot analysis was employed to the expression of p65 and p-p65. (A) A representative result for Western blot analysis p65. (B) Semi-quantitative analysis of 10 animals studied in each group. The relative amounts of p-p65 and p65 in each group of rats were normalized by β-actin and presented as a ratio between p-p65 and p65. *p < .05 (IRI vs. Sham); #p < .05 (Cur vs. IRI).
![Figure 3. Effects of Curcumin pretreatment on the expression of p65 and p-p65 after renal ischemia-reperfusion injury. Western blot analysis was employed to the expression of p65 and p-p65. (A) A representative result for Western blot analysis p65. (B) Semi-quantitative analysis of 10 animals studied in each group. The relative amounts of p-p65 and p65 in each group of rats were normalized by β-actin and presented as a ratio between p-p65 and p65. *p < .05 (IRI vs. Sham); #p < .05 (Cur vs. IRI).](/cms/asset/77563779-0e3c-4580-86f0-9ce0edfcfc94/irnf_a_1544565_f0003_b.jpg)
Figure 4. Effects of Curcumin pretreatment on the JAK2/STAT3 signaling after renal ischemia-reperfusion injury. Western blot analysis was employed to the expression of JAK2, p-JAK2, STAT3, and p-STATA3. (A) A representative result for Western blot analysis p-JAK2, STAT3, and p-STATA3. (B) Semi-quantitative analysis of 10 animals studied in each group. The relative amounts of p-JAK2, JAK2, STAT3, and p-STATA3 in each group of rats were normalized by β-actin and presented as a ratio between p-JAK2/JAK2 and p-STAT3/STAT3. *p<.05 (IRI vs. Sham); #p<.05 (Curcumin vs. IRI). (IRI vs. Sham); #p<.05 (Cur vs. IRI).
![Figure 4. Effects of Curcumin pretreatment on the JAK2/STAT3 signaling after renal ischemia-reperfusion injury. Western blot analysis was employed to the expression of JAK2, p-JAK2, STAT3, and p-STATA3. (A) A representative result for Western blot analysis p-JAK2, STAT3, and p-STATA3. (B) Semi-quantitative analysis of 10 animals studied in each group. The relative amounts of p-JAK2, JAK2, STAT3, and p-STATA3 in each group of rats were normalized by β-actin and presented as a ratio between p-JAK2/JAK2 and p-STAT3/STAT3. *p<.05 (IRI vs. Sham); #p<.05 (Curcumin vs. IRI). (IRI vs. Sham); #p<.05 (Cur vs. IRI).](/cms/asset/16f1d33f-c0b6-4ba3-9aae-47a812f04cdc/irnf_a_1544565_f0004_b.jpg)