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Laboratory Study

Paricalcitol may improve oxidative DNA damage on experimental amikacin-induced nephrotoxicity model

, , , , , & show all
Pages 751-758 | Received 04 Jan 2016, Accepted 17 Feb 2016, Published online: 16 Mar 2016

Figures & data

Table 1. Renal function parameters in the four treatment groups (n = 8 each).

Table 2. Oxidative stress biomarkers of four treatment groups (n = 8 each).

Figure 1. Renal histology of the study groups (haematoxylin and eosin staining, original magnification, x400). Normal histology in (a) control and (c) paricalcitol groups. (b) Tubular necrosis areas and proteinaceous casts of Group A. (d) Healthy tubular cells of Group A + P.

Figure 1. Renal histology of the study groups (haematoxylin and eosin staining, original magnification, x400). Normal histology in (a) control and (c) paricalcitol groups. (b) Tubular necrosis areas and proteinaceous casts of Group A. (d) Healthy tubular cells of Group A + P.

Table 3. Histology and immunohistochemistry in the four treatment groups (n = 8 each).

Figure 2. Immunoexpression of VEGF in the four treatment groups (X400). No VEGF expression in the renal tubular cells in the (a) control, (c) paricalcitol and (d) paricalcitol treated amikacin-induced nephrotoxicity groups. (b) Intense expression of VEGF of amikacin-induced nephrotoxicity group.

Figure 2. Immunoexpression of VEGF in the four treatment groups (X400). No VEGF expression in the renal tubular cells in the (a) control, (c) paricalcitol and (d) paricalcitol treated amikacin-induced nephrotoxicity groups. (b) Intense expression of VEGF of amikacin-induced nephrotoxicity group.

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