The effect of poly (ADP-ribose) polymerase inhibition on aminoglycoside-induced acute tubular necrosis in rats

摘要

Introduction: Aminoglycosides (AG) cause nephrotoxicity in 10 - 20% of patients. One of the mechanisms is by generating reactive oxygen species (ROS), leading to DNA destruction and activation of poly(ADPribose) polymerase (PARP) causing necrotic tubular cell death. PARP inhibition on gentamicin- induced nephrotoxicity was studied. Methods: 19 female Wistar-Kyoto rats divided into 3 groups: control (3 rats receiving no treatment); gentamicin-treated group (8 rats); and 8 rats treated with gentamicin combined with 3-aminobenzamide (3 AB). Kidney functions, protein, and gentamicin levels as well as urinary trypsin inhibitory activity (TIA) were measured. Tissue microscopic examination and immunohistochemical study for proliferative cell nuclear antigen (PCNA) were determined. The effect of PARP inhibitor on the bactericidal activity of gentamicin was also assessed. Results: The following results were statistically significant: urea (mg/dL) 39.9 +/- 5.86, 88.3 +/- 50.3, and 48.5 +/- 12.7 (p = 0.048); serum creatinine (mg/dL): 0.6 +/- 0.26, 1.05 +/- 0.7, 0.6 +/- 0.06 (p = 0.043); proteinuria (mg/24-hours): 7.27 +/- 3.65, 41.2 +/- 18.1, and 17.6 +/- 13.9 (p = 0.050); the number of tubular macronuclei (per 10 mm(2)): 18.33 +/- 16.07, 218 +/- 101.8, 41.7 +/- 36.2 (p = 0.012); the number of dilated tubes (per 10 mm2): 61.67 +/- 12.58, 276.3 +/- 112.7, 140.0 +/- 90.9 (p = 0.04); and the number of PCNA positive nuclei (per 10 mm2): 223.3 +/- 95.69, 3,585 +/- 2,215.3, 626.7 +/- 236.9 (p = 0.034) in the control, gentamicin, and gentamicin+3AB-treated groups, respectively. The following biochemical and histologic parameters were also examined, however, they showed no statistically significant difference: TIA (p = 0.055), mitoses (p = 0.14), mononuclear infiltrate (p = 0.188), and intratubular cast formation (p = 0.084). No effect on bactericidal activity was observed. Conclusion: This study illustrates that PARP inhibitor significantly attenuates gentamicin-induced nephrotoxicity in rats with no effect on the bactericidal activity.