Author/Authors :
Köse, Evren School of Medicine - Inonu University - Malatya, Turkey , Oğuz, Fatih School of Medicine - Inonu University - Malatya, Turkey , Sarihan, Mehmet Ediz School of Medicine - Inonu University - Malatya, Turkey , Beytur, Ali School of Medicine - Inonu University - Malatya, Turkey , Yücel, Aytaç School of Medicine - Inonu University - Malatya, Turkey , Vardi, Nigar Department of Histology-Embryology - School of Medicine - Inonu University - Malatya, Turkey , Polat, Alaadin Department of Physiology - School of Medicine - Inonu University - Malatya, Turkey , Eki̇nci̇, Nihat Department of Anatomy - School of Medicine - Erciyes University - Kayseri, Turkey
Abstract :
The current study was designed to investigate the therapeutic and protective effects of
montelukast (ML) against doxorubicin (DOX)-induced acute kidney damage in rats.
Materials and Methods: Thirty-five Wistar albino female rats were randomly divided into 5 groups
as follows: Group I: Control; Group II: Control+ML; Group III: DOX; Group IV: DOX+ML; Group V:
ML+DOX. At the end of the experiment, the kidney tissues of rats were collected. Thiobarbituric acid
reactive substance (TBARS), reduced glutathione, superoxide dismutase (SOD), and catalase levels
were determined from the kidney tissues. In addition, the kidney tissues were examined histologically.
Results: DOX induced a significant increase in the kidney TBARS levels, whereas SOD contents
significantly decreased when compared with the control group. On the other hand, ML administration
before and after DOX injection caused significant decreases in TBARS production and also increases in
SOD levels. Histologically, the most remarkable damage was glomerulosclerosis and tubular changes
in the DOX group. Moreover, marked tubular necrosis and swelling in tubular epithelial cells were
observed in this group. Contrarily, although glomerulosclerosis was recognized as alleviated also in
both DOX+ML and ML+DOX groups, the lesions did not completely ameliorate. However, treatment
with ML after DOX injection was more effective than treatment with ML before DOX injection with
respect to the protection of tubular structures.
Conclusion: It was determined that ML treatment after DOX injection caused therapeutic effects
against DOX-induced kidney damage. Thence, ML treatment is of some clinical properties for oxidative
stress damage in kidney tissues.
Keywords :
Doxorubicin , TBARS , Histology , Kidney , Leukotrienes , Oxidative stress