Efficacy of poly(adenosine diphosphate-ribose) polymerase inhibition in extracorporeal shock wave-induced renal injury

被引:1
|
作者
Malkoc, Ercan [1 ]
Alp, Bilal Firat [2 ]
Demirer, Zafer [3 ]
Guragac, Ali [2 ]
Dursun, Furkan [1 ]
Ates, Ferhat [1 ]
Yildirim, Ibrahim [2 ]
Yuksel, Ramazan [4 ]
Uysal, Bulent [4 ]
Topal, Turgut [4 ]
Kurt, Yasemin Gulcan [5 ]
Ozcan, Ayhan [5 ]
Guven, Ahmet [6 ]
机构
[1] Gulhane Mil Med Acad Haydarpasa Training Hosp, Dept Urol, Istanbul, Turkey
[2] Gulhane Mil Med Acad, Dept Urol, Ankara, Turkey
[3] Eskisehir Mil Hosp, Dept Urol, Eskisehir, Turkey
[4] Gulhane Mil Med Acad, Dept Physiol, Ankara, Turkey
[5] Gulhane Mil Med Acad, Dept Clin Biochem, Ankara, Turkey
[6] Gulhane Mil Med Acad, Dept Pediat Surg, Ankara, Turkey
关键词
3-aminobenzamide; extracorporeal shock wave lithotripsy; oxidative stress; PARP inhibition; renal injury; ADP-RIBOSE; OXIDATIVE STRESS; ISCHEMIA/REPERFUSION INJURY; PARP ACTIVATION; NITRIC-OXIDE; IN-VIVO; INFLAMMATION; LITHOTRIPSY; RAT; NEOPTERIN;
D O I
10.3109/0886022X.2014.962423
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Extracorporeal shock wave lithotripsy (ESW) induces renal damage by excessive production of free oxygen radicals. Free Oxygen radicals cause cellular injury by inducing nicks in DNA. The enzyme poly(adenosine diphosphate-ribose) polymerase (PARP) involved in the process of repair of DNA in damaged cells. However, its activation in damaged cells can lead to adenosine triphosphate depletion and death. Thus, we designed a study to evaluate the efficacy of 3-aminobenzamide (3-AB), a PARP inhibitor, against extracorporeal shock wave induced renal injury. Methods: Twenty-four Sprague-Dawley rats were divided into three groups: control, ESW, ESW + 3-AB groups. All groups except control group were subjected to ESW procedure. ESW + 3-AB group received 20 mg/kg/day 3-aminobenzamide intraperitoneally at 2 h before ESW and continued once a day for consecutive 3 days. The surviving animals were sacrificed at the 4th day and their kidneys were harvested for biochemical and histopathologic analysis. Blood samples from animals were also obtained. Results: Serum ALT and AST levels, serum neopterin and tissue oxidative stress parameters were increased in the ESW group and almost came to control values in the treatment group (p<0.05, ESW vs. ESW + 3-AB). Histopathological injury score were significantly lower in treatment group than the ESW group (p<0.05, ESW vs. ESW + 3-AB). Conclusion: Our data showed that PARP inhibition protected renal tissue against ESW induced renal injury. These findings suggest that it would be possible to improve the outcome of ESW induced renal injury by using PARP inhibitors as a preventive therapy.
引用
收藏
页码:1564 / 1569
页数:6
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