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Zoledronic acid aggravates kidney damage during ischemia reperfusion injury in rat

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info:eu-repo/semantics/closedAccess

Date

2015

Author

Şehitoğlu, İbrahim
Tümkaya, Levent
Bedir, Recep
Kalkan, Yıldıray
Cüre, Medine Cumhur
Yücel, Ahmet Fikret
Zorba, Orhan Ünal
Yüce, Süleyman
Cüre, Erkan

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Citation

Sehitoglu, I., Tumkaya, L., Bedir, R., Kalkan, Y., Cure, M. C., Yucel, A. F., Zorba, O. U., Yuce, S., & Cure, E. (2015). Zoledronic acid aggravates kidney damage during ischemia reperfusion injury in rat. Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer, 34(1), 53–61. https://doi.org/10.1615/jenvironpatholtoxicoloncol.2015012424

Abstract

Introduction: Zoledronic acid (ZA), a bisphosphonate, increases the levels of cytokines, such as interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-?), and reactive oxygen species (ROS) in subjects without cancer. Increased production of ROS, TNF-?, and IL-6 during ischemia and reperfusion (I/R) injury stimulates apoptosis that leads to renal injury. We aimed to investigate whether ZA treatment has a protective effect on renal tissues during I/R. Materials and Methods: Twenty-four Sprague-Dawley rats were used in this study, and they were subdivided randomly into three groups, each containing eight rats. Infrarenal abdominal aortic cross ligation was performed on the I/R group. After 2 h of ischemia, 2 h of reperfusion was applied. A single dose of 100 µg/kg ZA was administered intraperitoneally to the ZA group. I/R was performed after 48 h. Results: Whereas TNF-?, IL-6, and nitric oxide (NO) levels of the I/R group were higher than those of the control group, TNF-?, IL-6, and NO levels of the ZA group were higher than those of the I/R group [TNF-? (p=0.038), IL-6 (p=0.012), NO (p=0.002), and caspase-3 (p=0.037)] and the control group [TNF-? (p<0.001), IL-6 (p<0.001), NO (p<0.001), and caspase-3 (p<0.001)]. Whereas the carbonic anhydrase II (CA-II) level of the ZA group was lower than that of the control group (p=0.040), the CA-II level of the I/R group was higher than that of the control group (p=0.020). Conclusion: ZA may aggravate renal injury during I/R by increasing cytokine production and apoptosis. It may also increase renal injury and metabolic acidosis during I/R by suppressing CA-II enzyme activities. © 2015 by Begell House, Inc.

Source

Journal of Environmental Pathology, Toxicology and Oncology

Volume

34

Issue

1

URI

https://doi.org/10.1615/JEnvironPatholToxicolOncol.2015012424
https://hdl.handle.net/11436/4365

Collections

  • PubMed İndeksli Yayınlar Koleksiyonu [2443]
  • Scopus İndeksli Yayınlar Koleksiyonu [6026]
  • TF, Cerrahi Tıp Bilimleri Bölümü Koleksiyonu [1225]
  • TF, Dahili Tıp Bilimleri Bölümü Koleksiyonu [1573]
  • TF, Temel Tıp Bilimleri Bölümü Koleksiyonu [700]



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