The Protective Effect of Adalimumab on Renal Injury in a Model of Abdominal Aorta Cross Clamping       
Yazarlar (9)
Medine C. Cure
Recep Tayyip Erdogan University, Türkiye
Erkan Cure
Recep Tayyip Erdogan University, Türkiye
Yildiray Kalkan
Recep Tayyip Erdogan University, Türkiye
Levent Tumkaya
Recep Tayyip Erdogan University, Türkiye
Ibrahim Aydin
Recep Tayyip Erdogan University, Türkiye
Prof. Dr. Aynur KIRBAŞ Recep Tayyip Erdogan University, Türkiye
Hasan Efe
Recep Tayyip Erdogan University, Türkiye
Aysel Kurt
Recep Tayyip Erdogan University, Türkiye
Suleyman Yuce
Recep Tayyip Erdogan University, Türkiye
Makale Türü Açık Erişim Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale
Dergi Adı Advances in Clinical and Experimental Medicine
Dergi ISSN 1899-5276 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce
Basım Tarihi 03-2016
Cilt No 25
Sayı 2
Sayfalar 219 / 226
DOI Numarası 10.17219/acem/33250
Makale Linki http://www.advances.am.wroc.pl/strona.php?id=11&n=1882&lang=en
Özet
Background. Adalimumab (ADA) is a potent inhibitor of tumor necrosis factor (TNF-alpha). ADA treatment suppresses proinflammatory cytokines, leading to a decrease or inhibition of the inflammatory process.
Objectives. The aim of this study was to investigate the possible protective effects of ADA on oxidative stress and cellular damage on rat kidney tissue after ischemia/reperfusion (I/R).
Material and Methods. A total of 30 male Wistar albino rats were divided into three groups: control, I/R, and I/R plus ADA (I/R + ADA); each group comprised 10 animals. The control group underwent laparotomy without I/R injury. After undergoing laparotomy, I/R groups underwent two hours of infrarenal abdominal aortic cross ligation, which was followed by two hours of reperfusion. ADA (50 mg/kg) was administered as a single dose, intraperitoneally, to the I/R + ADA group, 5 days before I/R.
Results. The I/R group's TNF-alpha (1150.9 +/- 145.6 pg/mg protein), IL-1 beta (287.0 +/- 32.4 pg/mg protein) and IL-6 (1085.6 +/- 56.7 pg/mg protein) levels were significantly higher than those of the control (916.1 +/- 88.7 pg/mg protein, + ADA groups (864.2 +/- 169.4 pg/mg protein, p = 0.003; 241.4 +/- 33.4 pg/mg protein, p = 0.010; 987.7 +/- 66.5 pg/mg protein, p = 0.004, respectively). To date, a few histopathological changes have been reported regarding renal I/R injury in rats due to ADA treatment whereas I/R caused severe histopathological injury to kidney tissue.
Conclusions. ADA treatment significantly attenuated the severity of kidney I/R injury, inhibiting I/R-induced oxidative stress and renal damage. Because of its anti-inflammatory and antioxidant effects, ADA pretreatment may have protective effects on experimental kidney injury
Anahtar Kelimeler
ischemia | reperfusion injury | adalimumab | carbonic anhydrases | tumor necrosis factor alpha