Nigella sativa protects against ischaemia/reperfusion injury in rat kidneys

被引:76
作者
Bayrak, Omer [1 ]
Bavbek, Nuket [2 ]
Karatas, Omer Faruk [1 ]
Bayrak, Reyhan [3 ]
Catal, Ferhat [4 ]
Cimentepe, Ersin [1 ]
Akbas, Ali [5 ]
Yildirim, Erol [1 ]
Unal, Dogan [1 ]
Akcay, Ali [2 ]
机构
[1] Fatih Univ, Sch Med, Dept Urol, Ankara, Turkey
[2] Fatih Univ, Sch Med, Dept Nephrol, Ankara, Turkey
[3] Fatih Univ, Sch Med, Dept Pathol, Ankara, Turkey
[4] Fatih Univ, Sch Med, Dept Pediat, Ankara, Turkey
[5] Gaziosmanpasa Univ, Sch Med, Dept Biochem, Tokat, Turkey
关键词
ischaemia/reperfusion injury; kidney; Nigella sativa oil; rat model;
D O I
10.1093/ndt/gfm953
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background: Renal ischaemia followed by reperfusion leads to acute renal failure in both native kidneys and renal allografts, which is a complex pathophysiologic process involving hypoxia and free radical (FR) damage. The oil of Nigella sativa (NSO) has been subjected to considerable pharmacological investigations that have revealed its antioxidant activity in different conditions. But there is no previously reported study about its effect on ischaemia/reperfusion (I/R) injury of kidneys. The aim of this study was to investigate the possible effects of NSO in I/R-induced renal injury in rats. Methods: Thirty healthy male Wistar albino rats were randomly assigned to one of the following groups: control, sham, I/R, NSO+I/R, I/R+NSO and NSO. I/R, NSO+I/R and I/R+NSO rats were subjected to bilateral renal ischaemia followed by reperfusion and then all the rats were killed and kidney function tests, serum and tissue oxidants and antioxidants were determined and histopathological examinations were performed. Results: Pre- and post-treatment with NSO produced reduction in serum levels of blood urea nitrogen (BUN) and creatinine caused by I/R and significantly improved serum enzymatic activities of superoxide dismutase (SOD) and glutathion peroxidase (GSH-Px) and also tissue enzymatic activities of catalase (CAT), SOD and GSH-Px. NSO treatment resulted in lower total oxidant status (TOS) and higher total antioxidant capacity (TAC) levels and also significant reduction in serum and tissue malondialdehyde (MDA), nitric oxide (NO) and protein carbonyl content (PCC) that were increased by renal I/R injury. The kidneys of untreated ischaemic rats had a higher histopathological score, while treatment with NSO nearly preserved the normal morphology of the kidney. Conclusions: In view of previous observations and our data, with the potent FR scavenger and antioxidant properties, NSO seems to be a highly promising agent for protecting tissues from oxidative damage and preventing organ damage due to renal I/R.
引用
收藏
页码:2206 / 2212
页数:7
相关论文
共 50 条
  • [31] Effects of aminoguanidine against renal ischaemia-reperfusion injury in rats
    Sahna, E
    Parlakpinar, H
    Cihan, OF
    Turkoz, Y
    Acet, A
    CELL BIOCHEMISTRY AND FUNCTION, 2006, 24 (02) : 137 - 141
  • [32] Effect of sevoflurane preconditioning on ischaemia/reperfusion injury in the rat kidney in vivo
    Obal, D
    Dettwiler, S
    Favoccia, C
    Rascher, K
    Preckel, B
    Schlack, W
    EUROPEAN JOURNAL OF ANAESTHESIOLOGY, 2006, 23 (04) : 319 - 326
  • [33] Downregulation of microRNA-29 by antisense inhibitors and a PPAR-γ agonist protects against myocardial ischaemia-reperfusion injury
    Ye, Yumei
    Hu, Zhaoyong
    Lin, Yu
    Zhang, Congfang
    Perez-Polo, Jose R.
    CARDIOVASCULAR RESEARCH, 2010, 87 (03) : 535 - 544
  • [34] Mycophenolate mofetil attenuates uterine ischaemia/reperfusion injury in a rat model
    Ersoy, Gulcin Sahin
    Eken, Meryem Kurek
    Cevik, Ozge
    Cilingir, Ozlem T.
    Tal, Reshef
    REPRODUCTIVE BIOMEDICINE ONLINE, 2017, 34 (02) : 115 - 123
  • [35] Dexmedetomidine protects against myocardial ischaemia/reperfusion-induced renal damage in rats
    Assad, Osama M.
    Labib, Dina A. Aly
    Rashed, Laila Ahmed
    EGYPTIAN JOURNAL OF ANAESTHESIA, 2018, 34 (01) : 33 - 39
  • [36] Biliverdin Protects against Liver Ischemia Reperfusion Injury in Swine
    Andria, Barbara
    Bracco, Adele
    Attanasio, Chiara
    Castaldo, Sigismondo
    Cerrito, Maria Grazia
    Cozzolino, Santolo
    Di Napoli, Daniele
    Giovannoni, Roberto
    Mancini, Antonio
    Musumeci, Antonino
    Mezza, Ernesto
    Nasti, Mario
    Scuderi, Vincenzo
    Staibano, Stefania
    Lavitrano, Marialuisa
    Otterbein, Leo E.
    Calise, Fulvio
    PLOS ONE, 2013, 8 (07):
  • [37] Montelukast protects against renal ischemia/reperfusion injury in rats
    Sener, Goksel
    Sehirli, Ozer
    Velioglu-Ogunc, Ayliz
    Cetinel, Sule
    Gedik, Nursal
    Caner, Metin
    Sakarcan, Abdullah
    Yegen, Berrak C.
    PHARMACOLOGICAL RESEARCH, 2006, 54 (01) : 65 - 71
  • [38] Prion Protein Protects against Renal Ischemia/Reperfusion Injury
    Zhang, Bo
    Cowden, Daniel
    Zhang, Fan
    Yuan, Jue
    Siedlak, Sandra
    Abouelsaad, Mai
    Zeng, Liang
    Zhou, Xuefeng
    O'Toole, John
    Das, Alvin S.
    Kofskey, Diane
    Warren, Miriam
    Bian, Zehua
    Cui, Yuqi
    Tan, Tao
    Kresak, Adam
    Wyza, Robert E.
    Petersen, Robert B.
    Wang, Gong-Xian
    Kong, Qingzhong
    Wang, Xinglong
    Sedor, John
    Zhu, Xiongwei
    Zhu, Hua
    Zou, Wen-Quan
    PLOS ONE, 2015, 10 (09):
  • [39] HGF-MSP chimera protects kidneys from ischemia-reperfusion injury
    Xue, Feng
    Isaka, Yoshitaka
    Takahara, Terumi
    Imamura, Ryoichi
    Suzuki, Chigure
    Ichimaru, Naotsugu
    Michieli, Paolo
    Takahara, Shiro
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 363 (02) : 451 - 456
  • [40] Carbamylated erythropoietin improves angiogenesis and protects the kidneys from ischemia-reperfusion injury
    Imamura, Ryoichi
    Okumi, Masayoshi
    Isaka, Yoshitaka
    Ichimaru, Naotsugu
    Moriyarna, Toshiki
    Imai, Enyu
    Nonomura, Norio
    Takahara, Shiro
    Okuyama, Akihiko
    CELL TRANSPLANTATION, 2008, 17 (1-2) : 135 - 141