Luteolin Treatment Protects against Renal Ischemia-Reperfusion Injury in Rats

被引:51
作者
Hong, Xin [1 ]
Zhao, Xiaojing [1 ]
Wang, Gang [1 ]
Zhang, Zhengliang [1 ]
Pei, Honghong [1 ]
Liu, Zhong [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Emergency Med, Affiliated Hosp 2, Xian 710004, Shaanxi, Peoples R China
关键词
ENDOPLASMIC-RETICULUM STRESS; OXIDATIVE STRESS; ISCHEMIA/REPERFUSION INJURY; INDUCED NEPHROTOXICITY; KIDNEY; APOPTOSIS; PATHOPHYSIOLOGY; INFLAMMATION; NEUTROPHILS; INHIBITION;
D O I
10.1155/2017/9783893
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Renal ischemia-reperfusion (I/R) injury is a common but severe scientific problem. Luteolin has great anti-inflammatory and antioxidant effects. In this study, we studied the effect of luteolin on renal I/R injury in rats. Intragastric administration of luteolin or saline was performed in Sprague-Dawley rats before (40 mg/kg for three days) and after (one day) renal I/R modeling. Kidney and blood samples were harvested to detect the severity of renal injury 24 hours after operation. The results showed that luteolin-treated rats exhibited milder histomorphological changes with lower scores of renal histological lesions; lower blood urea nitrogen and creatinine levels; lower renal malondialdehyde (MDA), 8-oxo-deoxyguanosine (8-OHdG), and myeloperoxidase (MPO) levels; and higher superoxide dismutase (SOD) and catalase (CAT) activities in the kidney. Luteolin attenuated the increased levels of serum and renal tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, and IL-6, renal high mobility group box-1 (HMGB1), and nuclear factor kappa beta (NF-kappa B) expression levels in I/R rats. Furthermore, luteolin treatment significantly reduced renal cell apoptosis and endoplasmic reticulum (ER) stress caused by renal I/R injury. In conclusion, luteolin improved renal function in I/R rats by reducing oxidative stress, neutrophil infiltration, inflammation, renal cell apoptosis, and expression of HMGB1 and NF-kappa B, and ER stress.
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页数:10
相关论文
共 40 条
[1]   Luteolin ameliorates colistin-induced nephrotoxicity in the rat models [J].
Arslan, Birsen Yigit ;
Arslan, Ferhat ;
Erkalp, Kerem ;
Alagol, Aysin ;
Sevdi, Mehmet Salih ;
Yildiz, Gunes ;
Kucuk, Suat Hayri ;
Altinay, Serdar .
RENAL FAILURE, 2016, 38 (10) :1735-1740
[2]   Endoplasmic reticulum stress [J].
Banhegyi, Gabor ;
Baumeister, Peter ;
Benedetti, Angelo ;
Dong, Dezheng ;
Fu, Yong ;
Lee, Amy S. ;
Li, Jianze ;
Mao, Changhui ;
Margittai, Eva ;
Ni, Min ;
Paschen, Wulf ;
Piccirella, Simona ;
Senesi, Silvia ;
Sitia, Roberto ;
Wang, Miao ;
Yang, Wei .
STRESS RESPONSES IN BIOLOGY AND MEDICINE: STRESS OF LIFE IN MOLECULES, CELLS, ORGANISMS, AND PSYCHOSOCIAL COMMUNITIES, 2007, 1113 :58-71
[3]   Neutrophils in acute kidney injury: not neutral any more [J].
Bolisetty, Subhashini ;
Agarwal, Anupam .
KIDNEY INTERNATIONAL, 2009, 75 (07) :674-676
[4]   In vivo transfection of NF-κB decoy oligodeoxynucleotides attenuate renal ischemia/reperfusion injury in rats [J].
Cao, CC ;
Ding, XQ ;
Ou, ZL ;
Liu, CF ;
Li, P ;
Wang, L ;
Zhu, CF .
KIDNEY INTERNATIONAL, 2004, 65 (03) :834-845
[5]   Luteolin exhibits anti-inflammatory effects by blocking the activity of heat shock protein 90 in macrophages [J].
Chen, Dan ;
Bi, Aijing ;
Dong, Xiaoliang ;
Jiang, Yi ;
Rui, Bing ;
Liu, Jinjiao ;
Yin, Zhimin ;
Luo, Lan .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2014, 443 (01) :326-332
[6]   The role of high mobility group box 1 (HMGB1) in the pathogenesis of kidney diseases [J].
Chen, Qingjie ;
Guan, Xiaofeng ;
Zuo, Xiaocong ;
Wang, Jianglin ;
Yin, Wenjun .
ACTA PHARMACEUTICA SINICA B, 2016, 6 (03) :183-188
[7]  
Daemen MARC, 2002, TRANSPLANTATION, V73, P1693
[8]   Luteolin ameliorates cisplatin-induced nephrotoxicity in mice through inhibition of platinum accumulation, inflammation and apoptosis in the kidney [J].
Domitrovic, Robert ;
Cvijanovic, Olga ;
Pugel, Ester Pernjak ;
Zagorac, Gordana Blagojevic ;
Mahmutefendic, Hana ;
Skoda, Marko .
TOXICOLOGY, 2013, 310 :115-123
[9]   Dose- and time-dependent effects of luteolin on carbon tetrachloride-induced hepatotoxicity in mice [J].
Domitrovic, Robert ;
Jakovac, Hrvoje ;
Milin, Cedomila ;
Radosevic-Stasic, Biserka .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2009, 61 (06) :581-589
[10]   eNOS/iNOS and endoplasmic reticulum stress-induced apoptosis in the placentas of patients with preeclampsia [J].
Du, L. ;
He, F. ;
Kuang, L. ;
Tang, W. ;
Li, Y. ;
Chen, D. .
JOURNAL OF HUMAN HYPERTENSION, 2017, 31 (01) :49-55