Danshen protects kidney grafts from ischemia/reperfusion injury after experimental transplantation

被引:14
作者
Guan, Xiaohai [1 ]
Dei-Anane, Genevieve [1 ]
Bruns, Helge [1 ]
Chen, Jing [2 ]
Nickkholgh, Arash [1 ]
Liang, Rui [1 ]
Gross, Marie-Luise [3 ]
Kern, Michael [3 ]
Ludwig, Jochen [4 ]
Buechler, Markus W. [1 ]
Schemmer, Peter [1 ]
机构
[1] Univ Heidelberg, Dept Gen Surg, D-69120 Heidelberg, Germany
[2] Univ Heidelberg, Dept Clin Neurobiol, D-69120 Heidelberg, Germany
[3] Univ Heidelberg, Dept Pathol, D-69120 Heidelberg, Germany
[4] Univ Heidelberg, Dept Internal Med & Clin Chem 1, D-69120 Heidelberg, Germany
关键词
anti-oxidation; apoptosis; cold storage; Danshen; kidney transplantation; regeneration; reperfusion injury; tubular damage; TUMOR-NECROSIS-FACTOR; ACUTE-RENAL-FAILURE; NITRIC-OXIDE; SALVIAE-MILTIORRHIZAE; REPERFUSION INJURY; RAT-KIDNEY; LIVER-TRANSPLANTATION; TAURINE PROTECTS; KUPFFER CELLS; ISCHEMIA;
D O I
10.1111/j.1432-2277.2008.00770.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Danshen (DS) is used for treatment of various ischemic events in the traditional Chinese medicine. Hence, this study was designed to investigate its effect on ischemia/reperfusion injury (IRI) after experimental kidney transplantation (eKTx). Nephrectomized Sprague-Dawley rats underwent eKTx. Some animals were infused with 1.5 ml DS 10 min before surgery. Kidney grafts were transplanted after cold storage for 20 h in Histidine-Tryptophane-Ketoglutarate solution. After reperfusion blood samples were collected for blood urinary nitrogen (BUN), creatinine, lactate dehydrogenase (LDH), and alanine transaminase. Further, tissue was assessed for morphologic and pathophysiologic changes. Donor preconditioning with DS (DS-d) significantly decreased BUN, creatinine, LDH, and aspartate aminotransferase to 65-97% of controls while preconditioning of the recipient (DS-r) decreased values to 58-82% (P < 0.05). Tubular damage and caspase-3 decreased significantly in both DS-d and DS-r (DS-d: 96% and 67%, DS-r: 83% and 75% of controls) while heat shock protein 72 and superoxide dismutase increased significantly (DS-d: 143% and 173%, DS-r: 166% and 194% of controls). Further, inducible nitric oxide synthase and tumor necrosis factor-alpha decreased (DS-d: 84% and 61%, DS-r: 79% and 67% of controls) after DS. Preconditioning of both donors and recipients with DS significantly reduces IRI and thus improves graft function after eKTx.
引用
收藏
页码:232 / 241
页数:10
相关论文
共 47 条
[1]  
Bergmeyer HU., 1988, METHODS ENZYMATIC AN
[2]   PASSIVE-IMMUNIZATION AGAINST CACHECTIN TUMOR NECROSIS FACTOR PROTECTS MICE FROM LETHAL EFFECT OF ENDOTOXIN [J].
BEUTLER, B ;
MILSARK, IW ;
CERAMI, AC .
SCIENCE, 1985, 229 (4716) :869-871
[3]   ENDOTHELIAL-LEUKOCYTE ADHESION MOLECULES IN HUMAN-DISEASE [J].
BEVILACQUA, MP ;
NELSON, RM ;
MANNORI, G ;
CECCONI, O .
ANNUAL REVIEW OF MEDICINE, 1994, 45 :361-378
[4]   Gene transfer-induced local heme oxygenase-1 overexpression protects rat kidney transplants from ischemia/reperfusion injury [J].
Blydt-Hansen, TD ;
Katori, M ;
Lassman, C ;
Ke, B ;
Coito, AJ ;
Iyer, S ;
Ettenger, R ;
Busuttil, RW ;
Kupiec-Weglinski, JW ;
Buelow, R .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (03) :745-754
[5]  
CANADA A T, 1986, Journal of Free Radicals in Biology and Medicine, V2, P327, DOI 10.1016/S0748-5514(86)80032-0
[6]  
CAO T, 1999, CHIN J ULTRASON MED, V15, P457
[7]  
Chang TH, 2002, ACTA PHARMACOL SIN, V23, P769
[8]   Inhibition of inducible nitric oxide synthase reduces renal ischemia/reperfusion injury [J].
Chatterjee, PK ;
Patel, NSA ;
Kvale, EO ;
Cuzzocrea, S ;
Brown, PAJ ;
Stewart, KN ;
Mota-Filipe, H ;
Thiemermann, C .
KIDNEY INTERNATIONAL, 2002, 61 (03) :862-871
[9]   Calpain inhibitor-1 reduces renal ischemia/reperfusion injury in the rat [J].
Chatterjee, PK ;
Brown, PAJ ;
Cuzzocrea, S ;
Zacharowski, K ;
Stewart, KN ;
Mota-Filipe, H ;
McDonald, MC ;
Thiemermann, C .
KIDNEY INTERNATIONAL, 2001, 59 (06) :2073-2083
[10]  
CHUNG HY, 1986, CHEM PHARM BULL, V34, P3818