Hemorheological changes in patients with living-donor renal transplantation

被引:9
作者
Du, Yuan [1 ]
Yao, Weijuan [2 ]
Qian, Yeyong [3 ]
Han, Mengxia [3 ]
Wen, Zongyao [2 ]
Ma, Lulin [1 ]
机构
[1] Peking Univ Third Hosp, Dept Urol, Beijing 100191, Peoples R China
[2] Peking Univ, Dept Biophys, Hlth Sci Ctr, Hemorheol Ctr, Beijing 100191, Peoples R China
[3] 309th Hosp PLA, Dept Urol, Beijing, Peoples R China
基金
美国国家科学基金会;
关键词
Living-donor renal transplantation; Hemorheology; Erythrocyte membrane protein; BLOOD-CELL-DEFORMABILITY; ERYTHROCYTE-MEMBRANE; OSMOTIC FRAGILITY; UREMIC PATIENTS; FAILURE; DIALYSIS; MICROCIRCULATION; AGGREGATION; THROMBOSIS; VISCOSITY;
D O I
10.3233/CH-2010-1381
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Living-donor renal transplantation is the preferred treatment for patients with end stage renal disease since it affords earlier transplantation and better graft for long term survival. The aim of the present study was to explore the hemorheological changes in patients undergone living-donor renal transplantation. We investigated the dynamic changes in the hemorheological properties of blood taken from the patients before renal transplantation and at 1 week, 2 week, 3 week and >1 month after the operation. As compared with pre-operation, the whole blood viscosity at different shear rates decreased significantly; the erythrocyte aggregation index decreased; the erythrocyte deformation index (DI) and integrated deformation index (IDI) had a remarkable improvement; the erythrocyte electrophoresis rate was rasied. We also found that the osmotic fragility of RBCs at 145 mOsm/kg was greatly decreased after renal transplantation. Importantly, the ratio of erythrocyte membrane protein 4.1a to 4.1b decreased, which may explain the changes in DI, IDI, and osmotic fragility. Our results suggest that these hemorheological changes may greatly improve the organ microcirculation, which would play a critical role in reduce the ischemia-reperfusion injury in the graft.
引用
收藏
页码:199 / 209
页数:11
相关论文
共 41 条
[1]  
BAREFORD D, 1986, CLIN HEMORHEOL, V6, P501
[2]   New guidelines for hemorheological laboratory techniques [J].
Baskurt, Oguz K. ;
Boynard, Michel ;
Cokelet, Giles C. ;
Connes, Philippe ;
Cooke, Brian M. ;
Forconi, Sandro ;
Liao, Fulong ;
Hardeman, Max R. ;
Jung, Friedrich ;
Meiselman, Herbert J. ;
Nash, Gerard ;
Nemeth, Norbert ;
Neu, Bjoern ;
Sandhagen, Bo ;
Shin, Sehyun ;
Thurston, George ;
Wautier, Jean Luc .
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2009, 42 (02) :75-97
[3]   Elastase, myeloperoxidase, nitric oxide metabolites and oxidative status in subjects with clinical stable chronic renal failure on conservative treatment [J].
Caimi, Gregorio ;
Carollo, Caterina ;
Montana, Maria ;
Vaccaro, Francesco ;
Lo Presti, Rosalia .
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2009, 43 (03) :251-256
[4]  
Cicco G, 2005, ADV EXP MED BIOL, V566, P363
[5]   An overview about erythrocyte membrane [J].
de Oliveira, Sofia ;
Saldanha, Carlota .
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2010, 44 (01) :63-74
[6]  
DOCCI D, 1985, CLIN NEPHROL, V23, P68
[7]  
DORINI S, 1997, 10 EUR C CLIN HAEM L
[8]  
DUCHESNEGUEGUEN M, 1988, CLIN HEMORHEOL, V8, P407
[9]   Influence of non-Newtonian behavior of blood on flow in an elastic artery model [J].
Dutta, A ;
Tarbell, JM .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1996, 118 (01) :111-119
[10]   ELECTROPHORETIC ANALYSIS OF MAJOR POLYPEPTIDES OF HUMAN ERYTHROCYTE MEMBRANE [J].
FAIRBANKS, G ;
STECK, TL ;
WALLACH, DFH .
BIOCHEMISTRY, 1971, 10 (13) :2606-+