Early Detection of Metabolic Changes Using Microdialysis During and After Experimental Kidney Transplantation in a Porcine Model

被引:15
作者
Fonouni, Hamidreza [1 ]
Esmaeilzadeh, Majid [1 ]
Jarahian, Parvin [1 ]
Rad, Morva Tahmasbi [1 ]
Golriz, Mohammad [1 ]
Faridar, Alireza [1 ]
Hafezi, Mohammadreza [1 ]
Jafarieh, Shadi [1 ]
Kashfi, Arash [1 ]
Yazdi, Seid Hashem Fani [1 ]
Soleimani, Mehrdad [1 ]
Longerich, Thomas [2 ]
Shevchenko, Maxim [1 ]
Sakowitz, Oliver [3 ]
Schmidt, Jan [1 ]
Mehrabi, Arianeb [1 ]
机构
[1] Heidelberg Univ, Dept Gen Visceral & Transplantat Surg, Heidelberg, Germany
[2] Heidelberg Univ, Dept Pathol, D-6900 Heidelberg, Germany
[3] Heidelberg Univ, Dept Neurosurg, Heidelberg, Germany
关键词
kidney transplantation; microdialysis; metabolic changes; ISCHEMIA-REPERFUSION INJURY; EXCITATORY AMINO-ACIDS; WARM ISCHEMIA; INTRACEREBRAL MICRODIALYSIS; PHOSPHOLIPID DEGRADATION; LIVER-TRANSPLANTATION; GRAFT-SURVIVAL; RENAL ISCHEMIA; COLD-STORAGE; BRAIN;
D O I
10.1177/1553350610392063
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Microdialysis (MD) can detect organ-related metabolic changes before they become measurable in plasma through the biochemical parameters. This study aims to evaluate the early detection of metabolic changes during experimental kidney transplantation (KTx). Material and methods: During preparation of 8 donor kidneys, one MD catheter was inserted in the renal cortex and samples were collected. After a 6-hour cold ischemia time (CIT), kidneys were implanted in the 8 recipient pigs. Throughout the warm ischemia time (WIT) and after reperfusion, kidneys were monitored. The interstitial glucose, lactate, pyruvate, glutamate, and glycerol concentrations were evaluated. Results: A significant decline in glucose level was observed at the end of CIT. The lactate level was reduced to the minimum point of 0.35 +/- 0.08 mmol/L in CIT. After reperfusion, lactate values raised significantly. During the WIT, the pyruvate level increased, continued until the end of the WIT. For glutamate, a steady increase was noted during explantation, CIT, WIT, and early reperfusion phases. The increase of glycerol value continued in the early postreperfusion, which was then followed by a sharp decline. Conclusion: MD is a fast and simple minimally invasive method for measurement of metabolic substrates in renal parenchyma during KTx. MD offers the option of detecting minor changes of interstitial glucose, lactate, pyruvate, glutamate, and glycerol in every stage of KTx. Through the use of MD, metabolic changes can be continuously monitored during the entire procedure of KTx.
引用
收藏
页码:321 / 328
页数:8
相关论文
共 40 条
[1]   ESTIMATION OF RENAL INTERSTITIAL ADENOSINE AND PURINE METABOLITES BY MICRODIALYSIS [J].
BARANOWSKI, RL ;
WESTENFELDER, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (01) :F174-F182
[2]   Microdialysis assessment of shock wave lithotripsy-induced renal injury [J].
Brown, SA ;
Munver, R ;
Delvecchio, FC ;
Kuo, RL ;
Zhong, P ;
Preminger, GM .
UROLOGY, 2000, 56 (03) :364-368
[3]  
CHAN PH, 1984, FED PROC, V43, P210
[4]   PHOSPHOLIPID DEGRADATION AND CELLULAR EDEMA INDUCED BY FREE-RADICALS IN BRAIN CORTICAL SLICES [J].
CHAN, PH ;
YURKO, M ;
FISHMAN, RA .
JOURNAL OF NEUROCHEMISTRY, 1982, 38 (02) :525-531
[5]  
Daemen J-WUC, 1995, TRANSPLANT REV, V9, P159
[6]  
Gutierrez A, 1999, EUR J CLIN INVEST, V29, P947
[7]   ISCHEMIA-INDUCED SHIFT OF INHIBITORY AND EXCITATORY AMINO-ACIDS FROM INTRACELLULAR TO EXTRACELLULAR COMPARTMENTS [J].
HAGBERG, H ;
LEHMANN, A ;
SANDBERG, M ;
NYSTROM, B ;
JACOBSON, I ;
HAMBERGER, A .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1985, 5 (03) :413-419
[8]   Neurochemical monitoring of the acutely injured human brain [J].
Hillered, L ;
Persson, L .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1999, 59 :9-18
[9]   Interstitial glycerol as a marker for membrane phospholipid degradation in the acutely injured human brain [J].
Hillered, L ;
Valtysson, J ;
Enblad, P ;
Persson, L .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1998, 64 (04) :486-491
[10]   THE NEUROCHEMICAL AND METABOLIC CASCADE FOLLOWING BRAIN INJURY - MOVING FROM ANIMAL-MODELS TO MAN [J].
HOVDA, DA ;
LEE, SM ;
SMITH, ML ;
VONSTUCK, S ;
BERGSNEIDER, M ;
KELLY, D ;
SHALMON, E ;
MARTIN, N ;
CARON, M ;
MAZZIOTTA, J ;
PHELPS, M ;
BECKER, DP .
JOURNAL OF NEUROTRAUMA, 1995, 12 (05) :903-906