Time-dependent impairment of mitochondrial function after storage and transplantation of rabbit kidneys

被引:41
作者
Sammut, IA
Burton, K
Balogun, E
Sarathchandra, P
Brooks, KJ
Bates, TE
Green, CJ
机构
[1] Northwick Pk Hosp & Clin Res Ctr, Northwick Pk Inst Med Res, Dept Surg Res, Harrow HA1 3UJ, Middx, England
[2] Univ London, Neurol Inst, Dept Neurochem, London WC1N 3BG, England
关键词
D O I
10.1097/00007890-200004150-00011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The mitochondrial respiratory chain is implicated as a major target of kidney damage after ischemia-reperfusion. This study measures changes in integrated mitochondrial function and in the activity of enzymes of the respiratory chain after cold storage and transplantation-reperfusion in vivo. Methods. Mitochondrial oxygen consumption and activities of respiratory chain enzymes and citrate synthase were measured in cortical mitochondria isolated from rabbit kidneys after 1-48 hr of cold ischemia with or without transplantation-reperfusion. Results. State 4 mitochondrial oxygen consumption was significantly increased after 48 hr of ischemia or 24-48 hr of ischemia with transplantation. Prolonged (24 or 48 hr) ischemic storage with and without transplantation caused a significant decrease in state 3 oxygen consumption, as did transplantation after 1, 24, and 48 hr of cold storage. Complex I and complex II-III activity decreased after 24 or 48 hr of ischemia, with transplantation having little additional effect. Complex IV activity was significantly decreased after 48 hr of ischemia, this decrease being exacerbated by transplantation-reperfusion. Complex V activity decreased significantly after 1 hr of ischemia and continued to decrease after 24-48 hr of ischemia. Transplantation after 1-24 hr (but not 48 hr) of ischemia resulted in partial recovery of complex V activity. Citrate synthase activity was decreased significantly only after 48 hr of:ischemia and reperfusion, consistent with the loss of mitochondrial membrane integrity seen in electron micrographs of the transplanted 48-hr group. Conclusions. These data suggest that individual rabbit kidney mitochondrial complexes have different susceptibilities to cold ischemic and reperfusion damage.
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页码:1265 / 1275
页数:11
相关论文
共 49 条
[1]  
ALLEN KL, 1995, J NEUROCHEM, V64, P2222
[2]  
ALMEIDA A, 1995, J NEUROCHEM, V65, P1698
[3]   Mitochondrial nitric oxide synthase: A ubiquitous regulator of oxidative phosphorylation? [J].
Bates, TE ;
Loesch, A ;
Burnstock, G ;
Clark, JB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 218 (01) :40-44
[4]   POSTNATAL-DEVELOPMENT OF THE COMPLEXES OF THE ELECTRON-TRANSPORT CHAIN IN ISOLATED RAT-BRAIN MITOCHONDRIA [J].
BATES, TE ;
ALMEIDA, A ;
HEALES, SJR ;
CLARK, JB .
DEVELOPMENTAL NEUROSCIENCE, 1994, 16 (5-6) :321-327
[5]  
BAUMANN M, 1989, MOL CELL BIOCHEM, V87, P137
[6]   In vivo heat shock protects rat myocardial mitochondria [J].
Bornman, L ;
Steinmann, CML ;
Gericke, GS ;
Polla, BS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 246 (03) :836-840
[7]   The mitochondrial membrane permeability transition induced by inorganic phosphate or inorganic arsenate. A comparative study [J].
Bravo, C ;
Chavez, E ;
Rodriguez, JS ;
MorenoSanchez, R .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1997, 117 (01) :93-99
[8]   Nitric oxide and peroxynitrite-dependent aconitase inactivation and iron-regulatory protein-1 activation in mammalian fibroblasts [J].
Castro, LA ;
Robalinho, RL ;
Cayota, A ;
Meneghini, R ;
Radi, R .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 359 (02) :215-224
[9]  
Cecka J M, 1995, Clin Transpl, P1
[10]  
Davey GP, 1996, J NEUROCHEM, V66, P1617