Evidence for a protective role played by the Na+/Ca2+ exchanger in cerebral ischemia induced by middle cerebral artery occlusion in male rats

被引:82
作者
Pignataro, G
Tortiglione, A
Scorziello, A
Giaccio, L
Secondo, A
Severino, B
Santagada, V
Caliendo, G
Amoroso, S
Di Renzo, G
Annunziato, L
机构
[1] Univ Naples Federico II, Dept Neurosci, Div Pharmacol, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dept Toxicol & Pharmaceut Chem, I-80131 Naples, Italy
关键词
Na+/Ca2+ exchanger; focal ischemia; pMCAO; Fe3+ ion; XIP; CB-DMB;
D O I
10.1016/j.neuropharm.2003.09.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the present paper, the role played by Na+/Ca2+ exchanger (NCX) in focal cerebral ischemia was investigated. To this aim, permanent middle cerebral artery occlusion (pMCAO) was performed in male rats. The effects on the infarct volume of some inhibitors, such as tyrosine-6 glycosylated form of the exchanger inhibitory peptide (GLU-XIP), benzamil derivative (CB-DMB) and diarylaminopropylamine derivative (bepridil), and of the NCX activator, FeCl3, were examined. FeCl3, CB-DMB, bepridil and GLU-XIP, a modified peptide synthesized in our laboratory in order to facilitate its entrance into the cells through the glucose transporter, were intracerebroventricularly (icv) infused. FeCl3 (10 mug/kg) was able to reduce the extenson of brain infarct volume. This effect was counteracted by the concomitant icv administration of CB-DMB (120 mug/kg). All NCX inhibitors, GLU-XIP, CB-DMB and bepridil, caused a worsening of the brain infarct lesion. These results suggest that a stimulation of NCX activity may help neurons and glial cells that are not irreversibly damaged in the penumbral zone to survive, whereas its pharmacological blockade can compromise their survival. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:439 / 448
页数:10
相关论文
共 37 条
[1]  
AMOROSO S, 1993, J PHARMACOL EXP THER, V264, P515
[2]   Pharmacological evidence that the activation of the Na+-Ca2+ exchanger protects C6 glioma cells during chemical hypoxia [J].
Amoroso, S ;
DeMaio, M ;
Russo, GM ;
Catalano, A ;
Bassi, A ;
Montagnani, S ;
DiRenzo, G ;
Annunziato, L .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (02) :303-309
[3]   Sodium nitroprusside prevents chemical hypoxia-induced cell death through iron ions stimulating the activity of the Na+-Ca2+ exchanger in C6 glioma cells [J].
Amoroso, S ;
Tortiglione, A ;
Secondo, A ;
Catalano, A ;
Montagnani, S ;
Di Renzo, G ;
Annunziato, L .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (04) :1505-1513
[4]   INHIBITION OF NA+/CA2+ EXCHANGE ENHANCES DELAYED NEURONAL DEATH ELICITED BY GLUTAMATE IN CEREBELLAR GRANULE CELL-CULTURES [J].
ANDREEVA, N ;
KHODOROV, B ;
STELMASHOOK, E ;
CRAGOE, E ;
VICTOROV, I .
BRAIN RESEARCH, 1991, 548 (1-2) :322-325
[5]   THRESHOLDS IN CEREBRAL-ISCHEMIA - THE ISCHEMIC PENUMBRA [J].
ASTRUP, J ;
SIESJO, BK ;
SYMON, L .
STROKE, 1981, 12 (06) :723-725
[6]   EVALUATION OF 2, 3, 5-TRIPHENYLTETRAZOLIUM CHLORIDE AS A STAIN FOR DETECTION AND QUANTIFICATION OF EXPERIMENTAL CEREBRAL INFARCTION IN RATS [J].
BEDERSON, JB ;
PITTS, LH ;
GERMANO, SM ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, HM .
STROKE, 1986, 17 (06) :1304-1308
[7]   Sodium calcium exchange: Its physiological implications [J].
Blaustein, MP ;
Lederer, WJ .
PHYSIOLOGICAL REVIEWS, 1999, 79 (03) :763-854
[8]   IN-VIVO DETECTION OF SUPEROXIDE ANION PRODUCTION BY THE BRAIN USING A CYTOCHROME-C ELECTRODE [J].
FABIAN, RH ;
DEWITT, DS ;
KENT, TA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1995, 15 (02) :242-247
[9]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[10]   A novel isothiourea derivative selectively inhibits the reverse mode of Na+/Ca2+ exchange in cells expressing NCX1 [J].
Iwamoto, T ;
Watano, T ;
Shigekawa, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (37) :22391-22397