Ischemia-induced increase in long-term potentiation is warded off by specific calpain inhibitor PD 150606

被引:21
作者
Farkas, B
Tantos, A
Schlett, K
Világi, I
Friedrich, P
机构
[1] Eotvos Lorand Univ, Dept Physiol & Neurobiol, H-1117 Budapest, Hungary
[2] Hungarian Acad Sci, Biol Res Ctr, Inst Enzymol, H-1113 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
calpain inhibition; carotid ligation; cell culture; hippocampal slice; LTP; calpain activity;
D O I
10.1016/j.brainres.2004.07.059
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the present study, the effect of specific, membrane-permeable calpain inhibitor, PD150606, was analysed on synaptic efficacy in in vitro brain slices experiments after ischemic insult of rats in vivo, and on cell viability in a glutamate excitotoxicity test in mouse cell culture. Bilateral common carotid artery ligation (BCCL) for 24 h markedly increased calpain activity and enhanced LTP induction in rat hippocampus, although the CA1 layer significantly shrank. The enhancement of Up could be diminished by short-term application of PD150606 (40 muM) into the perfusion solution. Intracerebroventricular administration of PD150606 (100 muM) parallel with ischemic insult prevented UP and effectively inhibited hippocampal calpain activity. Intracerebroventricularly applied PD150606 inhibited the CA1 layer shrinkage after common carotid ligation. High level of exogenous glutamate caused marked decrease of cell viability in mouse cerebellar granule cell cultures, which could be partly warded off by 20 muM PD150606. Our data witness that calpain action is intricately involved in the regulation of synaptic efficacy. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:150 / 158
页数:9
相关论文
共 61 条
[1]   Models of brain injury and alterations in synaptic plasticity [J].
Albensi, BC .
JOURNAL OF NEUROSCIENCE RESEARCH, 2001, 65 (04) :279-283
[2]  
Alexa A, 1996, J NEUROSCI RES, V44, P438, DOI 10.1002/(SICI)1097-4547(19960601)44:5<438::AID-JNR4>3.0.CO
[3]  
2-G
[4]   Autolysis parallels activation of mu-calpain [J].
Baki, A ;
Tompa, P ;
Alexa, A ;
Molnar, O ;
Friedrich, P .
BIOCHEMICAL JOURNAL, 1996, 318 :897-901
[5]   POSTISCHEMIC ADMINISTRATION OF AK275, A CALPAIN INHIBITOR, PROVIDES SUBSTANTIAL PROTECTION AGAINST FOCAL ISCHEMIC BRAIN-DAMAGE [J].
BARTUS, RT ;
BAKER, KL ;
HEISER, AD ;
SAWYER, SD ;
DEAN, RL ;
ELLIOTT, PJ ;
STRAUB, JA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1994, 14 (04) :537-544
[6]   Calcium signalling: Dynamics, homeostasis and remodelling [J].
Berridge, MJ ;
Bootman, MD ;
Roderick, HL .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (07) :517-529
[7]   Developmental changes in calpain activity, GluR1 receptors and in the effect of kainic acid treatment in rat brain [J].
Bi, X ;
Chen, J ;
Baudry, M .
NEUROSCIENCE, 1997, 81 (04) :1123-1135
[8]   Regional distribution and time-course of calpain activation following kainate-induced seizure activity in adult rat brain [J].
Bi, XN ;
Chang, V ;
Siman, R ;
Tocco, G ;
Baudry, M .
BRAIN RESEARCH, 1996, 726 (1-2) :98-108
[9]   Calpain-mediated regulation of NMDA receptor structure and function [J].
Bi, XN ;
Rong, YQ ;
Chen, J ;
Dang, SD ;
Wang, Z ;
Baudry, M .
BRAIN RESEARCH, 1998, 790 (1-2) :245-253
[10]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3