Neuroprotective effects of adenosine in cerebral ischemia, window of opportunity

被引:122
作者
Sweeney, MI [1 ]
机构
[1] UNIV SASKATCHEWAN, SASKATCHEWAN STROKE RES CTR, SASKATOON, SK S7N 5E5, CANADA
关键词
endogenous adenosine; adenosine deaminase inhibitors; adenosine uptake inhibitors; delayed neuronal death; hypoxic pre-conditioning; ischemia stroke; adenosine receptor desensitization; side effects; brain;
D O I
10.1016/S0149-7634(96)00011-5
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The inhibitory neuromodulator adenosine is neuroprotective against damage induced by cerebral ischemia. Its vasodilator effects add to its suitability as a possible anti-stroke agent, but also account for unwanted side effects following systemic administration of adenosine receptor agonists. ATP breakdown during ischemia produces adenosine which effluxes out of the neuron. This review will focus on endogenously produced adenosine and its subsequent protection against ischemia-induced neuronal damage in some stroke models, bur will also highlight possible disadvantages to increasing adenosine concentrations. In the advantages column, therapeutic benefits have been obtained by enhancing synaptic concentrations of endogenous adenosine using the adenosine uptake inhibitor propentofylline, but not dipyridamole. There is an emerging role for endogenous adenosine in preventing delayed cell death, e.g. following hypoxic pre-conditioning. One of the cons associated with enhancing the synaptic concentration of adenosine is the appearance of adenosine receptor desensitization over time. Thus, there is a therapeutic window of opportunity during which activation of an adenosine A(1) receptor is beneficial to an ischemic neuron. (C) 1997 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:207 / 217
页数:11
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