Consequences of transient focal cerebral ischaemia for second messenger and neurotransmitter binding in the rat: Quantitative autoradiographic analysis of forskolin, dopamine D-1 receptor binding and cerebral blood flow changes

被引:7
作者
Gartshore, G
Dawson, D
Patterson, J
Macrae, IM
机构
[1] UNIV GLASGOW,HUGH FRASER NEUROSCI LABS,GLASGOW G61 1QH,LANARK,SCOTLAND
[2] SO GEN HOSP,INST NEUROL SCI,DEPT CLIN PHYS,GLASGOW G51 4TF,LANARK,SCOTLAND
基金
英国惠康基金;
关键词
endothelin; HMPAO; iodoantipyrine; cerebral blood flow; receptor binding;
D O I
10.1111/j.1460-9568.1996.tb01232.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In order to study the consequences of reperfusion for ischaemic brain injury, quantitative ligand binding autoradiography was carried out in a model of reversible focal cerebral ischaemia. Endothelin-l applied to the abluminal surface of the middle cerebral artery in anaesthetized Sprague-Dawley rats induced severe focal ischaemia and subsequent reperfusion (assessed by blood flow tracers [Tc-99m]HMpAO and [C-14]iodoantipyrine respectively) by 2 h after insult. Ligand binding autoradiography on consecutive sections demonstrated these blood flow changes to be associated with a significant reduction in forskolin binding throughout the middle cerebral artery territory (e.g. 25% in parietal cortex, 11% in dorsolateral caudate nucleus). The most marked losses in forskolin binding were in areas where ischaemia was severe and reperfusion was poor, However, the same changes in cerebral blood flow had no significant effect on D-1 dopamine receptor binding (e,g. <2% reduction in the caudate nucleus). These data demonstrate that ligand binding characteristics are significantly affected as early as 2 h after insult, with evidence of differential sensitivity for forskolin and D-1 dopamine binding. With regard to the consequences of reperfusion, comparison with our previous study of 2 h maintained ischaemia demonstrates reperfusion-related salvage of dopamine and forskolin binding in the caudate nucleus but possible exacerbation of forskolin binding loss in the cortex.
引用
收藏
页码:486 / 493
页数:8
相关论文
共 42 条
[1]  
ANDERSEN A R, 1989, Cerebrovascular and Brain Metabolism Reviews, V1, P288
[2]   POSTISCHEMIC ALTERATION OF [H-3] FORSKOLIN BINDING-SITES IN SELECTIVELY VULNERABLE AREAS - AN AUTORADIOGRAPHIC STUDY OF GERBIL BRAIN [J].
ARAKI, T ;
KATO, H ;
HARA, H ;
KOGURE, K .
NEUROSCIENCE LETTERS, 1991, 125 (02) :159-162
[3]   GRADED BIOASSAY FOR DEMONSTRATION OF BRAIN RESCUE FROM EXPERIMENTAL ACUTE-ISCHEMIA IN RATS [J].
ARONOWSKI, J ;
OSTROW, P ;
SAMWAYS, E ;
STRONG, R ;
ZIVIN, JA ;
GROTTA, JC .
STROKE, 1994, 25 (11) :2235-2240
[4]   HUMAN CDNA CLONES FOR 4 SPECIES OF G-ALPHA-S SIGNAL TRANSDUCTION PROTEIN [J].
BRAY, P ;
CARTER, A ;
SIMONS, C ;
GUO, V ;
PUCKETT, C ;
KAMHOLZ, J ;
SPIEGEL, A ;
NIRENBERG, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (23) :8893-8897
[5]   PROTECTIVE EFFECT OF CYCLOHEXYLADENOSINE ON ADENOSINE-A1-RECEPTORS, GUANINE-NUCLEOTIDE AND FORSKOLIN BINDING-SITES FOLLOWING TRANSIENT BRAIN ISCHEMIA - A QUANTITATIVE AUTORADIOGRAPHIC STUDY [J].
DAVAL, JL ;
VONLUBITZ, DKJE ;
DECKERT, J ;
REDMOND, DJ ;
MARANGOS, PJ .
BRAIN RESEARCH, 1989, 491 (02) :212-226
[6]   ANTIISCHEMIC EFFICACY OF A NITRIC-OXIDE SYNTHASE INHIBITOR AND A N-METHYL-D-ASPARTATE RECEPTOR ANTAGONIST IN MODELS OF TRANSIENT AND PERMANENT FOCAL CEREBRAL-ISCHEMIA [J].
DAWSON, DA ;
GRAHAM, DI ;
MCCULLOCH, J ;
MACRAE, IM .
BRITISH JOURNAL OF PHARMACOLOGY, 1994, 113 (01) :247-253
[7]   AUTORADIOGRAPHIC EVALUATION OF FORSKOLIN AND D1-DOPAMINE RECEPTOR-BINDING IN A RAT MODEL OF FOCAL CEREBRAL-ISCHEMIA [J].
DAWSON, DA ;
ROBINSON, MJ ;
MACRAE, IM ;
REID, JL ;
MCCULLOCH, J .
BRAIN RESEARCH, 1992, 577 (02) :210-217
[8]  
DAWSON DA, 1995, NEUROSCI LETT, V185, P1
[9]  
DRINNAN S L, 1991, Molecular and Cellular Neuroscience, V2, P66, DOI 10.1016/1044-7431(91)90040-U
[10]   NEURONAL NECROSIS AFTER MIDDLE CEREBRAL-ARTERY OCCLUSION IN WISTAR RATS PROGRESSES AT DIFFERENT TIME INTERVALS IN THE CAUDOPUTAMEN AND THE CORTEX [J].
GARCIA, JH ;
LIU, KF ;
HO, KL .
STROKE, 1995, 26 (04) :636-642