Chronic administration of adenosine A3 receptor agonist and cerebral ischemia:: neuronal and glial effects

被引:51
作者
Von Lubitz, DKJE
Lin, RCS
Boyd, M
Bischofberger, N
Jacobson, KA
机构
[1] NIDDK, Mol Recognit Sect, NIH, Bethesda, MD USA
[2] Allegheny Univ Hlth Sci, Dept Anat & Neurobiol, Philadelphia, PA 19102 USA
[3] Gilead Sci Inc, Foster City, CA 94404 USA
关键词
ischemia; adenosine A(3) receptor; GFAP (glial fibrillary acidic protein); MAP-2 (microtubule associated protein); nitric oxide (NO); synthase; (gerbil);
D O I
10.1016/S0014-2999(98)00977-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have previously shown that chronic administration of the selective A, receptor agonist N-6-(3-iodobenzyl)-5'-N-methylcarboxoamidoadenosine (IB-MECA) leads to a significant improvement of postocclusive cerebral blood flow, and protects against neuronal damage and mortality induced by severe forebrain ischemia in gerbils. Using immunocytochemical methods we now show that chronic with IB-MECA results in a significant preservation of ischemia-sensitive microtubule associated protein 2 (MAP-2), enhancement of the expression of glial fibrillary acidic protein (GFAP), and a very intense depression of nitric oxide synthase in the brain of postischemic gerbils. These changes demonstrate that the cerebroprotective actions of chronically administered IB-MECA involve both neurons and glial cells, and indicate the possibility of distinct mechanisms that are affected in the course of chronic administration of the drug. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:157 / 163
页数:7
相关论文
共 42 条
[1]  
ABBRACCHIO MP, 1995, ADENOSINE AND ADENINE NUCLEOTIDES: FROM MOLECULAR BIOLOGY TO INTEGRATIVE PHYSIOLOGY, P271
[2]  
Abbracchio MP, 1995, MOL PHARMACOL, V48, P1038
[3]  
[Anonymous], 1974, STEREOTAXIC ATLAS MO, DOI DOI 10.1007/s00429-016-1259-0
[4]   NITRIC-OXIDE - AN ATTRACTIVE SIGNALING MOLECULE [J].
AOKI, E ;
TAKEUCHI, IK ;
SHOJI, R .
ACTA HISTOCHEMICA ET CYTOCHEMICA, 1995, 28 (02) :97-106
[5]  
CERUTI S, 1996, DRUG DEVELOP RES, V3, P177
[6]   DUAL ROLE OF NITRIC-OXIDE IN FOCAL CEREBRAL-ISCHEMIA [J].
DALKARA, T ;
YOSHIDA, T ;
IRIKURA, K ;
MOSKOWITZ, MA .
NEUROPHARMACOLOGY, 1994, 33 (11) :1447-1452
[7]   NITRIC-OXIDE MEDIATES GLUTAMATE NEUROTOXICITY IN PRIMARY CORTICAL CULTURES [J].
DAWSON, VL ;
DAWSON, TM ;
LONDON, ED ;
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (14) :6368-6371
[8]   AN ELEMENTARY INTRODUCTION TO STEREOLOGY (QUANTITATIVE MICROSCOPY) [J].
ELIAS, H ;
HYDE, DM .
AMERICAN JOURNAL OF ANATOMY, 1980, 159 (04) :411-446
[9]   EXPRESSION OF THE INDUCIBLE FORM OF NITRIC-OXIDE SYNTHASE BY REACTIVE ASTROCYTES AFTER TRANSIENT GLOBAL-ISCHEMIA [J].
ENDOH, M ;
MAIESE, K ;
WAGNER, J .
BRAIN RESEARCH, 1994, 651 (1-2) :92-100
[10]   THE NEURAL CELL SPECTRIN SKELETON - A REVIEW [J].
GOODMAN, SR ;
ZAGON, IS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 250 (03) :C347-C360