CHARACTERIZATION OF THE PHARMACOLOGY AND REGIONAL DISTRIBUTION OF (S)-[H-3]-5-FLUOROWILLARDIINE BINDING IN RAT-BRAIN

被引:57
作者
HAWKINS, LM
BEAVER, KM
JANE, DE
TAYLOR, PM
SUNTER, DC
ROBERTS, PJ
机构
[1] UNIV BRISTOL,DEPT PHARMACOL,BRISTOL BS8 1TD,AVON,ENGLAND
[2] TOCRIS COOKSON LTD,BRISTOL BS18 7DY,AVON,ENGLAND
关键词
ALPHA-AMINO-3-HYDROXY-5-METHYL-4-ISOXAZOLEPROPIONIC ACID (AMPA) RECEPTOR; (S)-[H-3]-5-FLUOROWILLARDIINE; RAT BRAIN SYNAPTIC MEMBRANES; RECEPTOR AUTORADIOGRAPHY;
D O I
10.1111/j.1476-5381.1995.tb16408.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 This study examined the binding of the new radioligand (S)-[H-3]-5-fluorowillardiine to rat brain synaptic membranes. Specific binding represented greater than 80% of the total binding and was increased by 10% in the presence of 100 mM potassium thiocyanate (KSCN). 2 In the absence of KSCN, (S)-[H-3]-5-fluorowillardiine identified two binding sites with K-D1 = 22.5 nM, B-max1 = 1.4 pmol mg(-1) protein and K-D2 = 1.5 mu M, B-max2 = 10.8 pmol mg(-1) protein. In the presence of 100 mM KSCN the affinities of both the binding sites were increased, yielding values of K-D1 = 6.9 nM and K-D2 = 0.4 mu M KSCN was without effect on the B-max values. 3 (S)-[H-3]-5-fluorowillardiine binding was displaced by non-NMDA receptor ligands with the rank order of potency: 2,3-dihydroxy-6-nitro-7-sulphamoyl-benzo(F)quinoxaline (NBQX) > domoate > (S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazoleproionic acid (AMPA) approximate to L-glutamate > 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) > kainate >> (R)-5-fluorowillardiine. In contrast, both N-methyl-D-aspartate (NMDA) and the metabotropic glutamate receptor agonist, (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (ACPD) were inactive. 4 By use of quantitative autoradiography the regional distribution of (S)-[H-3]-5-fluorowillardiine binding in rat brain was assessed. The highest levels of binding were in the dentate gyrus and the CA1 region of the hippocampus. Lower levels of binding were detected in the cerebral cortex: olfactory system, lateral septum, caudate putamen and nucleus accumbens. 5 We conclude that the pharmacological profile and regional distribution of (S)-[H-3]-5-fluorowillardiine binding is consistent with its specific interaction with AMPA receptors. The advantages of high percentage specific binding and recognition of the two binding sites, in the absence of KSCN, suggest that (S)-[H-3]-5-fluorowillardiine may be the ligand of choice for the future study of AMPA receptors.
引用
收藏
页码:2033 / 2039
页数:7
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