Alkylxanthines as research tools

被引:47
作者
Daly, JW [1 ]
机构
[1] NIDDKD, Sect Pharmacodynam, Bioorgan Chem Lab, NIH, Bethesda, MD 20892 USA
来源
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM | 2000年 / 81卷 / 1-3期
关键词
caffeine; methylxanthines; pharmacological effects;
D O I
10.1016/S0165-1838(00)00110-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
(1) The methylxanthine caffeine has many pharmacological effects, most of which can be Linked to blockade of adenosine receptors, inhibition of phosphodiesterases, and augmentation of calcium-dependent release of calcium from intracellular stores. (2) A variety of xanthines have been developed as potent and/or selective antagonists for adenosine receptors. (3) Several xanthines have been developed that are more potent and more selective inhibitors of cyclic nucleotide phosphodiesterase than caffeine or theophylline. (4) Caffeine remains the xanthine of choice for activation of intracellular calcium-sensitive calcium release channels although millimolar concentrations are required, which can have effects on other aspects of calcium regulation. (C) 2000 Elsevier Science BN. All rights reserved.
引用
收藏
页码:44 / 52
页数:9
相关论文
共 105 条
[1]  
AKASU T, 1980, J PHARMACOL EXP THER, V213, P586
[2]  
ALI H, 1991, J PHARMACOL EXP THER, V258, P954
[3]   CAFFEINE-INDUCED TRANSMITTER RELEASE IS MEDIATED VIA RYANODINE-SENSITIVE CHANNEL [J].
AVIDOR, T ;
CLEMENTI, E ;
SCHWARTZ, L ;
ATLAS, D .
NEUROSCIENCE LETTERS, 1994, 165 (1-2) :133-136
[4]  
Baraldi PG, 1995, CURR MED CHEM, V2, P707
[5]  
BEAVO JA, 1970, MOL PHARMACOL, V6, P597
[6]   PRIMARY SEQUENCE OF CYCLIC-NUCLEOTIDE PHOSPHODIESTERASE ISOZYMES AND THE DESIGN OF SELECTIVE INHIBITORS [J].
BEAVO, JA ;
REIFSNYDER, DH .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1990, 11 (04) :150-155
[7]   EFFECT OF CAFFEINE ON RADIOCALCIUM MOVEMENT IN FROG SARTORIUS [J].
BIANCHI, CP .
JOURNAL OF GENERAL PHYSIOLOGY, 1961, 44 (05) :845-&
[8]   THE OPENING OF THE INOSITOL 1,4,5-TRISPHOSPHATE-SENSITIVE CA2+ CHANNEL IN RAT CEREBELLUM IS INHIBITED BY CAFFEINE [J].
BROWN, GR ;
SAYERS, LG ;
KIRK, CJ ;
MICHELL, RH ;
MICHELANGELI, F .
BIOCHEMICAL JOURNAL, 1992, 282 :309-312
[9]   ADENOSINE ANTAGONISM BY PURINES, PTERIDINES AND BENZOPTERIDINES IN HUMAN-FIBROBLASTS [J].
BRUNS, RF .
BIOCHEMICAL PHARMACOLOGY, 1981, 30 (04) :325-333
[10]   ADENOSINE RECEPTORS IN BRAIN MEMBRANES - BINDING OF N6-CYCLOHEXYL[H-3]ADENOSINE AND 1,3-DIETHYL-8-[H-3]PHENYLXANTHINE [J].
BRUNS, RF ;
DALY, JW ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (09) :5547-5551