Further pharmacological characterization of the adenosine receptor subtype mediating inhibition of oxidative burst in human isolated neutrophils
- 1 April 1998
- journal article
- research article
- Published by Wiley in Drug Development Research
- Vol. 43 (4) , 214-224
- https://doi.org/10.1002/(sici)1098-2299(199804)43:4<214::aid-ddr5>3.0.co;2-l
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- Activation of adenosine A3 receptors on macrophages inhibits tumor necrosis factor-αEuropean Journal of Pharmacology, 1996
- 2-Chloroadenosine Inhibits the MHC-Unrestricted Cytolytic Activity of Anti-CD3-Activated Killer Cells: Evidence for the Involvement of a Non-A1/A2 Cell-Surface Adenosine ReceptorCellular Immunology, 1994
- Cloned adenosine A3 receptors: Pharmacological properties, species differences and receptor functionsTrends in Pharmacological Sciences, 1994
- Binding of the Adenosine A2 Receptor Ligand [3H]CGS 21680 to Human and Rat Brain: Evidence for Multiple Affinity SitesJournal of Neurochemistry, 1990
- The adenosine/neutrophil paradox resolved: human neutrophils possess both A1 and A2 receptors that promote chemotaxis and inhibit O2 generation, respectively.Journal of Clinical Investigation, 1990
- Adenosine promotes neutrophil chemotaxis.The Journal of Experimental Medicine, 1988
- Adenosine A1 receptors in mammalian brain: Species differences in their interactions with agonists and antagonistsDrug Development Research, 1986
- [3H]Adenosine binding to rat mast cells — pharmacologic and functional characterizationInflammation Research, 1985
- 1,3-Dialkyl-8-(p-sulfophenyl)xanthines: potent water-soluble antagonists for A1- and A2-adenosine receptorsJournal of Medicinal Chemistry, 1985
- Adenosine: a physiological modulator of superoxide anion generation by human neutrophils.The Journal of Experimental Medicine, 1983