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Department of Medicine, University of Virginia, Charlottesville, Virginia
Received February 3, 2005; accepted February 9, 2005
| Abstract |
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| Increases in Oxygen Supply/Demand Ratio |
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| Ischemic Preconditioning and Postconditioning |
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Anti-Inflammatory Responses. Many recent studies indicate that adenosine acting on A2A receptors can powerfully inhibit inflammation and reperfusion injury. The A2A adenosine receptor is found on most bone-marrowderived cells and produces cellular effects that in general inhibit inflammation. The cellular responses seem to be mediated predominately by cyclic AMP and result in inhibition of oxidative burst in neutrophils (Fredholm et al., 1996
), reduced TNF
release by monocytes (Link et al., 2000
), reduced platelet activation (Hourani, 1996
), and inhibition of lymphocyte activation (Lappas et al., 2005
). In aggregate, these responses prevent the release of pro-inflammatory cytokines and oxygen radicals, prevent endothelial cell activation, and greatly reduce microvascular occlusion, which can exacerbate tissue injury during reperfusion of previously ischemic tissues.
A2B Receptors are Proinflammatory. Both A2A and A2B receptors couple to the heterotrimeric G protein, Gs; in many cell types, however, A2B receptors have been found to be dually coupled to Gs and Gq. Signaling through Gq results in calcium mobilization and activation of phospholipase C and mitogen-activated protein kinase (Gao et al., 1999
). This signaling pathway seems to be responsible for pro-inflammatory actions of adenosine mediated by A2B receptors that results in facilitation by adenosine of antigen-induced deregulation of canine or human but not rodent mast cells (Feoktistov and Biaggioni, 1995
; Auchampach et al., 1997
). In addition, activation of A2B receptors has been shown to increase the release of interleukin 6 from epithelial cells, astrocytes, and fibroblasts (Schwaninger et al., 1997
; Sitaraman et al., 2001
; Zhong et al., 2005
). Hence, the activation of adenosine receptors is not invariably protective of tissues. In fact, A2B blockers may be useful as anti-inflammatory agents.
| Angiogenesis |
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| Conclusion |
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| Footnotes |
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Please see the related article on page page 1406.
ABBREVIATIONS: ZM241385, 4-{2-[7-amino-2-(2-furyl)[1,2,4]triazolo-[2,3-a][1,3,5]triazin-5-ylamino]ethyl}phenol.
Address correspondence to: Dr. Joel Linden, Department of Medicine, University of Virginia, Charlottesville, VA 22908. E-mail: jlinden{at}virginia.edu
| References |
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