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Adenosine signaling during acute and chronic disease states

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TLDR
Key observations are discussed that define the beneficial and detrimental aspects of adenosine signaling during acute and chronic disease states with an emphasis on cellular processes, such as inflammatory cell regulation, vascular barrier function, and tissue fibrosis.
Abstract
Adenosine is a signaling nucleoside that is produced following tissue injury, particularly injury involving ischemia and hypoxia. The production of extracellular adenosine and its subsequent signaling through adenosine receptors plays an important role in orchestrating injury responses in multiple organs. There are four adenosine receptors that are widely distributed on immune, epithelial, endothelial, neuronal,and stromal cells throughout the body. Interestingly, these receptors are subject to altered regulation following injury. Studies in mouse models and human cells and tissues have identified that the production of adenosine and its subsequent signaling through its receptors plays largely beneficial roles in acute disease states, with the exception of brain injury. In contrast, if elevated adenosine levels are sustained beyond the acute injury phase, adenosine responses can become detrimental by activating pathways that promote tissue injury and fibrosis. Understanding when during the course of disease adenosine signaling is beneficial as opposed to detrimental and defining the mechanisms involved will be critical for the advancement of adenosine-based therapies for acute and chronic diseases. The purpose of this review is to discuss key observations that define the beneficial and detrimental aspects of adenosine signaling during acute and chronic disease states with an emphasis on cellular processes, such as inflammatory cell regulation, vascular barrier function, and tissue fibrosis.

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References
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Journal ArticleDOI

The Reno-Vascular A2B Adenosine Receptor Protects the Kidney from Ischemia

TL;DR: The A2BAR is identified as a novel therapeutic target for providing potent protection from renal ischemia using ischemic preconditioning (IP) and is associated with corresponding changes in tissue inflammation and nitric oxide production.
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Adenosine A2A receptors play a role in the pathogenesis of hepatic cirrhosis

TL;DR: It is demonstrated that hepatic adenosine A2A receptors play an active role in the pathogenesis of hepatic fibrosis, and a novel therapeutic target is suggested in the treatment and prevention of Hepatic cirrhosis.
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Selective A2A adenosine receptor activation reduces ischemia-reperfusion injury in rat kidney

TL;DR: It is concluded that selective A2A-AR activation by DWH-146e reduces ischemia-reperfusion injury in rat kidneys, and the protective effects are mediated by preventing injury during the reperfusion period.
Journal ArticleDOI

Protection from ischemic liver injury by activation of A2A adenosine receptors during reperfusion: inhibition of chemokine induction.

TL;DR: It is concluded that most damage after hepatic ischemia occurs during reperfusion and can be blocked by A(2A)AR activation.
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