Targeting Purinergic Signaling for Perioperative Organ Protection
Eltzschig, Holger K. M.D., Ph.D.
“Despite [our] remarkable progress, acute organ injury remains one of the leading causes for morbidity and mortality in surgical patients.”
ADVANCEMENTS in the field of anesthesia have led to significant improvements in our monitoring capabilities, safer anesthetic drugs, and improved pain control. Despite this remarkable progress, acute organ injury remains one of the leading causes for morbidity and mortality in surgical patients. Patients who require a major surgical intervention—such as cardiothoracic, vascular, general surgery, or solid organ transplantation—may have had a “perfect” operation but are threatened during their perioperative course by the development of acute organ injury. For example, acute kidney injury, myocardial infarction, intestinal ischemia, and reperfusion injury or stroke are some of the threats that are among the leading causes of perioperative morbidity and mortality.1
A recent review article published in the New England Journal of Medicine
discussed “Purinergic Signaling during Inflammation,”2
provides an update on how signaling events through extracellular receptors for the purines adenosine triphosphate (ATP) and adenosine can be targeted to alter inflammatory endpoints. As discussed in this review article, recent studies implicate purinergic signaling via
ATP or adenosine receptors as important therapeutic targets to prevent or treat acute organ injury in perioperative patients.
In many instances, perioperative organ injury is caused by ischemia and concomitant hypoxia-induced inflammation.3
Hypoxia and inflammation share an interdependent relationship, where inflammatory diseases such as intestinal inflammation or acute lung injury can cause inflamed areas to become severely hypoxic. This typically occurs because of increased metabolic demand of resident and inflammatory cells while metabolic supply is simultaneously decreased. However, diseases that are attributed primarily to hypoxia and ischemia will undergo secondary inflammatory changes that—in the context of ischemia and reperfusion injury—contribute significantly to organ injury (fig. 1
During hypoxic or inflammatory disease states, many cells release ATP from their intracellular toward the extracellular compartment. In the extracellular space, ATP can activate extracellular ATP receptors, which are classified as P2 receptors. They function as G-protein coupled receptors (P2Y receptors) or as ligand-gated ion channels (P2X receptors). Activation of P2 receptors has been shown to cause inflammatory activation and organ injury during ischemia or inflammation, and therapeutic strategies to dampen ATP receptor activation have been implicated in the treatment of inflammatory diseases.4–6
In the extracellular compartment, ATP is rapidly converted to adenosine. In contrast to the proinflammatory functions of ATP receptors, adenosine receptors have been shown to attenuate hypoxic inflammation,7
provide metabolic tissue adaptation to increase ischemia tolerance,8
and to promote injury resolution.9–11
Therefore, treatment approaches to enhance ATP conversion to adenosine represents an experimental therapeutic strategy to dampen acute organ injury. Conversion of ATP to adenosine is controlled by a two-step enzymatic system. The first step is the conversion of ATP to adenosine monophosphate by the ectonucleoside triphosphate diphosphohydrolase 1 (CD39). The subsequent second step in the extracellular generation of adenosine is catalyzed by the ecto-5′-nucleotidase CD73. Conditions of inflammatory hypoxia result in the induction of both enzymes (fig. 2
). CD39 is transcriptionally induced by the Sp1 transcription factor,12
whereas CD73 is induced by hypoxia-inducible factor (HIF)—the key transcription factor for hypoxia adaptation.13
For example, HIF is known to regulate the transcriptional activity of the erythropoietin promoter. Conditions of hypoxia, ischemia, or anemia will lead to tissue hypoxia and subsequent stabilization of HIF. Binding of HIF to the erythropoietin promoter results in transcriptional induction of erythropoietin, leading to increases in erythropoiesis. Indeed, HIF activators have been implicated in treating inflammatory hypoxia via
increasing tissue expression of CD73, thereby promoting the extracellular generation of adenosine.5
Once generated in the extracellular compartment, adenosine can activate four distinct adenosine receptors. These are G-protein coupled receptors that differ in their sensitivity for adenosine, and the type of second message response they elicit. The Adora1 and Adora3 are known to inhibit adenylate cyclase, thereby leading to decreased intracellular cyclic adenosine monophosphate levels. In contrast, the Adora2a and Adora2b are known to activate adenylate cyclase and thereby increase cyclic adenosine monophosphate levels.15
In the context of organ protection, activation of Adora2a receptors expressed on inflammatory cells has been shown to provide tissue protection. Moreover, the Adora2b receptor is transcriptionally induced by HIF during conditions of ischemia or hypoxia,16
and has been shown to protect the tissues from the detrimental effects of hypoxia-driven inflammation (fig. 2
In summary, current experimental evidence indicates that purinergic signaling events can be targeted to treat or prevent acute organ injury such as occurs during the perioperative period. These studies suggest the following pharmacologic approaches:
* Inhibition of signaling events through ATP receptors (e.g. P2Y or P2X receptors) by ATP receptor antagonists.
* Pharmacologic approaches that promote the extracellular conversion of ATP to adenosine, such as apyrase treatment (conversion of ATP to adenosine monophosphate) or nucleotidase treatment (conversion of adenosine monophosphate to adenosine). Several other pharmacologic compounds that are used in the treatment of inflammatory diseases (e.g. methotrexate or sulfasalazine) are known to exhibit their antiinflammatory properties by stimulating CD73-dependent adenosine production.
* Pharmacologic approaches to activate adenosine receptors, particularly the Adora2a or the Adora2b. For example, a highly selective Adora2b agonist has recently been characterized to function in murine or human tissues.8
This compound (BAY 60–6483) has been shown to have organ-protective functions in a wide range of disease models from the field of ischemia and reperfusion injury, for example intestinal ischemia13
or renal ischemia.10
* Pharmacologic approaches to indirectly increase extracellular adenosine signaling effects. This can be achieved for example by adenosine transport inhibitors19
or by inhibitors of the metabolic breakdown of adenosine.20
* Pharmacologic strategies to enhance transcriptional pathways that result in increased ATP to adenosine turnover and increased expression of adenosine receptors. This can be achieved for example by pharmacologic activators of the transcription factor HIF.
Most of these pharmacologic interventions have been identified and described in animal models. However, several pharmacologic agents that modulate purinergic signaling are being used in patients. For example, the antiinflammatory medications methotrexate or sulfasalazine are known to increase extracellular adenosine levels via
activation of CD73. Similarly, the adenosine uptake inhibitor dipyridamole is used in patients during stress echocardiography. Finally, clinical studies have used HIF activators in patients without safety concerns.21
As such, we are hoping that several of these pharmacologic interventions can be used for the prevention of organ injury in surgical patients in the near future. However, efforts to go forward with translational studies, such as clinical randomized trials in perioperative patients will be required to make progress on this front.
The author acknowledges Shelley A. Eltzschig, B.S.B.A., artist, Mucosal Inflammation Program, University of Colorado School of Medicine, Aurora, Colorado, for artwork that inspired the figures included in this Editorial.
Holger K. Eltzschig, M.D., Ph.D.
, Mucosal Inflammation Program, Department of Anesthesiology, University of Colorado School of Medicine, Aurora, Colorado. firstname.lastname@example.org
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