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Adenosine A2A Receptor Stimulation: A New Strategy for the Treatment of Periodontitis Volume 13 - Issue 5

Giacomo Picciolo, Natasha Irrera, Giuseppe Picciolo and Francesco Squadrito*

  • Department of Clinical and Experimental Medicine, Italy

Received: January 21, 2019;   Published: January 30, 2019

*Corresponding author: Francesco Squadrito, Department of Clinical and Experimental Medicine, Italy

DOI: 10.26717/BJSTR.2019.13.002457

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Periodontitis is an unpleasant clinical condition in which an exaggerated inflammatory reaction occurs in the extravascular gingival tissue. Inflammatory cells release cytokines that amplify tissue inflammation and create the condition for periodontal tissue damage. Adenosine is a mediator that is released under several pathological conditions including ischemia and inflammation and participates in the regulation of inflammatory reaction. Among the several adenosine receptors, the adenosine A2A subtype plays a key role in resolving gingival inflammation and in protecting the periodontal tissues from damage. PDRN (polydeoxyribonuclotide) binds selectively the A2A subtype and exerts curative effect, suggesting that adenosine A2A receptor stimulation might be an innovative strategy for the treatment of periodontitis.

Keywords: Adenosine A2A Receptor; Periodontitis; PDRN


Periodontitis is common diseases of the oral cavity [1]. It is a devastating inflammatory condition that takes place at the level of the soft and hard tissues surrounding the teeth [2] and it is one of the leading cause of teeth loss worldwide [3]. Modifiable and diffuse risk factors (e.g., elevated blood pressure, increased blood cholesterol, metabolic syndrome) and unhealthy behaviors (poor physical activity, smoking and consumption of high fat rich food) may significantly influence the development of the disease [4]. An exaggerated inflammatory reaction represents the hallmark of the periodontitis pathogenesis. Bacteria overloading in the gingival sulcus induces accumulation of Polymorphonuclear Neutrophils (PMNs) and monocytes. PMNs and monocytes work in concert with epithelial cells of gingivae to cause the production of Interleukin (IL)-1β, Tumour Necrosis Factor α (TNF-α), IL-6 and High Mobility Group Box 1 protein (HMGB-1). These pro-inflammatory cytokines trigger the expression of adhesion molecules such as intercellular adhesion molecule 1 (ICAM-1) that favors the adhesion and accumulation of the inflammatory leukocytes (PMNs and monocytes) to the endothelium and augment the cross-talk between the several cell types leading to the leakage of leukocytes into the infected tissues [5].

This cascade of events causes macrophages, that have been recruited in the inflammatory zone, to release Prostaglandin 2 (PGE2). This prostanoid and the inflammatory cytokine IL-1β prompt the accumulation of PMNs and monocytes to endothelial cells, thus amplifying and empowering inflammation; finally, these two mediators together with IL-6 and TNF-α, cause osteoclasts to stimulate and reabsorb the alveolar bone [6,7]. Besides inflammation, apoptosis has been also shown to have a role in periodontitis: infact the pro-apoptotic protein BAX-1 is enhanced while the anti-apoptotic protein Bcl-2 is reduced, thus leading to an enhanced destruction of the alveolar bone.

Adenosine is a mediator that is released under several pathological conditions including ischemia and inflammation and participates in the regulation of inflammatory reaction [8]. Interestingly it has been proposed that adenosine may have an anti-inflammatory role. Adenosine is produced both in the intracellular and extracellular compartments through dephosphorylation of Adenosine Monophosphate (AMP) by ecto-5’-nuclotidates; then it is transformed to inosine via the activity of adenosine deaminase and finally degraded to uric acid [8]. Adenosine engages on cell membrane G protein coupled adenosine receptors that are localized in almost all mammalian cells. Four types of adenosine receptors have been identified and indicated as A1, A2A, A2B and A3.These receptors differ in affinity for adenosine and have a different level of expression in the several cell types.

It has been previously reported that adenosine receptors are present in both human gingival cells and fibroblasts and that their up-regulation or down-regulation may serve as signal mechanisms to orchestrate the production of other inflammatory mediators [9].Indeed, previous experimental work has suggested that the expression of A2A, and A2B receptors are enhanced in periodontitis while A3 expression is reduced and A1 expression is unchanged. Regarding the finalistic meaning of these changes, it is generally accepted that over-expression of the A2A, and A2B receptors may serve as a brake to halt the inflammatory cascade [9]. This leads to hypothesize that activation of one or both of these two types of Adenosine Receptors (A2A, and A2B) may represent a rational strategy to design new drugs for the treatment of periodontitis.

PDRN (polydeoxyribonuclotide) is prepared from DNA and it is made by fragments of deoxyribonucleotides [10]. It binds selectively the A2A subtype that has a key role in down-regulating and resolving inflammation [10]. Theoretically PDRN might be beneficial in periodontitis where an inflammation cascade develops in soft tissues close to the bone. In experimental animals (e.g., rats and mice), the “pathology” may be induced and transferred by ligating the lower first molar cervix. This experimental procedure provides a valuable and reproducible “experimental paradigm” that can be used to test the preclinical efficacy of investigational drugs. A gel solution of 0.74% PDRN was studied in a rat model of periodontitis. The gel was topically administered for seven consecutive days alone or together with an A2A subtype receptor antagonist. A control “arm” of rats with periodontitis received the vehicle gel. At the end of the experimental period, animals were suppressed and the periodontium and surrounding gingival tissue were harvested to perform histological studies and molecular evaluation of inflammatory (TNF-α , IL-6) and apoptotic proteins (BAX and Bcl-2).

The administration of PDRN succeeded in blunting the severe histological damage, reduced in the inflamed tissue the expression of the several pro-inflammatory protein and rebalanced the apoptotic system towards augmenting the expression of Bcl-2 [11]. To confirm the PDRN mode of action, concomitant treatment with an adenosine A2A subtype antagonist abolished all these protective effects. Indeed, topical application of the PDRN gel significantly preserved bone resorption and improved alveolar bone quality. This strongly points out that PDRN may also cause bone formation and regeneration.

Recently the Wnt/β-catenin signaling has been suggested to stimulate formation of alveolar bone. Wnt can be activated by A2A receptor through an increase in intracellular cAMP, which is a wellknown intracellular second messenger that boosts Wnt signaling [12]. Once triggered, the intracytoplasmic Wnt cascade causes β-catenin to translocate to the nucleus, where it binds to genes that codify for bone forming proteins. Unpublished findings from our laboratory suggest that PDRN activates Wnt/β-catenin signaling in alveolar bone, thus offering a valid explanation for the positive effects of PDRN on alveolar bone during periodontitis.

In conclusion, the available data so far produced suggest that A2A receptor stimulation might be an innovative strategy for the treatment of periodontitis. However, this experimental evidence deserves to be validated and confirmed in patients suffering from periodontitis. Since PDRN is available in the market in Europe and South Corea with different therapeutic indication, the design of a clinical trial aiming at confirming the pre-clinical evidence could be easily designed and performed.


  1. Albandar JM (2005) Epidemiology and risk factors of periodontal diseases. Dent Clin North Am 49(3): 517-532.
  2. Bueno AC, Ferreira RC, Cota LO, Silva GC, Magalhães CS, et al. (2015) Comparison of different criteria for periodontitis case definition in head and neck cancer individuals. Support Care Cancer 23(9): 2599-2604.
  3. Albandar JM, Rams TE (2002) Global epidemiology of periodontal diseases: An overview. Periodontology 2000 29(1): 7-10.
  4. Reynolds MA (2014) Modifiable risk factors in periodontitis: At the intersection of aging and disease. Periodontology 2000 64(1): 7-19.
  5. Ford PJ, Gamonal J, Seymour GJ (2010) Immunological differences and similarities between chronic periodontitis and aggressive periodontitis. Periodontology 2000 53: 111-123.
  6. Dosseva-Panova VT, Popova CL, Panov VE (2014) Subgingival microbial profile and production of proinflammatory cytokines in chronic periodontitis. Folia Med 56: 152-160.
  7. Meyle J, Chapple I (2015) Molecular aspects of the pathogenesis of periodontitis. Periodontology 2000 69: 7-17.
  8. Bours MJ, Swennen EL, Di Virgilio F, Cronstein BN, Dagnelie PC (2006) Adenosine 5’-triphosphate and adenosine as endogenous signaling molecules in immunity and inflammation. Pharmacol Ther 112(2): 358- 404.
  9. Murakami S, Terakura M, Kamatani T, Hashikawa T, Saho T, et al. (2000) Adenosine regulates the production of interleukin-6 by human gingival fibroblasts via cyclic AMP/protein kinase A pathway. J Periodontal Res 35(2): 93-101.
  10. Squadrito F, Bitto A, Irrera N, Pizzino G, Pallio G, et al. (2017) Pharmacological activity and clinical use of PDRN. Front Pharmacol 26(8): pp. 224.
  11. Bitto A, Oteri G, Pisano M, Polito F, Irrera N, et al. (2013) Adenosine receptor stimulation by polynucleotides (PDRN) reduces inflammation in experimental periodontitis. J Clin Periodontol 40(1): 26-32.
  12. Shaikh G, Zhang J, Perez-Aso M, Mediero A, Cronstein B (2016) Adenosine A(2A) receptor promotes collagen type III synthesis via β-catenin activation in human dermal fibroblasts. Br J Pharmacol 173(23): 3279- 3291.