A3 Adenosine Receptor Allosteric Modulator Induces an Anti-Inflammatory Effect: In Vivo Studies and Molecular Mechanism of Action

The A3 adenosine receptor (A3AR) is overexpressed in inflammatory cells and in the peripheral blood mononuclear cells of individuals with inflammatory conditions. Agonists to the A3AR are known to induce specific anti-inflammatory effects upon chronic treatment. LUF6000 is an allosteric compound kno...

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Main Authors: Shira Cohen, Faina Barer, Sara Bar-Yehuda, Adriaan P. IJzerman, Kenneth A. Jacobson, Pnina Fishman
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2014/708746
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author Shira Cohen
Faina Barer
Sara Bar-Yehuda
Adriaan P. IJzerman
Kenneth A. Jacobson
Pnina Fishman
author_facet Shira Cohen
Faina Barer
Sara Bar-Yehuda
Adriaan P. IJzerman
Kenneth A. Jacobson
Pnina Fishman
author_sort Shira Cohen
collection DOAJ
description The A3 adenosine receptor (A3AR) is overexpressed in inflammatory cells and in the peripheral blood mononuclear cells of individuals with inflammatory conditions. Agonists to the A3AR are known to induce specific anti-inflammatory effects upon chronic treatment. LUF6000 is an allosteric compound known to modulate the A3AR and render the endogenous ligand adenosine to bind to the receptor with higher affinity. The advantage of allosteric modulators is their capability to target specifically areas where adenosine levels are increased such as inflammatory and tumor sites, whereas normal body cells and tissues are refractory to the allosteric modulators due to low adenosine levels. LUF6000 administration induced anti-inflammatory effect in 3 experimental animal models of rat adjuvant induced arthritis, monoiodoacetate induced osteoarthritis, and concanavalin A induced liver inflammation in mice. The molecular mechanism of action points to deregulation of signaling proteins including PI3K, IKK, IκB, Jak-2, and STAT-1, resulting in decreased levels of NF-κB, known to mediate inflammatory effects. Moreover, LUF6000 induced a slight stimulatory effect on the number of normal white blood cells and neutrophils. The anti-inflammatory effect of LUF6000, mechanism of action, and the differential effects on inflammatory and normal cells position this allosteric modulator as an attractive and unique drug candidate.
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institution Kabale University
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publishDate 2014-01-01
publisher Wiley
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series Mediators of Inflammation
spelling doaj-art-0677634340754e048807810c00a0fc972025-02-03T01:20:03ZengWileyMediators of Inflammation0962-93511466-18612014-01-01201410.1155/2014/708746708746A3 Adenosine Receptor Allosteric Modulator Induces an Anti-Inflammatory Effect: In Vivo Studies and Molecular Mechanism of ActionShira Cohen0Faina Barer1Sara Bar-Yehuda2Adriaan P. IJzerman3Kenneth A. Jacobson4Pnina Fishman5Can-Fite BioPharma Ltd., Kiryat-Matalon, 10 Bareket Street, P.O. Box 7537, 49170 Petach Tikva, IsraelCan-Fite BioPharma Ltd., Kiryat-Matalon, 10 Bareket Street, P.O. Box 7537, 49170 Petach Tikva, IsraelCan-Fite BioPharma Ltd., Kiryat-Matalon, 10 Bareket Street, P.O. Box 7537, 49170 Petach Tikva, IsraelDivision of Medicinal Chemistry, Leiden Academic Centre for Drug Research, Leiden University, P.O. Box 9502, 2300 RA Leiden, The NetherlandsMolecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0810, USACan-Fite BioPharma Ltd., Kiryat-Matalon, 10 Bareket Street, P.O. Box 7537, 49170 Petach Tikva, IsraelThe A3 adenosine receptor (A3AR) is overexpressed in inflammatory cells and in the peripheral blood mononuclear cells of individuals with inflammatory conditions. Agonists to the A3AR are known to induce specific anti-inflammatory effects upon chronic treatment. LUF6000 is an allosteric compound known to modulate the A3AR and render the endogenous ligand adenosine to bind to the receptor with higher affinity. The advantage of allosteric modulators is their capability to target specifically areas where adenosine levels are increased such as inflammatory and tumor sites, whereas normal body cells and tissues are refractory to the allosteric modulators due to low adenosine levels. LUF6000 administration induced anti-inflammatory effect in 3 experimental animal models of rat adjuvant induced arthritis, monoiodoacetate induced osteoarthritis, and concanavalin A induced liver inflammation in mice. The molecular mechanism of action points to deregulation of signaling proteins including PI3K, IKK, IκB, Jak-2, and STAT-1, resulting in decreased levels of NF-κB, known to mediate inflammatory effects. Moreover, LUF6000 induced a slight stimulatory effect on the number of normal white blood cells and neutrophils. The anti-inflammatory effect of LUF6000, mechanism of action, and the differential effects on inflammatory and normal cells position this allosteric modulator as an attractive and unique drug candidate.http://dx.doi.org/10.1155/2014/708746
spellingShingle Shira Cohen
Faina Barer
Sara Bar-Yehuda
Adriaan P. IJzerman
Kenneth A. Jacobson
Pnina Fishman
A3 Adenosine Receptor Allosteric Modulator Induces an Anti-Inflammatory Effect: In Vivo Studies and Molecular Mechanism of Action
Mediators of Inflammation
title A3 Adenosine Receptor Allosteric Modulator Induces an Anti-Inflammatory Effect: In Vivo Studies and Molecular Mechanism of Action
title_full A3 Adenosine Receptor Allosteric Modulator Induces an Anti-Inflammatory Effect: In Vivo Studies and Molecular Mechanism of Action
title_fullStr A3 Adenosine Receptor Allosteric Modulator Induces an Anti-Inflammatory Effect: In Vivo Studies and Molecular Mechanism of Action
title_full_unstemmed A3 Adenosine Receptor Allosteric Modulator Induces an Anti-Inflammatory Effect: In Vivo Studies and Molecular Mechanism of Action
title_short A3 Adenosine Receptor Allosteric Modulator Induces an Anti-Inflammatory Effect: In Vivo Studies and Molecular Mechanism of Action
title_sort a3 adenosine receptor allosteric modulator induces an anti inflammatory effect in vivo studies and molecular mechanism of action
url http://dx.doi.org/10.1155/2014/708746
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