TY - JOUR
T1 - Immunomodulatory and neuroprotective effects of inosine
AU - Haskó, György
AU - Sitkovsky, Michail V.
AU - Szabó, Csaba
N1 - Funding Information:
This work was supported by the National Institutes of Health (R01GM66189 to G. Haskó and R43GM59676 to C. Szabó).
PY - 2004/3
Y1 - 2004/3
N2 - Adenosine has been considered as a potential immunomodulatory and neuroprotective agent for 30 years. Inosine, a major degradation product of adenosine, was thought originally to have no biological effects. However, recent studies demonstrate that inosine has potent immunomodulatory and neuroprotective effects. Inosine enhances mast-cell degranulation, attenuates the production of pro-inflammatory mediators by macrophages, lymphocytes and neutrophils, and is protective in animal models of sepsis, ischemia-reperfusion and autoimmunity. Inosine preserves the viability of glial cells and neuronal cells during hypoxia, and stimulates axonal regrowth after injury. The biological actions of inosine might involve effects on adenosine receptors, poly(ADP-ribose) polymerase and cellular energy levels. In this article, we review recent observations indicating that it might be possible to exploit inosine therapeutically for the treatment of tissue damage caused by inflammation and ischemia.
AB - Adenosine has been considered as a potential immunomodulatory and neuroprotective agent for 30 years. Inosine, a major degradation product of adenosine, was thought originally to have no biological effects. However, recent studies demonstrate that inosine has potent immunomodulatory and neuroprotective effects. Inosine enhances mast-cell degranulation, attenuates the production of pro-inflammatory mediators by macrophages, lymphocytes and neutrophils, and is protective in animal models of sepsis, ischemia-reperfusion and autoimmunity. Inosine preserves the viability of glial cells and neuronal cells during hypoxia, and stimulates axonal regrowth after injury. The biological actions of inosine might involve effects on adenosine receptors, poly(ADP-ribose) polymerase and cellular energy levels. In this article, we review recent observations indicating that it might be possible to exploit inosine therapeutically for the treatment of tissue damage caused by inflammation and ischemia.
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U2 - 10.1016/j.tips.2004.01.006
DO - 10.1016/j.tips.2004.01.006
M3 - Review article
C2 - 15019271
AN - SCOPUS:1342264245
SN - 0165-6147
VL - 25
SP - 152
EP - 157
JO - Trends in Pharmacological Sciences
JF - Trends in Pharmacological Sciences
IS - 3
ER -