4.3 Article

Signaling pathways underlying the antidepressant-like effect of inosine in mice

Journal

PURINERGIC SIGNALLING
Volume 13, Issue 2, Pages 203-214

Publisher

SPRINGER
DOI: 10.1007/s11302-016-9551-2

Keywords

Inosine; Depression; Signaling pathways; Protein kinases; CREB

Funding

  1. National Council for Scientific and Technological Development (CNPq) Brazil [308459/2013-0, 481523/2013-8, 308723/2013-9]
  2. National Coordination for the Training and Improvement of Higher Education Personnel (CAPES/MINCyT) [249/14]
  3. Santa Catarina State Research Foundation (FAPESC/PRONEX Program-NENASC Project) [1262/2012-9]
  4. INCT-National Institute of Science and Technology
  5. Santa Catarina Program for the Training for Special Education (PROESP/CAPES) [1509/2009]
  6. CNPq
  7. CAPES Foundation, Ministry of Education of Brazil

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Inosine is a purine nucleoside formed by the breakdown of adenosine that elicits an antidepressant-like effect in mice through activation of adenosine A(1) and A(2A) receptors. However, the signaling pathways underlying this effect are largely unknown. To address this issue, the present study investigated the influence of extracellular-regulated protein kinase (ERK)1/2, Ca2+/calmoduline-dependent protein kinase (CaMKII), protein kinase A (PKA), phosphoinositide 3-kinase (PI3K)/Akt, and glycogen synthase kinase 3beta (GSK-3 beta) modulation in the antiimmobility effect of inosine in the tail suspension test (TST) in mice. In addition, we attempted to verify if inosine treatment was capable of altering the immunocontent and phosphorylation of the transcription factor cyclic adenosine monophosphatate (cAMP) response-binding element protein (CREB) in mouse prefrontal cortex and hippocampus. Intracerebroventricular administration of U0126 (5 mu g/mouse, MEK1/2 inhibitor), KN-62 (1 mu g/mouse, CaMKII inhibitor), H-89 (1 mu g/mouse, PKA inhibitor), and wortmannin (0.1 mu g/mouse, PI3K inhibitor) prevented the antiimmobility effect of inosine (10 mg/kg, intraperitoneal (i.p.)) in the TST. Also, administration of a sub-effective dose of inosine (0.1 mg/kg, i.p.) in combination with a sub-effective dose of AR-A014418 (0.001 mu g/mouse, GSK-3 beta inhibitor) induced a synergic antidepressant-like effect. None of the treatments altered locomotor activity of mice. Moreover, 24 h after a single administration of inosine (10 mg/kg, i.p.), CREB phosphorylation was increased in the hippocampus. Our findings provided new evidence that the antidepressant-like effect of inosine in the TST involves the activation of PKA, PI3K/Akt, ERK1/2, and CaMKII and the inhibition of GSK-3 beta. These results contribute to the comprehension of the mechanisms underlying the purinergic system modulation and indicate the intracellular signaling pathways involved in the antidepressant-like effect of inosine in a preclinical test of depression.

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