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The protective effect of tianeptine on Gp120‐induced apoptosis in astroglial cells: role of GS and NOS, and NF‐κB suppression
Author(s) -
Janda Elzbieta,
Visalli Valeria,
Colica Carmela,
Aprigliano Serafina,
Musolino Vincenzo,
Vadalà Nuria,
Muscoli Carolina,
Sacco Iolanda,
Ian Michelangelo,
Rotiroti Domenicantonio,
Spedding Michael,
Mollace Vincenzo
Publication year - 2011
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.2010.01172.x
Subject(s) - tianeptine , pharmacology , proinflammatory cytokine , nitric oxide synthase , apoptosis , chemistry , nitric oxide , inflammation , biology , immunology , endocrinology , biochemistry , hippocampus , antidepressant
BACKGROUND AND PURPOSE Tianeptine is an antidepressant affecting the glutamatergic system. In spite of its proven clinical efficacy, molecular effects of tianeptine are not entirely clear. Tianeptine modulates cytokine expression in the CNS and protects the hippocampus from chronic stress effects. HIV infection is associated with inflammation and neuronal loss, causing HIV‐associated dementia (HAD). The human immunodeficiency virus type‐1 glycoprotein gp120 has been proposed as a likely aetiological agent of HAD. In this study, we determined whether tianeptine protects astroglial cells from the neurodegenerative effects of gp120. EXPERIMENTAL APPROACH Human astroglial cells were treated with gp120 and tianeptine, and viability and apoptosis was monitored by TUNEL, annexin V, and activated caspase‐3 staining and flow cytometry. Protein levels of glutamine synthase (GS), inducible and constitutive nitric oxide synthases (iNOS, cNOS) and nuclear factor κB (NF‐κB) pathway were determined by Western blot analysis. The respective activities were assessed indirectly by measuring glutamine and nitrite concentrations or by luciferase reporter assays. KEY RESULTS Tianeptine showed an anti‐apoptotic effect and prevented caspase‐3 activation by gp120. The mechanism of tianeptine's action involved GS and cNOS stabilization and iNOS suppression. Moreover, tianeptine increased IκB‐α levels in the absence of gp120 and blocked its degradation in response to gp120. This correlated with the suppression of basal and gp120‐induced NF‐κB transcriptional activity. CONCLUSIONS AND IMPLICATIONS Tianeptine clearly exerts neuroprotective effects in vitro by suppressing the molecular pro‐inflammatory effects of gp120. Studies in animal models should be performed to evaluate the potential of tianeptine as a treatment for HAD.