N-3 polyunsaturated fatty acids and clozapine abrogates poly I: C-induced immune alterations in primary hippocampal neurons

• Published in: Progress in neuro-psychopharmacology & biological psychiatry 2019-03, Vol.90, p.186-196
• Main Authors: Ribeiro, Bruna Mara Machado, Chaves Filho, Adriano José Maia, Costa, Deiziane Viana da Silva, de Menezes, Antônio Teles, da Fonseca, Anna Carolina Carvalho, Gama, Clarissa S., Moura Neto, Vivaldo, de Lucena, David Freitas, Vale, Mariana Lima, Macêdo, Danielle S.
• Format: Article
• Language: English
• Subjects: Clozapine; Hippocampus; n3 PUFAs; Neuroinflammation; NFkB; Poly I:C
• ISSN: 0278-5846; 1878-4216
• DOI: 10.1016/j.pnpbp.2018.11.022

The viral mimetic polyinosinic:polycytidylic acid (poly I:C) is an important tool to study the consequences of viral infection to the development of neuropsychiatric disorders. Here, based on the premise of omega-3 polyunsaturated fatty acids (n3 PUFAs) as supplemental treatment to antipsychotics in schizophrenia, we investigated the involvement of NFkB pathway in the effects of n3 PUFAs or of the atypical antipsychotic clozapine in hippocampal poly I:C-challenged neurons. Primary hippocampal neuronal cultures were exposed to n3 PUFAs (DHA4.35 μM/EPA7.10 μM, DHA 8.7 μM/EPA14.21 μM or DHA17.4 μM/EPA28.42 μM) or clozapine (1.5 or 3 μM) in the presence or absence of poly I:C. MTT assay revealed that poly I:C-induced reduction in cell viability was prevented by n3 PUFAs or clozapine. N3 PUFAs (DHA 8.7 μM/EPA14.21 μM) or clozapine (3 μM) significantly reduced poly I:C-induced increase in iNOS, NFkB (p50/p65), IL-6 and nitrite when compared to non-treated cells. Only n3 PUFAs prevented poly I:C-induced deficits in BDNF. On the other hand, poly I:C caused a marked reduction in DCX immunoexpression, which was prevented only by clozapine. Thus, n3 PUFAs and clozapine exert in vitro neuroprotective effects against poly I:C immune challenge in hippocampal neurons, by mechanisms possibly involving the inhibition of canonical NFkB pathway. The present study adds further evidences to the mechanisms underlying n3 PUFAs and clozapine neuroprotective effects against viral immune challenges. Since n3 PUFAs is a safe strategy for use during pregnancy, our results also add further evidence for the use of this supplement in order to prevent alterations induced by viral hits during this developmental period. •Poly(I:C) increases iNOS, NFkB (p50/p65), IL-6, nitrite in hippocampal neuronal cells.•Poly(I:C) causes deficits in neuronal hippocampal mechanisms.•N3 PUFAs or clozapine prevented neuroinflammatory alterations induced by poly(I:C).•N3 PUFAs prevented the deficits in BDNF, while clozapine increased DCX-immunoexpression.•N3 PUFAs and clozapine are neuroprotective effects against poly(I:C) neurotoxic effects.