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037 _ _ |a DZNE-2026-00098
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Costa, Vivian V.
|b 0
245 _ _ |a N -Methyl- d -Aspartate (NMDA) Receptor Blockade Prevents Neuronal Death Induced by Zika Virus Infection
260 _ _ |a Washington, DC
|c 2017
|b American Society for Microbiology
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520 _ _ |a Zika virus (ZIKV) infection is a global health emergency that causes significant neurodegeneration. Neurodegenerative processes may be exacerbated by N-methyl-d-aspartate receptor (NMDAR)-dependent neuronal excitoxicity. Here, we have exploited the hypothesis that ZIKV-induced neurodegeneration can be rescued by blocking NMDA overstimulation with memantine. Our results show that ZIKV actively replicates in primary neurons and that virus replication is directly associated with massive neuronal cell death. Interestingly, treatment with memantine or other NMDAR blockers, including dizocilpine (MK-801), agmatine sulfate, or ifenprodil, prevents neuronal death without interfering with the ability of ZIKV to replicate in these cells. Moreover, in vivo experiments demonstrate that therapeutic memantine treatment prevents the increase of intraocular pressure (IOP) induced by infection and massively reduces neurodegeneration and microgliosis in the brain of infected mice. Our results indicate that the blockade of NMDARs by memantine provides potent neuroprotective effects against ZIKV-induced neuronal damage, suggesting it could be a viable treatment for patients at risk for ZIKV infection-induced neurodegeneration.IMPORTANCE Zika virus (ZIKV) infection is a global health emergency associated with serious neurological complications, including microcephaly and Guillain-Barré syndrome. Infection of experimental animals with ZIKV causes significant neuronal damage and microgliosis. Treatment with drugs that block NMDARs prevented neuronal damage both in vitro and in vivo These results suggest that overactivation of NMDARs contributes significantly to the neuronal damage induced by ZIKV infection, and this is amenable to inhibition by drug treatment.
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650 _ 7 |a NMDA receptor
|2 Other
650 _ 7 |a Zika virus
|2 Other
650 _ 7 |a intraocular pressure
|2 Other
650 _ 7 |a memantine
|2 Other
650 _ 7 |a microgliosis
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650 _ 7 |a mouse model
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650 _ 7 |a neuronal death
|2 Other
650 _ 7 |a Neuroprotective Agents
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650 _ 7 |a Receptors, N-Methyl-D-Aspartate
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Disease Models, Animal
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Neurodegenerative Diseases: drug therapy
|2 MeSH
650 _ 2 |a Neurodegenerative Diseases: pathology
|2 MeSH
650 _ 2 |a Neuroprotective Agents: administration & dosage
|2 MeSH
650 _ 2 |a Receptors, N-Methyl-D-Aspartate: antagonists & inhibitors
|2 MeSH
650 _ 2 |a Treatment Outcome
|2 MeSH
650 _ 2 |a Zika Virus: growth & development
|2 MeSH
650 _ 2 |a Zika Virus Infection: complications
|2 MeSH
650 _ 2 |a Zika Virus Infection: pathology
|2 MeSH
700 1 _ |a Del Sarto, Juliana L.
|b 1
700 1 _ |a Rocha, Rebeca F.
|b 2
700 1 _ |a Silva, Flavia R.
|b 3
700 1 _ |a Doria, Juliana G.
|b 4
700 1 _ |a Olmo, Isabella G.
|b 5
700 1 _ |a Marques, Rafael E.
|b 6
700 1 _ |a Queiroz-Junior, Celso M.
|b 7
700 1 _ |a Foureaux, Giselle
|b 8
700 1 _ |a Araújo, Julia Maria S.
|b 9
700 1 _ |a Cramer, Allysson
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700 1 _ |a Real, Ana Luíza C. V.
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700 1 _ |a Secchim Ribeiro, Lucas
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700 1 _ |a Sardi, Silvia I.
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700 1 _ |a Ferreira, Anderson J.
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700 1 _ |a Machado, Fabiana S.
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700 1 _ |a de Oliveira, Antônio C.
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700 1 _ |a Teixeira, Antônio L.
|b 17
700 1 _ |a Nakaya, Helder I.
|b 18
700 1 _ |a Souza, Danielle G.
|b 19
700 1 _ |a Ribeiro, Fabiola M.
|b 20
700 1 _ |a Teixeira, Mauro M.
|b 21
773 _ _ |a 10.1128/mBio.00350-17
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