Interactions of pannexin 1 with NMDA and P2X7 receptors in central nervous system pathologies: Possible role on chronic pain
Author
dc.contributor.author
Bravo, D.
Author
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Maturana, C. J.
Author
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Pelissier Serrano, Teresa
Author
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Hernández, A.
Author
dc.contributor.author
Constandil, L.
Admission date
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2015-12-28T17:59:16Z
Available date
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2015-12-28T17:59:16Z
Publication date
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2015
Cita de ítem
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Pharmacological Research 101 (2015) 86–93
en_US
Identifier
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1043-6618
Identifier
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DOI: 10.1016/j.phrs.2015.07.016
Identifier
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https://repositorio.uchile.cl/handle/2250/135993
General note
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Artículo de publicación ISI
en_US
Abstract
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Pannexin 1 (Panx1) is a glycoprotein that acts as a membrane channel in a wide variety of tissues in mammals. In the central nervous system (CNS) Panx1 is expressed in neurons, astrocytes and microglia, participating in the pathophysiology of some CNS diseases, such as epilepsy, anoxic depolarization after stroke and neuroinflammation. In these conditions Panx1 acts as an important modulator of the neuroinflammatory response, by secreting ATP, by interacting with the P2X7 receptor (P2X7R), and as an amplifier of NMDA receptor (NMDAR) currents, particularly in conditions of pathological neuronal hyperexcitability. Here, we briefly reviewed the current evidences that support the interaction of Panx1 with NMDAR and P2X7R in pathological contexts of the CNS, with special focus in recent data supporting that Panx1 is involved in chronic pain signaling by interacting with NMDAR in neurons and with P2X7R in glia. The participation of Panx1 in chronic pain constitutes a novel topic for research in the field of clinical neurosciences and a potential target for pharmacological interventions in chronic pain.