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Acute neurotoxicant exposure induces hyperexcitability in mouse lumbar spinal motor neurons.
Sceniak, Michael P; Spitsbergen, Jake B; Sabo, Shasta L; Yuan, Yukun; Atchison, William D.
Afiliación
  • Sceniak MP; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.
  • Spitsbergen JB; Department of Biology, Central Michigan University, Mount Pleasant, Michigan.
  • Sabo SL; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.
  • Yuan Y; Department of Biology, Central Michigan University, Mount Pleasant, Michigan.
  • Atchison WD; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.
J Neurophysiol ; 123(4): 1448-1459, 2020 04 01.
Article en En | MEDLINE | ID: mdl-32159428
ABSTRACT
Spinal motor neurons (MNs) are susceptible to glutamatergic excitotoxicity, an effect associated with lumbar MN degeneration in amyotrophic lateral sclerosis (ALS). MN susceptibility to environmental toxicant exposure, one prospective contributor to sporadic ALS, has not been systematically studied. The goal of this study was to test the ability of a well-known environmental neurotoxicant to induce hyperexcitability in mouse lumbar MNs. Methylmercury (MeHg) causes neurotoxicity through mechanisms involving elevated intracellular Ca2+ concentration ([Ca2+]i), a hallmark of excitotoxicity. We tested whether acute exposure to MeHg induces hyperexcitability in MNs by altering synaptic transmission, using whole cell patch-clamp recordings of lumbar spinal MNs in vitro. Acute MeHg exposure (20 µM) led to an increase in the frequency of both spontaneous excitatory postsynaptic currents (EPSCs) and miniature EPSCs. The frequency of inhibitory postsynaptic currents (IPSCs) was also increased by MeHg. Action potential firing rates, both spontaneous and evoked, were increased by MeHg, despite increases in both EPSCs and IPSCs, indicating a shift toward hyperexcitability. Also consistent with hyperexcitability, fluo 4-AM microfluorimetry indicated that MeHg exposure induced an increase in [Ca2+]i. Spinal cord hyperexcitability is partially mediated by Ca2+-permeable AMPA receptors, as MeHg-dependent increases in EPSCs were blocked by 1-napthyl spermine. Therefore, spinal MNs appear highly susceptible to MeHg exposure, leading to significant increases in spontaneous network excitability and disruption of normal function. Prolonged hyperexcitability could lead to eventual neurodegeneration and loss of motor function as observed in spinal cord after MeHg exposure in vivo and may contribute to MeHg-induced acceleration of ALS symptoms.NEW & NOTEWORTHY Spinal motor neurons (MN) are susceptible to glutamatergic excitotoxicity, an effect associated with lumbar MN degeneration in amyotrophic lateral sclerosis (ALS). This study investigated MN susceptibility to environmental toxicant exposure, one prospective contributor to sporadic ALS. Spinal MNs appear highly susceptible to methylmercury exposure, leading to significant increases in spontaneous network excitability and disruption of normal function. Prolonged hyperexcitability could lead to neurodegeneration and loss of motor function as observed in ALS spinal cord symptoms.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_quimicos_contaminacion Asunto principal: Médula Espinal / Transmisión Sináptica / Ácido Glutámico / Potenciales Postsinápticos Excitadores / Potenciales Postsinápticos Inhibidores / Compuestos de Metilmercurio / Neuronas Motoras / Red Nerviosa Límite: Animals Idioma: En Revista: J Neurophysiol Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_quimicos_contaminacion Asunto principal: Médula Espinal / Transmisión Sináptica / Ácido Glutámico / Potenciales Postsinápticos Excitadores / Potenciales Postsinápticos Inhibidores / Compuestos de Metilmercurio / Neuronas Motoras / Red Nerviosa Límite: Animals Idioma: En Revista: J Neurophysiol Año: 2020 Tipo del documento: Article
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