دورية أكاديمية

Synaptic effects of xenon on NMDA receptor-mediated response in rat spinal neuron.

التفاصيل البيبلوغرافية
العنوان: Synaptic effects of xenon on NMDA receptor-mediated response in rat spinal neuron.
المؤلفون: Nonaka, Kiku, Nakamura, Michiko, Noda, Mami, Yamaga, Toshitaka, Jang, Il-Sung, Akaike, Norio
المصدر: Neurosci Lett ; ISSN:1872-7972
بيانات النشر: Elsevier Science
سنة النشر: 2024
المجموعة: PubMed Central (PMC)
مصطلحات موضوعية: AMPA/KA receptor, NMDA receptor, Pre- and/or postsynaptic action, Whole-cell patch-clamp technique, Xenon, spinal sacral dorsal commissural nucleus (SDCN) neurons
الوصف: To investigate the precise mechanism of xenon (Xe), pharmacologically isolated AMPA/KA and NMDA receptor-mediated spontaneous (s) and evoked (e) excitatory postsynaptic currents (s/eEPSCAMPA/KA and s/eEPSCNMDA) were recorded from mechanically isolated single spinal sacral dorsal commissural nucleus (SDCN) neurons attached with glutamatergic nerve endings (boutons) using conventional whole-cell patch-clamp technique. We analysed kinetic properties of both s/eEPSCAMPA/KA and s/eEPSCNMDA by focal single- and/or paired-pulse electrical stimulation to compare them. The s/eEPSCNMDA showed smaller amplitude, slower rise time, and slower 1/e decay time constant (τDecay) than those of s/eEPSCAMPA/KA. We previously examined how Xe modulates s/eEPSCAMPA/KA, therefore, examined the effects on s/eEPSCNMDA in the present study. Xe decreased the frequency and amplitude of sEPSCNMDA, and decreased the amplitude but increased the failure rate and paired-pulse ratio of eEPSCNMDA without affecting their τDecay. It was concluded that Xe might suppress NMDA receptor-mediated synaptic transmission via both presynaptic and postsynaptic mechanisms.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: https://doi.org/10.1016/j.neulet.2024.137885Test; https://pubmed.ncbi.nlm.nih.gov/38914276Test
DOI: 10.1016/j.neulet.2024.137885
الإتاحة: https://doi.org/10.1016/j.neulet.2024.137885Test
https://pubmed.ncbi.nlm.nih.gov/38914276Test
حقوق: Copyright © 2024. Published by Elsevier B.V.
رقم الانضمام: edsbas.CCDA2C33
قاعدة البيانات: BASE