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題名 Differential inhibitory effects of resveratrol on excitotoxicity and synaptic plasticity: involvement of NMDA receptor subtypes
作者 詹銘煥
Chan, Ming-Huan
Hsieh, Chung-Pin
Chang, Wei-Tang
Chen, Linyi
Chen, Hwei-Hsien
貢獻者 神科所
日期 2021-07
上傳時間 27-Oct-2021 10:57:07 (UTC+8)
摘要 Objectives: The neuroprotective effects of resveratrol against excitatory neurotoxicity have been associated with N-methyl-D-aspartate receptor (NMDAR) inhibition. This study examined the differential inhibitory effects of resveratrol on NMDAR-mediated responses in neuronal cells with different NMDAR subtype composition. Methods: The effects of resveratrol on NMDA-induced cell death and calcium influx in immature and mature rat primary cortical neurons were determined and compared. Moreover, the potencies and efficacies of resveratrol to inhibit NR1/NR2A, NR1/NR2B, NR1/NR2C, and NR1/NR2D NMDAR expressed in HEK 293 cells were evaluated. Results: Resveratrol significantly attenuated NMDA-induced cell death in mature neurons, but not in immature neurons. Resveratrol also concentration-dependently reduced NMDA-induced calcium influx among all NMDAR subtypes, but displayed NR2 subunit selectivity, with a potency rank order of NR2B = NR2D > NR2A = NR2C and an efficacy rank order of NR2B = NR2C > NR2A = NR2D. Data show the stronger inhibitory effects of resveratrol on NR1/NR2B than other subtypes. Moreover, resveratrol did not affect hippocampal long-term potentiation (LTP), but impaired long-term depression (LTD). Discussion: These findings reveal the specific NMDAR modulating profile of resveratrol, providing further insight into potential mechanisms underlying the protective effects of resveratrol on neurological disorders.
關聯 Nutritional Neuroscience, Vol.24, No.6, pp.443-458
資料類型 article
DOI https://doi.org/10.1080/1028415X.2019.1641995
dc.contributor 神科所-
dc.creator (作者) 詹銘煥-
dc.creator (作者) Chan, Ming-Huan-
dc.creator (作者) Hsieh, Chung-Pin-
dc.creator (作者) Chang, Wei-Tang-
dc.creator (作者) Chen, Linyi-
dc.creator (作者) Chen, Hwei-Hsien-
dc.date (日期) 2021-07-
dc.date.accessioned 27-Oct-2021 10:57:07 (UTC+8)-
dc.date.available 27-Oct-2021 10:57:07 (UTC+8)-
dc.date.issued (上傳時間) 27-Oct-2021 10:57:07 (UTC+8)-
dc.identifier.uri (URI) http://nccur.lib.nccu.edu.tw/handle/140.119/137550-
dc.description.abstract (摘要) Objectives: The neuroprotective effects of resveratrol against excitatory neurotoxicity have been associated with N-methyl-D-aspartate receptor (NMDAR) inhibition. This study examined the differential inhibitory effects of resveratrol on NMDAR-mediated responses in neuronal cells with different NMDAR subtype composition. Methods: The effects of resveratrol on NMDA-induced cell death and calcium influx in immature and mature rat primary cortical neurons were determined and compared. Moreover, the potencies and efficacies of resveratrol to inhibit NR1/NR2A, NR1/NR2B, NR1/NR2C, and NR1/NR2D NMDAR expressed in HEK 293 cells were evaluated. Results: Resveratrol significantly attenuated NMDA-induced cell death in mature neurons, but not in immature neurons. Resveratrol also concentration-dependently reduced NMDA-induced calcium influx among all NMDAR subtypes, but displayed NR2 subunit selectivity, with a potency rank order of NR2B = NR2D > NR2A = NR2C and an efficacy rank order of NR2B = NR2C > NR2A = NR2D. Data show the stronger inhibitory effects of resveratrol on NR1/NR2B than other subtypes. Moreover, resveratrol did not affect hippocampal long-term potentiation (LTP), but impaired long-term depression (LTD). Discussion: These findings reveal the specific NMDAR modulating profile of resveratrol, providing further insight into potential mechanisms underlying the protective effects of resveratrol on neurological disorders.-
dc.format.extent 2946916 bytes-
dc.format.mimetype application/pdf-
dc.relation (關聯) Nutritional Neuroscience, Vol.24, No.6, pp.443-458-
dc.title (題名) Differential inhibitory effects of resveratrol on excitotoxicity and synaptic plasticity: involvement of NMDA receptor subtypes-
dc.type (資料類型) article-
dc.identifier.doi (DOI) 10.1080/1028415X.2019.1641995-
dc.doi.uri (DOI) https://doi.org/10.1080/1028415X.2019.1641995-