Zhan, Lb., Sui, H., Lu, Xg. et al. Effects of Zibu Piyin Recipe (滋补脾阴方药) on SNK-SPAR pathway in neuron injury induced by glutamate., Chin. J. Integr. Med. 14, 117–122 (2008). https://doi.org/10.1007/s11655-008-0117-1
Li-bin Zhan, Hua Sui, Xiao-guang Lu, et al. Effects of Zibu Piyin Recipe (滋补脾阴方药) on SNK-SPAR pathway in neuron injury induced by glutamate[J]. Chinese Journal of Integrative Medicine, 2008,14(2):117-122.
Zhan, Lb., Sui, H., Lu, Xg. et al. Effects of Zibu Piyin Recipe (滋补脾阴方药) on SNK-SPAR pathway in neuron injury induced by glutamate., Chin. J. Integr. Med. 14, 117–122 (2008). https://doi.org/10.1007/s11655-008-0117-1DOI:
Li-bin Zhan, Hua Sui, Xiao-guang Lu, et al. Effects of Zibu Piyin Recipe (滋补脾阴方药) on SNK-SPAR pathway in neuron injury induced by glutamate[J]. Chinese Journal of Integrative Medicine, 2008,14(2):117-122. DOI: 10.1007/s11655-008-0117-1.
Effects of Zibu Piyin Recipe (滋补脾阴方药) on SNK-SPAR pathway in neuron injury induced by glutamate
摘要
To investigate the relationship between the excitotoxicity and serum-inducible kinase (SNK) and spine-associated Rap GTPase-activating protein (SPAR) pathway in primary hippocampal neuron injury induced by glutamate and furthermore
to explore the molecular mechanism of neuroprotection of Zibu Piyin Recipe (滋补脾阴方药
ZBPYR) and the relationship between ZBPYR and the morphological regulation of dendritic spines. The serum containing ZBPYR was prepared by seropharmacology. Reverse transcription and polymerase chain reaction (RT-PCR) was used to detect the expression of mRNA for SNK
SPAR
postsynaptic density protein 95 (PSD-95) and N-methyl-D-aspartate (NMDA) receptor subunits (NR1
NR2A and NR2B) in primary rat hippocampal neuron cultures after pretreatment with 10 μmol/L glutamate and ZBPYR serum. ZBPYR serum pretreatment resulted in a significant down-regulation of glutamate-induced SNK mRNA expression (P<0.05). Significant up-regulation was seen on the mRNA expression of SPAR and PSD-95 (P<0.05). All these changes were dose-dependent. The mRNA expression of NR1
NR2A and NR2B was down-regulated to different degrees (P<0.05). The mechanism of effect of ZBPYR on glutamate-induced excitotoxicity may be related to the regulation of SNK-SPAR signal pathway. ZBPYR may play a role in protecting and maintaining the normal morphology and structure of dendritic spines
which may be achieved by inhibiting the excessive activation of NMDA receptors.
Abstract
To investigate the relationship between the excitotoxicity and serum-inducible kinase (SNK) and spine-associated Rap GTPase-activating protein (SPAR) pathway in primary hippocampal neuron injury induced by glutamate and furthermore
to explore the molecular mechanism of neuroprotection of Zibu Piyin Recipe (滋补脾阴方药
ZBPYR) and the relationship between ZBPYR and the morphological regulation of dendritic spines. The serum containing ZBPYR was prepared by seropharmacology. Reverse transcription and polymerase chain reaction (RT-PCR) was used to detect the expression of mRNA for SNK
SPAR
postsynaptic density protein 95 (PSD-95) and N-methyl-D-aspartate (NMDA) receptor subunits (NR1
NR2A and NR2B) in primary rat hippocampal neuron cultures after pretreatment with 10 μmol/L glutamate and ZBPYR serum. ZBPYR serum pretreatment resulted in a significant down-regulation of glutamate-induced SNK mRNA expression (P<0.05). Significant up-regulation was seen on the mRNA expression of SPAR and PSD-95 (P<0.05). All these changes were dose-dependent. The mRNA expression of NR1
NR2A and NR2B was down-regulated to different degrees (P<0.05). The mechanism of effect of ZBPYR on glutamate-induced excitotoxicity may be related to the regulation of SNK-SPAR signal pathway. ZBPYR may play a role in protecting and maintaining the normal morphology and structure of dendritic spines
which may be achieved by inhibiting the excessive activation of NMDA receptors.
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相关机构
National Key Lab of Available Utilization of Chemical Resources, Beijing University of Chemical Industry
Haici Medical Group of Qingdao City
Xiyuan Hospital, China Academy of Chinese Medical Sciences
Department of Geriatrics, Fuzhou General Hospital of Nanjing Military District
Research Center of Rehabilitation Science and Technology, School of Life Science and Technology, Xi’an Jiaotong University