首页> 美国卫生研究院文献>Biomedicines >The Modulation of NMDA and AMPA/Kainate Receptors by Tocotrienol-Rich Fraction and Α-Tocopherol in Glutamate-Induced Injury of Primary Astrocytes
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The Modulation of NMDA and AMPA/Kainate Receptors by Tocotrienol-Rich Fraction and Α-Tocopherol in Glutamate-Induced Injury of Primary Astrocytes

机译:富含谷三烯酚的组分和α-生育酚对谷氨酸诱导的原代星形胶质细胞损伤的NMDA和AMPA / Kainate受体的调节。

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摘要

Astrocytes are known as structural and supporting cells in the central nervous system (CNS). Glutamate, as a main excitatory amino acid neurotransmitter in the mammalian central nervous system, can be excitotoxic, playing a key role in many chronic neurodegenerative diseases. The aim of the current study was to elucidate the potential of vitamin E in protecting glutamate-injured primary astrocytes. Hence, primary astrocytes were isolated from mixed glial cells of C57BL/6 mice by applying the EasySep® Mouse CD11b Positive Selection Kit, cultured in Dulbecco’s modified Eagle medium (DMEM) and supplemented with special nutrients. The IC20 and IC50 values of glutamate, as well as the cell viability of primary astrocytes, were assessed with 100 ng/mL, 200 ng/mL, and 300 ng/mL of tocotrienol-rich fraction (TRF) and alpha-tocopherol (α-TCP), as determined by an 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The mitochondrial membrane potential (MMP) detected in primary astrocytes was assessed with the same concentrations of TRF and α-TCP. The expression levels of the ionotropic glutamate receptor genes (Gria2, Grin2A, GRIK1) were independently determined using RT-PCR. The purification rate of astrocytes was measured by a flow-cytometer as circa 79.4%. The IC20 and IC50 values of glutamate were determined as 10 mM and 100 mM, respectively. Exposure to 100 mM of glutamate in primary astrocytes caused the inhibition of cell viability of approximately 64.75% and 61.10% in pre- and post-study, respectively (p < 0.05). Both TRF and α-TCP (at the lowest and highest concentrations, respectively) were able to increase the MMP to 88.46% and 93.31% pre-treatment, and 78.43% and 81.22% post-treatment, respectively. Additionally, the findings showed a similar pattern for the expression level of the ionotropic glutamate receptor genes. Increased extracellular calcium concentrations were also observed, indicating that the presence of vitamin E altered the polarization of astrocytes. In conclusion, α-TCP showed better recovery and prophylactic effects as compared to TRF in the pre-treatment of glutamate-injured primary astrocytes.
机译:星形胶质细胞是中枢神经系统(CNS)中的结构性细胞和支持细胞。谷氨酸,作为哺乳动物中枢神经系统中主要的兴奋性氨基酸神经递质,可能具有兴奋性毒性,在许多慢性神经退行性疾病中起关键作用。本研究的目的是阐明维生素E在保护谷氨酸损伤的原代星形胶质细胞中的潜力。因此,通过使用EasySep ®小鼠CD11b阳性选择试剂盒,从C57BL / 6小鼠的混合神经胶质细胞中分离出原代星形胶质细胞,并在Dulbecco改良的Eagle培养基(DMEM)中进行培养,并补充特殊营养素。用100 ng / mL,200 ng / mL和300 ng / mL富含生育三烯酚的馏分(TRF)和α-生育酚(α)评估谷氨酸的IC20和IC50值,以及原代星形胶质细胞的细胞活力。 -TCP),通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MTT)分析确定。用相同浓度的TRF和α-TCP评估在原代星形胶质细胞中检测到的线粒体膜电位(MMP)。使用RT-PCR独立确定离子型谷氨酸受体基因(Gria2,Grin2A,GRIK1)的表达水平。用流式细胞仪测量星形胶质细胞的纯化率约为79.4%。谷氨酸的IC20和IC50值分别确定为10 mM和100 mM。在研究前和研究后,暴露于原代星形胶质细胞的100 mM谷氨酸导致细胞活力的抑制分别约为64.75%和61.10%(p <0.05)。 TRF和α-TCP(分别处于最低和最高浓度)都能够将MMP分别提高至治疗前的88.46%和93.31%,以及治疗后的78.43%和81.22%。此外,研究结果表明离子型谷氨酸受体基因的表达水平具有相似的模式。还观察到增加的细胞外钙浓度,表明维生素E的存在改变了星形胶质细胞的极化。总之,在谷氨酸损伤的原代星形胶质细胞的预处理中,与TRF相比,α-TCP具有更好的恢复和预防作用。

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