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[氧糖剥夺诱导原代培养星形胶质细胞释放谷氨酸]

[Oxygen glucose deprivation induced glutamate release in primary cultured astrocytes].

作者信息

Liu Wei, Jiang Shan, Liu Yi, Pan Huajiang, Chen Lei, Xiao Jianxin

机构信息

118 Hospital of PLA, Wenzhou 325000, China.

First Affiliated Hospital, Chinese PLA General Hospital, Beijing 100048, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2014 Jun;30(6):569-72.

Abstract

OBJECTIVE

To investigate the effect of oxygen glucose deprivation (OGD) on the glutamate release and the role of connexin 43 (Cx43) hemichannels in the OGD-induced glutamate release in primary cultured astrocytes.

METHODS

The astrocytes were randomly divided into four groups: normal control, OGD group, Gap26 (Cx43 hemichannel blocker) plus OGD group, Cx43-specific antisense oligodeoxynucleotide (ASODN) plus OGD group. In the OGD group, the astrocytes were cultured in the oxygen- and glucose-free culture medium (950 mL/L N₂ and 50 mL/L CO₂) for different durations (0, 15, 30, 60, 90, 120 minutes) at 37 Degrees Celsius, while the astrocytes in the control group were cultured in the ordinary culture medium. In the Gap26 plus OGD group or Cx43-ASODN plus OGD group, the astrocytes were incubated with Gap26 or Cx43-ASODN before and during the OGD. The extracelluar glutamate level was measured by high performance liquid chromatography (HPLC).

RESULTS

After OGD, the extracelluar glutamte level significantly increased, and reached the maximum (5.00±0.30) nmol/mL at 90 minutes of OGD, which was significantly higher than that of the normal control (2.36±0.15) nmol/mL(P<0.05). After treatment by Cx43-ASODN or Gap26, the increase was inhibited. At 90 minutes of OGD, the extracellular glutamate levels were respectively (4.02±0.18) nmol/mL and (3.93±0.32) nmol/mL. They were signficalty lower than that of the OGD group at the same time (P<0.05).

CONCLUSION

OGD induced glutamate release through Cx43 hemichannel in primary cultured astrocytes.

摘要

目的

探讨氧糖剥夺(OGD)对原代培养星形胶质细胞谷氨酸释放的影响以及连接蛋白43(Cx43)半通道在OGD诱导的谷氨酸释放中的作用。

方法

将星形胶质细胞随机分为四组:正常对照组、OGD组、Gap26(Cx43半通道阻滞剂)+OGD组、Cx43特异性反义寡脱氧核苷酸(ASODN)+OGD组。OGD组星形胶质细胞于37℃在无氧无糖培养基(950 mL/L N₂和50 mL/L CO₂)中培养不同时间(0、15、30、60、90、120分钟),而对照组星形胶质细胞在普通培养基中培养。在Gap26+OGD组或Cx43-ASODN+OGD组中,星形胶质细胞在OGD前及OGD期间用Gap26或Cx43-ASODN孵育。采用高效液相色谱法(HPLC)检测细胞外谷氨酸水平。

结果

OGD后,细胞外谷氨酸水平显著升高,在OGD 90分钟时达到最高(5.00±0.30)nmol/mL,显著高于正常对照组(2.36±0.15)nmol/mL(P<0.05)。经Cx43-ASODN或Gap26处理后,升高受到抑制。在OGD 90分钟时,细胞外谷氨酸水平分别为(4.02±0.18)nmol/mL和(3.93±0.32)nmol/mL。它们显著低于同一时间的OGD组(P<0.05)。

结论

OGD通过原代培养星形胶质细胞中的Cx43半通道诱导谷氨酸释放。

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