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银杏内酯和银杏黄酮苷元对 TNF-α 诱导的大鼠海马神经元凋亡的保护作用及其机制的体外研究。

The protective mechanism of Ginkgolides and Ginkgo flavonoids on the TNF-α induced apoptosis of rat hippocampal neurons and its mechanisms in vitro.

机构信息

School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 300193, China.

出版信息

Heliyon. 2015 Sep 21;1(1):e00020. doi: 10.1016/j.heliyon.2015.e00020. eCollection 2015 Sep.

Abstract

OBJECTIVE

To explore the neuroprotective mechanism of Ginkgolides or Ginkgo flavonoids on the TNF-α induced apoptosis of cultured rat hippocampal neurons.

MATERIALS AND METHODS

Primary hippocampal neurons were isolated from rat brains and cultured with (model group) or without (control group) addition of tumor necrosis factor-α (TNF-α, final concentration of 40 ng/ml) to induce apoptosis. TNF-α induced cultures were divided into model group, Ginkgolides pre-treatment group (20 μg/ml) and Ginkgo flavonoids pre-treatment group (12 μg/ml). CCK8 was used to assess cell viability while Hoechst 33258 staining, Flow cytometry and TUNEL kits were all employed to determine apoptotic neurons. Expression levels of Bcl-2, Bax, Caspase-3, Caspase-7, Caspase-8, Caspase-9 and Cytc were estimated by qRT-PCR.

RESULTS

Cell viability was significantly improved in Ginkgolides pre-treatment group or Ginkgo flavonoids pre-treatment group compared with that in model group. Apoptotic neurons were significantly less in Ginkgolides pre-treatment group or Ginkgo flavonoids pre-treatment group than those in model group. Transcription levels of caspase-7, caspase-8, caspase-3, caspase-9, Bax and Cytc were down-regulated, while transcription levels of Bcl-2 was up-regulated in Ginkgolides pre-treatment or Ginkgo flavonoids pre-treatment group than those in model group.

CONCLUSIONS

Ginkgolides and Ginkgo flavonoids might protect against apoptosis of hippocampal neurons through inhibiting death receptor pathway or mitochondrial pathway under TNF-α background.

摘要

目的

探讨银杏内酯或银杏黄酮对 TNF-α诱导培养大鼠海马神经元凋亡的神经保护作用机制。

材料与方法

原代海马神经元从大鼠脑中分离出来,与(模型组)或不添加(对照组)肿瘤坏死因子-α(TNF-α,终浓度为 40ng/ml)一起培养以诱导凋亡。TNF-α 诱导的培养物分为模型组、银杏内酯预处理组(20μg/ml)和银杏黄酮预处理组(12μg/ml)。CCK8 用于评估细胞活力,而 Hoechst 33258 染色、流式细胞术和 TUNEL 试剂盒均用于确定凋亡神经元。通过 qRT-PCR 估计 Bcl-2、Bax、Caspase-3、Caspase-7、Caspase-8、Caspase-9 和 Cytc 的表达水平。

结果

与模型组相比,银杏内酯预处理组或银杏黄酮预处理组的细胞活力显著提高。银杏内酯预处理组或银杏黄酮预处理组的凋亡神经元明显少于模型组。与模型组相比,银杏内酯预处理组或银杏黄酮预处理组的 caspase-7、caspase-8、caspase-3、caspase-9、Bax 和 Cytc 的转录水平下调,而 Bcl-2 的转录水平上调。

结论

银杏内酯和银杏黄酮可能通过抑制 TNF-α 背景下的死亡受体途径或线粒体途径来保护海马神经元免受凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49bb/4939806/4128ffc76082/gr1.jpg

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