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银杏内酯B通过抑制钙内流和细胞内钙释放维持缺氧海马神经元的钙稳态。

Ginkgolide B Maintains Calcium Homeostasis in Hypoxic Hippocampal Neurons by Inhibiting Calcium Influx and Intracellular Calcium Release.

作者信息

Wang Li, Lei Quan, Zhao Shuai, Xu WenJuan, Dong Wei, Ran JiHua, Shi QingHai, Fu JianFeng

机构信息

Clinical Laboratory Diagnostic Center, General Hospital of Xinjiang Military Command, Urumqi, China.

The Department of Medical Administration, General Hospital of Xinjiang Military Command, Urumqi, China.

出版信息

Front Cell Neurosci. 2021 Feb 10;14:627846. doi: 10.3389/fncel.2020.627846. eCollection 2020.

Abstract

Ginkgolide B (GB), a terpene lactone and active ingredient of , shows protective effects in neuronal cells subjected to hypoxia. We investigated whether GB might protect neurons from hypoxic injury through regulation of neuronal Ca homeostasis. Primary hippocampal neurons subjected to chemical hypoxia (0.7 mM CoCl) exhibited an increase in cytoplasmic Ca (measured from the fluorescence of fluo-4), but this effect was significantly diminished by pre-treatment with 0.4 mM GB. Electrophysiological recordings from the brain slices of rats exposed to hypoxia revealed increases in spontaneous discharge frequency, action potential frequency and calcium current magnitude, and all these effects of hypoxia were suppressed by pre-treatment with 12 mg/kg GB. Western blot analysis demonstrated that hypoxia was associated with enhanced mRNA and protein expressions of Ca1.2 (a voltage-gated Ca channel), STIM1 (a regulator of store-operated Ca entry) and RyR2 (isoforms of Ryanodine Receptor which mediates sarcoplasmic reticulum Ca release), and these actions of hypoxia were suppressed by GB. Taken together, our and data suggest that GB might protect neurons from hypoxia, in part, by regulating Ca influx and intracellular Ca release to maintain Ca homeostasis.

摘要

银杏内酯B(GB)是银杏的一种萜类内酯和活性成分,对缺氧的神经元细胞具有保护作用。我们研究了GB是否可能通过调节神经元钙稳态来保护神经元免受缺氧损伤。经化学性缺氧(0.7 mM 氯化钴)处理的原代海马神经元细胞质钙(通过fluo-4荧光测量)增加,但用0.4 mM GB预处理可显著减弱这种效应。对暴露于缺氧环境的大鼠脑片进行电生理记录显示,自发放电频率、动作电位频率和钙电流幅度增加,而用12 mg/kg GB预处理可抑制缺氧的所有这些效应。蛋白质免疫印迹分析表明,缺氧与Ca1.2(一种电压门控钙通道)、STIM1(一种储存操纵性钙内流调节剂)和RyR2(介导肌浆网钙释放的兰尼碱受体亚型)的mRNA和蛋白质表达增强有关,而GB可抑制缺氧的这些作用。综上所述,我们的实验和数据表明,GB可能部分通过调节钙内流和细胞内钙释放来维持钙稳态,从而保护神经元免受缺氧损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b2e/7928385/b38cb98e5c10/fncel-14-627846-g0001.jpg

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