中国神经再生研究(英文版) ›› 2020, Vol. 15 ›› Issue (6): 1086-1093.doi: 10.4103/1673-5374.270317

• 原著:脑损伤修复保护与再生 • 上一篇    下一篇

牛膝多肽抑制谷氨酸电流在培养海马神经元发挥抗凋亡作用

  

  • 出版日期:2020-06-15 发布日期:2020-07-02
  • 基金资助:
    国家自然科学基金(81073079);江苏省高等教育学院自然科学基金(18KJA180009);南通市科学基金(MS12018043)

Achyranthes bidentata polypeptides prevent apoptosis by inhibiting the glutamate current in cultured hippocampal neurons

Rong-Lu Pan 1, Wen-Qing Hu 1, 2, Jie Pan 1 , Li Huang1 , Cheng-Cheng Luan1 , Hong-Mei Shen1, 3   

  1. 1 Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education and Institute of Nautical Medicine, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China
    2 Department of Neurobiology, Physiology and Behavior, College of Biological Science, Davis, CA, USA
    3 Affiliated Mental Health Center of Nantong University, Nantong Brain Hospital, Nantong, Jiangsu Province, China
  • Online:2020-06-15 Published:2020-07-02
  • Contact: Hong-Mei Shen, MD, PhD,shmhu@ntu.edu.cn.
  • Supported by:
    This work was supported by the National Natural Science Foundation of China, No. 81073079 (to HMS); the Natural Science Foundation of the Jiangsu Higher Education Institute of China, No. 18KJA180009 (to HMS); the Science Foundation of Nantong City of China, No. MS12018043 (to HMS).

摘要:

谷氨酸兴奋毒性是大脑中动脉阻塞引发神经功能损伤的关键因素。研究结果表明,牛膝多肽对大脑中动脉阻塞导致神经功能损伤具有明显的保护作用,但是其具体神经保护机制,特别是与谷氨酸兴奋毒性的相关性还没有得到证实。因此,实验旨在解释牛膝多肽对大鼠海马神经元谷氨酸兴奋毒性是否具有保护作用。(1)实验首先采用含300 µM谷氨酸无镁细胞外液置换细胞培养液培养,并持续作用大鼠海马神经元3 h建立谷氨酸毒性模型设为谷氨酸损伤组;无镁细胞外液置换细胞培养液,持续相同时间为正常组;含不同浓度牛膝多肽和300 µM谷氨酸无镁细胞外液置换细胞培养液培养大鼠海马神经元,持续相同时间为牛膝多肽处理组;(2)在谷氨酸损伤后24 h,MTT检测和Hoechst 33258染色分别测定神经元活性和细胞核形态,Western Blot检测激活型Caspase-3蛋白表达,比色酶法检测Caspase-3酶活性。采用H2DCF-DA对细胞内的活性氧进行实时检测,Rhodamine 123染色对线粒体膜电位进行实时检测。采用电生理记录技术记录培养海马神经元谷氨酸诱导的内向电流,观察牛膝多肽对谷氨酸电流的影响;(3)实验结果显示,牛膝多肽能降低谷氨酸引起的海马神经元凋亡数目增加,降低谷氨酸引起的激活型Caspase-3蛋白表达及其活性的增加,抑制谷氨酸导致线粒体功能损伤引起的活性氧生成增加、线粒体膜电位下降,降低谷氨酸诱导的内向电流幅度;(4)因此,上述结果揭示,牛膝多肽调节谷氨酸受体的过度激活,使Caspase-3依赖性线粒体途径实现了其抗凋亡作用。

orcid: 0000-0003-0048-4554 (Hong-Mei Shen)

关键词: 牛膝多肽, 兴奋毒性, 谷氨酸受体, 自由基氧化产物, 线粒体膜电位, 线粒体功能损伤, caspase-3, 星形孢菌素, 神经保护, 调亡

Abstract: Glutamate-induced excitotoxicity plays a critical role in the neurological impairment caused by middle cerebral artery occlusion. Achyran- thes bidentata polypeptides have been shown to protect against neurological functional damage caused by middle cerebral artery occlusion, but the underlying neuroprotective mechanisms and the relationship to glutamate-induced excitotoxicity remain unclear. Therefore, in the current study, we investigated the protective effects of Achyranthes bidentata polypeptides against glutamate-induced excitotoxicity in cultured hippocampal neurons. Hippocampal neurons were treated with Mg 2+ -free extracellular solution containing glutamate (300 µM) for 3 hours as a model of glutamate-mediated excitotoxicity (glutamate group). In the normal group, hippocampal neurons were incu- bated in Mg 2+ -free extracellular solution. In the Achyranthes bidentata polypeptide group, hippocampal neurons were incubated in Mg 2+ - free extracellular solution containing glutamate (300 µM) and Achyranthes bidentata polypeptide at different concentrations. At 24 hours after exposure to the agents, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and Hoechst 33258 staining were used to assess neuronal viability and nuclear morphology, respectively. Caspase-3 expression and activity were evaluated using western blot assay and colorimetric enzymatic assay, respectively. At various time points after glutamate treatment, reactive oxygen species in cells were detected by H2DCF-DA, and mitochondrial membrane potential was detected by rhodamine 123 staining. To examine the effect of Achy- ranthes bidentata polypeptides on glutamate receptors, electrophysiological recording was used to measure the glutamate-induced inward current in cultured hippocampal neurons. Achyranthes bidentata polypeptide decreased the percentage of apoptotic cells and reduced the changes in caspase-3 expression and activity induced by glutamate. In addition, Achyranthes bidentata polypeptide attenuated the ampli- tude of the glutamate-induced current. Furthermore, the glutamate-induced increase in intracellular reactive oxygen species and reduction in mitochondrial membrane potential were attenuated by Achyranthes bidentata polypeptide treatment. These findings collectively suggest that Achyranthes bidentata polypeptides exert a neuroprotective effect in cultured hippocampal neurons by suppressing the overactivation of glutamate receptors and inhibiting the caspase-3-dependent mitochondrial apoptotic pathway. All animal studies were approved by the Animal Care and Use Committee, Nantong University, China (approval No. 20120216-001) on February 16, 2012.

Key words: Achyranthes bidentata polypeptides, apoptosis, caspase-3, excitotoxicity, glutamate receptors, mitochondrial dysfunction, mitochondrial membrane potential, neuroprotection, reactive oxygen species, staurosporine