神经药理学报

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半枝莲黄酮对抗Aβ25-35 所致N2a 细胞损伤的作用

蔡红玲,程建军,樊琪,缪红,商亚珍

  1. 河北省中医药抗痴呆重点研究室,河北省中药研究与开发重点实验室,承德医学院中药研所,承德,067000,中国
  • 出版日期:2017-10-26发布日期:2017-12-01
  • 通讯作者:商亚珍,女,博士,硕士生导师,教授;研究方向:中药抗痴呆;Tel:+86-0313-2290616,E-mail:shangyz1018@sina.com
  • 作者简介:蔡红玲,女,硕士研究生;研究方向:神经药理学;Tel:+86-0313-2290616,E-mail:1225820994@qq.com
  • 基金资助:
    河北省自然基金资助项目(No.C2009001007、No.H2014406048),河北省中医药管理局资助项目(No.05027、No.2014062)

The Effect of Scutellaria Barbata Flavonoid Against N2a Cells Injury Induced by Aβ25-35

CAI Hong-ling,CHENG Jian-jun,PAN Qi,MIAO Hong,SHANG Ya-zhen

  1. Hebei Province Key Research Office of Traditional Chinese Medicine Against Dementia,Hebei Provincial Key Laboratory of Traditional Chinese Medicine Research and Development,Institute of Traditional Chinese Medicine,Chengde Medical College,Chengde,067000,China
  • Online:2017-10-26Published:2017-12-01
  • Contact:商亚珍,女,博士,硕士生导师,教授;研究方向:中药抗痴呆;Tel:+86-0313-2290616,E-mail:shangyz1018@sina.com
  • About author:蔡红玲,女,硕士研究生;研究方向:神经药理学;Tel:+86-0313-2290616,E-mail:1225820994@qq.com
  • Supported by:
    河北省自然基金资助项目(No.C2009001007、No.H2014406048),河北省中医药管理局资助项目(No.05027、No.2014062)

摘要:

目的:探讨半枝莲黄酮对抗β- 淀粉样蛋白25-35(β-amyloid protein 25-35,Aβ25-35)所致小鼠脑神经瘤细胞(Neuro-2a,N2a)损伤的作用。方法:体外培养N2a 细胞,随机分为空白组、模型组、半枝莲黄酮(scutellaria barbata flavonoids,SBF)1.125 μg·mL-1、2.250 μg·mL-1 和4.500 μg·mL-1 剂量组。药物作用细胞12 h 后,模型组和SBF 组分别加入终浓度为35 μmol·L-1 的Aβ25-35 作用24 h。倒置显微镜下观察细胞形态学变化,分光光度法测定细胞培养液中乳酸脱氢酶(lactate dehydrogenase,LDH)的水平,噻唑蓝(methyl thiazolyl tetrazolium,MTT)比色法测定细胞存活率。结果:与空白组比较,模型组N2a 细胞形态结构明显受损,细胞与细胞之间链接破坏,部分细胞聚团,折光性降低;细胞培养液中LDH 水平明显增加(P<0.01);细胞存活率显著下降(P<0.01)。与模型组比较,三剂量SBF 不同程度地降低Aβ25-35 所致N2a 细胞结构受损的程度,细胞突起增加,细胞之间结构清晰,折光性增强;培养液中LDH 释放量也不同程度地降低(P<0.05),细胞的存活率亦明显增加(P<0.01)。结论:SBF 能够对抗Aβ25-35 所致的N2a 细胞的损伤。

关键词:半枝莲黄酮,β- 淀粉样蛋白25-35,N2a 细胞,乳酸脱氢酶,细胞存活率

Abstract:

Objective:To investigate the effect of scutellaria barbata fl avonoid against N2a cells injury induced by β-amyloid protein 25-35 (Aβ25-35). Methods:N2a cells were cultured in vitro and randomly divided into control group,model group,scutellaria barbata flavonoid (SBF)1.125 μg·mL-1,2.250 μg·mL-1 and 4.500 μg·mL-1 group. After the N2a cells of three doses of group were treated by 1.125 μg·mL-1,2.250 μg·mL-1 and 4.500 μg·mL-1 SBF for 12 h,the
model and SBF group cells were exposed to Aβ25-35 at the end concentration of 35 μmol·L-1. The morphology of N2a cells was observed and photographed under an inverted microscope. The level of lactate dehydrogenase (LDH) in the culture medium was measured by spectrophotography. The
cell viability was determined by thiazolyl blue tetrazolium bromide (MTT). Results:Compared with control group,the N2a cells were found markedly injured in morphology and structure, including the damage of the link between cells and cells,some sells agglomeration and refractive index decrease,the level of LDH in the culture medium of N2a cells significantly increased (P<0.01) and the N2a cell viability obviously reduced (P<0.01) in model group. Compared with the model group,three dose of SBF could dramatically oppose the cells injured in morphology, including the cells neurite growth,cell structure clearness and refractive index increase,lower the level of LDH of the cells’ culture medium (P<0.05) and add the cell viability (P<0.01).
Conclusion:SBF can significantly oppose the injury of N2a cells induced by Aβ25-35.

Key words:scutellaria barbata flavonoid,β-amyloid protein 25-35(Aβ25-35),N2a cells,lactate dehydrogenase,cell viability

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