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Liriodendrin protects SH-SY5Y cells from dopamine-induced cytotoxicity

Da-Long Zhao, Da-Wei Shen, Yu-Tao Chi, Fang Liu, Li-Bo Zou, Hai-Bo Zhu*   

  1. 1. Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine affiliated Ministry of Education, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China;
    2.Shenyang Pharmaceutial University, Shenyang 110016, China;
    3.Yanbian University, Yanji 133000, China
  • Received:2007-04-06 Revised:2007-11-10 Online:2007-12-15 Published:2007-12-15
  • Contact: Hai-Bo Zhu*

Abstract:

Aim To investigate the effect of liriodendrin, an extract from Fraxinus sielboldiana blume belonging to the Oleaceae family, on dopamine-induced cytotoxicity in human neuroblastoma SH-SY5Y cells. Methods Cell viability was processed when treated with 50 μmol·L–1 of dopamine for 24 h by MTT assay. Early apoptosis, late apoptosis/necrosis were analyzed by flow cytometry using Annexin V-FITC and propidium iodide (PI) double-staining, respectively. Generation of reactive oxygen species (ROS) was assessed by DCFH-DA, an oxidation-sensitive fluorescent probe. To evaluate mitochondrion membrane potential (ΔΨm) using flow cytometry with the fluorescent dye Rhodamine 123. The transcriptional level of P53 was studied using RTPCR. Results The dopamine-induced loss of cell viability was significantly attenuated by liriodendrin treatment at the concentration of 10–8, 10–7, 10–6, 10–5 and 10–4 mol·L–1. The protective effects of liriodendrin (10–7, 10–6 and 10–5 mol·L–1) on dopamine-induced cytotoxicity may be ascribed to its anti-oxidative properties by reducing ROS level and anti-apoptotic effect via protection of ΔΨm. In addition, the effect of liriodendrin may involve the P53 pathway in apoptosis. Conclusion Liriodendrin may provide a useful therapeutic strategy for the treatment of neurodegenerative diseases such as Parkinson’s disease (PD).

Key words: Liriodendrin, Liriodendrin, Parkinson's disease, Parkinson's disease, Dopamine, Dopamine, Apoptosis, Apoptosis, ROS, ROS, Mitochondrion membrane potential, Mitochondrion membrane potential, P53, P53

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