神经药理学报››2014,Vol. 4››Issue (1): 11-16.

• 研究论文 •上一篇下一篇

甲氨蝶呤治疗大鼠脊髓挫伤对急性期脂质过氧化的影响

张 思1,顾 兵1 ,王烁宇2 ,李华南2,张国福2,张水印1

  1. 1江西科技师范大学生命科学学院南昌,330013中国
    2江西中医药大学附属医院脊柱外科南昌,330006中国
  • 出版日期:2014-02-26发布日期:2014-06-06
  • 通讯作者:顾兵,男,博士后,教授,硕士生导师;研究方向:神经精神药物学;E-mail: bguemory@hotmail.com
  • 作者简介:张思,女,硕士生;研究方向:化学生物学;E-mail: 847404553 @qq.com
  • 基金资助:

    国家自然科学基金项目(No.30960448),江西省自然科学基金项目(No.20114BAB205033),江西省教育厅科技项目(No.GJJ11596、GJJ12584)

Effects of Methotrexate on Acute Phrase of Spinal Cord Contusion-Induced Lipid Peroxidation in Rats

ZHANG Si1, GU Bing1, WANG Shuo-yu2, LI Hua-nan2, ZHANG Guo-fu2, ZHANG Shui-yin1

  1. 1.College of Life Science, Jiangxi Science & Technology Normal University, Nanchang, 330013, China2.Department of Spine Surgery, The Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China
  • Online:2014-02-26Published:2014-06-06
  • Contact:顾兵,男,博士后,教授,硕士生导师;研究方向:神经精神药物学;E-mail: bguemory@hotmail.com
  • About author:张思,女,硕士生;研究方向:化学生物学;E-mail: 847404553 @qq.com
  • Supported by:

    国家自然科学基金项目(No.30960448),江西省自然科学基金项目(No.20114BAB205033),江西省教育厅科技项目(No.GJJ11596、GJJ12584)

摘要:目的:观察甲氨蝶呤对大鼠脊髓挫伤后脂质过氧化的影响,探讨其急性期抗氧化神经保护机制。方法:采用PinPointTM精密皮质撞击器制备大鼠脊髓挫伤模型。伤后30 min皮下注射甲氨蝶呤(0.5 mg·kg-1·BW)。采用酶联免疫吸附法检测血浆中丙二醛(malondialdehyde,MDA)和8-异前列腺素F(8-iso-prostaglandin F,8-iso-PGF)的含量以及损伤组织中4-羟基壬烯醛-His加合物(4-hydroxynonenal-His adduct,HNE)的含量。结果:伤后1,3,6,12,24,48,72 h,甲氨蝶呤组MDA、8-iso-PGF以及HNE的含量均低于模型组。尤其在伤后6,12 h,甲氨蝶呤组血浆中MDA和脊髓组织中HNE含量均显著低于模型组(P<0.05);在伤后12 h,血浆中8-iso-PGF含量也显著低于模型组(P<0.05)。结论:合适剂量的甲氨蝶呤防止脊髓继发性损伤可能与抑制或减轻脂质过氧化有关。

关键词:甲氨蝶呤,创伤性脊髓损伤,急性期,脂质过氧化,酶联免疫吸附法

Abstract:Objective:This study examined the effect of methotrexate on acute phrase of spinal cord contusion-induced lipid peroxidation in rats and the neuroprotective mechanism of its anti-oxidant action.Methods:Rat spinal cord contusion model was prepared by Pinpoint Precision Cortical Impactor™ apparatus and then methotrexate (0.5mg•kg-1•BW)
was subcutaneously administrated at posttraumatic 30 min. ELISA method was used to determine the content of malondialdehyde(MDA)and 8-iso-PGFin plasma and 4-hydroxynonenal-His adduct (HNE) in injury tissue.Results:Posttraumatic 1, 3, 6, 12, 24, 48, 72 h, the contents of MDA, 8-iso-PGFand HNE in the methotrexate group were all lower than those in the model group, which achieved statistical significance at posttraumatic 6, 12 h (P<0.05). At posttraumatic 12 h, the content of 8-iso-PGF2α in plasma was also significantly lower than that in the model group (P<0.05).Conclusion:The appropriate doses, methotrexate could prevent secondary injury of spinal cord, which may be related to inhibiting or reducing the lipid peroxidation.

Key words:methotrexate,traumatic spinal cord injury,acute phase,lipid peroxidation,enzyme linked immunosorbent assay

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