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中国临床药理学与治疗学 ›› 2004, Vol. 9 ›› Issue (1): 80-82.

• 研究原著 • 上一篇    下一篇

大鼠脑出血后一氧化氮合酶阳性神经元数目的时程变化及果糖二磷酸钠镁干预作用

陈友香, 董志, 曾凡新1   

  1. 重庆医科大学药理教研室, 重庆 400016;
    1重庆医药工业研究院药理毒理室, 重庆 400061
  • 收稿日期:2002-12-17 修回日期:2003-03-22 出版日期:2004-01-26 发布日期:2020-11-16
  • 通讯作者: 陈友香,女, 医学硕士, 讲师, 主要从事神经药理研究。Tel:023-68481938  E-mail:zlixia2000 @163.com
  • 作者简介:董志, 男, 医学博士, 教授, 博士生导师, 研究方向:神经药理学。

Timed number of nitric oxide synthase-positive cells in brain of rats with intracerebral hemorrhage and influence of sodium magnesium fructose diphosphate

CHEN You-Xiang, DONG Zhi, ZENG Fan-Xin1   

  1. Department of Pharmacology, Chongqing University of Medical Sciences, Chongqing 400016, China;
    1Department of Pharmacology and Toxicology, Chongqing Pharmaceutical Research Institute, Chongqing, 400061, China
  • Received:2002-12-17 Revised:2003-03-22 Online:2004-01-26 Published:2020-11-16

摘要: 目的: 研究脑出血后一氧化氮合酶(NOS) 阳性神经元的时程变化, 以及果糖二磷酸钠镁(FDPM)的干预作用。方法: 以胶原酶诱导法制备大鼠脑出血模型, 应用NADPH 黄递酶组织化学方法, 观察脑出血后NOS 阳性神经元随时间的变化过程, 并观察FDPM 对其影响。结果: 脑出血后NOS 阳性神经元2 h 时明显增多, 6 h 有轻度下降, 12 h 再度增多, 24~ 72 h 达高峰, 7 d (168 h) 下降, 但仍明显高于正常。脑出血后使用400 mg·kg-1 FDPM 可显著减少NOS 阳性神经元, 其作用优于相似剂量的1, 6-二磷酸果糖(FDP) 和硫酸镁, 而133 mg·kg-1 的FDPM 没有明显作用。结论: 脑出血后NOS 活性变化呈双峰现象;抑制NOS 活性可能是FDPM 保护脑出血的重要机制之一。

关键词: 脑出血, 一氧化氮合酶, 果糖二磷酸钠镁, 1, 6-二磷酸果糖, 硫酸镁

Abstract: AIM: To study the timed number of nitric oxide synthase (NOS)-positive cells and the effects of sodium magnesium fructose diphophate (FDPM).METHODS: Rat model of intracerebral hemorrhage (ICH) was induced by collagenase, the timed number of NOS-positive cells and the effects of FDPM on it was determined by NADPH histochemical staining.RESULTS: After the onset of ICH, the number of NOS-positive cells increased obviously at 2 hours, decreased lightly at 6 hours, increased again at 12 hours, peaked during from 24 hours to 3 days, and decreased again at 7 days, but was till higher than that of normal condition.Application of FDPM decreased significantly the number of NOS-positive cells after ICH, and the effect of FDPM was superior to that of fructose-1, 6-diphophate or magnesium sulfate.CONCLUSION: The change of NOS activity shows two peaks after ICH, and inhibition of NOS activity may be one of the important protective mechanisms of FDPM from ICH.

Key words: intracerebral hemorrhage, nitric oxide synthase, sodium magnesium fructose diphophate, fructose-1, 6-diphophate, magnesium sulfate

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